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克服BRAF突变癌症中对BRAF或MEK抑制剂获得性耐药的潜在治疗策略。

Potential therapeutic strategies to overcome acquired resistance to BRAF or MEK inhibitors in BRAF mutant cancers.

作者信息

Corcoran Ryan B, Settleman Jeffrey, Engelman Jeffrey A

机构信息

Massachusetts General Hospital Cancer Center, Boston, MA 02129, USA.

出版信息

Oncotarget. 2011 Apr;2(4):336-46. doi: 10.18632/oncotarget.262.

Abstract

Recent clinical trials with selective inhibitors of the BRAF and MEK kinases have shown promising results in patients with tumors harboring BRAF V600 mutations. However, as has been observed previously with similarly successful targeted therapies, acquired resistance to these agents is an emerging problem that limits their clinical benefit. Several recent studies from our laboratory and others have investigated the causes of acquired resistance to BRAF and MEK inhibitors, and multiple resistance mechanisms have been identified. Here, we review these mechanisms and suggest that they can be broadly grouped into two main classes: ERK-dependent and ERK-independent. We also propose distinct therapeutic strategies that might be employed to overcome each class of acquired resistance..

摘要

近期针对BRAF和MEK激酶选择性抑制剂开展的临床试验表明,对于携带BRAF V600突变的肿瘤患者,这些抑制剂显示出了有前景的结果。然而,正如之前在同样成功的靶向治疗中所观察到的那样,对这些药物产生获得性耐药是一个新出现的问题,限制了它们的临床获益。我们实验室和其他机构最近的几项研究调查了对BRAF和MEK抑制剂产生获得性耐药的原因,并确定了多种耐药机制。在此,我们综述这些机制,并提出它们可大致分为两大类:ERK依赖性和ERK非依赖性。我们还提出了可能用于克服每种获得性耐药类型的不同治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a85/3248170/e50158d2c213/oncotarget-02-336-g001.jpg

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