Sodium bicarbonate, an inorganic salt and a potential active agent for cancer therapy

Sodium bicarbonate, an inorganic salt and a potential active agent for cancer therapy

PDF

Yue Wang^a^,¹, Xueer Zhou^a^,¹, Wenxuan Wang^a, Yongyao Wu^a, Zhiyong Qian^b, Qiang Peng^a^,^*

Chinese Chemical Letters | 2021, 32(12) : 3687 - 3695

Less

Chinese Chemical Letters | 2021, 32(12): 3687-3695

• Review •

Sodium bicarbonate, an inorganic salt and a potential active agent for cancer therapy

Full

Yue Wang^a^,¹, Xueer Zhou^a^,¹, Wenxuan Wang^a, Yongyao Wu^a, Zhiyong Qian^b, Qiang Peng^a^,^*

Affiliations

^a State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China

^b State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center, Chengdu 610041, China

Published: 2021-12-15 doi: 10.1016/j.cclet.2021.06.032

Outline

Abstract

Less

Cancer is a serious threat to humans due to its high mortality. The efforts to fully understand cancer and to fight against it have never been stopped. The traditional therapies, such as surgery, radiotherapy and chemotherapy, are useful but cannot meet the increasing demands of patients. As such, novel approaches against cancer are urgently required. It has been found that the acidic tumor microenvironment plays important roles in promoting the cancer progression. In recent years, sodium bicarbonate (NaHCO₃), a simple inorganic salt, has been found to be able to reverse the pH of tumor microenvironment and inhibit the invasion, metastasis, immune evasion, drug resistance and hypoxia of tumor cells. Thus, NaHCO₃-based therapy is a potential approach for the treatment of cancer, and the related studies have been increasingly reported. Herein, we aim to provide a comprehensive understanding of the acidic tumor microenvironment and summarize the applications and mechanisms of NaHCO₃ in cancer therapy. The combination of NaHCO₃ with chemotherapy, immunotherapy or nanoparticles systems is discussed. In addition, the concerns of NaHCO₃ in clinical use and the potential ways to use NaHCO₃ for cancer therapy are also discussed.

Key words

Sodium bicarbonate / Cancer / Tumor microenvironment / Acidosis / Pharmacology

Cite this Article

Yue Wang, Xueer Zhou, Wenxuan Wang, Yongyao Wu, Zhiyong Qian, Qiang Peng. Sodium bicarbonate, an inorganic salt and a potential active agent for cancer therapy[J]. Chinese Chemical Letters, 2021 , 32 (12) : 3687 -3695 . DOI: 10.1016/j.cclet.2021.06.032

Full Text

Less

1 Introduction

Less

Cancer, a serious threat to human health, is considered as the second leading cause of death worldwide [1]. It is estimated that 20% people develop cancer during their lifetime, and 1/8 men and 1/11 women die from caner (10 million total cancer deaths in 2020) [2]. With the rapid population growth and aging tendency, the incidence of malignant tumors is on the rise [3]. Although significant progresses have been made in cancer therapy, it is still of the greatest challenge to treat cancer in a satisfying manner.

To date, surgery, radiotherapy and chemotherapy are still the most common cancer therapies in clinic. In recent years, some novel approaches, such as targeted therapy, gene therapy, immunotherapy and phototherapy, are (being) developed [4, 5]. However, their applications are largely limited by the undesired side effects, such as drug resistance, cardiotoxicity and immune disorders [6-8]. As such, much attention has been paid to seek novel, safe and effective approaches for cancer therapy.

It has long been known that cancer is a single-cell disease in which mutations in proto-oncogenes and tumor suppressor genes determine the carcinogenesis and tumor progression [9]. Although Stephen Paget proposed the "seed and soil" hypothesis emphasizing the influence of tumor microenvironment on its development as early as 1889, researchers lacked enthusiasm and innovation in studying tumor microenvironment until the 1980s [10]. The change in attitudes began with the discovery that tumor microenvironment can reprogram the phenotype of tumor cells to facilitate their growth, invasion, and metastasis [11].

Cells together with the physical conditions in the tumor microenvironment promote the tumor development. The anaerobic glycolysis caused by hypoxia (Pasteur effect) produces a large amount of lactate [12]. In addition, under aerobic or moderate hypoxia conditions, tumor cells undergo aerobic respiration and produce carbon dioxide (CO₂). Lactate fermentation and decomposition of hydrated CO₂ produce a large number of protons, which are transported into the tumor microenvironment through various transporters, ultimately resulting in the extracellular acidosis [13]. The extracellular pH (pH_e) in tumor tissues is between 6.5 and 7.0 while pH_e in normal tissues is between 7.2 and 7.5 [14, 15]. Meanwhile, the intracellular pH (pH_i) in cancer cells is usually higher (pH_i > 7.4) than that in normal cells (pH_i ~7.2) [16]. Tumor acidosis can cause drug resistance, immune evasion and chronic autophagy, promote the decomposition of tumor matrix and the epithelial mesenchymal transformation, and thus accelerate tumor invasion and metastasis [17, 18]. In this regard, regulating the tumor pH_e is a potential approach for cancer treatment.

Sodium bicarbonate (NaHCO₃), a simple and readily available inorganic salt, has been used to correct the acidosis of tumor microenvironment and shown significant and positive effects on cancer therapy [19]. Basically, NaHCO₃ can be used alone or combined with other therapies, such as chemotherapy [20]. It is undoubted that NaHCO₃ can play significant roles in regulating tumor microenvironment and in the ultimate cancer therapy. In this review, therefore, we aim to provide a comprehensive understanding of the acidic tumor microenvironment (tumor acidosis), summarize the applications and mechanisms of NaHCO₃ in cancer therapy, and discuss the potential combination of NaHCO₃ with chemotherapy, immunotherapy or nano-therapy (Fig. 1). In addition, the concerns of NaHCO₃ in clinical use and the potential ways to use NaHCO₃ for cancer therapy are also discussed.

2 Tumor acidosis

Less

Tumor acidosis has been experimentally proven and widely recognized. The sources of acid are mainly associated with lactate produced by glycolysis and CO₂ produced by respiration [21]. Acidosis can not only promote tumor cell proliferation, invasion, migration and other malignant biological behaviors, but also make tumor cells resistant to certain chemotherapeutic drugs, evade host immune surveillance, and promote autophagy and hypoxia [22].

2.1 Biogenesis of tumor acidosis

2.1.1 Lactate-derived acidosis

Due to the heterogeneity of tumors, hypoxia caused by insufficient perfusion and increased oxygen consumption is widely accepted [23]. Hypoxia leads to an increase in the expression of HIF1α, which leads to an increase in the expression of glucose transporters, thereby accelerating the uptake of glucose by tumor cells [24]. At the same time, HIF1α promotes the expression of the enzyme that converts glucose to pyruvate and the enzyme that converts pyruvate to lactate, such as lactate dehydrogenase A (LDHA), which accelerates the production of pyruvate and lactate in cells [25]. Under the stimulation of hypoxia and acidic pH_i, the expression of the monocarboxylate transporter 4 (MCT4) that transports lactate and H⁺ ions to the outside of the cell increases, resulting in an increase in the concentration of extracellular H⁺ ions [26]. In addition to MCT4, there are many highly expressed H⁺ extruders on the tumor cell membranes for H⁺ ions efflux, including vacuolar H⁺-ATPase (V-ATPase), sodium-hydrogen exchangers (NHEs), sodium-bicarbonate cotransporters (NBCs), monocarboxylate transporters (MCTs), carbonic anhydrases (CAs) [27]. V-ATPase and NHEs use ATP hydrolysis and energy stored in Na⁺ gradient respectively to actively transport H⁺ ions against their gradient [28]. Tumor cells may also undergo glycolysis under aerobic conditions although it is still controversial [29].

