首页> 外文期刊>Expert opinion on investigational drugs >Entrectinib: a potent new TRK, ROS1, and ALK inhibitor
【24h】

Entrectinib: a potent new TRK, ROS1, and ALK inhibitor

机译:Entrectinib:一种有效的新型TRK,ROS1和ALK抑制剂

获取原文
获取原文并翻译 | 示例
       

摘要

Introduction: Receptor tyrosine kinases (RTKs) and their signaling pathways, control normal cellular processes; however, their deregulation play important roles in malignant transformation. In advanced non-small cell lung cancer (NSCLC), the recognition of oncogenic activation of specific RTKs, has led to the development of molecularly targeted agents that only benefit roughly 20% of patients. Entrectinib is a pan-TRK, ROS1 and ALK inhibitor that has shown potent anti-neoplastic activity and tolerability in various neoplastic conditions, particularly NSCLC.
机译:简介:受体酪氨酸激酶(RTKs)及其信号通路控制正常的细胞过程。然而,它们的放松调控在恶性转化中起着重要作用。在晚期非小细胞肺癌(NSCLC)中,对特定RTK致癌激活的认识导致了分子靶向药物的开发,该药物仅使大约20%的患者受益。 Entrectinib是一种pan-TRK,ROS1和ALK抑制剂,在各种赘生性疾病(尤其是NSCLC)中均显示出强大的抗肿瘤活性和耐受性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号