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Bioinformatic analysis of cancer-related microRNAs and their target genes

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  • 1. School of Chemistry and Biological Engineering, Nanjing Normal University Taizhou College, Taizhou 225300, China;
    2. Health Management Department of Daping Hospital, Third Military Medical University, Chongqing 400042,China;
    3. College of Life Science, Nanjing Normal University, Nanjing 210046, China

Received date: 2015-03-22

  Revised date: 2015-07-06

  Online published: 2015-09-20

Abstract

MicroRNAs (miRNAs) are a class of ~22 nucleotide endogenous noncoding RNAs which regulate gene expression by targeting complementary transcripts. Recent studies have found that miRNAs are closely related to tumorigenesis and can act as oncogenes or tumor suppressor genes to influence the occurrence and development of tumor. To further reveal characteristics of cancer-related miRNAs and the functions of miRNA targets, we obtained 475 miRNAs involved in cancer through database searching and information retrieval. We systematically analyzed and compared the features including conservation, SNP distribution, cancer spectrum width, and transcriptional regulation between cancer and non-cancer related miRNAs as well as between intergenic and intragenic miRNAs. Our results showed that cancer-related miRNAs have higher conservation and lower SNP frequency compared to non-cancer-related miRNAs, and the cancer spectrum of one miRNA is positively correlated with its conservation. Genome analysis showed that cancer-related miRNAs tend to present as clusters compared with non-cancer-related miRNAs. Further association analysis between cancer progression and host genes, cancer-related miRNAs or target genes found that the host genes of some non-cancer related miRNAs tend to be targeted by cancer-related miRNAs. This study provides theoretical basis for further understanding the relationship between miRNA and cancer progression as well as the miRNA-based cancer diagnosis.

Cite this article

Xue Zhou, Yilan Du, Ping Jin, Fei Ma . Bioinformatic analysis of cancer-related microRNAs and their target genes[J]. Hereditas(Beijing), 2015 , 37(9) : 855 -864 . DOI: 10.16288/j.yczz.14-439

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