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间变性淋巴瘤激酶抑制剂的研究进展

陈雅琳 李巍 汪天洋 周雪琴 刘东志

化工进展2016,Vol.35Issue(12):3985-3990,6.
化工进展2016,Vol.35Issue(12):3985-3990,6.DOI:10.16085/j.issn.1000-6613.2016.12.035

间变性淋巴瘤激酶抑制剂的研究进展

Advances in research on anaplastic lympgoma kinase inhibitors

陈雅琳 1李巍 2汪天洋 3周雪琴 1刘东志2

作者信息

  • 1. 天津大学化工学院,天津 300072
  • 2. 天津化学化工协同创新中心,天津 300072
  • 3. 天津市功能精细化学品技术工程中心,天津 300072
  • 折叠

摘要

Abstract

Researchers have found that multiple oncogenic driver multations are closely related with the progression and prognosis of NSCLC.In the era of molecular targeted treatment,rearrangements in anaplastic lymphoma kinase(ALK)gene and echinoderm microtubule-associated protein-like 4 (EML4)gene were applied in patients with non-small cell lung cancer(NSCLC). Crizotinib,an ALK inhibitor,is effective in treating advanced ALK-positive NSCLC,and the US Food and Drug Administration(FDA)approved it for treating ALK-positive NSCLC. Several mechanisms of acquired resistance to crizotinib have recently been reported. Second-generation ALK inhibitors were developed to overcome these resistance mechanisms and showed activity againstALKpositive NSCLC. The latest development of crizotinib,ceritinib,alectinibetc. were reviewed.

关键词

非小细胞肺癌/EML4-ALK基因重排/克唑替尼

Key words

non small cell lung cancer/echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase rearrangement/crizotinib

分类

信息技术与安全科学

引用本文复制引用

陈雅琳,李巍,汪天洋,周雪琴,刘东志..间变性淋巴瘤激酶抑制剂的研究进展[J].化工进展,2016,35(12):3985-3990,6.

基金项目

天津市科技创新平台计划(14TXGCCX00017)项目。 ()

化工进展

OA北大核心CSCDCSTPCD

1000-6613

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