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A Review on the Comparison of Vemurafenib and Dabrafenib in the treatment of Melanoma caused by Mutation of Braf

机译:vemureafenib和dabrafenib在BRAF突变引起的黑色素瘤治疗中的比较综述

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摘要

Metastatic melanoma is one of the most aggressive forms of skin cancer. The mortality rate of this cancer is high .Almost 60% of the melanomas are due to the mutation of BRAF gene. BRAF V600E mutations has been implicated in melanoma genesis by different mechanisms. It occurs due to the improper regulation of the activation of downstream MEK (mitogen activated protein kinase enzyme)/ERK (extra cellular signal related kinase) effectors. In order to overcome the increasing rate of this disease a comparative study has been performed between two ERK/MEK inhibitors namely vemurafenib and dabrafenib and also to understand the relative efficacy and toxicity effect between these two therapeutic modalities.
机译:转移性黑色素瘤是最具侵略性的皮肤癌形式之一。 这种癌症的死亡率很高。至于Melanomas的60%是由于BRAF基因的突变。 BRAF V600E突变通过不同机制涉及黑色素瘤的成因。 由于下游MEK(促丝糖原活化蛋白激酶酶)/ ERK(额外细胞信号相关激酶)效应器的激活的不适当的调节而发生的。 为了克服这种疾病的增加率,在两个ERK / MEK抑制剂之间进行了比较研究,即vemureafenib和dabrafenib,也可以了解这两种治疗方式之间的相对疗效和毒性效果。

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