Affiliated Foshan Maternity and Child Healthcare Hospital, Southern Medical University, Foshan 528000, PR China.
Department of Emergency, Affiliated Foshan Maternity and Child Healthcare Hospital, Southern Medical University, Foshan 528000, PR China.
Aging (Albany NY). 2022 Jul 19;14(14):5812-5837. doi: 10.18632/aging.204185.
Traditional Chinese medicine (TCM) is a promising strategy for effectively treating cancer by inducing cellular senescence with minimal side effects. Si-Wu-Tang (SWT) is a TCM composed of four herbs that is commonly used in China for the treatment of gynecological diseases; SWT can prevent breast cancer (BC), but the molecular mechanism by which SWT induces cellular senescence and its clinical application value remain unknown. We identified 335 differentially expressed genes (DEGs) in SWT-treated MCF-7 cells through Gene Expression Omnibus (GEO) dataset analysis. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses revealed the enrichment of biological processes and key signaling pathways including cellular senescence, the cell cycle, the MAPK signaling pathway, and the p53 signaling pathway. Additionally, SWT induced BC cell senescence by upregulating the expression of 33 aging/senescence-induced genes (ASIGs). According to LASSO regression analysis, NDRG1, ERRFI1, SOCS1, IRS2, IGFBP4, and BIRC3 levels were associated with BC prognosis and were used to develop risk scores. ERRFI1, SOCS1, IRS2, IGFBP4, and BIRC3 were identified as protective factors ( < 0.05, HR < 1), while NDRG1 was identified as a risk factor ( < 0.05, HR > 1). Notably, patients with low risk scores had increased senescence-associated secretory phenotypes (SASPs) and immune cell infiltration. Overall, we systematically integrated biological databases and biocomputational methods to reveal the mechanisms by which SWT induces senescence in breast cancer and its clinical value.
传统中药(TCM)通过诱导细胞衰老来有效治疗癌症,副作用极小,是一种很有前途的策略。四物汤(SWT)是一种由四种草药组成的中药,在中国常用于治疗妇科疾病;SWT 可以预防乳腺癌(BC),但其诱导细胞衰老的分子机制及其临床应用价值尚不清楚。我们通过基因表达综合数据库(GEO)数据集分析,鉴定出 SWT 处理 MCF-7 细胞中的 335 个差异表达基因(DEGs)。基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析显示,生物过程和关键信号通路包括细胞衰老、细胞周期、MAPK 信号通路和 p53 信号通路的富集。此外,SWT 通过上调 33 个衰老/衰老诱导基因(ASIGs)的表达诱导 BC 细胞衰老。根据 LASSO 回归分析,NDRG1、ERRFI1、SOCS1、IRS2、IGFBP4 和 BIRC3 的水平与 BC 预后相关,并用于开发风险评分。ERRFI1、SOCS1、IRS2、IGFBP4 和 BIRC3 被鉴定为保护因素(<0.05,HR<1),而 NDRG1 被鉴定为风险因素(<0.05,HR>1)。值得注意的是,风险评分低的患者具有增加的衰老相关分泌表型(SASPs)和免疫细胞浸润。总的来说,我们系统地整合了生物数据库和生物计算方法,揭示了 SWT 诱导乳腺癌衰老的机制及其临床价值。