Article(id=1322926852729352335, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926740955341011, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.10.014, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793339940483, onlineDateStr=2026-10-30, pubDate=1760025600000, pubDateStr=2025-10-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339940483, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339940483, creator=13701087609, updateTime=1793339940483, updator=13701087609, issue=Issue{id=1322926740955341011, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='10', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1760025600000', pubDateStr='2025-10-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339913834, creator='13701087609', updateTime=1793340753123, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322930261259846420, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926740955341011, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322930261259846421, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926740955341011, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=67, endPage=71, ext={EN=ArticleExt(id=1322926852993593488, articleId=1322926852729352335, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Effects of Ethanol Extract from Tengligen(Radix Actinidiae Chinensis)on Apoptosis and Malignant Biological Behavior of Non-Small Cell Lung Cancer, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective

To explore the effects of ethanol extract from Tengligen(Radix Actinidiae Chinensis)on apoptosis and malignant biological behavior of non-small cell lung cancer.

Methods

The logarithmic growth stage non-small cell lung cancer cells A549 were selected to add different concentrations ethanol extract of Tengligen(Radix Actinidiae Chinensis)(0,10,20,40 μg/mL).The proliferation inhibition rate of A549 cells was measured by using MTT assay.Annexin V-FITCwas used to measure of A549 cells apoptosis rate.Western Blot was used to determine the expressions of apoptotic proteins Bax and Bcl-2.The invasive ability of A549 cells was measured by using Transwell method.The scratch healing rate of A549 cells was measured by using scratch experiments.

Result

The cell proliferation inhibition rates of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis with the dose of 0μg/mL(P<0.05),and it showed a dose-dependent effect.The Bax grayscale values of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL,while the Bcl-2 grayscale values were lower than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL(P<0.05),and showed a dose-dependent effect.The cell invasion rate of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL(P<0.05),and it showed a dose-dependent effect.The scratch healing rate of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL(P<0.05),and it showed a dose-dependent effect.

Conclusion

Ethanol extract of Tengligen(Radix Actinidiae Chinensis)can inhibit cell proliferation,invasion and migration,and induce apoptosis in non-small cell lung cancer A549 cells.It was related to Bax expression up-regulation and Bcl-2 expression down-regulation.

, authors=Lina HUANG, Yan JIN, Mengjing CHEN, Fei LI, Xiaofang ZHOU, Zhangxuan SHOU, authorsList=Lina HUANG, Yan JIN, Mengjing CHEN, Fei LI, Xiaofang ZHOU, Zhangxuan SHOU, authorCompany=null, correspAuthors=Zhangxuan SHOU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322926856009298081, articleId=1322926852729352335, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的

探讨藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响。

方法

取对数生长期非小细胞肺癌细胞A549,加入不同浓度(0、10、20和40μg/mL)藤梨根乙醇提取物。采用MTT法测定A549细胞增殖抑制率;采用Annexin V-FITC测定A549细胞凋亡率;采用Western blot测定凋亡蛋白Bax和B淋巴细胞瘤-2基因(B-cell lymphoma-2,Bcl-2)表达;采用Transwell法测定A549细胞侵袭能力;采用划痕实验测定A549细胞划痕愈合率。

结果

10、20、40μg/mL的藤梨根乙醇提取物细胞增殖抑制率高于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物细胞凋亡率高于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物Bax灰度值高于0μg/mL藤梨根乙醇提取物,而Bcl-2灰度值低于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物细胞侵袭率低于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物划痕愈合率低于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。

结论

藤梨根乙醇提取物可抑制非小细胞肺癌A549细胞的增殖、侵袭和迁移,诱导其细胞凋亡,与上调Bax表达及下调Bcl-2表达有关。

, authors=黄丽娜, 金艳, 陈梦静, 李菲, 周晓芳, 寿张轩, authorsList=黄丽娜, 金艳, 陈梦静, 李菲, 周晓芳, 寿张轩, authorCompany=null, correspAuthors=寿张轩, authorNote=

