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Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia

AIM: microRNA-423 is an oncogenic factor which is frequently upregulated in cancer. However, associations with breast cancer risk remain inconsistent. Therefore, we investigated the prevalence of microRNA-423 rs6505162C>T gene variation with breast cancer susceptibility in Saudi women. METHODOLOG...

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Autores principales: Mir, R, Balawi, I A Al, Duhier, F M Abu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249472/
https://www.ncbi.nlm.nih.gov/pubmed/30256064
http://dx.doi.org/10.22034/APJCP.2018.19.9.2581
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author Mir, R
Balawi, I A Al
Duhier, F M Abu
author_facet Mir, R
Balawi, I A Al
Duhier, F M Abu
author_sort Mir, R
collection PubMed
description AIM: microRNA-423 is an oncogenic factor which is frequently upregulated in cancer. However, associations with breast cancer risk remain inconsistent. Therefore, we investigated the prevalence of microRNA-423 rs6505162C>T gene variation with breast cancer susceptibility in Saudi women. METHODOLOGY: This study was conducted on 100 breast cancer patients and 124 matched healthy individuals. Genotyping of the microRNA-423 rs6505162C/T gene variation was performed by using the amplification refractory mutation system PCR method (ARMS-PCR). RESULTS: A significant difference was observed in the genotype distribution between the breast cancer cases and controls (p=0.0001), the frequencies of the genotypes CC,CT and TT being 25%, 52% and 23% in patients and 65%,20% and 15% respectively, in controls. The microRNA-423 C>T variant was associated with an increased risk of breast cancer in codominant models for (OR = 6.73, 95 % CI, 3.50-12.97; RR 2.35(1.67-3.30, p=0.0001) the microRNA-423TT genotype and (OR = 4.14, 95 % CI, 1.93-8.87; p=0.0003) microRNA-423CT (OR= 6.73, 95% CI, 3.50-12.97; p=0.0001) and also with the dominant model (OR 5.6(3.14-1.01), p=0.0001) CT+TT vs CC) with a non-significant association for the recessive model (OR=1.75, 95%CI=0.08-3.44, P=0.139, TT vs CC+CT). The T allele significantly increased the risk of breast cancer (OR =2.63, 95 % CI, 1.77-3.91; p=0.001) compared to the C allele. Some 6.73 ,4.14 and 2.63 fold increased risk of developing breast cancer was associated with TT and CT genotypes and the T allele of microRNA-423 in the northwestern region of Saudi Arabia. CONCLUSION: Our findings indicate that the microRNA-423 TT genotype and the T allele are associated with an increased susceptibility, metastasis and advanced stage of breast cancer in Saudi Arabian patients. Further studies with larger sample sizes are necessary to confirm our findings.
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spelling pubmed-62494722018-12-07 Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia Mir, R Balawi, I A Al Duhier, F M Abu Asian Pac J Cancer Prev Research Article AIM: microRNA-423 is an oncogenic factor which is frequently upregulated in cancer. However, associations with breast cancer risk remain inconsistent. Therefore, we investigated the prevalence of microRNA-423 rs6505162C>T gene variation with breast cancer susceptibility in Saudi women. METHODOLOGY: This study was conducted on 100 breast cancer patients and 124 matched healthy individuals. Genotyping of the microRNA-423 rs6505162C/T gene variation was performed by using the amplification refractory mutation system PCR method (ARMS-PCR). RESULTS: A significant difference was observed in the genotype distribution between the breast cancer cases and controls (p=0.0001), the frequencies of the genotypes CC,CT and TT being 25%, 52% and 23% in patients and 65%,20% and 15% respectively, in controls. The microRNA-423 C>T variant was associated with an increased risk of breast cancer in codominant models for (OR = 6.73, 95 % CI, 3.50-12.97; RR 2.35(1.67-3.30, p=0.0001) the microRNA-423TT genotype and (OR = 4.14, 95 % CI, 1.93-8.87; p=0.0003) microRNA-423CT (OR= 6.73, 95% CI, 3.50-12.97; p=0.0001) and also with the dominant model (OR 5.6(3.14-1.01), p=0.0001) CT+TT vs CC) with a non-significant association for the recessive model (OR=1.75, 95%CI=0.08-3.44, P=0.139, TT vs CC+CT). The T allele significantly increased the risk of breast cancer (OR =2.63, 95 % CI, 1.77-3.91; p=0.001) compared to the C allele. Some 6.73 ,4.14 and 2.63 fold increased risk of developing breast cancer was associated with TT and CT genotypes and the T allele of microRNA-423 in the northwestern region of Saudi Arabia. CONCLUSION: Our findings indicate that the microRNA-423 TT genotype and the T allele are associated with an increased susceptibility, metastasis and advanced stage of breast cancer in Saudi Arabian patients. Further studies with larger sample sizes are necessary to confirm our findings. West Asia Organization for Cancer Prevention 2018 /pmc/articles/PMC6249472/ /pubmed/30256064 http://dx.doi.org/10.22034/APJCP.2018.19.9.2581 Text en Copyright: © Asian Pacific Journal of Cancer Prevention http://creativecommons.org/licenses/BY-SA/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Research Article
Mir, R
Balawi, I A Al
Duhier, F M Abu
Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia
title Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia
title_full Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia
title_fullStr Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia
title_full_unstemmed Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia
title_short Involvement of microRNA-423 Gene Variability in Breast Cancer Progression in Saudi Arabia
title_sort involvement of microrna-423 gene variability in breast cancer progression in saudi arabia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249472/
https://www.ncbi.nlm.nih.gov/pubmed/30256064
http://dx.doi.org/10.22034/APJCP.2018.19.9.2581
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