Targeting the RAS pathway in melanoma

被引:58
作者
Ji, Zhenyu [1 ,2 ]
Flaherty, Keith T. [3 ]
Tsao, Hensin [1 ,2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Wellman Ctr Photomed, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Dermatol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, MGH Canc Ctr, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
RECOMBINANT INTERLEUKIN-2 THERAPY; INHIBITOR AZD6244 ARRY-142886; KIT PROTEIN EXPRESSION; METASTATIC MELANOMA; CUTANEOUS MELANOMA; PHASE-II; IMATINIB MESYLATE; TUMOR-GROWTH; B-RAF; SELECTIVE INHIBITOR;
D O I
10.1016/j.molmed.2011.08.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metastatic melanoma is a highly lethal type of skin cancer and is often refractory to all traditional chemotherapeutic agents. Key insights into the genetic make-up of melanoma tumors have led to the development of promising targeted agents. An activated RAS pathway, anchored by oncogenic BRAF, appears to be the central motor driving melanoma proliferation. Although recent clinical trials have brought enormous hope to patients with melanoma, adverse effects and novel escape mechanisms of these inhibitors have already emerged. Definition of the limits of the first successful targeted therapies will provide the basis for further advances in management of disseminated melanoma. In this review, the current state of targeted therapy for melanoma is discussed, including the potent BRAF(V600E) inhibitor vemurafenib.
引用
收藏
页码:27 / 35
页数:9
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