基于顺铂的人类癌症化疗。

Journal of Cancer Science & Therapy Pub Date : 2019-01-01 Epub Date: 2019-04-08
Andrea Brown, Sanjay Kumar, Paul B Tchounwou
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引用次数: 0

摘要

顺铂(顺-二胺-二氯铂II)最初被发现可以阻止大肠杆菌的生长,并进一步被认为具有抗肿瘤和对癌细胞的细胞毒性作用。顺铂通过静脉给药给人,被用作诊断为各种恶性肿瘤的患者的一线化疗,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。一旦顺铂进入细胞,它就会失去一个氯配体,与DNA结合形成链内DNA加合物,抑制DNA合成和细胞生长,从而发挥细胞毒性作用。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)通路,阻止顺铂诱导的细胞死亡,从而通过NER(核切除修复系统)激活DNA修复反应。虽然治疗已被证明是有效的,但许多患者由于耐药而复发。因此,其他铂类化合物如奥沙利铂和卡铂已被使用,并显示出一定程度的有效性。在这篇综述中,顺铂的临床应用进行了讨论,特别强调其在癌症化疗中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cisplatin-Based Chemotherapy of Human Cancers.

Cisplatin-Based Chemotherapy of Human Cancers.

Cisplatin-Based Chemotherapy of Human Cancers.

Cisplatin (cis-diammine-dichloro-platinum II) was initially discovered to prevent the growth of Escherichia coli 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 via 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.

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