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Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer

OBJECTIVE: This study was conducted to find out the possible association of Vitamin D receptor, caudal-related homeobox 2 (VDR-Cdx2) polymorphism with cancer in the given study group. METHODS: In this study, 151 subjects (84 cases and 67 controls) were recruited from two local tertiary care hospital...

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Autores principales: Rehman, Madiha, Mahboob, Tabassum, Shahid, Syed M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Qassim Uninversity 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934131/
https://www.ncbi.nlm.nih.gov/pubmed/33708039
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author Rehman, Madiha
Mahboob, Tabassum
Shahid, Syed M.
author_facet Rehman, Madiha
Mahboob, Tabassum
Shahid, Syed M.
author_sort Rehman, Madiha
collection PubMed
description OBJECTIVE: This study was conducted to find out the possible association of Vitamin D receptor, caudal-related homeobox 2 (VDR-Cdx2) polymorphism with cancer in the given study group. METHODS: In this study, 151 subjects (84 cases and 67 controls) were recruited from two local tertiary care hospitals of Karachi, Pakistan, suffering from various cancers including gastric cancer (GC), rectal cancer (RC), colon cancer (CC), and multiple myeloma followed by ethical approval from institutions and informed consent from all the participants. The genotyping of VDR-Cdx2 polymorphism was performed using tetra-primer amplification refractory mutation system-polymerase chain reaction method. The genotypic assortment/distribution in the control and disease groups was according to Hardy-Weinberg’s equilibrium. RESULTS: The genotype frequencies of VDR-Cdx2 polymorphism in cancer patients were observed as: AA 1.2%, AG 32%, and GG 66.8% while in control group as; AA 7.5%, AG 50.7%, and GG was 41.8%. The results unveil that the genotype VDR-Cdx2 was found significantly different in cancer and control group (P < 0.01). The AG and GG genotypes were found to be associated with the cancer (P < 0.05). Therefore, these genotypes may be considered as the risk factors for cancer. However, the frequencies of “A” and “G” alleles were not significantly different between two groups. CONCLUSION: The observed single-nucleotide polymorphism of VDR-Cdx2 gene may be considered as a risk factor for the cancer in this study group. The AG and GG genotypes established an association with various cancers including GC, RC, CC, and multiple myeloma in Pakistani population. Further investigations examining large data are required to compare the role of VDR-Cdx2 polymorphism in cancer etiology in related population.
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spelling pubmed-79341312021-03-10 Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer Rehman, Madiha Mahboob, Tabassum Shahid, Syed M. Int J Health Sci (Qassim) Original Article OBJECTIVE: This study was conducted to find out the possible association of Vitamin D receptor, caudal-related homeobox 2 (VDR-Cdx2) polymorphism with cancer in the given study group. METHODS: In this study, 151 subjects (84 cases and 67 controls) were recruited from two local tertiary care hospitals of Karachi, Pakistan, suffering from various cancers including gastric cancer (GC), rectal cancer (RC), colon cancer (CC), and multiple myeloma followed by ethical approval from institutions and informed consent from all the participants. The genotyping of VDR-Cdx2 polymorphism was performed using tetra-primer amplification refractory mutation system-polymerase chain reaction method. The genotypic assortment/distribution in the control and disease groups was according to Hardy-Weinberg’s equilibrium. RESULTS: The genotype frequencies of VDR-Cdx2 polymorphism in cancer patients were observed as: AA 1.2%, AG 32%, and GG 66.8% while in control group as; AA 7.5%, AG 50.7%, and GG was 41.8%. The results unveil that the genotype VDR-Cdx2 was found significantly different in cancer and control group (P < 0.01). The AG and GG genotypes were found to be associated with the cancer (P < 0.05). Therefore, these genotypes may be considered as the risk factors for cancer. However, the frequencies of “A” and “G” alleles were not significantly different between two groups. CONCLUSION: The observed single-nucleotide polymorphism of VDR-Cdx2 gene may be considered as a risk factor for the cancer in this study group. The AG and GG genotypes established an association with various cancers including GC, RC, CC, and multiple myeloma in Pakistani population. Further investigations examining large data are required to compare the role of VDR-Cdx2 polymorphism in cancer etiology in related population. Qassim Uninversity 2021 /pmc/articles/PMC7934131/ /pubmed/33708039 Text en Copyright: © International Journal of Health Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Rehman, Madiha
Mahboob, Tabassum
Shahid, Syed M.
Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
title Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
title_full Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
title_fullStr Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
title_full_unstemmed Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
title_short Possible association of Vitamin D receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
title_sort possible association of vitamin d receptor, caudal-related homeobox 2 polymorphism with the risk of cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934131/
https://www.ncbi.nlm.nih.gov/pubmed/33708039
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