Article(id=1317115123811074187, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317115107243573307, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.04.004, 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=1791954316332, onlineDateStr=2026-10-14, pubDate=1775750400000, pubDateStr=2026-04-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1791954316332, onlineIssueDateStr=2026-10-14, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1791954316332, creator=13701087609, updateTime=1791954316332, updator=13701087609, issue=Issue{id=1317115107243573307, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='4', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1775750400000', pubDateStr='2026-04-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1791954312382, creator='13701087609', updateTime=1791958738709, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1317133672680116252, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317115107243573307, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1317133672680116253, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317115107243573307, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=17, endPage=20, ext={EN=ArticleExt(id=1317115124045955212, articleId=1317115123811074187, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Regulatory Effect of Astragalus Polysaccharide on Immune Function and Tumor Cell Growth of Lung Cancer Mice, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the regulation effect of astragalus polysaccharide on lung cancer-bearing mice in vivo immunity and tumor cell growth.
Methods A total of 72 SPF-grade C57BL/6J mice were randomly divided into a model group(treated with an equal volume of normal saline by gavage), a positive control group(treated with cisplatin 6.0 mg/kg via intraperitoneal injection), a low-dose group(treated with astragalus polysaccharide solution 50 mg/kg by gavage, at a concentration of 1.0 mg/mL)and a high-dose group(treated with astragalus polysaccharide solution 100 mg/kg by gavage, at a concentration of 1.0 mg/mL), with 18 mice in each group. The tumor volume, tumor mass, tumor inhibition rate, T lymphocyte count in peripheral blood and Survivin protein expression in tumor tissues were compared among the groups 14 days after modeling. Flow cytometry was used to detect the staging distribution of tumor cells in the tumor tissues of mice in each group.
Results Compared with those in the model group, the tumor volume and tumor mass in the positive control, low-dose and high-dose groups were all significantly lower(P<0.05). Specifically, the tumor volume and tumor mass in the positive control group were significantly lower than those in the low-dose and high-dose groups(P<0.05), while the tumor inhibition rate was significantly higher(P<0.05). Furthermore, the tumor volume and tumor mass in the high-dose group were lower than those in the low-dose group(P<0.05), and the tumor inhibition rate was higher(P<0.05). In terms of peripheral blood, the levels of CD4+ and CD4+/CD8+ in the low-dose and high-dose groups were higher than those in the model and positive control groups(P<0.05), while the CD8+ level was lower(P<0.05). Additionally, the levels of CD4+ and CD4+/CD8+ in the high-dose group were higher than those in the low-dose group(P<0.05), and the CD8+ level was lower(P<0.05). Regarding Survivin protein expression in tumor tissues, the scores in the positive control, low-dose and high-dose groups were all lower than those in the model group(P<0.05). Notably, the Survivin protein expression in the positive control group was lower than that in the low-dose and high-dose groups(P<0.05), and the expression in the high-dose group was lower than that in the low-dose group(P<0.05). Finally, the proportions of S-phase cells in tumor tissues were higher in the positive control, low-dose and high-dose groups compared to those in the model group(P<0.05). Specifically, the proportion of S-phase cells in the positive control group was higher than that in the low-dose and high-dose groups(P<0.05), and the proportion in the high-dose group was higher than that in the low-dose group(P<0.05).
Conclusion Astragalus polysaccharide can regulate the immune function and reduce the expression of Survivin protein in the treatment of lung cancer-bearing mice, thereby inhibiting the growth of tumor cells.
, authors=Jianguo TU
1, Wenmiao CAO
2, Buhai WANG
2, authorsList=Jianguo TU, Wenmiao CAO, Buhai WANG, authorCompany=null, correspAuthors=null, 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=1317115124402471053, articleId=1317115123811074187, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=黄芪多糖对肺癌荷瘤小鼠机体免疫功能、肿瘤细胞生长的调节作用, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 探讨黄芪多糖对肺癌荷瘤小鼠机体免疫、肿瘤细胞生长的调节作用。
方法 选取无特定病原体(specific pathogen free,SPF)级的C57BL/6J小鼠72只,随机分为模型组(等量生理盐水灌胃)、阳性对照组(顺铂6.0 mg/kg腹腔注射)、低剂量组(黄芪多糖溶液50 mg/kg灌胃,浓度为1.0 mg/mL)、高剂量组(黄芪多糖溶液100 mg/kg灌胃,浓度为1.0 mg/mL)各18只,对比各组小鼠造模后第14天肿瘤体积、肿瘤瘤体质量、抑瘤率、外周血中T淋巴细胞、肿瘤组织中Survivin蛋白表达,采用流式细胞技术检测各组小鼠肿瘤组织中肿瘤细胞的分期分布情况。
结果 阳性对照组、低剂量组、高剂量组的肿瘤体积、肿瘤质量与模型组比较均更低(P<0.05);阳性对照组的肿瘤体积、肿瘤质量与低剂量组、高剂量组小鼠比较明显更低(P<0.05),抑瘤率相较于低剂量组、高剂量组则明显更高(P<0.05);高剂量组的肿瘤体积、肿瘤质量均低于低剂量组(P<0.05),抑瘤率高于低剂量组(P<0.05);低剂量组、高剂量组外周血中CD4+T淋巴细胞(cluster of differentiation 4,CD4+)、CD4+/CD8+T淋巴细胞(cluster of differentiation 8,CD8+)高于模型组和阳性对照组(P<0.05),CD8+水平低于模型组和阳性对照组(P<0.05);高剂量组外周血中CD4+、CD4+/CD8+高于低剂量组(P<0.05),CD8+水平低于低剂量组(P<0.05);阳性对照组、低剂量组、高剂量组的肿瘤组织中Survivin蛋白评分低于模型组(P<0.05),阳性对照组的Survivin蛋白评分低于低剂量组、高剂量组(P<0.05),高剂量组Survivin蛋白评分低于低剂量组(P<0.05);阳性对照组、低剂量组、高剂量组的肿瘤组织中S期细胞占比高于模型组(P<0.05),阳性对照组的S期细胞占比高于低剂量组、高剂量组(P<0.05),高剂量组S期细胞占比高于低剂量组(P<0.05)。
结论 黄芪多糖通过调节肺癌荷瘤小鼠免疫功能、降低Survivin蛋白表达,达到抑制肿瘤细胞生长的效果。
, authors=涂建国
1, 曹文淼
2, 汪步海
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涂建国(1974-),男,江苏宝应人,主任医师,学士,研究方向:肺癌。
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