| Literature DB >> 22393467 |
Lloyd D Graham1, Susanne K Pedersen, Glenn S Brown, Thu Ho, Zena Kassir, Audrey T Moynihan, Emma K Vizgoft, Robert Dunne, Letitia Pimlott, Graeme P Young, Lawrence C Lapointe, Peter L Molloy.
Abstract
An uncharacterized gene locus (Chr16:hCG_1815491), now named colorectal neoplasia differentially expressed (gene symbol CRNDE), is activated early in colorectal neoplasia. The locus is unrelated to any known protein-coding gene. Microarray analysis of 454 tissue specimens (discovery) and 68 previously untested specimens (validation) showed elevated expression of CRNDE in >90% of colorectal adenomas and adenocarcinomas. These findings were confirmed and extended by exon microarray studies and RT-PCR assays. CRNDE transcription start sites were identified in CaCo2 and HCT116 cells by 5'-RACE. The major transcript isoforms in colorectal cancer (CRC) cell lines and colorectal tissue are CRNDE-a, -b, -d, -e, -f, -h, and -j. Except for CRNDE-d, the known CRNDE splice variants are upregulated in neoplastic colorectal tissue; expression levels for CRNDE-h alone demonstrate a sensitivity of 95% and specificity of 96% for adenoma versus normal tissue. A quantitative RT-PCR assay measuring CRNDE-h RNA levels in plasma was (with a threshold of 2(-ΔCt) = 2.8) positive for 13 of 15 CRC patients (87%) but only 1 of 15 healthy individuals (7%). We conclude that individual CRNDE transcripts show promise as tissue and plasma biomarkers, potentially exhibiting high sensitivity and specificity for colorectal adenomas and cancers.Entities:
Keywords: CRNDE; RNA biomarker; colorectal adenoma; colorectal cancer; colorectal neoplasia
Year: 2011 PMID: 22393467 PMCID: PMC3278902 DOI: 10.1177/1947601911431081
Source DB: PubMed Journal: Genes Cancer ISSN: 1947-6019