Lu Jiafeng, Li Zhaoyan, Liu Xingjing, Xu Bin, Zhang Weiyu
Department of Pharmacy, Ruijin Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
Department of Traditional Chinese Medicine, Ruijin Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
Cancer Manag Res. 2024 Sep 9;16:1189-1204. doi: 10.2147/CMAR.S477399. eCollection 2024.
The resistance to endocrine therapy can lead to recurrence and metastasis of breast cancer (BC), affecting the survival period. Tiaogan Bushen Xiaoji (TGBSXJ) Formula, a traditional Chinese medicine (TCM) decoction, has been widely used in the treatment of estrogen receptor-positive (ER) BC. However, the underlying mechanism of TGBSXJ Formula in ERBC treatment has not been totally elucidated.
Network pharmacology (NP) and RNA sequencing were used to predict the candidate ingredients and explore the potential targets of TGBSXJ Formula. Then, the results of NP and RNA sequencing were investigated by in vitro experiments.
Active ingredients of TGBSXJ Formula mainly included Mangiferin, Rutin, Anemarrhena asphodeloides saponin BII, Ganoderic acid A and Acacetin, etc. A protein-protein interaction (PPI) network was created based on the active ingredients of TGBSXJ Formula and target genes of ER BC, in which TGF-β, MMP2 and SMAD3 were defined as the hub genes. In vitro experiments showed that TGBSXJ Formula significantly inhibited the viability, colony ability and migration of ER BC cells, and significantly increased the sensitivity to TAM. Western blot analysis showed that TGBSXJ Formula significantly downregulated TGF-β, E-cadherin, MMP2, MMP9, N-cadherin, p-Smad2 and p-Smad3 in ER BC cells.
TGBSXJ Formula increases the sensitivity of ER BC cells to TAM by inhibiting the TGF-β/Smad signaling pathway.
内分泌治疗耐药可导致乳腺癌(BC)复发和转移,影响生存期。调肝补肾消积(TGBSXJ)方作为一种中药汤剂,已广泛应用于雌激素受体阳性(ER)乳腺癌的治疗。然而,TGBSXJ方治疗ER乳腺癌的潜在机制尚未完全阐明。
采用网络药理学(NP)和RNA测序来预测候选成分并探索TGBSXJ方的潜在靶点。然后,通过体外实验研究NP和RNA测序的结果。
TGBSXJ方的活性成分主要包括芒果苷、芦丁、知母皂苷BII、灵芝酸A和刺槐素等。基于TGBSXJ方的活性成分和ER乳腺癌的靶基因构建了蛋白质-蛋白质相互作用(PPI)网络,其中TGF-β、MMP2和SMAD3被确定为枢纽基因。体外实验表明,TGBSXJ方显著抑制ER乳腺癌细胞的活力、集落形成能力和迁移能力,并显著提高对他莫昔芬(TAM)的敏感性。蛋白质免疫印迹分析表明,TGBSXJ方显著下调ER乳腺癌细胞中TGF-β、E-钙黏蛋白、MMP2、MMP9、N-钙黏蛋白、p-Smad2和p-Smad3的表达。
TGBSXJ方通过抑制TGF-β/Smad信号通路增加ER乳腺癌细胞对TAM的敏感性。