Large-Scale Analysis of <i>KIT</i> Aberrations in Chinese Patients with Melanoma

Yan Kong(Oregon Health & Science University), Lu Si(Oregon Health & Science University), Yanyan Zhu(Oregon Health & Science University), Xiaowei Xu(Oregon Health & Science University), Christopher L. Corless(Oregon Health & Science University), Keith T. Flaherty(Oregon Health & Science University), Li Li(Oregon Health & Science University), Haifu Li(Oregon Health & Science University), Xinan Sheng(Oregon Health & Science University), Chuanliang Cui(Oregon Health & Science University), Zhihong Chi(Oregon Health & Science University), Siming Li(Oregon Health & Science University), Mei Han(Oregon Health & Science University), Lili Mao(Oregon Health & Science University), Aiping Lü(Oregon Health & Science University), Jun Guo(Oregon Health & Science University)
Clinical Cancer Research
February 16, 2011
Cited by 252

Abstract

PURPOSE: KIT aberrations were described in acral and mucosal melanomas in largely Caucasian populations. Asian populations are more prone to develop acral and mucosal than cutaneous melanomas, and may harbor a high frequency of KIT aberrations. EXPERIMENTAL DESIGN: Melanoma subtypes (n = 502) were analyzed histologically to determine melanoma subtype. Tissue samples were analyzed for mutations in exons 9, 11, 13, 17, and 18 of KIT gene in genomic DNA by PCR amplification and Sanger sequencing. The copy numbers of the KIT gene were analyzed by quantitative PCR, and protein expression levels of KIT (CD117) were determined by immunohistochemistry. RESULTS: The most common melanoma subtypes were acral (38.4%) and mucosal (33.3%) melanomas in this population. The overall incidence of somatic mutations within the KIT gene was 10.8% (54/502), and all subtypes of melanoma contained KIT mutations. Increases in KIT gene copy numbers were correlated to CD117 overexpression. The genetic mutations of KIT were unrelated to the age, gender, stage, thickness, and ulceration of primary melanomas. Importantly, the overall survival of melanoma patients with KIT mutations (P = 0.001) or with KIT aberrations (mutation plus amplification, P = 0.0002) was significantly shorter than that of patients without such alterations. CONCLUSION: In China, the prevalent melanomas are acral and mucosal melanomas. KIT mutations are detected in all melanoma subtypes. Our study suggests that increases in KIT gene copy numbers, but not KIT mutations, may be correlated to CD117 overexpression. For the first time, our study suggests that genetic KIT aberration is an adverse prognostic factor for melanoma.


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