黄丽娜(1981-),女,浙江诸暨人,主管中药师,硕士,研究方向:中医药抗肿瘤药理。

, correspAuthorsNote=
寿张轩(1968-),男,浙江杭州人,主任药师,硕士,研究方向:高龄老人骨质疏松防治。E-mail:。
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黄丽娜(1981-),女,浙江诸暨人,主管中药师,硕士,研究方向:中医药抗肿瘤药理。

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黄丽娜(1981-),女,浙江诸暨人,主管中药师,硕士,研究方向:中医药抗肿瘤药理。

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LncRNA IGF2-AS基因通过靶向miR-370-3p对肺癌细胞增殖和凋亡的影响[J]. 中国老年学杂志,2021,41(23):5308-5313., articleTitle=LncRNA IGF2-AS基因通过靶向miR-370-3p对肺癌细胞增殖和凋亡的影响, refAbstract=null), Reference(id=1322926865085772021, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, doi=null, pmid=null, pmcid=null, year=2023, volume=45, issue=22, pageStart=2363, pageEnd=2366,2465, url=null, language=null, rfNumber=[25], rfOrder=24, authorNames=郑思化, 赵学正, 高伟, journalName=浙江医学, refType=null, unstructuredReference=郑思化,赵学正,高伟. siRNA沉默CAPN1基因对人骨肉瘤细胞MG-63增殖、侵袭及Bcl-2和Bax表达的影响[J]. 浙江医学,2023,45(22):2363-2366,2465., articleTitle=siRNA沉默CAPN1基因对人骨肉瘤细胞MG-63增殖、侵袭及Bcl-2和Bax表达的影响, refAbstract=null), Reference(id=1322926865161269494, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, doi=null, pmid=null, pmcid=null, year=2023, volume=30, issue=6, pageStart=1070, pageEnd=1074, url=null, language=null, rfNumber=[26], rfOrder=25, authorNames=薛丕良, 李星宇, 王向伟, journalName=中国中医药科技, refType=null, unstructuredReference=薛丕良,李星宇,王向伟,等. 参芪蛭龙汤对膜性肾病小鼠肾组织凋亡因子Bcl-2、Bax、Caspase-3的影响[J]. 中国中医药科技,2023,30(6):1070-1074., articleTitle=参芪蛭龙汤对膜性肾病小鼠肾组织凋亡因子Bcl-2、Bax、Caspase-3的影响, refAbstract=null)], funds=[Fund(id=1322926861369618649, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, awardId=82204649, language=CN, fundingSource=国家自然科学基金项目(82204649), fundOrder=null, country=null), Fund(id=1322926861449310426, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, awardId=2023KY879, language=CN, fundingSource=浙江省医药卫生科技计划项目(2023KY879), fundOrder=null, country=null), Fund(id=1322926861545779419, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, awardId=2024ZL486; 2023ZR097, language=CN, fundingSource=浙江省中医药科技计划项目(2024ZL486; 2023ZR097), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1322926856336453794, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, xref=null, ext=[AuthorCompanyExt(id=1322926856349036707, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, companyId=1322926856336453794, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=The Second Affiliated Hospital of Zhejiang Chinese Medical University,Hangzhou 310005,Zhejiang,China), AuthorCompanyExt(id=1322926856357425316, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, companyId=1322926856336453794, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=浙江中医药大学附属第二医院,浙江 杭州 310005)])], figs=[ArticleFig(id=1322926858471354571, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, language=EN, label=null, caption=null, figureFileSmall=cKe9X52a8ZWc62UIPnR9aw==, figureFileBig=f8yGTi/zR+lphXZT+EWkHg==, tableContent=null), ArticleFig(id=1322926860073578700, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, language=CN, label=图1, caption=不同浓度藤梨根乙醇提取物对A549细胞凋亡率比较, figureFileSmall=cKe9X52a8ZWc62UIPnR9aw==, figureFileBig=f8yGTi/zR+lphXZT+EWkHg==, tableContent=null), ArticleFig(id=1322926860308459725, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, language=EN, label=null, caption=null, figureFileSmall=I717bQstQUZwYXo4W5Nf/A==, figureFileBig=TcV6LdKjZ8y9XcRyDRAdOg==, tableContent=null), ArticleFig(id=1322926860413317326, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, language=CN, label=图2, caption=不同浓度藤梨根乙醇提取物对凋亡蛋白表达, figureFileSmall=I717bQstQUZwYXo4W5Nf/A==, figureFileBig=TcV6LdKjZ8y9XcRyDRAdOg==, tableContent=null), ArticleFig(id=1322926860484620495, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别n(复孔)A549细胞增殖抑制率/(%)
0 μg/mL藤梨根乙醇提取物组30
10 μg/mL藤梨根乙醇提取物组317.86±4.15a
20 μg/mL藤梨根乙醇提取物组338.97±8.74ab
40 μg/mL藤梨根乙醇提取物组360.23±10.49abc
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不同浓度藤梨根乙醇提取物对A549细胞增殖抑制率比较()

