PMID- 19673870 OWN - NLM STAT- MEDLINE DCOM- 20100310 LR - 20211203 IS - 1365-2133 (Electronic) IS - 0007-0963 (Linking) VI - 161 IP - 5 DP - 2009 Nov TI - MYC gene numerical aberrations in actinic keratosis and cutaneous squamous cell carcinoma. PG - 1112-8 LID - 10.1111/j.1365-2133.2009.09351.x [doi] AB - BACKGROUND: The genetic alterations that drive the transition from actinic keratoses (AKs) to cutaneous squamous cell carcinomas (SCCs) have not been defined precisely. Amplification and/or overexpression of the MYC proto-oncogene have been demonstrated in several human, malignant tumours including head and neck SCCs. OBJECTIVES: To evaluate the presence of MYC genomic aberrations in both AKs and SCCs. METHODS: Skin biopsy specimens corresponding to AKs, SCCs and control samples were included in two paraffin-embedded tissue microarrays. MYC cytogenetic profile was evaluated by fluorescence in situ hybridization (FISH). The results obtained were compared with MYC immunohistochemical expression. RESULTS: Twenty-three AKs and 30 SCCs were evaluated. MYC numerical aberrations were observed in eight of 23 (35%) AKs and 19 of 30 (63%) SCCs (P = 0.05). MYC numerical aberrations were more frequent in moderately to poorly differentiated SCCs (77%) when compared with well-differentiated SCCs (25%; P = 0.027). A significant association between copy number gains of MYC by FISH analysis and MYC protein expression was demonstrated. CONCLUSIONS: MYC gains and amplifications are frequent cytogenetic abnormalities in SCCs and may play a relevant role in promoting SCC undifferentiation and tumoral progression. FAU - Toll, A AU - Toll A AD - Department of Dermatology, IMIM Hospital del Mar, Pg. 08003 Barcelona, Spain. 93828@imas.imim.es FAU - Salgado, R AU - Salgado R FAU - Yebenes, M AU - Yebenes M FAU - Martin-Ezquerra, G AU - Martin-Ezquerra G FAU - Gilaberte, M AU - Gilaberte M FAU - Baro, T AU - Baro T FAU - Sole, F AU - Sole F FAU - Alameda, F AU - Alameda F FAU - Espinet, B AU - Espinet B FAU - Pujol, R M AU - Pujol RM LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20090611 PL - England TA - Br J Dermatol JT - The British journal of dermatology JID - 0004041 SB - IM MH - Aged MH - Aged, 80 and over MH - Biopsy MH - Carcinoma, Squamous Cell/*genetics/pathology MH - *Chromosome Aberrations MH - *Disease Progression MH - Female MH - Genes, myc/*genetics MH - Humans MH - Immunohistochemistry MH - In Situ Hybridization, Fluorescence MH - Keratosis, Actinic/*genetics/pathology MH - Male MH - Microarray Analysis MH - Middle Aged MH - Proto-Oncogene Mas MH - Skin Neoplasms/*genetics/pathology EDAT- 2009/08/14 09:00 MHDA- 2010/03/11 06:00 CRDT- 2009/08/14 09:00 PHST- 2009/08/14 09:00 [entrez] PHST- 2009/08/14 09:00 [pubmed] PHST- 2010/03/11 06:00 [medline] AID - BJD9351 [pii] AID - 10.1111/j.1365-2133.2009.09351.x [doi] PST - ppublish SO - Br J Dermatol. 2009 Nov;161(5):1112-8. doi: 10.1111/j.1365-2133.2009.09351.x. Epub 2009 Jun 11.