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非小细胞肺癌中培美曲塞耐药的机制

Mechanisms of resistance to pemetrexed in non-small cell lung cancer.

作者信息

Liang Jiaqi, Lu Tao, Chen Zhencong, Zhan Cheng, Wang Qun

机构信息

Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

出版信息

Transl Lung Cancer Res. 2019 Dec;8(6):1107-1118. doi: 10.21037/tlcr.2019.10.14.

Abstract

Currently, lung cancer has remained the most common cause of cancer death while non-small cell lung cancer (NSCLC) accounts for the most of all lung cancer cases. Regardless of multiple existing managements, chemotherapy regimens are still the mainstay of treatment for NSCLC, where pemetrexed has shown cytotoxic activity and has increasingly been used, especially for advanced cases. However, chemo-resistance may inhibit clinical efficacy after long-term use. Mechanisms responsible for chemo-resistance to pemetrexed in NSCLC are plethoric but can be separated into two categories to be discussed: tumor cells and their interactions with drugs. Phenomena relevant to tumor cells such as oncogene or oncoprotein alterations, DNA synthesis, DNA repair, and tumor cell biology behavior are discussed, as well as processes associated with drug dynamics, including drug uptake, drug elimination, and antifolate polyglutamylation. This review will focus on clinical trials and the basic biomedical mechanisms of NSCLC treated with pemetrexed and will describe the underlying mechanisms of resistance to facilitate more efficient clinical therapies to treat patients.

摘要

目前,肺癌仍然是癌症死亡的最常见原因,而非小细胞肺癌(NSCLC)占所有肺癌病例的大多数。尽管存在多种现有治疗方法,但化疗方案仍是NSCLC治疗的主要手段,培美曲塞已显示出细胞毒性活性并越来越多地被使用,尤其是对于晚期病例。然而,长期使用后化疗耐药可能会抑制临床疗效。NSCLC中对培美曲塞化疗耐药的机制众多,但可分为两类进行讨论:肿瘤细胞及其与药物的相互作用。本文讨论了与肿瘤细胞相关的现象,如癌基因或癌蛋白改变、DNA合成、DNA修复和肿瘤细胞生物学行为,以及与药物动力学相关的过程,包括药物摄取、药物消除和抗叶酸聚谷氨酸化。本综述将重点关注培美曲塞治疗NSCLC的临床试验和基础生物医学机制,并将描述耐药的潜在机制,以促进更有效的临床治疗来治疗患者。

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