Lee David A, Cohen Jason A, Twaddell William S, Palacios Gustavo, Gill Melissa, Levit Eyal, Halperin Alan J, Mones Joan, Busam Klaus J, Silvers David N, Celebi Julide Tok
Department of Dermatology, Columbia University Medical Center, New York, NY 10032, USA.
Cancer. 2006 Feb 15;106(4):907-13. doi: 10.1002/cncr.21686.
Although the majority of melanomas demonstrate high rates of mutations in B-RAF or N-RAS that result in constitutive activation of the mitogen-activated protein kinase-signaling pathway, emerging data suggest molecular differences among melanoma subtypes. In this study, the authors evaluated the contribution of B-RAF and N-RAS mutations to the pathogenesis of Spitzoid melanomas.
In total, 33 Spitzoid melanomas were analyzed for clinical and pathologic characteristics as well as for hot-spot mutations in the B-RAF and N-RAS genes. In the majority of patients (28 of 33 melanomas), the tumors were confined to the skin with no evidence of metastasis (average follow-up, 32.5 mos). There were five metastasizing melanomas (5 of 33 tumors) with regional or systemic spread.
Of 33 Spitzoid melanomas, only 1 showed the V600E mutation in the B-RAF gene (1 of 33 tumors; 3%). It was noteworthy that none of the metastatic Spitzoid melanomas (0 of 5 tumors; 0%), of which 2 resulted in fatal outcomes, demonstrated mutations in B-RAF or N-RAS.
In contrast to the majority of cutaneous melanomas, activating hot-spot mutations in B-RAF or N-RAS were not involved in the pathogenesis of Spitzoid melanoma. These data suggested that Spitzoid melanoma is a distinct form of melanoma with unknown genes and/or signaling pathways involved in its development.
尽管大多数黑色素瘤显示出B-RAF或N-RAS的高突变率,导致丝裂原活化蛋白激酶信号通路的组成性激活,但新出现的数据表明黑色素瘤亚型之间存在分子差异。在本研究中,作者评估了B-RAF和N-RAS突变对Spitzoid黑色素瘤发病机制的贡献。
总共分析了33例Spitzoid黑色素瘤的临床和病理特征以及B-RAF和N-RAS基因的热点突变。在大多数患者(33例黑色素瘤中的28例)中,肿瘤局限于皮肤,无转移证据(平均随访32.5个月)。有5例转移性黑色素瘤(33例肿瘤中的5例)发生区域或全身扩散。
在33例Spitzoid黑色素瘤中,只有1例显示B-RAF基因的V600E突变(33例肿瘤中的1例;3%)。值得注意的是,转移性Spitzoid黑色素瘤中无一例(5例肿瘤中的0例;0%)显示B-RAF或N-RAS突变,其中2例导致致命后果。
与大多数皮肤黑色素瘤不同,B-RAF或N-RAS中的激活热点突变不参与Spitzoid黑色素瘤的发病机制。这些数据表明,Spitzoid黑色素瘤是一种独特的黑色素瘤形式,其发育涉及未知的基因和/或信号通路。