Title of article :
Genetic expression profiles and chromosomal alterations in sporadic breast cancer in Mexican women
Author/Authors :
Valladares، نويسنده , , Adلn and Hernلndez، نويسنده , , Normand Garcيa and Gَmez، نويسنده , , Fabio Salamanca and Curiel-Quezada، نويسنده , , Everardo and Madrigal-Bujaidar، نويسنده , , Eduardo and Vergara، نويسنده , , Ma. Dolores and Martيnez، نويسنده , , Mَnica Sierra and Arenas Aranda، نويسنده , , Diego J.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
5
From page :
147
To page :
151
Abstract :
Breast cancer is the second-leading cause of death among Mexican women >35 years of age. At the molecular level, changes in many genetic pathways have been reported to be associated with this neoplasm. To analyze these changes, we determined gene expression profiles and chromosomal structural alterations in tumors from Mexican women. We obtained mRNA to identify expression profiles with microarray technology, and DNA to determine amplifications and deletions, in 10 fresh sporadic breast tumor biopsies without treatment, as well as in 10 nonaffected breast tissues. Expression profiles were compared with genetic changes observed by comparative genomic hybridization (CGH). We compared the expression profiles against the structural alterations from the studied genes by means of microarrays; at least 17 of these genes correlated with DNA copy number alterations. We found that the following genes were overexpressed: LAMC1, PCTK3, CCNC, CCND1, FGF3, PCTK2, L1CAM, BGN, and PLXNB3 (alias PLEXR). Underexpressed genes included CASP9, FGR, TP73, HSPG2, and ERCC1; genes turned off included FRAP1, EPHA2 (previously ECK), IL12A, E2F5, TNFRSF10B, TNFRSF10A, EFNB3, and BCL2. The results will allow us, in the near future, to outline genes that could serve as diagnostic, prognostic, or target therapy markers for the Mexican population.
Journal title :
Cancer Genetics and Cytogenetics
Serial Year :
2006
Journal title :
Cancer Genetics and Cytogenetics
Record number :
1828045
Link To Document :
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