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曲妥珠单抗-DM1(T-DM1)保留了曲妥珠单抗的所有作用机制,并能有效抑制拉帕替尼耐药的乳腺癌的生长。

Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer.

机构信息

Research Oncology, Genentech, Inc., 1 DNA Way, Mailstop 72, South San Francisco, CA 94080, USA.

出版信息

Breast Cancer Res Treat. 2011 Jul;128(2):347-56. doi: 10.1007/s10549-010-1090-x. Epub 2010 Aug 21.

Abstract

Trastuzumab (Herceptin(®)) is currently used as a treatment for patients whose breast tumors overexpress HER2/ErbB2. Trastuzumab-DM1 (T-DM1, trastuzumab emtansine) is designed to combine the clinical benefits of trastuzumab with a potent microtubule-disrupting drug, DM1 (a maytansine derivative). Currently T-DM1 is being tested in multiple clinical trials. The mechanisms of action for trastuzumab include inhibition of PI3K/AKT signaling pathway, inhibition of HER-2 shedding and Fcγ receptor mediated engagement of immune cells, which may result in antibody-dependent cellular cytotoxicity (ADCC). Here we report that T-DM1 retains the mechanisms of action of unconjugated trastuzumab and is active against lapatinib resistant cell lines and tumors.

摘要

曲妥珠单抗(赫赛汀(®))目前被用于治疗人表皮生长因子受体 2(HER2/ErbB2)过表达的乳腺癌患者。曲妥珠单抗-DM1(T-DM1,曲妥珠单抗-美坦新偶联物)旨在将曲妥珠单抗的临床获益与一种有效的微管破坏药物 DM1(美登素衍生物)相结合。目前,T-DM1 正在多项临床试验中进行测试。曲妥珠单抗的作用机制包括抑制 PI3K/AKT 信号通路、抑制 HER-2 脱落和 Fcγ 受体介导的免疫细胞结合,这可能导致抗体依赖性细胞毒性(ADCC)。在这里,我们报告 T-DM1 保留了未缀合曲妥珠单抗的作用机制,并且对拉帕替尼耐药的细胞系和肿瘤有效。

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