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Melanoma as a model for precision medicine in oncology

机译:黑色素瘤作为肿瘤精密医学的模型

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Advances in the understanding of the molecular profile of tumour cells and progress in systems biology and bioinformatics have led to the promise of precision medicine for treatment of human cancer. Melanoma has provided an opportunity for insights into both the potential benefit and limitations of precision medicine for cancer.In 2002, half of all human melanoma cells were shown to harbour mutations in the BRAF gene,1 the product of which has an important role in cell division, differentiation, and secretion through the MAPK or RAS-RAF-MEK-ERK pathways. Mutations in BRAF result in constitutive MAPK signalling and have been associated with a number of tumour types. The ability to detect mutations in BRAF from tumour biopsy specimens and the availability of highly specific BRAF inhibitors have begun to change the notion of the clinical management of patients with melanoma.
机译:在对肿瘤细胞的分子特征的理解以及系统生物学和生物信息学的进步方面,人们提出了用于治疗人类癌症的精密医学的希望。黑色素瘤为深入了解精密药物治疗癌症的潜在益处和局限性提供了机会.2002年,人类黑素瘤细胞的一半显示出具有BRAF基因突变,1该产物在细胞中具有重要作用通过MAPK或RAS-RAF-MEK-ERK途径进行分裂,分化和分泌。 BRAF中的突变导致组成型MAPK信号传导,并与多种肿瘤类型有关。从肿瘤活检样本中检测BRAF突变的能力和高度特异性的BRAF抑制剂的可用性已开始改变黑素瘤患者临床治疗的观念。

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