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Actinic Keratosis


Scientists at University of Tokushima, Institute of Health Bioscience report research in carcinoma genetics



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This article was published in Clinical Oncology Week, which you can subscribe to online.

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2009 JUN 15 - (NewsRx.com) -- Fresh data on carcinoma are presented in the report 'Activation of fibroblast growth factor receptor 3 and oncogene-induced senescence in skin tumours.' "The activation of oncogenes is an important step in tumorigenesis, and recently, oncogene-induced senescence (OIS) was proposed as a critical barrier against malignant transformation in normal primary cells. The aim of this study was to examine the activation of fibroblast growth factor receptor 3 (FGFR3) as an oncogene product and OIS in human skin tumours," scientists in Japan report.

"We investigated the activation of FGFR3 and OIS by mutation and immunohistochemical analysis in skin tumours, including seborrhoeic keratosis, actinic keratosis (AK), Bowen's disease (BD), basal cell carcinoma (BCC) and squamous cell carcinoma (SCC). Activated point mutations of FGFR3 were identified in four of 22 cases (18%) of seborrhoeic keratosis, but no mutation was detected in the other skin tumours. Twenty-seven of 31 cases (87%) of seborrhoeic keratosis showed moderately to strongly positive expression of the FGFR3 protein, but almost all the other skin tumours were negative. On the other hand, almost all the seborrhoeic keratoses showed negative immunoreactivity for antiphoshohistone H2AX (gamma-H2AX) as a marker of OIS, but 17 of 22 cases (77%) of AK were moderately to strongly positive. Immunoreactivity for gamma-H2AX was significantly greater in AK than in seborrhoeic keratosis, BD, BCC and SCC. The activation of FGFR3 might be a common feature in the tumorigenesis in seborrhoeic keratosis, although the activation does not induce a typical oncogenic signal in keratinocytes," wrote Y. Hida and colleagues, University of Tokushima, Institute of Health Bioscience.

The researchers concluded: "In addition, OIS due to some oncogenic signals rather than activation of FGFR3 might be involved in the early skin carcinogenesis related to chronic ultraviolet radiation exposure."

Hida and colleagues published their study in British Journal of Dermatology (Activation of fibroblast growth factor receptor 3 and oncogene-induced senescence in skin tumours. British Journal of Dermatology, 2009;160(6):1258-63).

For additional information, contact Y. Hida, The University of Tokushima Graduate School, Dept. of Dermatology, Institute of Health Biosciences, Japan.

The publisher's contact information for the British Journal of Dermatology is: Blackwell Publishing Inc., 350 Main St., Malden, MA 02148, USA.

Keywords: Japan, Carcinoma Genetics, Actinic Keratosis, Basal Cell Cancer, Basal Cell Carcinoma, Bowen Disease, Dermatology, Genetics, Oncology, Squamous Cell Carcinoma.

This article was prepared by Clinical Oncology Week editors from staff and other reports. Copyright 2009, Clinical Oncology Week via NewsRx.com.

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