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组别n(复孔)A549细胞增殖抑制率/(%)
0 μg/mL藤梨根乙醇提取物组30
10 μg/mL藤梨根乙醇提取物组317.86±4.15a
20 μg/mL藤梨根乙醇提取物组338.97±8.74ab
40 μg/mL藤梨根乙醇提取物组360.23±10.49abc
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组别n(复孔)A549细胞凋亡率/(%)
0 μg/mL藤梨根乙醇提取物组30
10 μg/mL藤梨根乙醇提取物组317.86±4.15a
20 μg/mL藤梨根乙醇提取物组338.97±8.74ab
40 μg/mL藤梨根乙醇提取物组360.23±10.49abc
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不同浓度藤梨根乙醇提取物对A549细胞凋亡率比较()

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组别n(复孔)A549细胞凋亡率/(%)
0 μg/mL藤梨根乙醇提取物组30
10 μg/mL藤梨根乙醇提取物组317.86±4.15a
20 μg/mL藤梨根乙醇提取物组338.97±8.74ab
40 μg/mL藤梨根乙醇提取物组360.23±10.49abc
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组别n(复孔)Bax灰度值Bcl-2灰度值
0 μg/mL藤梨根乙醇提取物组30.28±0.071.36±0.23
10 μg/mL藤梨根乙醇提取物组30.47±0.12a1.02±0.17a
20 μg/mL藤梨根乙醇提取物组30.78±0.24ab0.74±0.18ab
40 μg/mL藤梨根乙醇提取物组31.09±0.26abc0.37±0.09abc
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不同浓度藤梨根乙醇提取物对凋亡蛋白表达比较()

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组别n(复孔)Bax灰度值Bcl-2灰度值
0 μg/mL藤梨根乙醇提取物组30.28±0.071.36±0.23
10 μg/mL藤梨根乙醇提取物组30.47±0.12a1.02±0.17a
20 μg/mL藤梨根乙醇提取物组30.78±0.24ab0.74±0.18ab
40 μg/mL藤梨根乙醇提取物组31.09±0.26abc0.37±0.09abc
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组别n(复孔)A549细胞侵袭率/(%)
0 μg/mL藤梨根乙醇提取物组379.94±5.52
10 μg/mL藤梨根乙醇提取物组352.31±6.77a
20 μg/mL藤梨根乙醇提取物组332.16±7.38ab
40 μg/mL藤梨根乙醇提取物组315.52±3.46abc
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不同浓度藤梨根乙醇提取物对细胞侵袭率比较()

