» Articles » PMID: 24564330

Co-modulated Behavior and Effects of Differentially Expressed MiRNA in Colorectal Cancer

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2014 Feb 26
PMID 24564330
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Background: MicroRNAs (miRNAs) are short noncoding RNAs (approximately 22 nucleotides in length) that play important roles in colorectal cancer (CRC) progression through silencing gene expression. Numerous dysregulated miRNAs simultaneously participate in the process of colon cancer development. However, the detailed mechanisms and biological functions of co-expressed miRNA in colorectal carcinogenesis have yet to be fully elucidated.

Results: The objective of this study was to identify the dysfunctional miRNAs and their target mRNAs using a wet-lab experimental and dry-lab bioinformatics approach. The differentially expressed miRNA candidates were identified from 2 miRNA profiles, and were confirmed in CRC clinical samples using reported target genes of dysfunctional miRNAs to perform functional pathway enrichment analysis. Potential target gene candidates were predicted by an in silico search, and their expression levels between normal and colorectal tumor tissues were further analyzed using real-time polymerase chain reaction (RT-PCR).

Conclusion: Fifteen dysfunctional miRNAs were engaged in metastasis-associated pathways through comodulating 7 target genes, which were identified by using a multi-step approach. The roles of these candidate genes are worth further exploration in the progression of colon cancer, and could potentially be targets in future therapy.

Citing Articles

Long Noncoding RNA LOC550643 Acts as an Oncogene in the Growth Regulation of Colorectal Cancer Cells.

Wu H, Lu T, Lo Y, Tu Y, Chen Y, Lee M Cells. 2022; 11(7).

PMID: 35406629 PMC: 8997465. DOI: 10.3390/cells11071065.


Myosin Motors: Novel Regulators and Therapeutic Targets in Colorectal Cancer.

Naydenov N, Lechuga S, Huang E, Ivanov A Cancers (Basel). 2021; 13(4).

PMID: 33670106 PMC: 7916823. DOI: 10.3390/cancers13040741.


Downregulation of microRNA-126 is inversely correlated with insulin receptor substrate-1 protein expression in colorectal cancer and is associated with advanced stages of disease.

Ye S, Yu C, Zhang G, Shi F, Chen Y, Yang J Oncol Lett. 2020; 20(3):2411-2419.

PMID: 32782558 PMC: 7400408. DOI: 10.3892/ol.2020.11796.


TACCO, a Database Connecting Transcriptome Alterations, Pathway Alterations and Clinical Outcomes in Cancers.

Chou P, Liao W, Tsai K, Chen K, Yu J, Chen T Sci Rep. 2019; 9(1):3877.

PMID: 30846808 PMC: 6405743. DOI: 10.1038/s41598-019-40629-z.


Aberrantly Expressed Genes and miRNAs in Slow Transit Constipation Based on RNA-Seq Analysis.

Zhao S, Chen Q, Kang X, Kong B, Wang Z Biomed Res Int. 2018; 2018:2617432.

PMID: 30186855 PMC: 6112260. DOI: 10.1155/2018/2617432.


References
1.
Lai V, Ashraf M, Jiang S, Haider K . MicroRNA-143 is a critical regulator of cell cycle activity in stem cells with co-overexpression of Akt and angiopoietin-1 via transcriptional regulation of Erk5/cyclin D1 signaling. Cell Cycle. 2012; 11(4):767-77. PMC: 3318108. DOI: 10.4161/cc.11.4.19211. View

2.
Monzo M, Navarro A, Bandres E, Artells R, Moreno I, Gel B . Overlapping expression of microRNAs in human embryonic colon and colorectal cancer. Cell Res. 2008; 18(8):823-33. DOI: 10.1038/cr.2008.81. View

3.
Akao Y, Nakagawa Y, Naoe T . MicroRNA-143 and -145 in colon cancer. DNA Cell Biol. 2007; 26(5):311-20. DOI: 10.1089/dna.2006.0550. View

4.
Li X, Zhang G, Luo F, Ruan J, Huang D, Feng D . Identification of aberrantly expressed miRNAs in rectal cancer. Oncol Rep. 2012; 28(1):77-84. DOI: 10.3892/or.2012.1769. View

5.
Callari M, Dugo M, Musella V, Marchesi E, Chiorino G, Mello Grand M . Comparison of microarray platforms for measuring differential microRNA expression in paired normal/cancer colon tissues. PLoS One. 2012; 7(9):e45105. PMC: 3441572. DOI: 10.1371/journal.pone.0045105. View