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非小细胞肺癌中抗血管内皮生长因子治疗耐药的机制及克服耐药的策略

Mechanisms of and strategies for overcoming resistance to anti-vascular endothelial growth factor therapy in non-small cell lung cancer.

作者信息

Huang Yuhui, Carbone David P

机构信息

Cyrus Tang Hematology Center, Jiangsu Institute of Hematology, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, China; Department of Cancer Biology, Mayo Clinic Florida, Griffin Building Room 321B, 4500 San Pablo Road, Jacksonville, FL 32224, USA.

The Ohio State University Medical Center, Columbus, OH, USA.

出版信息

Biochim Biophys Acta. 2015 Apr;1855(2):193-201. doi: 10.1016/j.bbcan.2015.01.003. Epub 2015 Jan 15.

Abstract

Sustained angiogenesis is a hallmark of cancer. Because of the primary role of vascular endothelial growth factors (VEGFs) and their receptors in angiogenesis, VEGF-targeted agents have been developed to inhibit these signaling processes in non-small cell lung cancer (NSCLC). However, the clinical benefits are transient and resistance often rapidly develops. Insights into the molecular mechanisms of resistance would help to develop novel strategies to improve the efficacy of antiangiogenic therapies. This review discusses the mechanisms of resistance to anti-VEGF therapy and the postulated strategies to optimize antiangiogenic therapy. A number of multitargeted tyrosine kinase inhibitors currently in phase III clinical development for NSCLC are summarized. The emerging combination of antiangiogenic therapy with tumor immunotherapy is also discussed.

摘要

持续的血管生成是癌症的一个标志。由于血管内皮生长因子(VEGF)及其受体在血管生成中起主要作用,因此已开发出VEGF靶向药物来抑制非小细胞肺癌(NSCLC)中的这些信号传导过程。然而,临床益处是短暂的,且耐药性往往迅速出现。深入了解耐药的分子机制将有助于制定新策略以提高抗血管生成疗法的疗效。本综述讨论了抗VEGF治疗的耐药机制以及优化抗血管生成治疗的假定策略。总结了目前处于NSCLC III期临床开发阶段的多种多靶点酪氨酸激酶抑制剂。还讨论了抗血管生成疗法与肿瘤免疫疗法的新兴联合应用。

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