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In melanocytic lesions the fraction of BRAFV600E alleles is associated with sun exposure but unrelated to ERK phosphorylation

机译:在黑素细胞病变中,BRAFV600E等位基因的一部分与阳光照射有关,但与ERK磷酸化无关

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BRAFV600E mutation has been frequently reported in different types of melanocytic lesions, but its role in melanomagenesis is poorly understood, having been associated with either the proliferative-induced MAPK pathway activation or the acquisition of oncogene-driven senescence. The presence of BRAF alterations has been related to sun exposure, although the molecular mechanisms underlying this event are only partly known. To elucidate the relationships among BRAF/NRAS alterations, MAPK pathway activation, and sun exposure, we examined 22 acquired nevi and 18 cutaneus melanomas from 38 patients. Microdissected tissues from each lesion were subjected to BRAF/NRAS mutation analysis by sequencing, allele-specific PCR and pyrosequencing assay. The same lesions were also examined for the expression of phosphorylated ERK1/2. Phototype and an accurate history of sun exposure were evaluated for each patient. BRAFV600E mutation was detected in 50% of the acquired nevi and in 70% of the cutaneus melanomas in the absence of NRAS alterations. The fraction of alleles carrying BRAFV600E substitution was variable but strongly associated with sun exposure. In contrast, no relationship was evidenced between the presence of this mutation and patients' phototype, phosphorylated ERK1/2 expression, or Clark's level. Our findings indicate that in melanocytic lesions, BRAFV600E mutation can affect a subset of the cells and is associated with the type and quantity of sun exposure. This mutation is independent of the nevo-melanoma progression and unrelated to ERK phosphorylation, suggesting that alternative mechanisms to the MAPK activation are also involved in this type of transformation.
机译:BRAFV600E突变已在不同类型的黑素细胞病变中频繁报道,但其在黑色素瘤形成中的作用了解甚少,与增生诱导的MAPK途径激活或癌基因驱动的衰老的获得有关。 BRAF改变的存在与阳光暴晒有关,尽管此事件的分子机制只是部分已知。为了阐明BRAF / NRAS改变,MAPK途径激活和日晒之间的关系,我们检查了38名患者中22例获得性痣和18例皮肤黑素瘤。通过测序,等位基因特异性PCR和焦磷酸测序法对每个病变的显微组织进行BRAF / NRAS突变分析。还检查了相同的病变的磷酸化ERK1 / 2的表达。评估每位患者的照相类型和准确的日晒史。在没有NRAS改变的情况下,在50%的获得性痣和70%的皮肤黑素瘤中检测到BRAFV600E突变。携带BRAFV600E替代的等位基因比例可变,但与日照强烈相关。相反,该突变的存在与患者的照片类型,磷酸化的ERK1 / 2表达或克拉克水平之间没有关系。我们的发现表明,在黑素细胞病变中,BRAFV600E突变会影响一部分细胞,并且与日晒的类型和数量有关。该突变独立于黑色素瘤的进展,与ERK的磷酸化无关,这表明MAPK激活的其他机制也参与了这种类型的转化。

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