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Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan

We aimed to investigate the association between genotypes for mir146a and mir196a-2 and the risk of developing colorectal cancer (CRC). We used polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to determine the mir146a rs2910164 and mir196a-2 rs11614913 genotypes in 362 C...

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Autores principales: Yueh, Te-Cheng, Wang, Yun-Chi, Chin, Yu-Ting, Hung, Yi-Chih, Mong, Mei-Chin, Yang, Ya-Chen, Pei, Jen-Sheng, Gu, Jian, Tsai, Chia-Wen, Bau, Da-Tian, Chang, Wen-Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380589/
https://www.ncbi.nlm.nih.gov/pubmed/37511371
http://dx.doi.org/10.3390/ijms241411613
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author Yueh, Te-Cheng
Wang, Yun-Chi
Chin, Yu-Ting
Hung, Yi-Chih
Mong, Mei-Chin
Yang, Ya-Chen
Pei, Jen-Sheng
Gu, Jian
Tsai, Chia-Wen
Bau, Da-Tian
Chang, Wen-Shin
author_facet Yueh, Te-Cheng
Wang, Yun-Chi
Chin, Yu-Ting
Hung, Yi-Chih
Mong, Mei-Chin
Yang, Ya-Chen
Pei, Jen-Sheng
Gu, Jian
Tsai, Chia-Wen
Bau, Da-Tian
Chang, Wen-Shin
author_sort Yueh, Te-Cheng
collection PubMed
description We aimed to investigate the association between genotypes for mir146a and mir196a-2 and the risk of developing colorectal cancer (CRC). We used polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to determine the mir146a rs2910164 and mir196a-2 rs11614913 genotypes in 362 CRC patients and 362 controls. We also assessed the interactions between these genotypes and age, gender, smoking, alcohol consumption, and BMI status on CRC risk. Additionally, the serum expression level of mir196a-2 was quantified using quantitative reverse transcription-PCR. Our findings demonstrated that among the controls, the proportions of TT, CT, and CC genotypes of mir196a-2 rs11614913 were 32.3%, 48.1%, and 19.6%, respectively. As for the cases, the proportions were 24.6%, 45.0%, and 30.4%, respectively. Logistic regression analysis revealed that the CC genotype carriers had a 2.04-fold increased risk (95% confidence interval [CI] = 1.36–3.06, p = 0.0008). Furthermore, carriers of the CT + CC genotypes also exhibited a significant association with CRC risk (odds ratio [OR] = 1.46, 95% CI = 1.06–2.03, p = 0.0261). Moreover, carriers of the CC genotype had significantly higher serum levels of mir196a-2 compared to those with the TT genotype (p < 0.0001), indicating a genotype-phenotype correlation. No association was found regarding mir146a rs2910164. In conclusion, mir196a-2 rs2910164 genotypes, along with their associated expression, can serve as predictive markers for CRC risk.
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spelling pubmed-103805892023-07-29 Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan Yueh, Te-Cheng Wang, Yun-Chi Chin, Yu-Ting Hung, Yi-Chih Mong, Mei-Chin Yang, Ya-Chen Pei, Jen-Sheng Gu, Jian Tsai, Chia-Wen Bau, Da-Tian Chang, Wen-Shin Int J Mol Sci Article We aimed to investigate the association between genotypes for mir146a and mir196a-2 and the risk of developing colorectal cancer (CRC). We used polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to determine the mir146a rs2910164 and mir196a-2 rs11614913 genotypes in 362 CRC patients and 362 controls. We also assessed the interactions between these genotypes and age, gender, smoking, alcohol consumption, and BMI status on CRC risk. Additionally, the serum expression level of mir196a-2 was quantified using quantitative reverse transcription-PCR. Our findings demonstrated that among the controls, the proportions of TT, CT, and CC genotypes of mir196a-2 rs11614913 were 32.3%, 48.1%, and 19.6%, respectively. As for the cases, the proportions were 24.6%, 45.0%, and 30.4%, respectively. Logistic regression analysis revealed that the CC genotype carriers had a 2.04-fold increased risk (95% confidence interval [CI] = 1.36–3.06, p = 0.0008). Furthermore, carriers of the CT + CC genotypes also exhibited a significant association with CRC risk (odds ratio [OR] = 1.46, 95% CI = 1.06–2.03, p = 0.0261). Moreover, carriers of the CC genotype had significantly higher serum levels of mir196a-2 compared to those with the TT genotype (p < 0.0001), indicating a genotype-phenotype correlation. No association was found regarding mir146a rs2910164. In conclusion, mir196a-2 rs2910164 genotypes, along with their associated expression, can serve as predictive markers for CRC risk. MDPI 2023-07-18 /pmc/articles/PMC10380589/ /pubmed/37511371 http://dx.doi.org/10.3390/ijms241411613 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yueh, Te-Cheng
Wang, Yun-Chi
Chin, Yu-Ting
Hung, Yi-Chih
Mong, Mei-Chin
Yang, Ya-Chen
Pei, Jen-Sheng
Gu, Jian
Tsai, Chia-Wen
Bau, Da-Tian
Chang, Wen-Shin
Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan
title Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan
title_full Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan
title_fullStr Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan
title_full_unstemmed Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan
title_short Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan
title_sort impact of mir196a-2 genotypes on colorectal cancer risk in taiwan
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380589/
https://www.ncbi.nlm.nih.gov/pubmed/37511371
http://dx.doi.org/10.3390/ijms241411613
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