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组别n(复孔)A549细胞侵袭率/(%)
0 μg/mL藤梨根乙醇提取物组379.94±5.52
10 μg/mL藤梨根乙醇提取物组352.31±6.77a
20 μg/mL藤梨根乙醇提取物组332.16±7.38ab
40 μg/mL藤梨根乙醇提取物组315.52±3.46abc
), ArticleFig(id=1322926861201846487, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926852729352335, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别n(复孔)划痕愈合率/(%)
0 μg/mL藤梨根乙醇提取物组374.97±8.82
10 μg/mL藤梨根乙醇提取物组352.35±7.71a
20 μg/mL藤梨根乙醇提取物组338.86±6.68ab
40 μg/mL藤梨根乙醇提取物组322.31±5.34abc
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不同浓度藤梨根乙醇提取物对划痕愈合率比较()

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组别n(复孔)划痕愈合率/(%)
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10 μg/mL藤梨根乙醇提取物组352.35±7.71a
20 μg/mL藤梨根乙醇提取物组338.86±6.68ab
40 μg/mL藤梨根乙醇提取物组322.31±5.34abc
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藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响
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黄丽娜 , 金艳 , 陈梦静 , 李菲 , 周晓芳 , 寿张轩
中华中医药学刊 | 国家项目点击 2025,43(10): 67-71
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中华中医药学刊 |国家项目点击 2025 , 43 (10) : 67 -71
藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响
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黄丽娜, 金艳, 陈梦静, 李菲, 周晓芳, 寿张轩
作者信息
  • 浙江中医药大学附属第二医院,浙江 杭州 310005
通讯作者:
寿张轩(1968-),男,浙江杭州人,主任药师,硕士,研究方向:高龄老人骨质疏松防治。E-mail:。
作者简介:

黄丽娜(1981-),女,浙江诸暨人,主管中药师,硕士,研究方向:中医药抗肿瘤药理。

Effects of Ethanol Extract from Tengligen(Radix Actinidiae Chinensis)on Apoptosis and Malignant Biological Behavior of Non-Small Cell Lung Cancer
Lina HUANG, Yan JIN, Mengjing CHEN, Fei LI, Xiaofang ZHOU, Zhangxuan SHOU
Affiliations
  • The Second Affiliated Hospital of Zhejiang Chinese Medical University,Hangzhou 310005,Zhejiang,China
出版时间: 2025-10-10 doi: 10.13193/j.issn.1673-7717.2025.10.014
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目的

探讨藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响。

方法

取对数生长期非小细胞肺癌细胞A549,加入不同浓度(0、10、20和40μg/mL)藤梨根乙醇提取物。采用MTT法测定A549细胞增殖抑制率;采用Annexin V-FITC测定A549细胞凋亡率;采用Western blot测定凋亡蛋白Bax和B淋巴细胞瘤-2基因(B-cell lymphoma-2,Bcl-2)表达;采用Transwell法测定A549细胞侵袭能力;采用划痕实验测定A549细胞划痕愈合率。

结果

10、20、40μg/mL的藤梨根乙醇提取物细胞增殖抑制率高于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物细胞凋亡率高于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物Bax灰度值高于0μg/mL藤梨根乙醇提取物,而Bcl-2灰度值低于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物细胞侵袭率低于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。10、20、40μg/mL的藤梨根乙醇提取物划痕愈合率低于0μg/mL藤梨根乙醇提取物(P<0.05),且呈剂量依赖性。

结论

藤梨根乙醇提取物可抑制非小细胞肺癌A549细胞的增殖、侵袭和迁移,诱导其细胞凋亡,与上调Bax表达及下调Bcl-2表达有关。

藤梨根乙醇提取物  /  非小细胞肺癌  /  凋亡  /  恶性生物学行为
Objective

To explore the effects of ethanol extract from Tengligen(Radix Actinidiae Chinensis)on apoptosis and malignant biological behavior of non-small cell lung cancer.

Methods

The logarithmic growth stage non-small cell lung cancer cells A549 were selected to add different concentrations ethanol extract of Tengligen(Radix Actinidiae Chinensis)(0,10,20,40 μg/mL).The proliferation inhibition rate of A549 cells was measured by using MTT assay.Annexin V-FITCwas used to measure of A549 cells apoptosis rate.Western Blot was used to determine the expressions of apoptotic proteins Bax and Bcl-2.The invasive ability of A549 cells was measured by using Transwell method.The scratch healing rate of A549 cells was measured by using scratch experiments.

