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参芪固本方调控IL-17信号通路改善癌因性疲乏的作用机制

李鑫 方崇锴 黄越 李要轩 黄海福 吴先林 CHEN Zhesheng 李萌

中国药房2025,Vol.36Issue(14):1722-1729,8.
中国药房2025,Vol.36Issue(14):1722-1729,8.DOI:10.6039/j.issn.1001-0408.2025.14.06

参芪固本方调控IL-17信号通路改善癌因性疲乏的作用机制

Mechanism of Shenqi guben formula in improving cancer-related fatigue by regulating IL-17 signaling pathway

李鑫 1方崇锴 2黄越 3李要轩 3黄海福 3吴先林 4CHEN Zhesheng 5李萌3

作者信息

  • 1. 广州中医药大学深圳医院(福田)治未病中心,广东 深圳 518034
  • 2. 广州中医药大学科技创新中心,广州 510405
  • 3. 深圳市中医肿瘤医学中心,广东 深圳 518034||广州中医药大学深圳医院(福田)肿瘤科,广东 深圳 518034
  • 4. 深圳市中医肿瘤医学中心,广东 深圳 518034
  • 5. 圣约翰大学,美国纽约 11439
  • 折叠

摘要

Abstract

OBJECTIVE To explore the mechanism of Shenqi guben formula(SQGB)in improving cancer-related fatigue(CRF)based on network pharmacology and cellular experiments.METHODS Active components of SQGB and CRF-related targets were identified on the basis of databases such as the Traditional Chinese Medicine Systems Pharmacology platform.An in vitro CRF cell model was established by inducing A549 cells with interleukin-17(IL-17).Cells were treated with low(1.0 mg/mL)or high(1.5 mg/mL)concentrations of SQGB.The effects on cell viability,migration,apoptosis,inflammatory factors,mRNA expression,apoptosis-related proteins and key proteins of IL-17 signaling pathway were evaluated using scratch assay,flow cytometry,ELISA,real-time fluorescent quantitative PCR and Western blot analysis.RESULTS SQGB contained 84 active components acting on 209 potential CRF targets.Among these,quercetin,kaempferol,and luteolin were identified as the core components of the compound.Core targets included tumor protein p53,AKT serine/threonine kinase 1,IL-6,and tumor necrosis factor(TNF).IL-17,TNF and phosphatidylinositol-3-kinase-serine/threonine protein kinase(PI3K/Akt)signaling pathways were identified as crucial pathways.Compared with IL-17 intervention group,the cell migration rate,B-cell lymphoma 2(Bcl-2)protein expression,the levels of IL-6 and TNF-α in the supernatant,mRNA expression of IL-17 receptor A(IL-17RA),TNF-α,and IL-6,as well as the protein expression of IL-17RA and nuclear factor kappa-B p65 subunit(p65),and phosphorylated(p)-p65/p65 ratio in IL-17+SQGB low-and high-quality concentration groups were all significantly decreased or down-regulation(P<0.05);the apoptosis rate,expression levels of Bcl-2 associated X protein(Bax)and cleaved caspase-3 protein,the ratio of Bax/Bcl-2,the expression level of p-p38 protein,and the p-p38/p38 ratio were all significantly increased or up-regulated(P<0.05).Moreover,the improvement effects of these indicators were mostly better in the high-quality concentration groups compared to the low-quality concentration groups(P<0.05).CONCLUSIONS SQGB ameliorates CRF by regulating the IL-17 signaling pathway,inhibiting the expression of inflammatory factors,and activating p38 MAPK-dependent apoptosis pathway.

关键词

参芪固本方/网络药理学/癌因性疲乏/细胞实验

Key words

Shenqi guben formula/network pharmacology/cancer-related fatigue/cellular experiments

分类

医药卫生

引用本文复制引用

李鑫,方崇锴,黄越,李要轩,黄海福,吴先林,CHEN Zhesheng,李萌..参芪固本方调控IL-17信号通路改善癌因性疲乏的作用机制[J].中国药房,2025,36(14):1722-1729,8.

基金项目

国家自然科学基金面上项目(No.82374536) (No.82374536)

深圳市科技计划项目(No.JCYJ20230807120508018) (No.JCYJ20230807120508018)

深圳市"医疗卫生三名工程"周岱翰国医大师中医肿瘤学团队项目(No.SZZYSM202311-011) (No.SZZYSM202311-011)

广州中医药大学校院联合科技创新基金-深圳医院基金立项项目(No.GZYFT2024Y10) (No.GZYFT2024Y10)

广州中医药大学深圳医院(福田)科研专项(No.GZYSY2024016) (福田)

中国药房

OA北大核心

1001-0408

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