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肺癌中凋亡途径的靶向治疗。

Targeting apoptosis pathways in lung cancer.

机构信息

Department of Medical Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

出版信息

Cancer Lett. 2013 May 28;332(2):359-68. doi: 10.1016/j.canlet.2010.09.012. Epub 2010 Oct 25.

Abstract

Lung cancer is a devastating disease with a poor prognosis. Non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) represent different forms of lung cancer that are associated with distinct genetic causes and display different responses to therapy in the clinic. Whereas SCLC is often sensitive to chemotherapy at start of treatment, NSCLC are less chemo-sensitive. In NSCLC different histological subtypes are distinguished and increasing efforts are made to identify subtypes that respond to specific therapies, such as those harbouring epidermal growth factor receptor (EGFR) mutations that have benefit from treatment with EGFR inhibitors. Targeting of the apoptotic machinery represents another approach that aims to selectively kill cancer cells while sparing normal ones. Here we describe different ways that are currently explored to induce apoptosis in lung cancer cells, specifically pathways controlled by TNF-related apoptosis-inducing ligand (TRAIL), BCL-2 family members and apoptosis inhibitory proteins (IAPs). Preclinical studies are discussed and for some agents results from early clinical studies and future perspectives are considered.

摘要

肺癌是一种预后不良的毁灭性疾病。非小细胞肺癌(NSCLC)和小细胞肺癌(SCLC)代表不同形式的肺癌,它们与不同的遗传原因相关,并在临床上对治疗有不同的反应。虽然 SCLC 在开始治疗时对化疗通常敏感,但 NSCLC 对化疗的敏感性较低。在 NSCLC 中,不同的组织学亚型被区分开来,并越来越努力地识别对特定治疗有反应的亚型,例如那些携带有表皮生长因子受体(EGFR)突变的亚型,这些突变对 EGFR 抑制剂的治疗有获益。凋亡机制的靶向是另一种旨在选择性杀死癌细胞而不伤害正常细胞的方法。在这里,我们描述了目前用于诱导肺癌细胞凋亡的不同方法,特别是受肿瘤坏死因子相关凋亡诱导配体(TRAIL)、BCL-2 家族成员和凋亡抑制蛋白(IAPs)控制的途径。讨论了临床前研究,对于一些药物,考虑了早期临床研究的结果和未来的展望。

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