Result

The cell proliferation inhibition rates of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis with the dose of 0μg/mL(P<0.05),and it showed a dose-dependent effect.The Bax grayscale values of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL,while the Bcl-2 grayscale values were lower than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL(P<0.05),and showed a dose-dependent effect.The cell invasion rate of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL(P<0.05),and it showed a dose-dependent effect.The scratch healing rate of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the doses of 10,20 and 40μg/mL were higher than that of ethanol extract of Tengligen(Radix Actinidiae Chinensis)with the dose of 0μg/mL(P<0.05),and it showed a dose-dependent effect.

Conclusion

Ethanol extract of Tengligen(Radix Actinidiae Chinensis)can inhibit cell proliferation,invasion and migration,and induce apoptosis in non-small cell lung cancer A549 cells.It was related to Bax expression up-regulation and Bcl-2 expression down-regulation.

ethanol extract of Tengligen(Radix Actinidiae Chinensis)  /  non-small cell lung cancer  /  apoptosis  /  malignant biological behavior
黄丽娜, 金艳, 陈梦静, 李菲, 周晓芳, 寿张轩. 藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响. 中华中医药学刊, 2025 , 43 (10) : 67 -71 . DOI: 10.13193/j.issn.1673-7717.2025.10.014
Lina HUANG, Yan JIN, Mengjing CHEN, Fei LI, Xiaofang ZHOU, Zhangxuan SHOU. Effects of Ethanol Extract from Tengligen(Radix Actinidiae Chinensis)on Apoptosis and Malignant Biological Behavior of Non-Small Cell Lung Cancer[J]. Chinese Archives of Traditional Chinese Medicine, 2025 , 43 (10) : 67 -71 . DOI: 10.13193/j.issn.1673-7717.2025.10.014
肺癌是常见的一种恶性肿瘤,其发病率呈逐年增高趋势[1]。非小细胞肺癌是肺癌最常见的一种病理类型,占肺癌发病的85%以上,5年生存率仅为20%左右,严重威胁人们生命健康[2-3]。尽管手术切除仍为治愈非小细胞肺癌的重要方法,但辅助治疗在预防非小细胞肺癌复发和转移方面尤为关键[4-5]。随着中医药相关领域深入研究,在非小细胞肺癌临床治疗中发挥重要作用。藤梨根是猕猴桃科植物猕猴桃的根,性寒、味甘酸,具有祛风除湿、清热解毒、利尿止血等功效,具有抗病毒、抗氧化和抗肿瘤等作用,广泛用于多种胃肠道恶性肿瘤中,关于其在肺癌方面研究甚少[6]。因此,本研究探讨藤梨根乙醇提取物诱导非小细胞肺癌凋亡及对恶性生物学行为的影响,深入了解其作用机制,以期为临床治疗提供新方案。
