Journal article
Mutations in KIT occur at low frequency in melanomas arising from anatomical sites associated with chronic and intermittent sun exposure
D Handolias, R Salemi, W Murray, A Tan, W Liu, A Viros, A Dobrovic, J Kelly, GA McArthur
Pigment Cell and Melanoma Research | Published : 2010
Abstract
In melanoma, mutations in KIT are most frequent in acral and mucosal subtypes and rarely reported in cutaneous melanomas particularly those associated with intermittent UV exposure. Conversely melanomas arising within chronic sun damaged skin are considered to harbour KIT mutations at higher rates. To characterize the frequency of KIT mutations in a representative melanoma population, 261 patients from two Australian melanoma centres were prospectively screened for mutations in exons 11, 13 and 17 of the KIT gene. A total of 257 patients had cutaneous melanoma arising from non-acral sites and four were acral melanomas. No mucosal or ocular melanomas were analysed. KIT mutations were identifi..
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Funding Acknowledgements
This work was supported by grants from the NHMRC and a Sir Edward Dunlop Clinical Research Fellowship from the Cancer Council of Victoria (G. A. McArthur), and an Australian Postgraduate Award from the University of Melbourne (D. Handolias).