2.1.2 CO₂-derived acidosis

In the case of aerobic or moderate hypoxia, tumor cells not only produce lactate, but also produce CO₂ through aerobic respiration using lactate and fatty acids as substrates [30]. CO₂ is hydrated into HCO₃⁻ and H⁺ ions by CAs, including CAIV, CAIX and CAXII, which are bound through the membrane [31]. Among them, CAIX is still active at very low pH and is considered to be a "pH regulator" responsible for acidifying tumor pH_e, whose high expression has been considered as a negative prognostic indicator in breast cancers [32]. The H⁺ ions are transported outside the cell through H⁺ extruders described above. In addition, because CO₂ can diffuse freely, when the concentration gradient inside and outside cells is sufficient, it can also directly diffuse outside cells to affect tumor pH_e, which is still controversial [33].

2.2 Consequences of tumor acidosis

The acidic tumor extracellular microenvironment is toxic to the peritumoral normal tissues, including promoting cell necrosis or apoptosis through a p53-dependent pathway initiated by caspase activation, and reducing genomic stability through chromosome fragmentation and translocations [34]. Interestingly, tumor cells not only adapted to the acidosis, but also used it for further growth and invasion [35]. Epithelial mesenchymal transformation (EMT) and extracellular matrix decomposition play an important role in acidosis-induced tumor invasion and metastasis. Furthermore, tumor acidosis also promotes immune evasion, drug resistance, autophagy and hypoxia (Fig. 2).

2.2.1 Tumor invasion and metastasis

Tumor acidosis favors tumor invasion and metastasis. The exact mechanism has not been clarified, but several existing evidences suggest its relation with EMT and extracellular matrix degradation, as described below.

Epithelial cells lose epithelial properties and gain mesenchymal features during the process of EMT, which facilitates cancer cells migration [36]. The present study shows that tumor cells undergo phenotypic transformation during reverse switch from EMT to mesenchymal-epithelial transition (MET) to adapt to acidosis, favoring tumor cell proliferation [37]. In addition, recent findings show that acid-sensing ion channels 1 (ASIC1) and ASIC3 increase the intracellular Ca²⁺ concentration and RhoA activity under acidosis conditions, thus initiating EMT of pancreatic cancer cells, which can provide a new target for tumor invasion inhibition [38].

Tumor acidosis also induces extracellular matrix degradation by enhancing activity of proteolytic enzymes and release of exosomes. Acidosis promotes proteolytic enzymes release of nearby normal cells (fibroblasts and macrophages), such as cathepsin B [39]. Moreover, acidosis can increase exosomes secretion, which is also strongly associated with tumor invasion [40]. For example, acidosis-induced exosomal miR-21 and miR-10b favor cancer cells proliferation and metastasis, thus considered as therapeutic targets for liver cancer [41]. In addition, acidosis will also promote the release of vascular endothelial growth factor (VEGF) to accelerate angiogenesis and facilitate tumor invasion [42].

2.2.2 Immune evasion

Tumor acidosis plays an important role in immune evasion [43]. Acidosis suppresses T-cell receptor activation [44], inhibits interferon gamma (IFN-γ) production by T cells and NK cells [45], impairs monocyte-derived tumor necrosis factor (TNF) [46] and induces dendritic cell (DC) phenotypic transition to a tumor-associated DC phenotype [47]. Meanwhile, there is evidence that acidosis influences other components of immune system, such as myeloid-derived suppressor cells and macrophages [48, 49].

2.2.3 Drug resistance

Drug resistance is a great challenge to chemotherapy and the development of chemicals with low or slowly-developed drug resistance is of great interest [50]. Acidosis may contribute to drug resistance via interference with drug entry and drug retention in tumor cells. A large number of anticancer drugs are weak bases that are quickly inactivated through neutralization by acidic tumor microenvironment or sequestrated into intracellular acidic vesicles, such as lysosomes [51]. Acidosis can also make the P-glycoprotein overexpressed on tumor cell surface, thus increasing drug efflux [52]. A possible strategy to reduce drug resistance is inhibition of ion pumps from acid effusions, such as proton pump inhibitors (PPI) [53]. Recently, there has been a self-assembled carbonic anhydrase inhibitor of nanofiber structures whose size increases with increased acidosis, resulting in damage to intracellular acid vesicles, against drug resistance [54].

2.2.4 Tumor survival

Tumor acidosis is associated with nutrient deficiency and poor perfusion, thus inducing autophagy. Through autophagy, cells break down cytoplasmic components into amino acids and ATP for tumor cells survival [55, 56]. Therefore, autophagy allows tumor cells to survive in a highly acidic environment. Autophagy regulation can be used in conjunction with conventional cancer treatments to improve therapy efficacy, such as the use of the lysosomal inhibitor ketone [57].

3 Common therapies for cancer

Less

As mentioned above, cancer is particularly dangerous. According to the 2020 global cancer report released by the world health organization (WHO), about one in five people will develop cancer during their lifetime, and one in eight men and one in ten women will die from cancer [2]. Nowadays, there are diverse treatments for different tumor types, including traditional therapies (surgery, chemotherapy and radiotherapy) and novel therapies (targeted therapy, immunotherapy, gene therapy, nano-therapy, sonodynamic therapy and multimodal therapy).

3.1 Traditional therapies

3.1.1 Surgy

Although tumor therapies have made great progress, surgical resection is still the most effective method for most solid tumors. However, surgery can also cause damage to normal tissues and organs, and postoperative complications or dysfunction may occur, affecting the quality of patient's life [58]. Rapid development of surgical techniques and equipment has translated into better outcomes for cancer patients, such as Da Vinci surgical robot and the application of liquid nitrogen during surgery [59, 60]. Due to more accurate preoperative staging and comprehensive treatment models, tumor surgery has entered the era of precise and microinvasive treatment.

3.1.2 Radiotherapy

Radiotherapy is used to treat malignant tumors and certain benign diseases by ionizing radiation to eliminate and eradicate local primary tumors or metastases [61]. It can cure at least 40% of cancers [60]. In recent years, assisted with improved radiotherapy equipment and technology, indications for radiotherapy have become wider and curative effect has been correspondingly more satisfactory, such as stereotactic body radiotherapy, carbon ion radiation treatment and proton beam therapy [62-65]. However, normal tissues are also irradiated inevitably in radiotherapy, leading to undesired side effects to surrounding tissues [66].

