Chang Xing, Liu Zi, Man Shuai, Roys Annie, Li Zengqiang, Zuo Daiying, Wu Yingliang
Department of Pharmacology, Shenyang Pharmaceutical University 103 Wenhua Road, Shenhe District Shenyang 110016 China
RSC Adv. 2019 Jun 7;9(31):17921-17932. doi: 10.1039/c9ra02258a. eCollection 2019 Jun 4.
The rearrangements of anaplastic lymphoma kinase (ALK) and the c-ros oncogene 1 (ROS1) have both been important driving factors in non-small-cell lung cancer (NSCLC). They have already been defined in 3-5% of NSCLC patients. ALK and ROS1 rearrangements are associated with unique clinical and pathological features, especially patients are usually younger, with milder or never smoking history, and adenocarcinoma histology. Also, they have both been found to contribute to the metastasis of NSCLC by cell migration and invasion. It has recently been recognized that the brain can be considered as a primary site for metastasis in cancers with ALK or ROS1 rearrangements. The present review summarizes the current status of NSCLC metastasis and possible mechanisms based on available evidence, and then we list possible therapeutic strategies so that an increase in control of ALK and ROS1 rearrangement of NSCLC metastases by combination therapy can be translated in an increase in overall survival and prognosis.
间变性淋巴瘤激酶(ALK)重排和原癌基因c-ros 1(ROS1)重排均是非小细胞肺癌(NSCLC)的重要驱动因素。它们已在3%-5%的NSCLC患者中被发现。ALK和ROS1重排与独特的临床和病理特征相关,尤其是患者通常较年轻,有较轻的吸烟史或从不吸烟,且组织学类型为腺癌。此外,二者均被发现可通过细胞迁移和侵袭促进NSCLC转移。最近人们认识到,对于具有ALK或ROS1重排的癌症,脑可被视为转移的主要部位。本综述基于现有证据总结了NSCLC转移的现状及可能机制,随后列出了可能的治疗策略,以便通过联合治疗加强对ALK和ROS1重排的NSCLC转移的控制,从而提高总生存率和改善预后。