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Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors
OBJECTIVE: This study was carried out to evaluate the relationship between mtDNA D-loop variations and the pathogenesis of a brain tumor. MATERIALS AND METHODS: In this experimental study, 25 specimens of brain tumor tissue with their adjacent tissues from patients and 454 blood samples from differe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582428/ https://www.ncbi.nlm.nih.gov/pubmed/31210442 http://dx.doi.org/10.22074/cellj.2019.5947 |
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author | Altafi, Donya Sadeghi, Soha Hojatian, Hamed Torabi Afra, Maryam Pakizeh Kar, Safoura Gorji, Mojtaba Houshmand, Massoud |
author_facet | Altafi, Donya Sadeghi, Soha Hojatian, Hamed Torabi Afra, Maryam Pakizeh Kar, Safoura Gorji, Mojtaba Houshmand, Massoud |
author_sort | Altafi, Donya |
collection | PubMed |
description | OBJECTIVE: This study was carried out to evaluate the relationship between mtDNA D-loop variations and the pathogenesis of a brain tumor. MATERIALS AND METHODS: In this experimental study, 25 specimens of brain tumor tissue with their adjacent tissues from patients and 454 blood samples from different ethnic groups of the Iranian population, as the control group, were analysed by the polymerase chain reaction (PCR)-sequencing method. RESULTS: Thirty-six variations of the D-loop area were observed in brain tumor tissues as well as the adjacent normal tissues. A significant difference of A750G (P=0.046), T15936C (P=0.013), C15884G (P=0.013), C16069T (P=0.049), T16126C (P=0.006), C16186T (P=0.022), T16189C (P=0.041), C16193T (P=0.045), C16223T (P=0.001), T16224C (P=0.013), C16234T (P=0.013), G16274A (P=0.009), T16311C (P=0.038), C16327T (P=0.045), C16355T (P=0.003), T16362C (P=0.006), G16384A (P=0.042), G16392A (P=0.013), G16394A (P=0.013), and G16477A (P=0.013) variants was found between the patients and the controls. CONCLUSION: The results indicated individuals with C16069T [odds ratio (OR): 2.048], T16126C (OR: 2.226), C16186T (OR: 3.586), G16274A (OR: 4.831), C16355T (OR: 7.322), and T16362C (OR: 6.682) variants with an OR more than one are probably associated with a brain tumor. However, given the multifactorial nature of cancer, more investigation needs to be done to confirm this association. |
format | Online Article Text |
id | pubmed-6582428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-65824282019-09-01 Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors Altafi, Donya Sadeghi, Soha Hojatian, Hamed Torabi Afra, Maryam Pakizeh Kar, Safoura Gorji, Mojtaba Houshmand, Massoud Cell J Original Article OBJECTIVE: This study was carried out to evaluate the relationship between mtDNA D-loop variations and the pathogenesis of a brain tumor. MATERIALS AND METHODS: In this experimental study, 25 specimens of brain tumor tissue with their adjacent tissues from patients and 454 blood samples from different ethnic groups of the Iranian population, as the control group, were analysed by the polymerase chain reaction (PCR)-sequencing method. RESULTS: Thirty-six variations of the D-loop area were observed in brain tumor tissues as well as the adjacent normal tissues. A significant difference of A750G (P=0.046), T15936C (P=0.013), C15884G (P=0.013), C16069T (P=0.049), T16126C (P=0.006), C16186T (P=0.022), T16189C (P=0.041), C16193T (P=0.045), C16223T (P=0.001), T16224C (P=0.013), C16234T (P=0.013), G16274A (P=0.009), T16311C (P=0.038), C16327T (P=0.045), C16355T (P=0.003), T16362C (P=0.006), G16384A (P=0.042), G16392A (P=0.013), G16394A (P=0.013), and G16477A (P=0.013) variants was found between the patients and the controls. CONCLUSION: The results indicated individuals with C16069T [odds ratio (OR): 2.048], T16126C (OR: 2.226), C16186T (OR: 3.586), G16274A (OR: 4.831), C16355T (OR: 7.322), and T16362C (OR: 6.682) variants with an OR more than one are probably associated with a brain tumor. However, given the multifactorial nature of cancer, more investigation needs to be done to confirm this association. Royan Institute 2019 2019-06-15 /pmc/articles/PMC6582428/ /pubmed/31210442 http://dx.doi.org/10.22074/cellj.2019.5947 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 Altafi, Donya Sadeghi, Soha Hojatian, Hamed Torabi Afra, Maryam Pakizeh Kar, Safoura Gorji, Mojtaba Houshmand, Massoud Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain Tumors |
title | Mitochondrial Polymorphisms, in The D-Loop Area, Are
Associated with Brain Tumors |
title_full | Mitochondrial Polymorphisms, in The D-Loop Area, Are
Associated with Brain Tumors |
title_fullStr | Mitochondrial Polymorphisms, in The D-Loop Area, Are
Associated with Brain Tumors |
title_full_unstemmed | Mitochondrial Polymorphisms, in The D-Loop Area, Are
Associated with Brain Tumors |
title_short | Mitochondrial Polymorphisms, in The D-Loop Area, Are
Associated with Brain Tumors |
title_sort | mitochondrial polymorphisms, in the d-loop area, are
associated with brain tumors |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582428/ https://www.ncbi.nlm.nih.gov/pubmed/31210442 http://dx.doi.org/10.22074/cellj.2019.5947 |
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