3.1.3 Chemotherapy

Chemotherapy uses cytotoxic drugs to kill tumor cells by affecting the structure and function of nucleic acids and proteins in cells, which is one of the main topics in anticancer research [67-69]. Following the availability of novel technologies that enable accurate delivery of drugs to targeted tumor or immune cells, the combination of chemotherapy, immunotherapy and targeted therapy has become increasingly prevalent for tumor treatment [70, 71]. Nowadays, the two greatest concerns regarding chemotherapy are drug resistance and damage to normal cells, such as gastrointestinal reactions and hair loss [72, 73].

3.2 Novel therapies

3-2-1 Gene therapy

Gene therapy transfers exogenous genes into human body, repairing and correcting structural and functional defects of tumor-related genes, or enhancing the host's defense mechanisms so as to kill tumors [74, 75]. The advent of CRISPER/Cas9 technology has improved the accuracy of targeted gene editing [76]. However, there are still many problems to be solved. For example, transferred genes cannot successfully enter target cells because they are degraded by enzymes during circulation. Correspondingly, nanoparticles are being developed to address this problem [77].

3.2.2 Immunotherapy

Immunotherapy is regarded as the therapeutic approach that achieves enhanced immunity by activating the host's immune defense mechanism, including immune checkpoint inhibition, adoptive cell transfer (ACT), immune modulator therapy and vaccination [78, 79]. The most common checkpoint proteins and their corresponding checkpoint inhibitors are PD-L1 and ipilimumab [80], CDLA-4 and nivolumab [81]. However, immunotherapy also has many side effects, such as immune-related adverse effects (irAEs) and cytokine release syndrome (CRS) [82]. These side effects often require special treatment, such as steroids and immunoregulatory therapy [83].

3.2.3 Targeted therapy

Molecular targeted therapy targets key molecules in tumor genesis and development, and uses effective blockers to interfere with signal transduction pathway and tumor microenvironment to achieve the purpose of treatment [84]. It is one of the most widely used and fastest growing tumor treatments. Some typical targeted therapies include cetuximab for BRAF-mutant colorectal cancer [85] and crizotinib for NSCLC with MET exon 14 alterations [86].

3.2.4 Nano-therapy

Nanotechnology is one of the fastest growing technologies, and an increasing number of nanomaterials are used for advanced drug delivery due to their great potentials in improving water solubility, enhancing targeting capacity, prolonging drug circulation time, and reducing drug resistance and side effects [87-95]. About a dozen anticancer nano-therapies have been approved, such as PEGylated liposomal doxorubicin (Caelyx®, Doxil®) [96]. In addition to the approved nano-therapeutics, some novel nanotechnologies and functionalized nanoparticles-based drug delivery systems have been used for regulating tumor microenvironment, realizing targeted radiotherapy and enhancing immunotherapy [97-100].

3.2.5 Sonodynamic therapy

Sonodynamic therapy (SDT) is a novel non-invasive and safe therapeutic technique involving the combination of low-intensity ultrasound and sonosensitizer, which avoids light damage in phototherapy and provides deeper penetration depth in soft tissue. Novel nanoparticle technologies are used in SDT to achieve targeted therapy with excellent drug loading, improved bioavailability and controlled release. For example, the multi-responsive nano-riceball NGR@DDP can significantly inhibit the growth of hepatocellular carcinoma with negligible side effects [101].

3.2.6 Multimodal therapy

As mentioned above, monotherapy has numerous side effects and often cannot cure cancer. Therefore, multimodal therapy based on the synergy of two or more therapies has become a promising novel therapeutic method. Multimodal therapy not only enhances the anti-cancer efficacy, but also reduces the side effects caused by high-dose drugs in monotherapy. Notably, nano-platforms play an important role in multimodal therapy. Wang et al. combined nano-platforms and photothermal therapy with the construction of titanium nitride nanoparticles, thus allowing complete tumor ablation using photothermal ablation in deeper regions [102].

4 NaHCO₃-based therapy

Less

The continuous progress of the above-mentioned therapies and their combination has significantly improved the efficacy of cancer therapy. But the outcome in many cases is still unsatisfying. In the past decades, NaHCO₃-based therapy targeting the acidic pH of tumor microenvironment has been developed and has shown a certain degree of promise in cancer therapy [103-105].

4.1 NaHCO₃ monotherapy

As an inorganic salt with alkalescence, NaHCO₃ is able to neutralize the weakly acidic pH in tumor microenvironment and thus can be used for cancer therapy directly. Robey and colleagues found that oral NaHCO₃ therapy in mice had no effect on primary tumor growth, but that NaHCO₃ therapy resulted in a significant reduction in the number and size of lung, bowel, and diaphragmatic tumor metastases [103]. They showed that in the experiment of 30-day period, the mice treated with NaHCO₃ had a total of 147 metastatic lung lesions (vs. 326 in control group), with an average lesion diameter of 4.5 mm (vs. 5.2 mm in control group). In the 60-day experiment, the treatment of NaHCO₃ reduced the average number of lesion pixels in mice to 74 (81% reduction), and half of the mice in the control group had more than 240 lesion pixels. In addition, the survival rate of mice in the NaHCO₃ group was greatly improved. In another work, Banerjee and colleagues achieved the initial burst release of NaHCO₃ with polycaprolactone coating in the calcium phosphate delivery system [106]. They found that the sharp increase in local pH_e reduced the proliferation capacity of osteosarcoma cells and the density of osteosarcoma, suggesting that NaHCO₃ could be used to increase the tumor pH_e after bone tumor surgery to reduce tumor invasion and metastasis.

4.2 Combined with immunotherapy

Immunotherapies for tumors include checkpoint inhibition and ACT of tumor-specific T cells [107]. However, tumor acidosis inhibits the activity of cancer-killing immune cells, such as T cells, dendritic cells and nature killer cells, and blocks the secretion of IFNγ and TNFα, resulting in immune escape [108]. It has been found that tumor acidosis promoted the polarization of tumor-associated macrophages into a non-inflammatory phenotype, thus promoting angiogenesis and supporting tumor growth and metastasis in the mouse models of melanoma [109]. Therefore, it is promising to improve the efficacy of immunotherapy by modulating pH_e with NaHCO₃.

Pilon-Thomas et al. showed that the addition of NaHCO₃ significantly inhibited tumor growth and improved the efficacy of immunotherapy [110]. They found that the efficacy of combining NaHCO₃ with anti-CTLA4 or anti-PD1 antibodies was equivalent to that of combining two checkpoint inhibitors in the B16 melanoma models. They also found that NaHCO₃ had a more significant inhibitory effect in the Panc02 pancreatic cancer model. NaHCO₃ or anti-PD1 antibody monotherapy had no effect on tumor growth, but their combination showed a significantly enhanced tumor growth inhibition rate (50% enhanced). Although there are no more relevant studies on the combination therapy of NaHCO₃ with immunotherapy, it is commonly recognized that tumor acidosis promotes the immune escape. Hence, the application of NaHCO₃ may be a promising approach to suppress immune escape and improve the immunotherapy.

