» Articles » PMID: 26722476

MiR-503 Inhibits Cell Proliferation and Induces Apoptosis in Colorectal Cancer Cells by Targeting E2F3

Overview
Specialty Pathology
Date 2016 Jan 2
PMID 26722476
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Colorectal cancer (CRC) is one of the major healthcare problems worldwide. A lot of miRNAs are aberrantly expressed in CRC and involved in its development and progression. The purpose of this study was to investigate the expression and function of miR-503 in CRC.

Methods: miR-503 expression was detected in CRC tissues and cell lines by Quantitative real-time PCR. Cell proliferation was assessed by MTT assay. Cell apoptosis and cell cycle distribution were measured by flow cytometry. Moreover, luciferase reporter assay and western blot were performed to determine the potential target of miR-503 in CRC cells.

Results: miR-503 was significantly decreased in CRC tissues and cell lines in comparison with controls. Overexpression of miR-503 in CRC cells remarkably inhibited cell proliferation and induced apoptosis. Furthermore, E2F3 was identified as a direct target of miR-503 in CRC cells and down-regulation of E2F3 had a similar effect as miR-503 overexpression on CRC cells. In addition, the expression of E2F3 was negatively correlated with miR-503 level in CRC tissues.

Conclusions: miR-503 inhibits cell proliferation and induces apoptosis by directly targeting E2F3 in CRC cells, indicating its potential application in CRC diagnosis and therapy.

Citing Articles

Role of non-coding RNAs as new therapeutic targets in regulating the EMT and apoptosis in metastatic gastric and colorectal cancers.

Ebrahimi N, Hakimzadeh A, Bozorgmand F, Speed S, Manavi M, Khorram R Cell Cycle. 2023; 22(20):2302-2323.

PMID: 38009668 PMC: 10730205. DOI: 10.1080/15384101.2023.2286804.


MiR-363 restrain the proliferation, migration and invasion of colorectal carcinoma cell by targeting E2F3.

Yang W, Yang X, Zhang Y, Li Y, Lv W J Cancer. 2023; 14(8):1362-1370.

PMID: 37283793 PMC: 10240674. DOI: 10.7150/jca.83897.


The Role and Interactions of Programmed Cell Death 4 and its Regulation by microRNA in Transformed Cells of the Gastrointestinal Tract.

Ferris W Front Oncol. 2022; 12:903374.

PMID: 35847932 PMC: 9277020. DOI: 10.3389/fonc.2022.903374.


Systematic Analysis of E2F Expression and Its Relation in Colorectal Cancer Prognosis.

Xu Z, Qu H, Ren Y, Gong Z, Ri H, Zhang F Int J Gen Med. 2022; 15:4849-4870.

PMID: 35585998 PMC: 9109810. DOI: 10.2147/IJGM.S352141.


Tumor-associated macrophages promote cholangiocarcinoma progression via exosomal Circ_0020256.

Chen S, Chen Z, Li Z, Li S, Wen Z, Cao L Cell Death Dis. 2022; 13(1):94.

PMID: 35091535 PMC: 8799724. DOI: 10.1038/s41419-022-04534-0.


References
1.
He L, Hannon G . MicroRNAs: small RNAs with a big role in gene regulation. Nat Rev Genet. 2004; 5(7):522-31. DOI: 10.1038/nrg1379. View

2.
Huang L, Luo J, Cai Q, Pan Q, Zeng H, Guo Z . MicroRNA-125b suppresses the development of bladder cancer by targeting E2F3. Int J Cancer. 2010; 128(8):1758-69. DOI: 10.1002/ijc.25509. View

3.
Yang Y, Gu X, Zhou M, Xiang J, Chen Z . Serum microRNAs: A new diagnostic method for colorectal cancer. Biomed Rep. 2014; 1(4):495-498. PMC: 3917018. DOI: 10.3892/br.2013.109. View

4.
Orang A, Barzegari A . MicroRNAs in colorectal cancer: from diagnosis to targeted therapy. Asian Pac J Cancer Prev. 2014; 15(17):6989-99. DOI: 10.7314/apjcp.2014.15.17.6989. View

5.
Raskov H, Pommergaard H, Burcharth J, Rosenberg J . Colorectal carcinogenesis--update and perspectives. World J Gastroenterol. 2015; 20(48):18151-64. PMC: 4277953. DOI: 10.3748/wjg.v20.i48.18151. View