人非小细胞肺癌A549细胞(中国科学院上海细胞库)。
藤梨根乙醇提取物(西安千草生物技术有限公司),胎牛血清(Gibco公司),胰酶(上海慧颖生物科技有限公司),MTT试剂(Gibco公司)、DMEM培养(Gibco公司),二甲基亚砜(Dimethyl sulfoxide,DMSO)(Sigma公司),磷酸盐缓冲液(上海慧颖生物科技有限公司),BCA蛋白试剂盒(碧云天生物技术有限公司),Bax多克隆抗体(北京百奥莱博科技有限公司),B淋巴细胞瘤-2基因(B-cell lymphoma-2,Bcl-2)多克隆抗体(北京百奥莱博科技有限公司),RIPA细胞裂解液(北京索莱宝生物公司)。
取非小细胞肺癌细胞A549,解冻,DMEM培养液稀释,离心8 min,弃上清;加入含10%胎牛血清培养,传代。
取对数生长期A549细胞,胰酶消化,按1×106密度细胞数,以100μL/孔接种于96孔培养板中,于37℃、5%CO2培养。将非小细胞肺癌细胞A549分为0、10、20、40μg/mL藤梨根乙醇提取物组,设3个复孔。分别加入含药物的培养基200μL,培养48 h,于培养结束前4 h,加入MTT 20μL/孔,培养4 h后,加入DMSO 150μL/孔,以波长490 nm在酶标仪上测定吸光度值。
取对数生长期非小细胞肺癌细胞A549,加入0、10、20、40μg/mL藤梨根乙醇提取物培养48 h后收集细胞,取1×106细胞,加入Annexin V缓冲液10μL悬浮细胞,再于各管中加入5μL Annexin V和5μL碘化丙啶,温和混匀,避光15 min,再加入500μL Annexin V缓冲液,离心8 min,采用流式细胞仪测定细胞凋亡率。
取对数生长期A549细胞,加入0、10、20、40μg/mL藤梨根乙醇提取物干预48 h。收集细胞,加入RIPA细胞裂解液,冰浴裂解30 min,提取总蛋白,离心8 min,取上清。运用BCA法测定蛋白含量。运用SDS-PAGE凝胶电泳,转膜,以3%BSA封闭60 min后,加入Bax(1∶1000)和Bcl-2(1∶1000),4℃过夜,以TBST漂洗,加入二抗,常温孵育60 min,漂洗,加入ECL工作液,显色,测定条带灰度值。
将Transwell小室提前铺上Matrigel基质胶。加入0、10、20、40μg/mL藤梨根乙醇提取物处理后,收集各组细胞并以1×106个/孔密度铺于小室的上室,培养48 h,再于下室加入10%胎牛血清培养液作为化学引诱物;然后再以磷酸盐缓冲液洗涤后,向每孔中加入1%结晶紫和多聚甲醛,显微镜下计算细胞侵袭率。
首先采用马克笔在铺板前于6孔板背面笔直画3条横线作为标记。加入0、10、20、40μg/mL藤梨根乙醇提取物处理后,收集各组细胞并以1×106个/孔密度培养于6孔板,于5% CO2培养箱中培养至细胞长满。然后再以20μL枪头垂直于孔板背面的横线画1条笔直的道痕,作为起始时刻拍照,再应用磷酸盐缓冲液洗涤,将培养板放于培养箱中培养24 h后拍照。A549细胞划痕愈合率应用Image J软件计算。细胞划痕愈合率=(划痕起始宽度-划痕端点宽度)/划痕起始宽度×100%。
运用SPSS25.0处理。计量资料采用表示,多组间采用方差分析,两两比较采用LSD-t检验。P<0.05表示差异有统计学意义。
10、20 、40 μg/mL的藤梨根乙醇提取物组细胞增殖抑制率高于0μg/mL藤梨根乙醇提取物组(P<0.05),且呈剂量依赖性。见表1。
10、20 、40 μg/mL的藤梨根乙醇提取物组细胞凋亡率高于0μg/mL藤梨根乙醇提取物组(P<0.05),且呈剂量依赖性。见表2、图1。
10、20 、40 μg/mL的藤梨根乙醇提取物组Bax灰度值高于0μg/mL藤梨根乙醇提取物组,而Bcl-2灰度值低于0μg/mL藤梨根乙醇提取物组(P<0.05),且呈剂量依赖性。见表3、图2。
10、20 、40 μg/mL的藤梨根乙醇提取物组细胞侵袭率低于0μg/mL藤梨根乙醇提取物组(P<0.05),且呈剂量依赖性。见表4。