4.3 Combined with chemotherapy

Combination of NaHCO₃ with anticancer drugs may be greatly promising to enhance the anticancer efficacy since pH directly affects the cellular uptake of ionizable drug molecules, especially the alkalescent drugs. Mitoxantrone, an alkalescent anticancer drug, is ionized by the acidic tumor microenvironment and thus is hard to be taken up into tumor cells [111]. It was found that mitoxantrone had a higher uptake by tumor cells and showed the higher cytotoxicity in alkaline (pH 7.4) environment than in acidic one (pH 6.6). In another work, Raghunand et al. showed that pre-administration of NaHCO₃ in tumor-bearing mice increased the tumor pH_e by 0.6 pH units and enhanced the therapeutic index of mitoxantrone by 3.3 folds [112].

Doxorubicin is also an alkaline drug and its anticancer efficacy can also be enhanced by NaHCO₃. Hanan et al. combined liposomal NaHCO₃ and doxorubicin and found that the viability of triple-negative breast cancer cells treated with single doxorubicin in an acidic pH_e condition was 48% and decreased to 12% when combined with liposomal NaHCO₃ [113]. Fluorescent microscopy and quantitative analysis showed that the uptake of doxorubicin by cancer cells was enhanced by two times in the presence of NaHCO₃ (Fig. 3). Interestingly, the NaHCO₃-induced efficacy enhancement of mitoxantrone is slightly less than that of doxorubicin in the MCF-7 tumor/SCID mouse models [114]. This suggests that the effect of NaHCO₃ on the efficacy of chemotherapy may be associated with the acidity coefficient (pKa) of drugs.

In a clinic trial, Hamaguchi et al. found that combining NaHCO₃ with epidermal growth factor receptor tyrosine kinase inhibitor could significantly increase the urine pH of patients with advanced pancreatic cancer and expanded the median overall survival (OS) to 16.1 months, an 11.4-month increase compared to the non-alkaline urine group [115]. Although the study did not measure the tumor pH_e changes, it still strongly proves that NaHCO₃ can enhance the efficacy of chemotherapy and prolong the survival of patients, even no less than efficacy of the standard cancer treatment for advanced pancreas cancer. A recent case-control study has also shown the similar results [116].

The role of NaHCO₃ in inhibiting drug resistance is also reflected in the enhancement of rapamycin efficacy. The complex 1 of the mechanistic target of rapamycin (mTORC1) is activated in cancer cells, ensuring unlimited proliferation of tumor cells [117]. Rapamycin is an mTORC1 inhibitor that inhibits tumor development by targeting mTORC1 [118]. Rapamycin significantly reduced the proliferation of HT29 colon cancer cells by 37.1% in physiological pH, but the inhibitory effect disappeared under acidic conditions, indicating that the acidic pH_e diminished the rapamycin inhibitory effect on mTORC1 [119]. Therefore, modulating pH_e is a very promising method to inhibit drug resistance. Compared with rapamycin monotherapy in mice bearing MC-38 tumors, the combination treatment of NaHCO₃ and rapamycin increased tumor pH_e, enhanced tumor growth inhibition by 26.4%, and improved the incidence of tumor cell apoptosis by 30% [104]. These results demonstrate that NaHCO₃ effectively increases the tumor pH_e, thereby enhancing the rapamycin anti-tumor effect and inhibiting drug resistance.

4.4 Combined with nano-therapy

Nanotechnology is one of the fastest growing technologies due to its excellent targeting properties, high bioavailability, and reduced side effects [120]. Combination of NaHCO₃ with nanomaterials has shown great potentials in cancer therapy. Basically, there are two ways to combine NaHCO₃ with nanotechnologies. One is delivering NaHCO₃ by nanocarriers to tumor extracellular microenvironment and thus alkalinize the acidosis, and the other is preparing pH-responsive nanocarriers with NaHCO₃, which can target the acidic tumor environment and release anti-tumor drugs [105, 121].

The targeted delivery of NaHCO₃ via nanotechnology will further enhance its alkalization ability, prolong the alkalization time, increase the immune cells number, inhibit tumor growth, and thereby inhibit acid-induced drug resistance. Abumanhal-Masarweh et al. showed that the liposomal NaHCO₃ could achieve an extracellular NaHCO₃ concentration of 3.7%, significantly higher than that of 0.17% achieved by free NaHCO₃, indicating a better tumor targeting capacity of liposomal NaHCO₃ [113]. In addition, the liposomal NaHCO₃ could further increase the number of CD45+ immune cells, T cells, B cells and macrophages.

NaHCO₃ can also be added to the nanoparticles to generate carbon dioxide gas in an acidic environment to destroy the nanoparticle shell and release the drug quickly. Kim et al. added NaHCO₃ to poly(lactide-co-glycolide) (PLGA) nanoparticles loaded with vaccine adjuvants to obtain the pH-responsive function [105]. Compared with conventional PLGA nanoparticles, the properties and efficacy of pH-responsive PLGA nanoparticles have been significantly improved, including the increase in the loading capacity, the number of CD4 T cells, NK cells and IFN-γ + NK cells, the antigen-specific CD8 T cell and natural killer (NK) cell responses, and the tumor volume inhibition rate. In summary, pH-responsive nanoparticles enhanced the anti-tumor effect of vaccine adjuvants, providing a promising delivery platform for cancer immunotherapy.

5 Mechanisms of NaHCO₃-based therapy

Less

The target of NaHCO₃-based therapy is the acidic tumor environment and its anticancer mechanisms may include inhibition of tumor invasion and metastasis, inhibition of immune evasion, inhibition of drug resistance, and inhibition of hypoxia and autophagy (Fig. 4).

5.1 Inhibition of tumor invasion and metastasis

Tumor acidosis has been shown to induce the expression and activity of many systems involved in matrix remodeling, including matrix metalloproteinases (MMP1, MMP2 and MMP9) and lysosomal proteases (cathepsin B, D or L) [122]. Robey and colleagues found that oral NaHCO₃ increased the tumor pH_e and inhibited the release and activity of cathepsin B which is mainly responsible for the metastasis of tumor cells [103]. This result explains why oral NaHCO₃ therapy in this experiment had no effect on primary tumor growth, but resulted in a significant reduction in the number and size of lung, bowel, and diaphragmatic tumor metastases.

The inhibition effect of NaHCO₃ on tumor metastasis also includes the reduction of the number of lymph node involvement and circulating tumor cells (CTC). It was found that 9 of 12 mice showed almost no tumor metastasis in the lymph nodes in the NaHCO₃ group, while 7 of 11 mice had a large number of metastatic tumors in their lymph nodes in the control group [123]. Accordingly, the average number of CTC was 5 ± 1 cells/mL in the 14 mice treated with NaHCO₃, but 13 ± 3 cells/mL in the 12 mice in the control group.

5.2 Inhibition of immune evasion

Tumor acidosis has been shown to inhibit the antitumor activity of immune cells, such as neutrophils, monocytes, macrophages, NK cells, CD4 T cells, CD8 T cells and myeloid dendritic cells [124]. The combination of NaHCO₃ therapy and immunotherapy has been reported to enhance the anticancer efficacy. It was found that ACT combined with NaHCO₃ reduced tumor growth rates and increased T-Cell persistence significantly [110]. In addition, NaHCO₃ therapy can lead to an increase in the number of immune cells. For example, NaHCO₃ resulted in a significant increase in the number of CD8β T cells infiltrating into Yumm 1.1 tumors [104]. The injection of liposomal NaHCO₃ in mice with breast cancer also resulted in an increase in the number of T cells, B cells and macrophages [113].

