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Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer

Lysine methyltransferase 2C (KMT2C) is a tumor-suppressor gene in several myeloid cells and epithelia and is linked with blood and solid tumor cancers. KMT2C single-nucleotide polymorphisms (SNPs) are also connected with several cancer types. Our study aimed to explore the potential genetic polymorp...

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Autores principales: Shieu, Mu-Kuei, Ho, Hsin-Yu, Lin, Shu-Hui, Lo, Yu-Sheng, Lin, Chia-Chieh, Chuang, Yi-Ching, Hsieh, Ming-Ju, Chen, Mu-Kuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997509/
https://www.ncbi.nlm.nih.gov/pubmed/35409657
http://dx.doi.org/10.3390/ijerph19073974
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author Shieu, Mu-Kuei
Ho, Hsin-Yu
Lin, Shu-Hui
Lo, Yu-Sheng
Lin, Chia-Chieh
Chuang, Yi-Ching
Hsieh, Ming-Ju
Chen, Mu-Kuan
author_facet Shieu, Mu-Kuei
Ho, Hsin-Yu
Lin, Shu-Hui
Lo, Yu-Sheng
Lin, Chia-Chieh
Chuang, Yi-Ching
Hsieh, Ming-Ju
Chen, Mu-Kuan
author_sort Shieu, Mu-Kuei
collection PubMed
description Lysine methyltransferase 2C (KMT2C) is a tumor-suppressor gene in several myeloid cells and epithelia and is linked with blood and solid tumor cancers. KMT2C single-nucleotide polymorphisms (SNPs) are also connected with several cancer types. Our study aimed to explore the potential genetic polymorphisms of KMT2C in oral cancer. Five KMT2C SNPs, including rs201834857, rs4725443, rs6464221, rs74483926, and rs6943984, were evaluated in 284 cancer-free controls and 284 oral squamous cell carcinoma (OSCC) cases. We found that individuals with the TC genotype or TC + CC genotype of rs4725443 had a higher risk of oral cancer incidence than those with the TT genotype. Further analysis of KMT2C SNP rs4725443 revealed that the TC + CC genotype of rs4725443 was associated with a significantly advanced tumor stage in the non-alcohol-drinking population. Moreover, the TC + CC genotype of rs4725443 was connected with poor cell differentiation in the alcohol-drinking population. Through analyzing a dataset from The Cancer Genome Atlas (TCGA), we found that reduced KMT2C levels were associated with advanced tumor stage, lymph node invasion, and poor cell differentiation in head and neck squamous cell carcinomas. Our data suggest that KMT2C SNP rs4725443 is a potential genetic marker for oral cancer patients in both non-alcohol-drinking and alcohol-drinking populations.
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spelling pubmed-89975092022-04-12 Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer Shieu, Mu-Kuei Ho, Hsin-Yu Lin, Shu-Hui Lo, Yu-Sheng Lin, Chia-Chieh Chuang, Yi-Ching Hsieh, Ming-Ju Chen, Mu-Kuan Int J Environ Res Public Health Article Lysine methyltransferase 2C (KMT2C) is a tumor-suppressor gene in several myeloid cells and epithelia and is linked with blood and solid tumor cancers. KMT2C single-nucleotide polymorphisms (SNPs) are also connected with several cancer types. Our study aimed to explore the potential genetic polymorphisms of KMT2C in oral cancer. Five KMT2C SNPs, including rs201834857, rs4725443, rs6464221, rs74483926, and rs6943984, were evaluated in 284 cancer-free controls and 284 oral squamous cell carcinoma (OSCC) cases. We found that individuals with the TC genotype or TC + CC genotype of rs4725443 had a higher risk of oral cancer incidence than those with the TT genotype. Further analysis of KMT2C SNP rs4725443 revealed that the TC + CC genotype of rs4725443 was associated with a significantly advanced tumor stage in the non-alcohol-drinking population. Moreover, the TC + CC genotype of rs4725443 was connected with poor cell differentiation in the alcohol-drinking population. Through analyzing a dataset from The Cancer Genome Atlas (TCGA), we found that reduced KMT2C levels were associated with advanced tumor stage, lymph node invasion, and poor cell differentiation in head and neck squamous cell carcinomas. Our data suggest that KMT2C SNP rs4725443 is a potential genetic marker for oral cancer patients in both non-alcohol-drinking and alcohol-drinking populations. MDPI 2022-03-27 /pmc/articles/PMC8997509/ /pubmed/35409657 http://dx.doi.org/10.3390/ijerph19073974 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shieu, Mu-Kuei
Ho, Hsin-Yu
Lin, Shu-Hui
Lo, Yu-Sheng
Lin, Chia-Chieh
Chuang, Yi-Ching
Hsieh, Ming-Ju
Chen, Mu-Kuan
Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer
title Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer
title_full Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer
title_fullStr Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer
title_full_unstemmed Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer
title_short Association of KMT2C Genetic Variants with the Clinicopathologic Development of Oral Cancer
title_sort association of kmt2c genetic variants with the clinicopathologic development of oral cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997509/
https://www.ncbi.nlm.nih.gov/pubmed/35409657
http://dx.doi.org/10.3390/ijerph19073974
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