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Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk

Several studies examined the impact of miR-34b/c rs4938723 polymorphism and cancer risk, but the findings are inconsistent. However, no study has been conducted to inspect the impact of miR-34b/c polymorphism on bladder cancer. This study aimed to assess possible association between rs4938723 polymo...

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Autores principales: Hashemi, Mohammad, Hasanpour, Vahed, Danesh, Hiva, Bizhani, Fatemeh, Narouie, Behzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352879/
https://www.ncbi.nlm.nih.gov/pubmed/30190447
http://dx.doi.org/10.7555/JBR.31.20170044
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author Hashemi, Mohammad
Hasanpour, Vahed
Danesh, Hiva
Bizhani, Fatemeh
Narouie, Behzad
author_facet Hashemi, Mohammad
Hasanpour, Vahed
Danesh, Hiva
Bizhani, Fatemeh
Narouie, Behzad
author_sort Hashemi, Mohammad
collection PubMed
description Several studies examined the impact of miR-34b/c rs4938723 polymorphism and cancer risk, but the findings are inconsistent. However, no study has been conducted to inspect the impact of miR-34b/c polymorphism on bladder cancer. This study aimed to assess possible association between rs4938723 polymorphism and bladder cancer risk. This case-control study was done on 136 pathologically proven bladder cancer patients and 144 controls. Genotyping of Pri-miR-34b/c rs4938723 polymorphism was achieved by using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method. Our findings did not show any statistically significant differences in genotype and allele frequencies between bladder cancer and controls. Larger sample sizes with diverse ethnicities are required to validate our findings.
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spelling pubmed-63528792019-03-16 Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk Hashemi, Mohammad Hasanpour, Vahed Danesh, Hiva Bizhani, Fatemeh Narouie, Behzad J Biomed Res Original Article Several studies examined the impact of miR-34b/c rs4938723 polymorphism and cancer risk, but the findings are inconsistent. However, no study has been conducted to inspect the impact of miR-34b/c polymorphism on bladder cancer. This study aimed to assess possible association between rs4938723 polymorphism and bladder cancer risk. This case-control study was done on 136 pathologically proven bladder cancer patients and 144 controls. Genotyping of Pri-miR-34b/c rs4938723 polymorphism was achieved by using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method. Our findings did not show any statistically significant differences in genotype and allele frequencies between bladder cancer and controls. Larger sample sizes with diverse ethnicities are required to validate our findings. Editorial Department of Journal of Biomedical Research 2019 2017-10-10 /pmc/articles/PMC6352879/ /pubmed/30190447 http://dx.doi.org/10.7555/JBR.31.20170044 Text en /creativecommons.org/licenses/by/4.0/ This is an open access article under the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited
spellingShingle Original Article
Hashemi, Mohammad
Hasanpour, Vahed
Danesh, Hiva
Bizhani, Fatemeh
Narouie, Behzad
Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk
title Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk
title_full Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk
title_fullStr Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk
title_full_unstemmed Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk
title_short Association between Pri-miR-34b/c rs4938723 polymorphism and bladder cancer risk
title_sort association between pri-mir-34b/c rs4938723 polymorphism and bladder cancer risk
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352879/
https://www.ncbi.nlm.nih.gov/pubmed/30190447
http://dx.doi.org/10.7555/JBR.31.20170044
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