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柴胡皂苷A通过下调CXCR4抑制三阴性乳腺癌的生长和转移。

Saikosaponin A Inhibits Triple-Negative Breast Cancer Growth and Metastasis Through Downregulation of CXCR4.

作者信息

Wang Ying, Zhao Liang, Han Xianghui, Wang Yahui, Mi Jinxia, Wang Changhong, Sun Duxin, Fu Yunfei, Zhao Xiaodong, Guo Haidong, Wang Qiangli

机构信息

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Department of Pharmacy, Shanghai Baoshan Luodian Hospital, Shanghai, China.

出版信息

Front Oncol. 2020 Jan 28;9:1487. doi: 10.3389/fonc.2019.01487. eCollection 2019.

Abstract

Due to a lack of recognized molecular targets for therapy, patients with triple-negative breast cancer (TNBC), unlike other subtypes of breast cancers, generally have not benefited from the advances made with targeted agents. The CXCR4/SDF-1 axis is involved in tumor growth and metastasis of TNBC. Therefore, down-regulation of the expression of CXCR4 in cancer cells is a potential therapeutic strategy for inhibiting primary tumor growth and metastasis of TNBC. In order to identify bioactive compounds that inhibit the expression of CXCR4 in traditional Chinese medicines, we investigated the capacity of saikosaponin A (SSA), one of the active ingredients isolated from Radix bupleuri, to affect CXCR4 expression and function in TNBC cells. Analyses of cell growth, migration, invasion, and protein expression were performed. Knockdowns by small interfering RNA (siRNA) and non-invasive bioluminescence were also used. SSA reduced proliferation and colony formation of SUM149 and MDA-MB-231 cells. SSA inhibited migration and invasion of TNBC cells. For mice, SSA inhibited primary tumor growth and reduced lung metastasis of highly metastatic, triple-negative 4T1-luc cells. SSA inhibited CXCR4 expression but did not regulate CXCR7 expression and . The inhibitory effects on the migration and invasion of TNBC cells were reversed by down-regulation of CXCR4 expression. In addition, SSA inactivated the Akt/mTOR signaling pathway and inhibited MMP-9 and MMP-2 expression. The results show that SSA exerts an anti-TNBC effect through the inhibition of CXCR4 expression and thus has the potential to be a candidate therapeutic agent for TNBC patients.

摘要

由于缺乏公认的治疗分子靶点,与其他亚型乳腺癌患者不同,三阴性乳腺癌(TNBC)患者一般未从靶向药物取得的进展中获益。CXCR4/SDF-1轴参与TNBC的肿瘤生长和转移。因此,下调癌细胞中CXCR4的表达是抑制TNBC原发肿瘤生长和转移的一种潜在治疗策略。为了在中药中鉴定出抑制CXCR4表达的生物活性化合物,我们研究了从柴胡中分离出的活性成分之一柴胡皂苷A(SSA)影响TNBC细胞中CXCR4表达和功能的能力。进行了细胞生长、迁移、侵袭和蛋白质表达分析。还使用了小干扰RNA(siRNA)敲低和非侵入性生物发光技术。SSA降低了SUM149和MDA-MB-231细胞的增殖和集落形成。SSA抑制TNBC细胞的迁移和侵袭。对于小鼠,SSA抑制原发肿瘤生长并减少高转移性三阴性4T1-luc细胞的肺转移。SSA抑制CXCR4表达,但不调节CXCR7表达。CXCR4表达下调可逆转对TNBC细胞迁移和侵袭的抑制作用。此外,SSA使Akt/mTOR信号通路失活并抑制MMP-9和MMP-2表达。结果表明,SSA通过抑制CXCR4表达发挥抗TNBC作用,因此有潜力成为TNBC患者的候选治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/981c/6997291/cc317a10140a/fonc-09-01487-g0001.jpg

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