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Merck

High-density array comparative genomic hybridization detects novel copy number alterations in gastric adenocarcinoma.

Anticancer research (2014-11-05)
Aline Damasceno Seabra, Taíssa Maíra Thomaz Araújo, Fernando Augusto Rodrigues Mello Junior, Diego Di Felipe Ávila Alcântara, Amanda Paiva De Barros, Paulo Pimentel De Assumpção, Raquel Carvalho Montenegro, Adriana Costa Guimarães, Samia Demachki, Rommel Mario Rodríguez Burbano, André Salim Khayat
RESUMEN

To investigate frequent quantitative alterations of intestinal-type gastric adenocarcinoma. We analyzed genome-wide DNA copy numbers of 22 samples and using CytoScan® HD Array. We identified 22 gene alterations that to the best of our knowledge have not been described for gastric cancer, including of v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4 (ERBB4), SRY (sex determining region Y)-box 6 (SOX6), regulator of telomere elongation helicase 1 (RTEL1) and UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 5 (B4GALT5). The most significant alterations related to peritoneal invasion involved the regions 13q21.1 (gain) and 15q15.1, 17q23.1, 19q13.2 and 20q11.22 (loss of heterozygozity; LOH), where we found LOH of erythrocyte membrane protein band 4.1-like 1 (EPB41L1) gene. In relation to early age of onset, the most significant alterations were gains in the regions Xq26 and Xp22.31 and a loss in the region 11p15.4. These quantitative changes may play a role in the development of this type of neoplasia and may be used as markers in evaluating poor prognosis, as well as act as potential therapeutic targets for gastric cancer.

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