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Mol Med. 2016 May 23;22. doi: 10.2119/molmed.2016.00020.

Low miR-187 expression promotes resistance to chemoradiation therapy in vitro and correlates with treatment failure in patients with esophageal adenocarcinoma.

Author information

1
University of Dublin Trinity College, Dublin, Ireland.
2
University of Hull, Hull, Kingston upon Hull, United Kingdom of Great Britain and Northern Ireland.
3
Arup Institute for Clinical and Experimental Pathology, United States.
4
University of Utah and ARUP Laboratories, United States.

Abstract

Esophageal adenocarcinoma (EAC) has a poor prognosis and is increasing in incidence in many western populations. Neoadjuvant chemoradiation therapy (CRT) followed by surgery is increasingly the standard of care for locally advanced EAC; however, resistance to treatment is a significant clinical problem. The identification of both novel biomarkers predicting response to treatment and novel therapeutic targets to enhance the efficacy of CRT are key to improving survival rates in EAC. In this study we performed global microRNA (miRNA) profiling of pre-treatment EAC biopsies and identified 67 miRNA significantly altered in patients who are resistant to CRT. One of these miRNA, miR-187, was significantly decreased in pre-treatment EAC tumors from patients having a poor response to neoadjuvant CRT, highlighting downregulation of miR-187 as a potential mechanism of treatment resistance in EAC. In vitro, miR-187 was demonstrated to play a functional role in modulating sensitivity to X-ray radiation and cisplatin in EAC and its dysregulation was demonstrated to be due to chromosomal alterations. In vitro, miR-187 altered expression of a diverse array of pathways, including the immune regulator complement component 3 (C3), serum levels of which we have previously demonstrated to predict patient response to CRT. In vivo, expression of C3 was significantly increased in tumors from patients having a poor response to CRT. This study highlights for the first time a role for miR-187 as a novel biomarker of response to CRT and a potential therapeutic target for enhancing the efficacy of CRT in EAC.

KEYWORDS:

Chemoradiation Therapy; Predictive biomarker; gastroenterology; microRNA; oncology

PMID:
27254108
PMCID:
PMC5072404
DOI:
10.2119/molmed.2016.00020
[Indexed for MEDLINE]
Free PMC Article

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