5.3 Inhibition of drug resistance

The tumor acidic pH ionizes the weak-base anticancer drugs and reduces their uptake by tumor cells, resulting in the development of drug resistance. NaHCO₃ is an alkaline salt and thus can neutralize the acidic pH and inhibit drug resistance. It has been shown that the slight increase in pH_e significantly reduced doxorubicin ionization by 76%, thus increasing its uptake by tumor cells and improving the anticancer efficacy [125]. Similarly, the liposomal NaHCO₃ was found to increase the tumor pH_e by about 0.25 pH units, thereby enhancing the activity of doxorubicin in 4T1 breast cancer cells [113]. The NaHCO₃-caused enhancement of antitumor activity of doxorubicin may be related to the pH_e-induced changes in subcellular distribution and topoisomerase activity [112].

Tumor acidosis can also attenuate the rapamycin inhibition on mTORC1, resulting in drug resistance. NaHCO₃ is able to reduce the activity of mTORC1 through alkalization of the acidic pH, thus reducing drug resistance. It has been shown that NaHCO₃ can induce the alkalization of tumor pH and thus enhance the activity of rapamycin and also promote its uptake by tumor cells [104].

5.4 Inhibition of hypoxia and autophagy

As mentioned above, there is a bidirectional promotion relationship between HIF-1 and acidic tumor microenvironment. It is reported that tumor microenvironment acidity reduces the transport of ascorbic acid into cells by suppressing the activity of sodium vitamin C cotransporter 2 (SVCT2) and causes the suboptimal intracellular ascorbic acid content [126]. McCarty et al. pointed out that NaHCO₃ has the potential to enhance the activity of SVCT2 and increase the uptake of ascorbic acid into cells, thus achieving the optimal intracellular concentration of ascorbic acid [127]. Optimal intracellular ascorbic acid content can further inhibit the transcriptional activity and expression of HIF-1 and suppress NF-κB activity to slow tumor invasion and metastasis.

In addition, autophagy is an important means for tumor cells to adapt to acidic environment [128]. Oral NaHCO₃ was found to reduce the expression of pro-autophagy signals in MDA-MB-231 xenograft tumor-bearing mice, but the role of NaHCO₃ in autophagy has not been fully disclosed [129].

As discussed above, NaHCO₃ can increase extracellular pH to inhibit tumor progression. The mechanisms include the inhibition of protease activity, immune escape, drug resistance, hypoxia and autophagy. In addition to NaHCO₃, some other buffers with pKa of ~7 may also have comparable or better results than NaHCO₃, such as cholamine chloride, BES and TES [130].

6 Advances and concerns of NaHCO₃-based therapy

Less

Basically, the antitumor therapies focus on tumor itself aiming at killing tumor cells directly [131]. However, the associated problems, such as drug resistance and immune escape, largely limit the efficacy. One of the reasons for these problems may be the tumor heterogeneity [132]. In contrast, NaHCO₃-based therapy targets the tumor acidic microenvironment, which is a common phenotype of tumors, and inhibits tumor growth by increasing the tumor pH_e. In this regard, NaHCO₃-based therapy may be more versatile than the others [133]. It is worth mentioning that NaHCO₃ has an obvious effect in inhibiting early metastasis of primary tumors, but not in non-highly glycolytic sensitive tumors treatment because their metastasis is considered to be pH independent [134]. It is estimated that the non-highly glycolytic sensitive tumor accounts for only ~10% in all kinds of tumor [135]. Thus, most patients with glycolytic tumor types can be benefit from NaHCO₃-based therapy. In addition, NaHCO₃ is readily available and non-toxic, which ensures the NaHCO₃-based therapy affordable and safe [136].

However, there are also some limitations in the clinical use of NaHCO₃. First, since it does not fully neutralize the large amount of acid produced by large tumors, NaHCO₃-based therapy may be ineffective for large solid tumor [137]. Second, NaHCO₃ should be avoided in combination with weakly acidic or neutral anticancer drugs, because their combination will reduce the anticancer efficacy, such as 5-fluouracil and cisplatin [138]. Also, there has been a case of metabolic alkalosis and hypernatremia caused by overdose and carelessness in use of NaHCO₃ [139]. In addition, the unsatisfying taste of NaHCO₃ may lead to poor patient compliance [140].

7 Conclusion and perspectives

Less

Tumor acidosis-mediated tumor metastasis, drug resistance, immune invasion, aggravated hypoxia and increased autophagy are important reasons for the unsatisfying prognosis and high mortality. NaHCO₃ has shown great potentials in cancer treatment due to its ready availability, safety and ability to neutralize the tumor acidic microenvironment. The anticancer mechanisms of NaHCO₃ include (1) inhibition of tumor invasion and metastasis; (2) inhibition of immune evasion; (3) inhibition of drug resistance; and (4) inhibition of hypoxia and autophagy.

Despite the great potentials and progress of NaHCO₃ in cancer treatment, many aspects of NaHCO₃-based therapy need to be further explored. First of all, the mechanisms of the antitumor effect caused by the alkalization of the tumor acidosis by NaHCO₃ need to be further disclosed. For example, it can be further confirmed whether NaHCO₃ inhibits exosomes secretion and reduces the activation of the multidrug transporter P-glycoprotein. Second, the combination of drugs that target the production of acids with NaHCO₃ may be a promising strategy to improve efficacy and avoid deficiencies. Third, the enhanced efficacy of radiotherapy is related to the increase in oxygen partial pressure. Therefore, NaHCO₃ may be combined with radiotherapy since it can inhibit the tumor hypoxia. In addition, the possibility of combining NaHCO₃ with phototherapy, such as photothermal therapy and photodynamic therapy, may be a direction in the future. The delivery of NaHCO₃, including the delivery routes and formulations, is also of great importance for deep investigation.

NaHCO₃ can be used alone and also in combination with other therapies, such as immunotherapy and chemotherapy. The practical use of NaHCO₃ is simple since there are several potential approaches for using it in clinic. The general administration routes may include oral delivery, intravenous injection and intratumor injection. NaHCO₃ can be used in the form of solution directly or in the form of advanced delivery systems, such as nanoparticles. In summary, NaHCO₃ is much more than a simple inorganic salt and has great potentials in cancer therapy as an active agent.

Declaration of competing interest

Less

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgments

Less

This work was supported by the National Natural Science Foundation of China (No. 81973261), the Foundation of West China Hospital of Stomatology (No. RD-02–201903), and the Research Funding from West China School/Hospital of Stomatology, Sichuan University (No. RCDWJS2020–7).

References

Less

[1]

F. Bray, J. Ferlay, I. Soerjomataram, et al., CA Cancer J. Clin. 68 (2018) 394–424

[2]

GLOBOCAN 2020: new cancer data, https://www.uicc.org/news/globocan-2020-new-cancer-data, last accessed on 17/12/2020.

