Doctoral Programme in Sciences with Major in Applied Cellular and Molecular Biology, Universidad de La Frontera, Temuco 4811230, Chile.
Center of Molecular Biology and Pharmacogenetics, Scientific and Technological Bioresource Nucleus, Universidad de La Frontera, Temuco 4811230, Chile.
Biomolecules. 2022 Sep 24;12(10):1365. doi: 10.3390/biom12101365.
Cisplatin (CDDP) is the drug of choice against different types of cancer. However, tumor cells can acquire resistance to the damage caused by cisplatin, generating genetic and epigenetic changes that lead to the generation of resistance and the activation of intrinsic resistance mechanisms in cancer cells. Among them, we can find mutations, alternative splicing, epigenetic-driven expression changes, and even post-translational modifications of proteins. However, the molecular mechanisms by which CDDP resistance develops are not clear but are believed to be multi-factorial. This article highlights a description of cisplatin, which includes action mechanism, resistance, and epigenetic factors involved in cisplatin resistance.
顺铂(CDDP)是治疗多种癌症的首选药物。然而,肿瘤细胞可以获得对顺铂引起的损伤的抵抗力,从而导致遗传和表观遗传变化,进而导致癌细胞产生耐药性和激活内在耐药机制。其中,我们可以发现突变、选择性剪接、表观遗传驱动的表达变化,甚至蛋白质的翻译后修饰。然而,顺铂耐药性发展的分子机制尚不清楚,但据信是多因素的。本文重点介绍了顺铂的描述,包括其作用机制、耐药性以及与顺铂耐药性相关的表观遗传因素。