Department of Molecular, Cellular, and Developmental Biology, and the Neuroscience Research Institute, University of California, Santa Barbara, CA 93106, USA.
Cancer Lett. 2011 Aug 28;307(2):113-8. doi: 10.1016/j.canlet.2011.03.017. Epub 2011 Apr 9.
Synthetic derivatives of the microtubule-targeted agent maytansine, commonly known as drug maytansinoids or DMs, are emerging as potential cancer therapeutics. DM1 is an antibody-conjugatable maytansinoid that was developed to overcome systemic toxicity associated with maytansine and to enhance tumor-specific delivery. Antibody-DM1 conjugates showed promising results in preclinical and clinical evaluations. However, the molecular mechanism of the drug component DM1 was largely unknown. Recently, researchers have examined the mechanism of DM1 at molecular and cellular levels. According to their findings, DM1 binds at the tips of microtubules and suppresses the dynamicity of microtubules. The antibody-DM1 conjugate cleaves inside cells and releases the active drug in a time-dependent manner. The suppression of microtubule dynamics by DM1 induces mitotic arrest and cell death.
微管靶向剂美登素的合成衍生物,通常被称为药物美登素或 DM,作为潜在的癌症治疗药物正在兴起。DM1 是一种可与抗体结合的美登素,旨在克服与美登素相关的全身毒性,并增强肿瘤特异性递送。抗体-DM1 缀合物在临床前和临床评估中显示出有希望的结果。然而,药物成分 DM1 的分子机制在很大程度上是未知的。最近,研究人员已经在分子和细胞水平上研究了 DM1 的作用机制。根据他们的发现,DM1 结合在微管的尖端并抑制微管的动态性。抗体-DM1 缀合物在细胞内裂解,并以时间依赖性方式释放活性药物。DM1 抑制微管动力学导致有丝分裂停滞和细胞死亡。