光化性角化病
医学
基因
角化病
基因表达
病理
活检
皮肤活检
皮肤病科
基底细胞
癌症研究
生物
遗传学
作者
R. Steven Padilla,Sheldon Sebastian,Zeyu Jiang,Ingo Nindl,Richard A. Larson
出处
期刊:Archives of Dermatology
[American Medical Association]
日期:2010-03-01
卷期号:146 (3)
被引量:114
标识
DOI:10.1001/archdermatol.2009.378
摘要
Objectives
To identify and compare the gene expression profiles of actinic keratosis (AK) and squamous cell carcinoma (SCC) and to further clarify critical genetic alterations in the evolution of SCC from normal sun-damaged human skin. Design
Observational study. Setting
University practice. Patients
Skin biopsy specimens were obtained from 16 patients. The specimens included 14 normal non–sun-exposed skin samples, 14 normal sun-exposed skin samples, 5 AKs, and 15 cutaneous SCCs. Main Outcome Measures
Gene expression profiles from normal non–sun-exposed skin, normal sun-exposed skin, AKs, and SCCs. Results
Using a highly astringent shrunken centroid threshold of 6.52 and the prediction analysis of microarrays, we identified 89 unique genes that most likely contribute to the molecular evolution of SCC. Our model was cross-validated using data from a separate study and clearly distinguishes between skin tumors (AK and SCC) and normal skin independent of sun exposure. Genes that were upregulated in AK and SCC were downregulated in normal skin, and genes that were downregulated in AK and SCC were upregulated in normal skin. Conclusions
The finding of similar differentially expressed genes in AK and SCC confirms that AK is a precursor lesion of SCC and indicates that they are closely related genetically. Clear elucidation of these relationships will be critical to improving therapeutic approaches.
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