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西罗莫司通过靶向 ErbB2/PKM2 通路抑制 ErbB2 过表达型乳腺癌。

Cerulenin suppresses ErbB2-overexpressing breast cancer by targeting ErbB2/PKM2 pathway.

机构信息

Department of Biochemistry and Molecular Biology, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, No. 17, Section 3, South Renmin Road, Chengdu, 610041, China.

Department of Physiology, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, 610041, China.

出版信息

Med Oncol. 2022 Oct 29;40(1):5. doi: 10.1007/s12032-022-01872-z.

Abstract

Cerulenin is a fungal metabolite and a specific inhibitor of fatty acid synthase (FASN), which has shown a potential anticancer activity. 20-25% of breast cancer patients with ErbB2-overexpressing develop resistance to treatment. Therefore, it is urgent to find an effective new target for the treatment of ErbB2-overexpressing breast cancer. Our previous study found that cerulenin inhibits the glycolysis and migration of SK-BR-3 cells, but the effect of cerulenin on other malignant phenotypes of breast cancer is still unknown. Furthermore, the mechanism by which cerulenin displays its inhibitory effects is not fully understood. In this study, we systematically investigate the inhibitory effects of cerulenin on proliferation, migration, invasion and glycolysis of ErbB2-overexpressing breast cancer cells and its molecular mechanism. We found that cerulenin obviously suppresses the proliferation, migration, invasion as well as glycolysis. Through bioinformatic analyses, we found that PKM2 might be a target of cerulenin. In addition, ErbB2 and its signaling pathway upregulated PKM2 protein levels. Furthermore, we demonstrated that cerulenin downregulated the protein levels of ErbB2, PKM2 and EMT markers (MMP9, MMP2 and Snail2) in a dose- and time-dependent manner. Finally, the inhibitory of cerulenin on colony formation, migration, invasion and glycolysis, as well as protein levels of EMT markers were rescued by replenishing with PKM2. These findings illustrated that cerulenin inhibits proliferation, migration, invasion and glycolysis by targeting ErbB2/PKM2 pathway in ErbB2-overexpressing breast cancer cells.

摘要

硫瑞宁是一种真菌代谢产物,也是脂肪酸合酶(FASN)的特异性抑制剂,具有潜在的抗癌活性。20-25%的 ErbB2 过表达的乳腺癌患者对治疗产生耐药性。因此,迫切需要寻找一种有效的新靶点来治疗 ErbB2 过表达的乳腺癌。我们之前的研究发现硫瑞宁抑制 SK-BR-3 细胞的糖酵解和迁移,但硫瑞宁对其他恶性表型的乳腺癌的影响尚不清楚。此外,硫瑞宁发挥抑制作用的机制尚不完全清楚。在本研究中,我们系统地研究了硫瑞宁对 ErbB2 过表达乳腺癌细胞增殖、迁移、侵袭和糖酵解的抑制作用及其分子机制。我们发现硫瑞宁明显抑制增殖、迁移、侵袭和糖酵解。通过生物信息学分析,我们发现 PKM2 可能是硫瑞宁的一个靶点。此外,ErbB2 及其信号通路上调了 PKM2 蛋白水平。此外,我们证明硫瑞宁以剂量和时间依赖的方式下调 ErbB2、PKM2 和 EMT 标志物(MMP9、MMP2 和 Snail2)的蛋白水平。最后,用 PKM2 补充可挽救硫瑞宁对集落形成、迁移、侵袭和糖酵解以及 EMT 标志物蛋白水平的抑制作用。这些发现表明,硫瑞宁通过靶向 ErbB2/PKM2 通路抑制 ErbB2 过表达乳腺癌细胞的增殖、迁移、侵袭和糖酵解。

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