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The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?

The polymorphism of killer cell immunoglobulin-like receptors (KIR) has been associated with several diseases, including infection, autoimmunity and cancer. KIR molecules are a family of receptors expressed on the surface of natural killer cells (NK), frontline defense of innate immunity against mic...

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Autor principal: Augusto, Danillo G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923111/
https://www.ncbi.nlm.nih.gov/pubmed/27446203
http://dx.doi.org/10.3389/fgene.2016.00121
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author Augusto, Danillo G.
author_facet Augusto, Danillo G.
author_sort Augusto, Danillo G.
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description The polymorphism of killer cell immunoglobulin-like receptors (KIR) has been associated with several diseases, including infection, autoimmunity and cancer. KIR molecules are a family of receptors expressed on the surface of natural killer cells (NK), frontline defense of innate immunity against microorganisms and neoplastic cells. Some studies have shown conflicting results concerning the role that KIR polymorphism plays in tumor susceptibility, particularly in leukemia and lymphoma. Interestingly, the presence of HLA ligands is sometimes strongly associated with several types of cancer and apparently is not related with their interaction with KIR. This manuscript briefly reviews the uncommon polymorphism of KIR and critically summarizes the recent findings with regards of the importance of KIR variation for cancer susceptibility.
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spelling pubmed-49231112016-07-21 The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined? Augusto, Danillo G. Front Genet Oncology The polymorphism of killer cell immunoglobulin-like receptors (KIR) has been associated with several diseases, including infection, autoimmunity and cancer. KIR molecules are a family of receptors expressed on the surface of natural killer cells (NK), frontline defense of innate immunity against microorganisms and neoplastic cells. Some studies have shown conflicting results concerning the role that KIR polymorphism plays in tumor susceptibility, particularly in leukemia and lymphoma. Interestingly, the presence of HLA ligands is sometimes strongly associated with several types of cancer and apparently is not related with their interaction with KIR. This manuscript briefly reviews the uncommon polymorphism of KIR and critically summarizes the recent findings with regards of the importance of KIR variation for cancer susceptibility. Frontiers Media S.A. 2016-06-28 /pmc/articles/PMC4923111/ /pubmed/27446203 http://dx.doi.org/10.3389/fgene.2016.00121 Text en Copyright © 2016 Augusto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Augusto, Danillo G.
The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?
title The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?
title_full The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?
title_fullStr The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?
title_full_unstemmed The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?
title_short The Impact of KIR Polymorphism on the Risk of Developing Cancer: Not as Strong as Imagined?
title_sort impact of kir polymorphism on the risk of developing cancer: not as strong as imagined?
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923111/
https://www.ncbi.nlm.nih.gov/pubmed/27446203
http://dx.doi.org/10.3389/fgene.2016.00121
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