[3]

M.C. White, D.M. Holman, J.E. Boehm, et al., Am. J. Prev. Med. 46 (2014) S7–S15

[4]

D. Jia, X. Ma, Y. Lu, et al., Chin. Chem. Lett. 32 (2021) 162–167

[5]

L. Shen, T. Zhou, Y. Fan, et al., Chin. Chem. Lett. 31 (2020) 1709–1716

[6]

J. Liu, N. Guo, C. Gao, et al., J. Biomed. Nanotechnol. 15 (2019) 531–543

[7]

J. Yang, D. Dai, L. Ma, Y.W. Yang, Chin. Chem. Lett. 32 (2021) 729–734

[8]

L.B. Kennedy, A.K.S. Salama, CA Cancer J. Clin. 70 (2020) 86–104

[9]

E. Rondeau, N. Larmonier, T. Pradeu, A. Bikfalvi, Elife8 (2019) e53755

[10]

S. Paget, Cancer Metastasis Rev. 8 (1989) 98–101

[11]

J. Pohl, A. Radler-Pohl, V. Schirrmacher, Cancer Metastasis Rev. 7 (1988) 347–356

[12]

A.M. Otto, Cancer Metab. 4 (2016) 5

[13]

K.A. White, B.K. Grillo-Hill, D.L. Barber, J. Cell Sci. 130 (2017) 663–669

[14]

J.R. Griffiths, Br. J. Cancer64 (1991) 425–427

[15]

P. Vaupel, F. Kallinowski, P. Okunieff, Cancer Res. 49 (1989) 6449–6465

[16]

B.A. Webb, M. Chimenti, M.P. Jacobson, D.L. Barber, Nat. Rev. Cancer11 (2011) 671–677

[17]

E.K. Rofstad, B. Mathiesen, K. Kindem, K. Galappathi, Cancer Res. 66 (2006) 6699–6707

[18]

V. Estrella, T. Chen, M. Lloyd, et al., Cancer Res. 73 (2013) 1524–1535

[19]

S.R. Pillai, M. Damaghi, Y. Marunaka, et al., Cancer Metastasis Rev. 38 (2019) 205–222

[20]

N. Sugandha, L. Mittal, A. Awasthi, S. Asthana, Recent advances in drug development targeting cancer metabolism, in: D. Kumar (Ed. ), Cancer Cell Metabolism: A Potential Target for Cancer Therapy, Springer Singapore, Singapore, 2020, pp. 103–126

[21]

J. Chiche, M.C. Brahimi-Horn, J. Pouysségur, J. Cell. Mol. Med. 14 (2010) 771–794

[22]

M. Wang, J. Zhao, L. Zhang, et al., J. Cancer8 (2017) 761–773

[23]

M. Hockel, P. Vaupel, J. Natl. Cancer Inst. 93 (2001) 266–276

[24]

C.M. Labak, P.Y. Wang, R. Arora, et al., Am. J. Cancer Res. 6 (2016) 1599

[25]

M.I. Koukourakis, C. Kakouratos, D. Kalamida, et al., Int. J. Radiat. Biol. 92 (2016) 353–363

[26]

K. Balamurugan, Int. J. Cancer138 (2016) 1058–1066

[27]

R.A. Cardone, K.O. Alfarouk, R.L. Elliott, et al., Int. J. Mol. Sci. 20 (2019) 3694

[28]

E.P. Spugnini, P. Sonveaux, C. Stock, et al., Biochim. Biophys. Acta Biomembranes1848 (2015) 2715–2726

[29]

B.I. Reinfeld, M.Z. Madden, M.M. Wolf, et al., Nature (2021), https://doi.org/10.1038/s41586-021-03442-1

[30]

S.A. Mookerjee, R.L. Goncalves, A.A. Gerencser, D.G. Nicholls, M.D. Brand, Biochim. Biophys. Acta Bioenerg. 1847 (2015) 171–181

[31]

S. Pastorekova, R.J. Gillies, Cancer Metastasis Rev. 38 (2019) 65–77

[32]

J.I. Kim, K.U. Choi, I.S. Lee, et al., Oncol. Lett. 9 (2015) 1699–1706

[33]

V. Endeward, M. Arias-Hidalgo, S. Al-Samir, G. Gros, Membranes7 (2017) 61

[34]

T. Morita, T. Nagaki, I. Fukuda, K. Okumura, Mutat. Res. 268 (1992) 297–305

[35]

R.A. Gatenby, E.T. Gawlinski, A.F. Gmitro, B. Kaylor, R.J. Gillies, Cancer Res. 66 (2006) 5216–5223

[36]

O. Thews, A. Riemann, Cancer Metastasis Rev. 38 (2019) 113–129

[37]

Y. Zhang, L. Xu, P. Wang, et al., Cell Cycle18 (2019) 1938–1947

[38]

S. Zhu, H.Y. Zhou, S.C. Deng, et al., Cell Death Dis. 8 (2017) e2806

[39]

J. Rozhin, M. Sameni, G. Ziegler, B.F. Sloane, Cancer Res. 54 (1994) 6517–6525

[40]

A. Abak, A. Abhari, S. Rahimzadeh, PeerJ6 (2018) e4763

[41]

X.P. Tian, C.Y. Wang, X.H. Jin, et al., Theranostics9 (2019) 1965–1979

[42]

P. Vaupel, G. Multhoff, Fatal alliance of hypoxia-/HIF-1α-driven microenvironmental traits promoting cancer progression, in: P.D. Ryy, J. LaManna, D. Harrison, S.S. Lee (Eds. ), Oxygen Transport to Tissue XLI. Advances in Experimental Medicine and Biology, Springer, 2020, vol. 1232, pp. 169–176.

[43]

D. Hanahan, R.A. Weinberg, Cell144 (2011) 646–674

[44]

Y.X. Zhang, Y.Y. Zhao, J. Shen, et al., Nano Lett. 19 (2019) 2774–2783

[45]

A. Brand, K. Singer, G.E. Koehl, et al., Cell Metab. 24 (2016) 657–671

[46]

K. Dietl, K. Renner, K. Dettmer, et al., J. Immunol. 184 (2010) 1200–1209

[47]

E. Gottfried, L.A. Kunz-Schughart, S. Ebner, et al., Blood107 (2006) 2013–2021

[48]

Z. Husain, Y. Huang, P. Seth, V.P. Sukhatme, J. Immunol. 191 (2013) 1486–1495

[49]

T. Ohashi, T. Akazawa, M. Aoki, et al., Int. J. Cancer133 (2013) 1107–1118

[50]

Y. Zhao, L.X. Zhang, T. Jiang, et al., Eur. J. Med. Chem. 203 (2020) 112570

[51]

B. Zhitomirsky, Y.G. Assaraf, Drug Resist. Updates24 (2016) 23–33

[52]

J. Marcoux, S.C. Wang, A. Politis, et al., Proc. Natl. Acad. Sci. U. S. A. 110 (2013) 9704–9709

[53]

E.P. Spugnini, S. Fais, Exp. Opin. Ther. Pat. 30 (2020) 15–25

[54]

