IL17A and IL17RA gene polymorphisms in Fanconi anemia

Abstract Fanconi anemia is a rare autosomal recessive disease. In this disease, cytokine pathways can induce the bone marrow failure that is observed in individuals with Fanconi anemia. Interleukin IL-17 exhibits a protective effect in organisms because it induces neutrophil recruitment and shows a pathological role in several models of autoimmune diseases, periodontal disease, cancer, allograft rejection, and graft versus host disease. Polymorphisms in the IL17A and IL17RA genes were evaluated from DNA in saliva, comparing individuals with or without Fanconi anemia, using models of genotypic transmission (additive, dominant, and recessive). Polymorphisms in the IL17A and IL17RA genes (rs2241044 [C allele], rs879577 [C allele], rs9606615 [T allele], and rs2241043 [C allele]) were risk factors for developing Fanconi anemia. We also performed an analysis of gene markers with clinical variables in the Fanconi group. Polymorphisms in the IL17A gene (rs3819025 [A allele] and rs2275913 [G allele], respectively) were associated with an age of less than 20 years (p = 0.026; RP 0.65) and the female sex (p = 0.043; RP 0.88). The IL17RA gene was also associated with age and the presence of leukoplakia (a potentially malignant oral disorder). An age of less than 20 years was associated with rs917864 (T allele; p = 0.036; RP 0.67). The presence of leukoplakia was associated with rs17606615 (T allele; p = 0.042; RP 0.47). To our knowledge, this is the first study that associates IL17A and IL17RA gene polymorphisms with Fanconi anemia and examines rs2241044 polymorphisms in scientific literature thus far.

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Main Authors: MOBILE,Rafael Zancan, MENDES,Monalisa Castilho, MACHADO-SOUZA,Cleber, QUEIROZ,Priscila de Mattos, BONFIM,Carmem Maria Sales, TORRES-PEREIRA,Cassius Carvalho, SCHUSSEL,Juliana Lucena
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Pesquisa Odontológica - SBPqO 2023
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242023000100209
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spelling oai:scielo:S1806-832420230001002092023-02-10IL17A and IL17RA gene polymorphisms in Fanconi anemiaMOBILE,Rafael ZancanMENDES,Monalisa CastilhoMACHADO-SOUZA,CleberQUEIROZ,Priscila de MattosBONFIM,Carmem Maria SalesTORRES-PEREIRA,Cassius CarvalhoSCHUSSEL,Juliana Lucena Fanconi Anemia Interleukin-17 Receptors, Interleukin-17 Abstract Fanconi anemia is a rare autosomal recessive disease. In this disease, cytokine pathways can induce the bone marrow failure that is observed in individuals with Fanconi anemia. Interleukin IL-17 exhibits a protective effect in organisms because it induces neutrophil recruitment and shows a pathological role in several models of autoimmune diseases, periodontal disease, cancer, allograft rejection, and graft versus host disease. Polymorphisms in the IL17A and IL17RA genes were evaluated from DNA in saliva, comparing individuals with or without Fanconi anemia, using models of genotypic transmission (additive, dominant, and recessive). Polymorphisms in the IL17A and IL17RA genes (rs2241044 [C allele], rs879577 [C allele], rs9606615 [T allele], and rs2241043 [C allele]) were risk factors for developing Fanconi anemia. We also performed an analysis of gene markers with clinical variables in the Fanconi group. Polymorphisms in the IL17A gene (rs3819025 [A allele] and rs2275913 [G allele], respectively) were associated with an age of less than 20 years (p = 0.026; RP 0.65) and the female sex (p = 0.043; RP 0.88). The IL17RA gene was also associated with age and the presence of leukoplakia (a potentially malignant oral disorder). An age of less than 20 years was associated with rs917864 (T allele; p = 0.036; RP 0.67). The presence of leukoplakia was associated with rs17606615 (T allele; p = 0.042; RP 0.47). To our knowledge, this is the first study that associates IL17A and IL17RA gene polymorphisms with Fanconi anemia and examines rs2241044 polymorphisms in scientific literature thus far.info:eu-repo/semantics/openAccessSociedade Brasileira de Pesquisa Odontológica - SBPqOBrazilian Oral Research v.37 20232023-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242023000100209en10.1590/1807-3107bor-2023.vol37.0012
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language English
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author MOBILE,Rafael Zancan
MENDES,Monalisa Castilho
MACHADO-SOUZA,Cleber
QUEIROZ,Priscila de Mattos
BONFIM,Carmem Maria Sales
TORRES-PEREIRA,Cassius Carvalho
SCHUSSEL,Juliana Lucena
spellingShingle MOBILE,Rafael Zancan
MENDES,Monalisa Castilho
MACHADO-SOUZA,Cleber
QUEIROZ,Priscila de Mattos
BONFIM,Carmem Maria Sales
TORRES-PEREIRA,Cassius Carvalho
SCHUSSEL,Juliana Lucena
IL17A and IL17RA gene polymorphisms in Fanconi anemia
author_facet MOBILE,Rafael Zancan
MENDES,Monalisa Castilho
MACHADO-SOUZA,Cleber
QUEIROZ,Priscila de Mattos
BONFIM,Carmem Maria Sales
TORRES-PEREIRA,Cassius Carvalho
SCHUSSEL,Juliana Lucena
author_sort MOBILE,Rafael Zancan
title IL17A and IL17RA gene polymorphisms in Fanconi anemia
title_short IL17A and IL17RA gene polymorphisms in Fanconi anemia
title_full IL17A and IL17RA gene polymorphisms in Fanconi anemia
title_fullStr IL17A and IL17RA gene polymorphisms in Fanconi anemia
title_full_unstemmed IL17A and IL17RA gene polymorphisms in Fanconi anemia
title_sort il17a and il17ra gene polymorphisms in fanconi anemia
description Abstract Fanconi anemia is a rare autosomal recessive disease. In this disease, cytokine pathways can induce the bone marrow failure that is observed in individuals with Fanconi anemia. Interleukin IL-17 exhibits a protective effect in organisms because it induces neutrophil recruitment and shows a pathological role in several models of autoimmune diseases, periodontal disease, cancer, allograft rejection, and graft versus host disease. Polymorphisms in the IL17A and IL17RA genes were evaluated from DNA in saliva, comparing individuals with or without Fanconi anemia, using models of genotypic transmission (additive, dominant, and recessive). Polymorphisms in the IL17A and IL17RA genes (rs2241044 [C allele], rs879577 [C allele], rs9606615 [T allele], and rs2241043 [C allele]) were risk factors for developing Fanconi anemia. We also performed an analysis of gene markers with clinical variables in the Fanconi group. Polymorphisms in the IL17A gene (rs3819025 [A allele] and rs2275913 [G allele], respectively) were associated with an age of less than 20 years (p = 0.026; RP 0.65) and the female sex (p = 0.043; RP 0.88). The IL17RA gene was also associated with age and the presence of leukoplakia (a potentially malignant oral disorder). An age of less than 20 years was associated with rs917864 (T allele; p = 0.036; RP 0.67). The presence of leukoplakia was associated with rs17606615 (T allele; p = 0.042; RP 0.47). To our knowledge, this is the first study that associates IL17A and IL17RA gene polymorphisms with Fanconi anemia and examines rs2241044 polymorphisms in scientific literature thus far.
publisher Sociedade Brasileira de Pesquisa Odontológica - SBPqO
publishDate 2023
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242023000100209
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