Brown Andrea, Kumar Sanjay, Tchounwou Paul B
Cellomics and Toxicogenomics Research Laboratory, NIH/NIMHD-RCMI Center for Environmental Health, College of Science, Engineering and Technology, Jackson State University, 1400 Lynch Street, Box18750, Jackson, Mississippi, MS 39217, USA.
J Cancer Sci Ther. 2019;11(4). Epub 2019 Apr 8.
Cisplatin (cis-diammine-dichloro-platinum II) was initially discovered to prevent the growth of and was further recognized for its anti-neoplastic and cytotoxic effects on cancer cells. Administered intravenously to humans, cisplatin is used as first-line chemotherapy treatment for patients diagnosed with various types of malignancies, such as leukemia, lymphomas, breast, testicular, ovarian, head and neck, and cervical cancers, and sarcomas. Once cisplatin enters the cell it exerts its cytotoxic effect by losing one chloride ligand, binding to DNA to form intra-strand DNA adducts, and inhibiting DNA synthesis and cell growth. The DNA lesions formed from cisplatin-induced DNA damage activate DNA repair response NER (nuclear excision repair system) by halting cisplatin-induced cell death by activation of ATM (ataxia telangiectasia mutated) pathway. Although treatment has been shown to be effective, many patients experience relapse due to drug resistance. As a result, other platinum compounds such as oxaliplatin and carboplatin have since been used and have shown some levels of effectiveness. In this review, the clinical applications of cisplatin are discussed with a special emphasis on its use in cancer chemotherapy.
顺铂(顺二氨二氯铂II)最初被发现可抑制生长,并因其对癌细胞的抗肿瘤和细胞毒性作用而得到进一步认可。静脉注射给人类后,顺铂被用作诊断为各种类型恶性肿瘤(如白血病、淋巴瘤、乳腺癌、睾丸癌、卵巢癌、头颈癌、宫颈癌和肉瘤)患者的一线化疗药物。顺铂一旦进入细胞,就会通过失去一个氯配体、与DNA结合形成链内DNA加合物以及抑制DNA合成和细胞生长来发挥其细胞毒性作用。由顺铂诱导的DNA损伤形成的DNA损伤通过激活ATM(共济失调毛细血管扩张突变)途径阻止顺铂诱导的细胞死亡,从而激活DNA修复反应NER(核切除修复系统)。尽管已证明该治疗有效,但许多患者由于耐药性而复发。因此,此后使用了其他铂类化合物,如奥沙利铂和卡铂,并显示出一定程度的有效性。在这篇综述中,讨论了顺铂的临床应用,特别强调了其在癌症化疗中的应用。