Cargando…

Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study

BACKGROUND: LOC105371267, also known as PR-lncRNA1, was reported to be a p53-regulated long noncoding RNA (lncRNA), which played an essential role in the pathogenesis of breast cancer (BC). We aimed to observe the potential association between LOC105371267 polymorphisms and BC risk in Northern Chine...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Linna, Huang, Congmei, Xing, Shishi, Li, Dandan, He, Chunjuan, He, Yongjun, Yang, Wei, Jin, Tianbo, Wang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407995/
https://www.ncbi.nlm.nih.gov/pubmed/34475952
http://dx.doi.org/10.1155/2021/4990695
_version_ 1783746732586172416
author Peng, Linna
Huang, Congmei
Xing, Shishi
Li, Dandan
He, Chunjuan
He, Yongjun
Yang, Wei
Jin, Tianbo
Wang, Li
author_facet Peng, Linna
Huang, Congmei
Xing, Shishi
Li, Dandan
He, Chunjuan
He, Yongjun
Yang, Wei
Jin, Tianbo
Wang, Li
author_sort Peng, Linna
collection PubMed
description BACKGROUND: LOC105371267, also known as PR-lncRNA1, was reported to be a p53-regulated long noncoding RNA (lncRNA), which played an essential role in the pathogenesis of breast cancer (BC). We aimed to observe the potential association between LOC105371267 polymorphisms and BC risk in Northern Chinese Han females. METHODS: Totally, 555 healthy individuals and 561 patients with BC were recruited. Five candidate SNPs (rs6499221, rs3931698, rs8044565, rs3852740, and rs111577197) of LOC105371267 were genotyped with the Agena MassARRAY system. Odds ratio (OR) and 95% confidence intervals (CIs) were applied to evaluate the relationship of LOC105371267 genetic polymorphisms with BC susceptibility. Additionally, stratification analysis based on clinical features and haplotype analysis were also conducted. Finally, multifactor dimensionality reduction (MDR) analysis was performed to assess the SNP-SNP interaction among LOC105371267 variants, and false-positive report probability (FPRP) analysis was used to validate the result of this study. RESULTS: In this study, rs3931698 was a protective factor of BC in total (GG homozygote: OR = 0.30, 95% CI: 0.11–0.82, p=0.018; recessive model: OR = 0.30, 95% CI: 0.11–0.84, p=0.021). In stratification analysis based on the average age of 52 years and clinical characteristics (PR status, III-IV TNM stage), rs3931698 was also demonstrated to be associated with BC susceptibility. In addition, rs6499221 and rs3852740 were also associated with BC susceptibility among patients at age <52 years and patients with BC in a positive status. Thus, the haplotype analysis had a negative result for the incidence of BC (p > 0.05), and haplotype consisting of rs8044565 and rs111577197 was nonsignificantly associated with the BC risk. Finally, MDR and FPRP analyses also validated the result of this study. CONCLUSION: Polymorphisms rs3931698, rs6499221, and rs3852740 of LOC105371267 were found to be associated with the risk of BC in total, and stratification analysis in the Northern Chinese Han females suggested that LOC105371267 variants might be helpful to predict BC progression.
format Online
Article
Text
id pubmed-8407995
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-84079952021-09-01 Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study Peng, Linna Huang, Congmei Xing, Shishi Li, Dandan He, Chunjuan He, Yongjun Yang, Wei Jin, Tianbo Wang, Li J Oncol Research Article BACKGROUND: LOC105371267, also known as PR-lncRNA1, was reported to be a p53-regulated long noncoding RNA (lncRNA), which played an essential role in the pathogenesis of breast cancer (BC). We aimed to observe the potential association between LOC105371267 polymorphisms and BC risk in Northern Chinese Han females. METHODS: Totally, 555 healthy individuals and 561 patients with BC were recruited. Five candidate SNPs (rs6499221, rs3931698, rs8044565, rs3852740, and rs111577197) of LOC105371267 were genotyped with the Agena MassARRAY system. Odds ratio (OR) and 95% confidence intervals (CIs) were applied to evaluate the relationship of LOC105371267 genetic polymorphisms with BC susceptibility. Additionally, stratification analysis based on clinical features and haplotype analysis were also conducted. Finally, multifactor dimensionality reduction (MDR) analysis was performed to assess the SNP-SNP interaction among LOC105371267 variants, and false-positive report probability (FPRP) analysis was used to validate the result of this study. RESULTS: In this study, rs3931698 was a protective factor of BC in total (GG homozygote: OR = 0.30, 95% CI: 0.11–0.82, p=0.018; recessive model: OR = 0.30, 95% CI: 0.11–0.84, p=0.021). In stratification analysis based on the average age of 52 years and clinical characteristics (PR status, III-IV TNM stage), rs3931698 was also demonstrated to be associated with BC susceptibility. In addition, rs6499221 and rs3852740 were also associated with BC susceptibility among patients at age <52 years and patients with BC in a positive status. Thus, the haplotype analysis had a negative result for the incidence of BC (p > 0.05), and haplotype consisting of rs8044565 and rs111577197 was nonsignificantly associated with the BC risk. Finally, MDR and FPRP analyses also validated the result of this study. CONCLUSION: Polymorphisms rs3931698, rs6499221, and rs3852740 of LOC105371267 were found to be associated with the risk of BC in total, and stratification analysis in the Northern Chinese Han females suggested that LOC105371267 variants might be helpful to predict BC progression. Hindawi 2021-08-28 /pmc/articles/PMC8407995/ /pubmed/34475952 http://dx.doi.org/10.1155/2021/4990695 Text en Copyright © 2021 Linna Peng et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Peng, Linna
Huang, Congmei
Xing, Shishi
Li, Dandan
He, Chunjuan
He, Yongjun
Yang, Wei
Jin, Tianbo
Wang, Li
Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study
title Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study
title_full Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study
title_fullStr Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study
title_full_unstemmed Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study
title_short Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study
title_sort impacts of loc105371267 variants on breast cancer susceptibility in northern chinese han females: a population-based case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407995/
https://www.ncbi.nlm.nih.gov/pubmed/34475952
http://dx.doi.org/10.1155/2021/4990695
work_keys_str_mv AT penglinna impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT huangcongmei impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT xingshishi impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT lidandan impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT hechunjuan impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT heyongjun impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT yangwei impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT jintianbo impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy
AT wangli impactsofloc105371267variantsonbreastcancersusceptibilityinnorthernchinesehanfemalesapopulationbasedcasecontrolstudy