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Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies

Breast cancer (BC) is one of the most common types of cancer in women worldwide. Several factors including genetic and environmental have been linked with susceptibility to development of BC. Her2 is a transmembrane protein with tyrosine kinase activity, overexpressed in several cancers including BC...

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Autores principales: Krishna, B. Madhu, Chaudhary, Sanjib, Panda, Aditya K., Mishra, Dipti Ranjan, Mishra, Sandip K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943262/
https://www.ncbi.nlm.nih.gov/pubmed/29743533
http://dx.doi.org/10.1038/s41598-018-25769-y
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author Krishna, B. Madhu
Chaudhary, Sanjib
Panda, Aditya K.
Mishra, Dipti Ranjan
Mishra, Sandip K.
author_facet Krishna, B. Madhu
Chaudhary, Sanjib
Panda, Aditya K.
Mishra, Dipti Ranjan
Mishra, Sandip K.
author_sort Krishna, B. Madhu
collection PubMed
description Breast cancer (BC) is one of the most common types of cancer in women worldwide. Several factors including genetic and environmental have been linked with susceptibility to development of BC. Her2 is a transmembrane protein with tyrosine kinase activity, overexpressed in several cancers including BC. Various studies in different populations have shown association of Her2 variants with susceptibility to BC, however these results were inconsistent, inconclusive and controversial. To obtain a common conclusive finding, we performed meta-analysis of 35 case-control studies reported earlier including 19, 220 cases and 22, 306 controls. We observed significant association of Her2 (Ile)655(Val) polymorphism with susceptibility to development of breast cancer (Overall allele Val vs Ile: OR = 1.130, 95% CI = 1.051–1.216, p = 0.001; Ile-Val vs Ile-Ile: OR = 1.100, 95% CI = 1.016–1.192, p = 0.019; Val-Val+Ile-Val vs Ile-Ile: OR = 1.127, 95% CI = 1.038–1.223, p = 0.004). Subgroup analysis indicated a significant association with susceptibility to breast cancer in African and Asian populations. However, such association was not observed in other ethnic groups. Our findings suggested that Her2 (Ile)655(Val) polymorphism is associated with breast cancer risk in overall, Asian and African populations, and can be used as diagnostic marker for BC.
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spelling pubmed-59432622018-05-14 Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies Krishna, B. Madhu Chaudhary, Sanjib Panda, Aditya K. Mishra, Dipti Ranjan Mishra, Sandip K. Sci Rep Article Breast cancer (BC) is one of the most common types of cancer in women worldwide. Several factors including genetic and environmental have been linked with susceptibility to development of BC. Her2 is a transmembrane protein with tyrosine kinase activity, overexpressed in several cancers including BC. Various studies in different populations have shown association of Her2 variants with susceptibility to BC, however these results were inconsistent, inconclusive and controversial. To obtain a common conclusive finding, we performed meta-analysis of 35 case-control studies reported earlier including 19, 220 cases and 22, 306 controls. We observed significant association of Her2 (Ile)655(Val) polymorphism with susceptibility to development of breast cancer (Overall allele Val vs Ile: OR = 1.130, 95% CI = 1.051–1.216, p = 0.001; Ile-Val vs Ile-Ile: OR = 1.100, 95% CI = 1.016–1.192, p = 0.019; Val-Val+Ile-Val vs Ile-Ile: OR = 1.127, 95% CI = 1.038–1.223, p = 0.004). Subgroup analysis indicated a significant association with susceptibility to breast cancer in African and Asian populations. However, such association was not observed in other ethnic groups. Our findings suggested that Her2 (Ile)655(Val) polymorphism is associated with breast cancer risk in overall, Asian and African populations, and can be used as diagnostic marker for BC. Nature Publishing Group UK 2018-05-09 /pmc/articles/PMC5943262/ /pubmed/29743533 http://dx.doi.org/10.1038/s41598-018-25769-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Krishna, B. Madhu
Chaudhary, Sanjib
Panda, Aditya K.
Mishra, Dipti Ranjan
Mishra, Sandip K.
Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
title Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
title_full Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
title_fullStr Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
title_full_unstemmed Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
title_short Her2(Ile)655(Val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
title_sort her2(ile)655(val) polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943262/
https://www.ncbi.nlm.nih.gov/pubmed/29743533
http://dx.doi.org/10.1038/s41598-018-25769-y
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