Exploring the Mechanism of Lianqiao Jinbei Decoction Inhibiting HER2-Positive Breast Cancer Based on Network Pharmacology and Experimental Verification.

IF 3.4 4区 医学 Q2 ONCOLOGY
Breast Cancer : Targets and Therapy Pub Date : 2025-07-14 eCollection Date: 2025-01-01 DOI:10.2147/BCTT.S522528
Dehui Li, Xukuo Liu, Huanfang Fan, Jingfei Dong, Liying Wei, Na Guo, Zhengrong Wang, Zhihua Du, Jiao Liu, Xiaohui Zhao, Xiaotong Tian, Changhui Han, Xujiong Yao
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引用次数: 0

Abstract

Purpose: Through network pharmacological prediction and in vitro experimental verification, the mechanism of action of Lianqiao Jinbei Decoction (LJD) in inhibiting HER2-positive breast cancer cells was clarified, providing experimental evidence for its treatment of HER2-positive breast cancer.

Methods: Network pharmacology method was used to construct the potential target network of LJD in the treatment of HER2+ breast cancer. After cell culture in vitro, the proliferation of HER2+ SK-BR3 breast cancer cells was investigated using CCK-8 technique. The apoptotic potential of SK-BR3 cells was detected by flow cytometry, and the migration of SK-BR3 cells was detected by cell scratch assay. The expression of HER2 protein in SK-BR3 breast cancer cells was detected by ELISA.

Results: HER2 was identified as the central gene and quercetin, β-sitosterol, and luteolin were the primary active ingredients using network pharmacology analysis. Serum-containing LJD medication can stop SK-BR3 cells from proliferating (P<0.05). Serum-containing LJD drugs at high, medium, and low concentrations may induce SK-BR3 cell death (P<0.05). LJD serum at high, medium, and low concentrations reduced the migration of SK-BR3 cells (P<0.05). The expression of HER2 protein was decreased by LJD high, medium, and low concentration drug-containing serum (P<0.05).

Conclusion: Regarding treating HER2-positive breast cancer, LJD has a multi-component, multi-target, and multi-pathway mode of action. The primary target of LJD's activity is the HER2 protein. Serum-containing LJD medication can prevent SK-BR3 cells from proliferating and migrating while encouraging their apoptosis. This effect may be attained by preventing HER2 protein expression.

基于网络药理学及实验验证的连翘金杯汤抑制her2阳性乳腺癌的机制探讨
目的:通过网络药理预测和体外实验验证,明确连翘金杯汤(LJD)抑制her2阳性乳腺癌细胞的作用机制,为其治疗her2阳性乳腺癌提供实验依据。方法:采用网络药理学方法构建LJD治疗HER2+乳腺癌的潜在靶点网络。细胞体外培养后,采用CCK-8技术研究HER2+ SK-BR3乳腺癌细胞的增殖情况。流式细胞术检测SK-BR3细胞的凋亡电位,细胞划痕法检测SK-BR3细胞的迁移。ELISA法检测SK-BR3乳腺癌细胞中HER2蛋白的表达。结果:网络药理学分析确定HER2为中心基因,槲皮素、β-谷甾醇、木犀草素为主要活性成分。含血清LJD用药可阻止SK-BR3细胞增殖(ppppp)结论:LJD治疗her2阳性乳腺癌具有多组分、多靶点、多通路的作用模式。LJD活性的主要靶点是HER2蛋白。含LJD的血清药物可以阻止SK-BR3细胞的增殖和迁移,同时促进其凋亡。这种作用可能通过阻止HER2蛋白表达来实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
40
审稿时长
16 weeks
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