Article(id=1322927087396467570, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926985957221241, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.11.017, 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=1793339996432, onlineDateStr=2026-10-30, pubDate=1762704000000, pubDateStr=2025-11-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339996432, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339996432, creator=13701087609, updateTime=1793339996432, updator=13701087609, issue=Issue{id=1322926985957221241, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='11', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1762704000000', pubDateStr='2025-11-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339972247, creator='13701087609', updateTime=1793340743335, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322930220201804556, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926985957221241, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322930220201804557, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926985957221241, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=74, endPage=77, ext={EN=ArticleExt(id=1322927087711040371, articleId=1322927087396467570, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Study on Synergistic Effect of Astragalus Polysaccharide in Chemotherapy of Cervical Cancer, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To study the synergistic effect of Astragalus polysaccharide(APS)on chemotherapy for cervical cancer transplanted tumor in nude mice,and to analyze its mechanism.
Methods Human cervical cancer Hela cells were cultured in vitro and inoculated into the subcutaneous area of the right back near the armpit of nude mice. The tumor-bearing mice were randomly divided into eight groups:blank group,chemotherapy group(cisplatin,DDP),APSlow dose group(50 mg/kg),APSmedium dose group(100 mg/kg),APShigh dose group(200 mg/kg),APSlow,medium and high dose+DDPgroup(combination group). The general condition and tumor growth of tumor-bearing nude mice were observed during treatment,the tumor growth inhibition rate was calculated,and the expressions of glucose-regulated protein 78(GRP78),C/EBP homologous protein(CHOP),Caspase-3 Cysteinyl aspartate specific protease 3),microtubule-associated protein light chain 3 beta typeⅡ(LC3-Ⅱ)proteins in immunohistochemical and western blot tumor tissues were detected.
Results Compared with DDP group,after APSintervention,the activity of nude mice increased,the glossiness of skin and hair increased,the degree of wasting improved significantly,and the body weight increased. The tumor mass of combination group decreased significantly(P<0.01). The number of nuclei in the tumor tissue of the combination group significantly decreased,with a large number of nuclei reduced and fragmented. The expression levels of GRP78,CHOP,Caspase-3 and LC3-II in the combination group showed a dose-dependent increase trend(P<0.01).
Conclusion APScan alleviate endoplasmic reticulum stress(ERS),stimulate mitochondria autophagy,promote tumor cell apoptosis,reduce chemotherapy resistance of cervical cancer cells,and has a synergistic and toxic effect.
, authors=Kaiyan CHEN
1, Wei YANG
2, Cai ZHAO
2, Juan QIN
3, authorsList=Kaiyan CHEN, Wei YANG, Cai ZHAO, Juan QIN, authorCompany=null, correspAuthors=Juan QIN, 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=1322927093872472970, articleId=1322927087396467570, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=黄芪多糖在宫颈癌化疗中增效作用的研究, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 研究黄芪多糖(Astragalus polysaccharide,APS)对宫颈癌裸鼠移植瘤化疗的增效作用,并分析其作用机制。
方法 体外培养人宫颈癌Hela细胞,接种于裸鼠右侧背部近腋窝处皮下,将荷瘤小鼠随机分为8组:空白组、化疗组[顺铂(Cisplatin,DDP)]、低剂量APS组(50 mg/kg)、中剂量APS组(100 mg/kg)、高剂量APS组(200 mg/kg)、(低、中、高剂量APS)+DDP组(联合组)。观察治疗期间荷瘤裸鼠的一般状况以及肿瘤生长情况,计算肿瘤生长抑制率,通过免疫组化(Immunohistochemistry,IHC)及蛋白质印迹法(Western blotting,WB)检测肿瘤组织中葡萄糖调节蛋白78(Glucose-regulated protein78,GRP78)、增强子结合蛋白同源蛋白(C/EBPhomologous protein,CHOP)、含半胱氨酸的天冬氨酸蛋白水解酶3(Cysteinyl aspartate specific protease 3,Caspase-3)、微管相关蛋白1轻链3-Ⅱ(Microtubule-associated protein light chain 3 beta typeⅡ,LC3-Ⅱ)蛋白的表达。
结果 与DDP组比较,经APS干预后的裸鼠活动增加,皮肤、毛发光泽度增加,消瘦程度明显好转、体质量增加;联合组的瘤体质量明显下降(P<0.01)。光镜见:联合组瘤体组织细胞核数量明显减少、大量细胞核减少、碎裂。联合组蛋白GRP78、CHOP、Caspase-3、LC3-Ⅱ表达水平均呈剂量依赖性增加趋势(P<0.01)。
结论 APS可通过减轻内质网应激(endoplasmic reticulum stress,ERS)、刺激线粒体发生自噬、促进肿瘤细胞凋亡,降低宫颈癌细胞的化疗耐药性,具有增效减毒作用。
, authors=陈开艳
1, 杨伟
2, 赵彩
2, 秦娟
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陈开艳(1984-),女,贵州贵阳人,主治医师,硕士在读,研究方向:妇科肿瘤与生殖内分泌。
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