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MicroRNA-320b promotes colorectal cancer proliferation and invasion by competing with its homologous microRNA-320a.

Abstract
Colorectal cancer metastasis is believed to be associated with microRNA dysregulation. However, little is known as to how microRNAs regulate colorectal cancer proliferation, invasion and metastasis. In the present study, we compared the microRNA expression profiles between patients of colorectal cancer at diagnosis with and without liver metastasis. MicroRNA-320b was found to be among those up-regulated in the patient group with metastasis. We subsequently found that microRNA-320b, opposite of its homolog, microRNA-320a that differs by only a single nucleotide, functions in promoting colorectal cancer cell proliferation and invasion. Moreover, we found that overexpression of exogenous microRNA-320b can up-regulate the target genes of microRNA-320a including β-catenin, Neuropilin-1 and Rac-1, which are all known to promote tumor proliferation, invasion and metastasis. These results suggest that microRNA-320b may function in competing with microRNA-320a. Thus, our study has proposed one novel mechanism for controlling colorectal cancer proliferation and invasion through homologous competition between microRNAs. This mechanism may be important for colorectal cancer metastasis.
AuthorsJiaojiao Zhou, Mengwen Zhang, Yanqing Huang, Lin Feng, Hailong Chen, Yiwang Hu, Huarong Chen, Kaitai Zhang, Lei Zheng, Shu Zheng
JournalCancer letters (Cancer Lett) Vol. 356 Issue 2 Pt B Pg. 669-75 (Jan 28 2015) ISSN: 1872-7980 [Electronic] Ireland
PMID25458952 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Biomarkers, Tumor
  • MIRN320 microRNA, human
  • MicroRNAs
  • RNA, Messenger
Topics
  • Apoptosis
  • Biomarkers, Tumor (genetics)
  • Blotting, Western
  • Cell Adhesion
  • Cell Movement
  • Cell Proliferation
  • Colorectal Neoplasms (genetics, pathology)
  • Gene Expression Profiling
  • Humans
  • Liver Neoplasms (genetics, secondary)
  • MicroRNAs (genetics)
  • Neoplasm Invasiveness
  • Neoplasm Staging
  • RNA, Messenger (genetics)
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Cells, Cultured

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