Identification of differential expressed transcripts in cervical cancer of Mexican patients
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The aim of this study was to identify the gene expression profile in biopsies of patients with cervical intraepithelial neoplasia (CIN) 1, CIN 2, CIN 3, and microinvasive cancer by suppression subtractive hybridization and Southern blotting. After analyzing 1,800 cDNA clones, we found 198 upregulated genes, 166 downregulated, and no significant change of gene expression in 86 clones (p=0.005). These results were validated by Northern blot analysis (p=0.0001) in the identification of 28 overexpressed and 7 downregulated transcripts. We observed a set of genes related to the Notch signaling pathway that may be involved in the transformation of cervical cells and in the development to malignancy. The differentially expressed genes may provide useful information about the molecular mechanisms involved in human cervical carcinoma and as diagnostic markers. © 2010 International Society of Oncology and BioMarkers (ISOBM).
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Cervical cancer; Gene expression; Mexican women; SSH complementary DNA; Notch receptor; apoptosis regulatory protein; CCAR1 protein, human; cell cycle protein; MYCN protein, human; Notch receptor; NOTCH3 protein, human; nuclear protein; oncoprotein; article; cancer grading; controlled study; DNA sequence; down regulation; female; gene expression profiling; gene expression regulation; gene identification; gene overexpression; human; human cell; human tissue; intracellular signaling; invasive carcinoma; Mexico; molecular cloning; molecular dynamics; Northern blotting; nucleotide sequence; priority journal; transcription regulation; upregulation; uterine cervix cancer; validation process; gene expression profiling; genetic transcription; genetics; Human papillomavirus type 16; isolation and purification; pathology; physiology; uterine cervix tumor; virology; Apoptosis Regulatory Proteins; Cell Cycle Proteins; Female; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Human papillomavirus 16; Humans; Mexico; Nuclear Proteins; Oncogene Proteins; Receptors, Notch; Transcription, Genetic; Uterine Cervical Neoplasms
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