10、20 、40 μg/mL的藤梨根乙醇提取物组划痕愈合率低于0μg/mL藤梨根乙醇提取物组(P<0.05),且呈剂量依赖性。见表5。
由于非小细胞肺癌早期无明显的症状及体征,发病隐匿,绝大多数患者确诊时均已是晚期,预后差[7-8]。若非小细胞肺癌发生远处转移,则患者中位生存期不超过6个月,而针对肺癌患者进行早期诊断会显著延长生存时间,甚至可能会治愈患者[9-10]。非小细胞肺癌的发生、发展与癌细胞迁移、增殖及凋亡等生物学过程密切相关,故而寻找有效促进癌细胞凋亡、抑制癌细胞增殖和迁移的药物对改善非小细胞肺癌预后尤为关键[11-13]。
藤梨根别名阳桃根,是猕猴桃科植物猕猴桃的根,主产于我国长江流域及西北、湖北和东北,归膀胱、肝、胃经,性寒,味甘酸,具有清热解毒、祛风除湿功效。药理研究表明,藤梨根乙醇提取物具有抗病毒、抗氧化、抗肿瘤作用[14-15]。王晓戎等[16]研究表明,结直肠癌细胞HCT-15、LoVo经藤梨根乙醇提取物处理后,细胞活力以剂量和时间依赖性下降;通过不同浓度藤梨根乙醇提取物处理后,细胞凋亡率提高,由此可见藤梨根乙醇提取物可发挥较强的抗肿瘤作用,且可显著诱导结直肠癌细胞凋亡[17-18]。本研究表明,10、20、40μg/mL的藤梨根乙醇提取物组细胞增殖抑制率高于0μg/mL藤梨根乙醇提取物组,且呈剂量依赖性,由此可见藤梨根乙醇提取物可显著抑制A549细胞增殖;10、20、40μg/mL的藤梨根乙醇提取物组细胞凋亡率高于0μg/mL藤梨根乙醇提取物组,且呈剂量依赖性,由此可见藤梨根乙醇提取物可显著诱导A549细胞凋亡;10、20、40μg/mL的藤梨根乙醇提取物组细胞侵袭率和划痕愈合率低于0μg/mL藤梨根乙醇提取物组,且呈剂量依赖性,由此可见藤梨根乙醇提取物可显著抑制A549细胞恶性生物学行为进展[19-20]。
诱导癌细胞凋亡是治疗非小细胞肺癌的有效策略[21-23]。在线粒体凋亡途径中,Bax被激活移位至线粒体膜,开放线粒体通道,导致Caspase活化因子释放增多,加速细胞凋亡。Bcl-2表达下调可诱导肿瘤细胞凋亡,发挥协同促凋亡效应[24-26]。本研究表明,10、20、40μg/mL的藤梨根乙醇提取物Bax灰度值高于0μg/mL藤梨根乙醇提取物组,而Bcl-2灰度值低于0μg/mL藤梨根乙醇提取物组,且呈剂量依赖性,由此可见藤梨根乙醇提取物可显著上调Bax表达及下调Bcl-2表达。
综上所述,藤梨根乙醇提取物可抑制细胞增殖、侵袭和迁移,诱导细胞凋亡,与上调Bax表达及下调Bcl-2表达有关。
  • 国家自然科学基金项目(82204649)
  • 浙江省医药卫生科技计划项目(2023KY879)
  • 浙江省中医药科技计划项目(2024ZL486; 2023ZR097)
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2025年第43卷第10期
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doi: 10.13193/j.issn.1673-7717.2025.10.014
  • 首发时间:2026-10-30
  • 出版时间:2025-10-10
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基金
国家自然科学基金项目(82204649)
浙江省医药卫生科技计划项目(2023KY879)
浙江省中医药科技计划项目(2024ZL486; 2023ZR097)
作者信息
    浙江中医药大学附属第二医院,浙江 杭州 310005

通讯作者:

寿张轩(1968-),男,浙江杭州人,主任药师,硕士,研究方向:高龄老人骨质疏松防治。E-mail:。
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https://castjournals.cast.org.cn/joweb/zhzyyxk/CN/10.13193/j.issn.1673-7717.2025.10.014
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2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
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