J. Li, K. Shi, Z.F. Sabet, et al., Sci. Adv. 5 (2019) eaax0937

[55]

C.J. Li, W.T. Liao, M.Y. Wu, P.Y. Chu, Int. J. Mol. Sci. 18 (2017) 1566

[56]

S. Yu, Y. Wang, L. Jing, et al., Cancer Lett. 411 (2017) 82–89

[57]

R.K. Amaravadi, A.C. Kimmelman, J. Cancer Discov. 9 (2019) 1167–1181

[58]

K. Moritani, Y. Kanemitsu, D. Shida, et al., Jpn. J. Clin. Oncol. 50 (2020) 89–93

[59]

H.B. Dai, Z.C. Wang, X.B. Feng, et al., World J. Surg. Oncol. 16 (2018) 41

[60]

T.T. Shah, M. Peters, D. Eldred-Evans, et al., Eur. Urol. 76 (2019) 98–105

[61]

D. Schaue, W.H. McBride, Nat. Rev. Clin. Oncol. 12 (2015) 527–540

[62]

R. Atun, D.A. Jaffray, M.B. Barton, et al., Lancet Oncol. 16 (2015) 1153–1186

[63]

J. Sia, R. Szmyd, E. Hau, H.E. Gee, Front. Cell Dev. Biol. 8 (2020) 41

[64]

T.D. Malouff, A. Mahajan, S. Krishnan, et al., Front. Oncol. 10 (2020) 82

[65]

O. Siddiqui, A. Pollock, S. Samanta, A. Kaiser, J.K. Molitoris, Curr. Oncol. Rep. 22 (2020) 30

[66]

Y. Gao, J. Gao, G. Mu, et al., Acta Pharm. Sin. B10 (2020) 2374–2383

[67]

Y. Tang, H. Liu, H. Chen, et al., J. Biomed. Nanotechnol. 16 (2020) 763–788

[68]

A. Pusuluri, D. Wu, S. Mitragotri, J. Control. Release305 (2019) 130–154

[69]

S. Guan, J. Wei, L. Huang, L. Wu, Eur. J. Med. Chem. 207 (2020) 112758

[70]

F. Combes, E. Meyer, N.N. Sanders, J. Control. Release327 (2020): 70–87

[71]

S. Nabergoj, I. Mlinarič-Raščan, Ž. Jakopin, Med. Res. Rev. 39 (2019) 1447–1484

[72]

R. Juza, P. Vlcek, E. Mezeiova, et al., Med. Res. Rev. 40 (2020) 1593–1678

[73]

Z.X. He, T.Q. Zhao, Y.P. Gong, et al., Eur. J. Med. Chem. 200 (2020) 112458

[74]

T. Wirth, N. Parker, S. Ylä-Herttuala, Gene525 (2013) 162–169

[75]

J. Liu, Z. Wang, S. Zhao, B. Ding, Nano Res. 11 (2018) 5017–5027

[76]

O. Shalem, N.E. Sanjana, E. Hartenian, et al., Science343 (2014) 84–87

[77]

L.M. Russell, C.H. Liu, P. Grodzinski, Biomaterials242 (2020) 119926

[78]

I. Mellman, G. Coukos, G. Dranoff, Nature480 (2011) 480–489

[79]

Y. Zhao, X. Yu, J. Li, Acta Pharm. Sin. B10 (2020) 2018–2036

[80]

J.A. Marin-Acevedo, B. Dholaria, A.E. Soyano, et al., J. Hematol. Oncol. 11 (2018) 39

[81]

S.S. Neelapu, S. Tummala, P. Kebriaei, et al., Nat. Rev. Clin. Oncol. 15 (2018) 47–62

[82]

J.A. Thompson, J. Natl. Compr. Cancer Netw. 16 (2018) 594–596

[83]

R.A. Harrison, S. Tummala, J. de Groot, Curr. Neurol. Neurosci. Rep. 20 (2020) 27

[84]

X. Ke, L. Shen, Front. Lab. Med. 1 (2017) 69–75

[85]

A. Gunjur, Lancet Oncol. 20 (2019) e618

[86]

A. Drilon, J.W. Clark, J. Weiss, et al., Nat. Med. 26 (2020) 47–51

[87]

J. Liu, J. Dong, T. Zhang, Q. Peng, J. Control. Release286 (2018) 64–73

[88]

W. Liao, Y. Du, C. Zhang, et al., Acta Biomater. 86 (2019) 1–14

[89]

Y. Li, T. Mei, S. Han, et al., Chin. Chem. Lett. 31 (2020) 3027–3040

[90]

G. Li, L. Chen, P. Xin, J. Huang, J. Wu, J. Biomed. Nanotechnol. 16 (2020) 1570–1587

[91]

T. Zhang, J.Z. Tang, X. Fei, et al., Acta Pharm. Sin. B11 (2021) 651–667

[92]

Y. Chen, K. Cheng, Nano Res. 13 (2020) 2617–2624

[93]

A.R. Khan, X. Yang, X. Du, et al., Carbohydr. Polym. 233 (2020) 115837

[94]

H. Li, D. Yin, W. Li, et al., Colloids Surf. B Biointerfaces199 (2021) 111502

[95]

Y. Gao, Y. Chen, Y. Cao, A. Mo, Q. Peng, Eur. J. Med. Chem. 213 (2021) 113056

[96]

D. Peer, J.M. Karp, S. Hong, et al., Nat. Nanotechnol. 2 (2007) 751–760

[97]

J. Li, D.J. Burgess, Acta Pharm. Sin. B10 (2020) 2110–2124

[98]

R.M. Pallares, R.J. Abergel, Nano Res. 13 (2020) 2887–2897

[99]

J. Yang, C. Wang, S. Shi, C. Dong, Nano Res. 13 (2020) 2595–2616

[100]

Z. Shi, Q. Li, L. Mei, Chin. Chem. Lett. 31 (2020) 1345–1356

[101]

X. Shi, Y. Zhang, Y. Tian, et al., Small Methods5 (2021) 2000416

[102]

C. Wang, C. Dai, Z. Hu, et al., Nanoscale Horiz. 4 (2019) 415–425

[103]

I.F. Robey, B.K. Baggett, N.D. Kirkpatrick, et al., Cancer Res. 69 (2009) 2260–2268

[104]

S. Faes, A.P. Duval, A. Planche, et al., Mol. Cancer15 (2016) 78

[105]

H. Kim, D. Sehgal, T.A. Kucaba, et al., Nanoscale10 (2018) 20851–20862

[106]

D. Banerjee, S. Bose, Mater. Today Chem. 12 (2019) 200–208

[107]

R. Houot, L.M. Schultz, A. Marabelle, H. Kohrt, Cancer Immunol. Res. 3 (2015) 1115–1122

[108]

S. Cassim, J. Pouyssegur, Int. J. Mol. Sci. 21 (2020) 157

[109]

T. Bohn, S. Rapp, N. Luther, et al., Nat. Immunol. 19 (2018) 1319–1329

[110]

S. Pilon-Thomas, K.N. Kodumudi, A.E. El-Kenawi, et al., Cancer Res. 76 (2016) 1381–1390

[111]

