Literature DB >> 22648208

Circulating miR-34a levels are reduced in colorectal cancer.

M Nugent1, N Miller, M J Kerin.   

Abstract

INTRODUCTION: MicroRNAs (miRNAs) are small, non-coding RNA segments that regulate gene expression via post-transcriptional inhibition and have roles in cell differentiation, proliferation, and apoptosis. Expression differs between tumor and normal tissue in several malignancies. Most work has focused on tissue and cell expression with few reports of circulating miRNAs in colorectal cancer. Available biomarkers for colorectal cancer have limited sensitivity and specificity, thus there is a need for new markers. AIMS: This study aimed to identify miRNAs that are differentially expressed in the blood of colorectal cancer patients compared to controls and to establish if this is specific to colorectal cancer and thus could be utilized as potential tumor markers.
METHODS: Blood samples were collected from 63 colorectal cancer patients and 45 controls. Expression of 7 target miRNAs (miR-143, miR-145, miR-21, miR-30a-3p, miR-31, miR-34a, and miR-92) was measured using RQ-PCR. Results were correlated with clinicopathological data and analyzed. Analysis of differentially expressed circulating miRNAs was expanded to include 62 patients with prostate, renal, breast, and melanoma cancers.
RESULTS: Analysis of the relative quantification of the target miRNAs showed significantly reduced expression (P = 0.004) of miR-34a in colorectal cancer. MiR-34a was also significantly reduced in breast cancer (P = 0.019).
CONCLUSION: This study demonstrates significantly reduced expression of circulating miR-34a in colorectal and breast cancer. This may have future application as part of a biomarker profile.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22648208     DOI: 10.1002/jso.23174

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  37 in total

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Journal:  World J Gastroenterol       Date:  2014-04-21       Impact factor: 5.742

Review 2.  Circulating microRNA testing for the early diagnosis and follow-up of colorectal cancer patients.

Authors:  Andrew Fesler; Jingting Jiang; Haiyan Zhai; Jingfang Ju
Journal:  Mol Diagn Ther       Date:  2014-06       Impact factor: 4.074

3.  MicroRNA-215 inhibits relapse of colorectal cancer patients following radical surgery.

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4.  Combination of circulating miR-19b-3p, miR-122-5p and miR-486-5p expressions correlates with risk and disease severity of knee osteoarthritis.

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5.  Circulating miR34a levels as a potential biomarker in the follow-up of Ewing sarcoma.

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Journal:  J Cell Commun Signal       Date:  2020-06-05       Impact factor: 5.782

6.  Circulating microRNA profiles reflect the presence of breast tumours but not the profiles of microRNAs within the tumours.

Authors:  Victoria J Cookson; Michael A Bentley; Brian V Hogan; Kieran Horgan; Bruce E Hayward; Lee D Hazelwood; Thomas A Hughes
Journal:  Cell Oncol (Dordr)       Date:  2012-07-21       Impact factor: 6.730

Review 7.  The tumor-suppressive and potential therapeutic functions of miR-34a in epithelial carcinomas.

Authors:  Brian D Adams; Christine Parsons; Frank J Slack
Journal:  Expert Opin Ther Targets       Date:  2015-12-11       Impact factor: 6.902

Review 8.  Role of microRNAs in the immune system, inflammation and cancer.

Authors:  Jennifer Raisch; Arlette Darfeuille-Michaud; Hang Thi Thu Nguyen
Journal:  World J Gastroenterol       Date:  2013-05-28       Impact factor: 5.742

9.  KLK6-regulated miRNA networks activate oncogenic pathways in breast cancer subtypes.

Authors:  Konstantinos G Sidiropoulos; Qiang Ding; Georgios Pampalakis; Nicole M A White; Peter Boulos; Georgia Sotiropoulou; George M Yousef
Journal:  Mol Oncol       Date:  2016-04-08       Impact factor: 6.603

Review 10.  Oncogenic and Tumor-Suppressive Roles of MicroRNAs with Special Reference to Apoptosis: Molecular Mechanisms and Therapeutic Potential.

Authors:  Dharambir Kashyap; Hardeep Singh Tuli; Vivek Kumar Garg; Neelam Goel; Anupam Bishayee
Journal:  Mol Diagn Ther       Date:  2018-04       Impact factor: 4.074

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