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CD44 Gene rs8193 C Allele Is Significantly Enriched in Gastric Cancer Patients
OBJECTIVE: Gastric cancer is a multifactorial disease. In addition to environmental factors, many genes are involved in this malignancy. One of the genes associated with gastric cancer is CD44 gene and its polymorphisms. CD44 gene plays role in regulating cell survival, growth and mobility. The sing...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722445/ https://www.ncbi.nlm.nih.gov/pubmed/31376327 http://dx.doi.org/10.22074/cellj.2020.6389 |
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author | Mokhtarian, Roya Tabatabaeian, Hossein Saadatmand, Pardis Azadeh, Mansoureh Balmeh, Negar Yakhchali, Bagher Ghaedi, Kamran |
author_facet | Mokhtarian, Roya Tabatabaeian, Hossein Saadatmand, Pardis Azadeh, Mansoureh Balmeh, Negar Yakhchali, Bagher Ghaedi, Kamran |
author_sort | Mokhtarian, Roya |
collection | PubMed |
description | OBJECTIVE: Gastric cancer is a multifactorial disease. In addition to environmental factors, many genes are involved in this malignancy. One of the genes associated with gastric cancer is CD44 gene and its polymorphisms. CD44 gene plays role in regulating cell survival, growth and mobility. The single nucleotide polymorphism (SNP) rs8193, located in the CD44 gene, has not been studied in gastric cancer patients of the Iranian population. The present study aims to study this polymorphism in 86 gastric cancer patients and 96 healthy individuals. MATERIALS AND METHODS: In this cross-sectional case-control study, rs8193 polymorphism was genotyped by allele specific primer polymerase chain reaction (ASP-PCR) technique. The obtained data were statistically analyzed. To find the potential mechanism of action, rs8193 was bioinformatically investigated. RESULTS: rs8193 C allele played a risk factor role for gastric cancer. Patients carrying this allele were more susceptible to have gastric cancer, with lymph node spread. On the other hand, rs8193 T allele, a protective factor, was associated with a higher chance of accumulation in the lower stages of cancer. C allele might impose its effect via destabilizing CD44 and miR-570 interaction. CONCLUSION: rs8193 is statistically associated with the risk of malignancy, lymph node spread and stage of gastric cancer in Iranian population. |
format | Online Article Text |
id | pubmed-6722445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-67224452020-01-01 CD44 Gene rs8193 C Allele Is Significantly Enriched in Gastric Cancer Patients Mokhtarian, Roya Tabatabaeian, Hossein Saadatmand, Pardis Azadeh, Mansoureh Balmeh, Negar Yakhchali, Bagher Ghaedi, Kamran Cell J Original Article OBJECTIVE: Gastric cancer is a multifactorial disease. In addition to environmental factors, many genes are involved in this malignancy. One of the genes associated with gastric cancer is CD44 gene and its polymorphisms. CD44 gene plays role in regulating cell survival, growth and mobility. The single nucleotide polymorphism (SNP) rs8193, located in the CD44 gene, has not been studied in gastric cancer patients of the Iranian population. The present study aims to study this polymorphism in 86 gastric cancer patients and 96 healthy individuals. MATERIALS AND METHODS: In this cross-sectional case-control study, rs8193 polymorphism was genotyped by allele specific primer polymerase chain reaction (ASP-PCR) technique. The obtained data were statistically analyzed. To find the potential mechanism of action, rs8193 was bioinformatically investigated. RESULTS: rs8193 C allele played a risk factor role for gastric cancer. Patients carrying this allele were more susceptible to have gastric cancer, with lymph node spread. On the other hand, rs8193 T allele, a protective factor, was associated with a higher chance of accumulation in the lower stages of cancer. C allele might impose its effect via destabilizing CD44 and miR-570 interaction. CONCLUSION: rs8193 is statistically associated with the risk of malignancy, lymph node spread and stage of gastric cancer in Iranian population. Royan Institute 2020 2019-07-31 /pmc/articles/PMC6722445/ /pubmed/31376327 http://dx.doi.org/10.22074/cellj.2020.6389 Text en The Cell Journal (Yakhteh) is an open access journal which means the articles are freely available online for any individual author to download and use the providing address. The journal is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported License which allows the author(s) to hold the copyright without restrictions that is permitting unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited. http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mokhtarian, Roya Tabatabaeian, Hossein Saadatmand, Pardis Azadeh, Mansoureh Balmeh, Negar Yakhchali, Bagher Ghaedi, Kamran CD44 Gene rs8193 C Allele Is Significantly Enriched in Gastric Cancer Patients |
title | CD44 Gene rs8193 C Allele Is Significantly Enriched in
Gastric Cancer Patients |
title_full | CD44 Gene rs8193 C Allele Is Significantly Enriched in
Gastric Cancer Patients |
title_fullStr | CD44 Gene rs8193 C Allele Is Significantly Enriched in
Gastric Cancer Patients |
title_full_unstemmed | CD44 Gene rs8193 C Allele Is Significantly Enriched in
Gastric Cancer Patients |
title_short | CD44 Gene rs8193 C Allele Is Significantly Enriched in
Gastric Cancer Patients |
title_sort | cd44 gene rs8193 c allele is significantly enriched in
gastric cancer patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722445/ https://www.ncbi.nlm.nih.gov/pubmed/31376327 http://dx.doi.org/10.22074/cellj.2020.6389 |
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