Tumor suppressor miR-375 regulates MYC expression via repression of CIP2A coding sequence through multiple miRNA-mRNA interactions

• Published in: Molecular biology of the cell Vol. 24; no. 11; pp. 1638 - 1648
• Main Authors: Jung, Hyun Min, Patel, Rushi S, Phillips, Brittany L, Wang, Hai, Cohen, Donald M, Reinhold, William C, Chang, Lung-Ji, Yang, Li-Jun, Chan, Edward K L
• Format: Journal Article
• Language: English
• Published: United States The American Society for Cell Biology 01-06-2013
• Subjects: Autoantigens - genetics; Autoantigens - metabolism; Base Sequence; Binding Sites; Carcinoma, Squamous Cell - genetics; Carcinoma, Squamous Cell - metabolism; Carcinoma, Squamous Cell - pathology; Cell Line, Tumor; Cell Movement; Cell Proliferation; Gene Expression Regulation, Neoplastic; Genes, Reporter; Humans; Luciferases - metabolism; Membrane Proteins - genetics; Membrane Proteins - metabolism; MicroRNAs - genetics; MicroRNAs - metabolism; Molecular Sequence Data; Mouth Neoplasms - genetics; Mouth Neoplasms - metabolism; Mouth Neoplasms - pathology; Mutation; Open Reading Frames; Primary Cell Culture; Proto-Oncogene Proteins c-myc - genetics; Proto-Oncogene Proteins c-myc - metabolism; RNA, Messenger - genetics; RNA, Messenger - metabolism; Signal Transduction; Tongue - metabolism; Tongue - pathology
• ISSN: 1059-1524; 1939-4586
• DOI: 10.1091/mbc.e12-12-0891

MicroRNAs (miRNAs) are small, noncoding RNAs involved in posttranscriptional regulation of protein-coding genes in various biological processes. In our preliminary miRNA microarray analysis, miR-375 was identified as the most underexpressed in human oral tumor versus controls. The purpose of the present study is to examine the function of miR-375 as a candidate tumor suppressor miRNA in oral cancer. Cancerous inhibitor of PP2A (CIP2A), a guardian of oncoprotein MYC, is identified as a candidate miR-375 target based on bioinformatics. Luciferase assay accompanied by target sequence mutagenesis elucidates five functional miR-375-binding sites clustered in the CIP2A coding sequence close to the C-terminal domain. Overexpression of CIP2A is clearly demonstrated in oral cancers, and inverse correlation between miR-375 and CIP2A is observed in the tumors, as well as in NCI-60 cell lines, indicating the potential generalized involvement of the miR-375-CIP2A relationship in many other cancers. Transient transfection of miR-375 in oral cancer cells reduces the expression of CIP2A, resulting in decrease of MYC protein levels and leading to reduced proliferation, colony formation, migration, and invasion. Therefore this study shows that underexpression of tumor suppressor miR-375 could lead to uncontrolled CIP2A expression and extended stability of MYC, which contributes to promoting cancerous phenotypes.