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Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population

Osteosarcoma is a malignant tumor that develops from a mesenchymal cell line and is caused by gene–environment interactions. This study aimed to explore whether TIMP2/TIMP3 polymorphisms influenced the osteosarcoma risk. The expression of the TIMP2 and TIMP3 genes in osteosarcoma histiocytes was ana...

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Autores principales: Wu, Zhongwei, Chen, Huali, Pan, Liwei, Yu, Weiyang, Lou, Chao, Chen, Jian, He, Dengwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982212/
https://www.ncbi.nlm.nih.gov/pubmed/33725949
http://dx.doi.org/10.1097/MD.0000000000024818
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author Wu, Zhongwei
Chen, Huali
Pan, Liwei
Yu, Weiyang
Lou, Chao
Chen, Jian
He, Dengwei
author_facet Wu, Zhongwei
Chen, Huali
Pan, Liwei
Yu, Weiyang
Lou, Chao
Chen, Jian
He, Dengwei
author_sort Wu, Zhongwei
collection PubMed
description Osteosarcoma is a malignant tumor that develops from a mesenchymal cell line and is caused by gene–environment interactions. This study aimed to explore whether TIMP2/TIMP3 polymorphisms influenced the osteosarcoma risk. The expression of the TIMP2 and TIMP3 genes in osteosarcoma histiocytes was analyzed by immunohistochemistry. In this case-control study, which includes samples from 499 patients and 500 healthy controls, 10 single-nucleotide polymorphisms (SNPs) in TIMP2 and TIMP3 were selected. Furthermore, we used the Agena MassARRAY platform for genotyping. The statistical analysis was performed using χ(2) test/Fisher exact test, and logistic regression analysis. The immunohistochemistry results showed that the expression of TIMP2 is obvious higher in osteosarcoma histiocytes than in the normal histiocytes. The association study indicated that the allele of rs2277698 and rs4789936 were protective SNPs reducing the risk of osteosarcoma (odds ratios  > 1, P < .05) by the χ(2) test. In the genetic model, logistic regression analyses revealed that the rs2277698 and rs4789936 were associated with decreasing the risk of osteosarcoma under the codominant model, dominant model, and log-additive model. Stratification analysis revealed that 2 SNPs (rs2277698 and rs4789936) were significantly associated with a reduced risk of osteosarcoma in allele and genetic model after stratification by gender or age (P < .05). In addition, the haplotype “T(rs2277698)C(rs2009169)C(rs7342880)” of TIMP2 was associated with decreasing the osteosarcoma risk. The “A(rs9609634)T(rs11547635)” of TIMP3 was associated with reducing the osteosarcoma risk. This finding shed new light on the high expression of TIMP2 polymorphisms may contribute to decreasing the osteosarcoma risk in Zhejiang populations.
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spelling pubmed-79822122021-03-23 Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population Wu, Zhongwei Chen, Huali Pan, Liwei Yu, Weiyang Lou, Chao Chen, Jian He, Dengwei Medicine (Baltimore) 3500 Osteosarcoma is a malignant tumor that develops from a mesenchymal cell line and is caused by gene–environment interactions. This study aimed to explore whether TIMP2/TIMP3 polymorphisms influenced the osteosarcoma risk. The expression of the TIMP2 and TIMP3 genes in osteosarcoma histiocytes was analyzed by immunohistochemistry. In this case-control study, which includes samples from 499 patients and 500 healthy controls, 10 single-nucleotide polymorphisms (SNPs) in TIMP2 and TIMP3 were selected. Furthermore, we used the Agena MassARRAY platform for genotyping. The statistical analysis was performed using χ(2) test/Fisher exact test, and logistic regression analysis. The immunohistochemistry results showed that the expression of TIMP2 is obvious higher in osteosarcoma histiocytes than in the normal histiocytes. The association study indicated that the allele of rs2277698 and rs4789936 were protective SNPs reducing the risk of osteosarcoma (odds ratios  > 1, P < .05) by the χ(2) test. In the genetic model, logistic regression analyses revealed that the rs2277698 and rs4789936 were associated with decreasing the risk of osteosarcoma under the codominant model, dominant model, and log-additive model. Stratification analysis revealed that 2 SNPs (rs2277698 and rs4789936) were significantly associated with a reduced risk of osteosarcoma in allele and genetic model after stratification by gender or age (P < .05). In addition, the haplotype “T(rs2277698)C(rs2009169)C(rs7342880)” of TIMP2 was associated with decreasing the osteosarcoma risk. The “A(rs9609634)T(rs11547635)” of TIMP3 was associated with reducing the osteosarcoma risk. This finding shed new light on the high expression of TIMP2 polymorphisms may contribute to decreasing the osteosarcoma risk in Zhejiang populations. Lippincott Williams & Wilkins 2021-03-19 /pmc/articles/PMC7982212/ /pubmed/33725949 http://dx.doi.org/10.1097/MD.0000000000024818 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3500
Wu, Zhongwei
Chen, Huali
Pan, Liwei
Yu, Weiyang
Lou, Chao
Chen, Jian
He, Dengwei
Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
title Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
title_full Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
title_fullStr Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
title_full_unstemmed Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
title_short Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
title_sort effect of timp2/timp3 genes on the risk of osteosarcoma in zhejiang population
topic 3500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982212/
https://www.ncbi.nlm.nih.gov/pubmed/33725949
http://dx.doi.org/10.1097/MD.0000000000024818
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