Abstract | BACKGROUND: AIMS: We reviewed studies that have investigated this to identify microRNAs with high biomarker potential for screening and disease monitoring in BE. METHODS: PubMed and EMBASE databases were searched for studies that quantified esophageal epithelial microRNAs. Publications reporting microRNA comparisons of normal, non-dysplastic BE, BE with high-grade dysplasia (HGD), and EAC tissues using both unbiased discovery and independent validation phases were reviewed. RESULTS: Eleven studies on microRNA expression differences between normal epithelium and non-dysplastic BE (seven studies), HGD (4) or EAC (7), or between non-dysplastic BE and HGD (3) or EAC (6) were identified, and the findings of their validation phase were analyzed. Increased miR-192, -194, and -215, and reduced miR-203 and -205 expression in BE compared to normal was noticed by all 4-6 of the seven studies that examined these microRNAs. In heterogeneity tests of the reported fold-change values, the I (2) statistics were 7.9-17.1 % (all P < 0.05). Elevated miR-192, -194, and -215, and diminished miR-203 and -205 levels were also noted for comparisons of HGD or EAC against normal. In contrast, a consistent microRNA expression difference was absent for the comparisons of HGD or EAC against BE. CONCLUSIONS:
MicroRNAs miR-192, -194, -203, -205, and -215 are promising tissue biomarkers for diagnosing BE. Cross-sectional data suggest that microRNAs may have a limited role in separating BE from HGD/EAC epithelia but need further testing in longitudinal follow-up studies.
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Authors | Reema Mallick, Santosh K Patnaik, Sachin Wani, Ajay Bansal |
Journal | Digestive diseases and sciences
(Dig Dis Sci)
Vol. 61
Issue 4
Pg. 1039-50
(Apr 2016)
ISSN: 1573-2568 [Electronic] United States |
PMID | 26572780
(Publication Type: Journal Article, Review, Systematic Review)
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Chemical References |
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Topics |
- Adenocarcinoma
(etiology, metabolism)
- Barrett Esophagus
(complications, diagnosis, metabolism)
- Biomarkers
(metabolism)
- Esophageal Neoplasms
(etiology, metabolism)
- Humans
- MicroRNAs
(metabolism)
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