N. Raghunand, B.P. Mahoney, R.J. Gillies, Biochem. Pharmacol. 66 (2003) 1219–1229

[112]

N. Raghunand, B. Mahoney, R. van Sluis, B. Baggett, R.J. Gillies, Neoplasia3 (2001) 227–235

[113]

H. Abumanhal-Masarweh, L. Koren, A. Zinger, et al., J. Control. Release296 (2019) 1–13

[114]

N. Raghunand, X. He, R. van Sluis, et al., Br. J. Cancer80 (1999) 1005–1011

[115]

R. Hamaguchi, R. Narui, H. Wada, Anticancer Res. 40 (2020) 873–880

[116]

R. Hamaguchi, T. Ito, R. Narui, et al., In Vivo34 (2020) 2623–2629

[117]

L.C. Kim, R.S. Cook, J. Chen, Oncogene36 (2017) 2191–2201

[118]

D.W. Lamming, Cold Spring Harbor Perspect. Med. 6 (2016) a025924

[119]

M.P. DeYoung, P. Horak, A. Sofer, D. Sgroi, L.W. Ellisen, Genes Dev. 22 (2008) 239–251

[120]

C.A. Cheng, T. Deng, F.C. Lin, Y. Cai, J.I. Zink, Theranostics9 (2019) 3341–3364

[121]

A. Som, R. Raliya, L. Tian, et al., Nanoscale8 (2016) 12639–12647

[122]

K. Ji, L. Mayernik, K. Moin, B.F. Sloane, Cancer Metastasis Rev. 38 (2019) 103–112

[123]

I.F. Robey, L.A. Nesbit, Biomed. Res. Int. 2013 (2013) 485196

[124]

F. Erra Díaz, E. Dantas, J. Geffner, Mediators Inflamm. 2018 (2018) 1218297

[125]

S.C. Yang, H.X. Ge, Y. Hu, X.Q. Jiang, C.Z. Yang, J. Appl. Polym. Sci. 78 (2000) 517–526

[126]

C. Kuiper, I.G. Molenaar, G.U. Dachs, et al., Cancer Res. 70 (2010) 5749–5758

[127]

M.F. McCarty, Med. Hypotheses81 (2013) 664–670

[128]

J.W. Wojtkowiak, J.M. Rothberg, V. Kumar, et al., Cancer Res. 72 (2012) 3938–3947

[129]

C. Corbet, O. Feron, Nat. Rev. Cancer17 (2017) 577–593

[130]

A.S. Silva, J.A. Yunes, R.J. Gillies, R.A. Gatenby, Cancer Res. 69 (2009) 2677–2684

[131]

J. Tchou, J. Conejo-Garcia, Adv. Pharmacol. 65 (2012) 45–61

[132]

D. Wu, D.C. Wang, Y. Cheng, et al., Semin. Cancer Biol. 42 (2017) 13–19

[133]

S. Fais, G. Venturi, B. Gatenby, Cancer Metastasis Rev. 33 (2014) 1095–1108

[134]

K.M. Bailey, J.W. Wojtkowiak, H.H. Cornnell, et al., Neoplasia16 (2014) 354–364

[135]

S.S. Gambhir, Nat. Rev. Cancer2 (2002) 683–693

[136]

S. Faes, O. Dormond, Med. Chem. 5 (2015) 540–544

[137]

A. Ibrahim-Hashim, V. Estrella, Cancer Metastasis Rev. 38 (2019) 149–155

[138]

J. Guindon, A.G. Hohmann, Neurosci. Lett. 544 (2013) 41–46

[139]

L.B. Galinko, S.H. Hsu, C. Gauran, et al., Am. J. Crit. Care26 (2017) 491–494

[140]

M. Yang, X. Zhong, Y. Yuan, Integr. Cancer Ther. 19 (2020) 1534735420922579

Appendix

Less

Year 2021 volume 32 Issue 12

PDF

Cite this Article

BibTeX

Article Info

doi: 10.1016/j.cclet.2021.06.032

Receive Date：2021-04-10
Online Date：2026-01-04
Published：2021-12-15

Article Data

Affiliations

History

Received：2021-04-10
Revised：2021-06-09
Accepted：2021-06-14

Affiliations

^a State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China

^b State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center, Chengdu 610041, China

References

Share

https://castjournals.cast.org.cn/joweb/ccl/EN/10.1016/j.cclet.2021.06.032

Share to

Scan QR to access full text

Cite this article

BibTeX

Citations

表12种不同金属材料的力学参数

科 Family	属数 Number of genus	种数 Number of species	占总种数比例 Percentage of total species (%)	属 Genus	种数 Number of species	占总种数比例 Percentage of total species (%)
鹅膏菌科Amanitaceae	2	11	5.26	鹅膏菌属 Amanita	10	4.78
小菇科 Mycenaceae	2	12	5.74	丝盖伞属 Inocybe	5	2.39
多孔菌科 Polyporaceae	8	14	6.70	蜡蘑属 Laccaria	5	2.39
红菇科 Russulaceae	3	23	11.00	小皮伞属 Marasmius	6	2.87
				小菇属 Mycena	11	5.26
				光柄菇属 Pluteus	5	2.39
				红菇属 Russula	17	8.13
				栓菌属 Trametes	5	2.39

关闭全屏

BibTeX
EndNote
RefWorks
TxT

Fig. 1 Schematic illustration of acidic tumor microenvironment and the applications and mechanisms of NaHCO₃-based cancer therapy.

Fig. 2 Tumor acidosis will result in the following results: Facilitating tumor invasion and metastasis by promoting EMT and matrix degradation; affecting immune cells function to promote immune escape; reducing drug entry into cells and increasing drug efflux by secreting exosomes to acquire drug resistance; chronic autophagy producing amino acids and ATP to promote tumor survival.

Fig. 3 Cellular uptake of doxorubicin in the presence or absence of NaHCO₃, examined by (A) fluorescent microscopy (scale bar: 20 μm), (B) flow cytometry and (C) quantifying intracellular doxorubicin. Reproduced with permission [113]. Copyright 2020, Elsevier Publishing Group.

Fig. 4 Schematics of the anticancer mechanisms of NaHCO₃-based therapy. (1) Inhibition of tumor invasion and metastasis: reduced lymph node involvement and circulating tumor cells (CTC), and inhibited cathepsin B activity; (2) inhibition of immune evasion: increased immune cells number, and improved ACT efficacy and checkpoint inhibition; (3) inhibition of drug resistance: decreased weak-base drug ionization, and restored mTORC1 sensitivity to rapamycin; (4) inhibition of hypoxia and autophagy: reduced expression of pro-autophagy signals, and enhanced SVCT2 activity to inhibit the activity of HIF-1α.

Articles: Latest Articles; Most Read; Collections

Updates: Events; News; Multimedia

About: About Us

Contact

No. 86 Xueyuan South Road, Haidian District, Beijing

100081

010-62199257

qkjq@cast.org.cn

Copyright © 2025 China Association for Science and Technology. All rights reserved. For all open access content, the relevant licensing terms apply.
Sponsored by the Office of the Leading Group for Cybersecurity and Informatization of CAST, and supported by Science and Technology Review Publishing House