Evaluation of common genetic variants in pre‐microRNA in susceptibility and prognosis of esophageal cancer. Issue 1 (12th June 2012)
- Record Type:
- Journal Article
- Title:
- Evaluation of common genetic variants in pre‐microRNA in susceptibility and prognosis of esophageal cancer. Issue 1 (12th June 2012)
- Main Title:
- Evaluation of common genetic variants in pre‐microRNA in susceptibility and prognosis of esophageal cancer
- Authors:
- Umar, Meenakshi
Upadhyay, Rohit
Prakash, Garima
Kumar, Shaleen
Ghoshal, Uday Chand
Mittal, Balraj
Angel, Joe - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="mc21931-sec-0001" sec-type="section"> <p>Genetic variants in micro‐RNAs (miRNA) have been shown to affect progression, diagnosis, and prognosis of various malignancies; however, their role in esophageal squamous cell carcinoma (ESCC) susceptibility is controversial. Therefore, we aimed to determine role of common genetic variants in cancer related pre‐miRNA in susceptibility and survival outcome of north Indian ESCC patients. We genotyped four common polymorphisms in pre‐miRNA: mir‐196a‐2C&gt;T, mir‐146aG&gt;C, mir‐499T&gt;C, and mir‐423C&gt;A in 289 incident ESCC cases (including 153 follow‐up cases) and 309 controls using PCR/PCR RFLP‐based methods. Binary logistic regression was applied for risk estimation, while Kaplan–Meier and Cox Regression tests were performed for survival analysis. We observed that none of the pre‐miRNA genetic variants were associated with ESCC or its clinical phenotypes independently, however, combined risk genotypes of four pre‐miRNA polymorphisms increased risk of ESCC in dose–response manner (<italic>P</italic><sub>trend</sub> = 0.011). Specifically, patients with 2–4 risk genotypes of pre‐miRNA polymorphisms had 1.4‐fold higher risk of ESCC compared to patients with 0–1 risk genotypes (OR = 1.43, 95% CI = 1.02–1.09, <italic>P</italic>‐value = 0.037). The risk was more pronounced in ESCC cases with upper‐third esophageal tumors. Moreover, cumulative but not<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="mc21931-sec-0001" sec-type="section"> <p>Genetic variants in micro‐RNAs (miRNA) have been shown to affect progression, diagnosis, and prognosis of various malignancies; however, their role in esophageal squamous cell carcinoma (ESCC) susceptibility is controversial. Therefore, we aimed to determine role of common genetic variants in cancer related pre‐miRNA in susceptibility and survival outcome of north Indian ESCC patients. We genotyped four common polymorphisms in pre‐miRNA: mir‐196a‐2C&gt;T, mir‐146aG&gt;C, mir‐499T&gt;C, and mir‐423C&gt;A in 289 incident ESCC cases (including 153 follow‐up cases) and 309 controls using PCR/PCR RFLP‐based methods. Binary logistic regression was applied for risk estimation, while Kaplan–Meier and Cox Regression tests were performed for survival analysis. We observed that none of the pre‐miRNA genetic variants were associated with ESCC or its clinical phenotypes independently, however, combined risk genotypes of four pre‐miRNA polymorphisms increased risk of ESCC in dose–response manner (<italic>P</italic><sub>trend</sub> = 0.011). Specifically, patients with 2–4 risk genotypes of pre‐miRNA polymorphisms had 1.4‐fold higher risk of ESCC compared to patients with 0–1 risk genotypes (OR = 1.43, 95% CI = 1.02–1.09, <italic>P</italic>‐value = 0.037). The risk was more pronounced in ESCC cases with upper‐third esophageal tumors. Moreover, cumulative but not independent effect of risk genotypes of pre‐miRNA polymorphisms was observed on survival outcome of ESCC patients. Cases with 2–4 risk genotypes had significantly lower median survival (11.60 vs. 30.2 months) and 2.3‐fold greater hazard of death compared to patients with 0–1 risk genotypes. In conclusion, the four studied common pre‐miRNA polymorphisms cumulatively affect susceptibility and survival of ESCC patients in north Indian population. © 2012 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Molecular carcinogenesis. Volume 52:Issue 1(2013:Jan.)
- Journal:
- Molecular carcinogenesis
- Issue:
- Volume 52:Issue 1(2013:Jan.)
- Issue Display:
- Volume 52, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 52
- Issue:
- 1
- Issue Sort Value:
- 2013-0052-0001-0000
- Page Start:
- 10
- Page End:
- 18
- Publication Date:
- 2012-06-12
- Subjects:
- Carcinogenesis -- Molecular aspects -- Periodicals
616.994071 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2744 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mc.21931 ↗
- Languages:
- English
- ISSNs:
- 0899-1987
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.802000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3997.xml