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A known expressed sequence tag, BM742401, is a potent lincRNA inhibiting cancer metastasis
Experimental & Molecular Medicine ; : e31-2013.
Article in English | WPRIM | ID: wpr-124615
ABSTRACT
Long intergenic non-coding RNAs (lincRNAs) have historically been ignored in cancer biology. However, thousands of lincRNAs have been identified in mammals using recently developed genomic tools, including microarray and high-throughput RNA sequencing (RNA-seq). Several of the lincRNAs identified have been well characterized for their functions in carcinogenesis. Here we performed RNA-seq experiments comparing gastric cancer with normal tissues to find differentially expressed transcripts in intergenic regions. By analyzing our own RNA-seq and public microarray data, we identified 31 transcripts, including a known expressed sequence tag, BM742401. BM742401 was downregulated in cancer, and its downregulation was associated with poor survival in gastric cancer patients. Ectopic overexpression of BM742401 inhibited metastasis-related phenotypes and decreased the concentration of extracellular MMP9. These results suggest that BM742401 is a potential lincRNA marker and therapeutic target.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Stomach Neoplasms / RNA, Messenger / Gene Expression Regulation, Neoplastic / Proportional Hazards Models / Survival Analysis / Multivariate Analysis / Reproducibility of Results / Genetic Predisposition to Disease / Expressed Sequence Tags Type of study: Prognostic study Limits: Animals / Humans / Male Language: English Journal: Experimental & Molecular Medicine Year: 2013 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Stomach Neoplasms / RNA, Messenger / Gene Expression Regulation, Neoplastic / Proportional Hazards Models / Survival Analysis / Multivariate Analysis / Reproducibility of Results / Genetic Predisposition to Disease / Expressed Sequence Tags Type of study: Prognostic study Limits: Animals / Humans / Male Language: English Journal: Experimental & Molecular Medicine Year: 2013 Type: Article