Analysis of mitochondrial ND1 gene in human colorectal cancer

Background: Colorectal cancer as a mortal disease affected both sexes of all ethnic and racial human groups. Former studies have indicated some mutations in the mitochondrial DNA (mtDNA) in different human cancers. Complex I NADH has the most subunits encoded by mtDNA. For a better understanding of...

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Main Authors: Mansoureh Akouchekian, Massoud Houshmand, Mohammad Hassan Hosseini Akbari, Behnam Kamalidehghan, Masoumeh Dehghan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2011-01-01
Series:Journal of Research in Medical Sciences
Subjects:
DNA
Online Access:http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2011;volume=16;issue=1;spage=50;epage=55;aulast=Akouchekian
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spelling doaj-8e2d04d6466446e4b4185101d6e1ecb92020-11-25T01:35:42ZengWolters Kluwer Medknow PublicationsJournal of Research in Medical Sciences1735-19951735-71362011-01-011615055Analysis of mitochondrial ND1 gene in human colorectal cancerMansoureh AkouchekianMassoud HoushmandMohammad Hassan Hosseini AkbariBehnam KamalidehghanMasoumeh DehghanBackground: Colorectal cancer as a mortal disease affected both sexes of all ethnic and racial human groups. Former studies have indicated some mutations in the mitochondrial DNA (mtDNA) in different human cancers. Complex I NADH has the most subunits encoded by mtDNA. For a better understanding of the mtDNA abnormality in colorectal cancer some genes of this complex is screened for existence of mutations. Methods: One of the main regions of the mtDNA encoding protein was screened by PCR-RFLP followed by DNA sequencing. The obtained sequences were aligned with the revised Cambridge Reference Sequence (rCRS). Each altera-tion recorded as single nucleotide polymorphisms (SNPs), deletions or insertions. Results: Eight mutations were found in 15 samples out of 30 studied populations and no mutation detected in other 15 samples. Among these 15 mutated samples, 7 different mutations were found in 7 patients, that means one mutation per patient and the 8th mutation (T4216C) was common in the rest of 8 samples; in other words T4216C mutation in 27% of tested samples was identified (8 patients out of 30 patients). The existence of T4216C mutation was found to be sig-nificantly different (p ≤ 0.05) between tumoral patient′s tissue and adjacent normal tissue. Conclusions: Results showed that a high frequency of somatic alterations of mtDNA occurs during the carcinogenesis and/or the progression of colorectal cancer. Based on the mtDNA mutation pattern observed in this study and other pre-viously studies it is believed that looking for somatic mutations in mtDNA would be one of the diagnostic values in early detection of cancer.http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2011;volume=16;issue=1;spage=50;epage=55;aulast=AkouchekianDNAMitochondrialColorectal NeoplasmsElectron Transport Complex IMT-ND1 ProteinHumanOxidative PhosphorylationReactive Oxygen Species
collection DOAJ
language English
format Article
sources DOAJ
author Mansoureh Akouchekian
Massoud Houshmand
Mohammad Hassan Hosseini Akbari
Behnam Kamalidehghan
Masoumeh Dehghan
spellingShingle Mansoureh Akouchekian
Massoud Houshmand
Mohammad Hassan Hosseini Akbari
Behnam Kamalidehghan
Masoumeh Dehghan
Analysis of mitochondrial ND1 gene in human colorectal cancer
Journal of Research in Medical Sciences
DNA
Mitochondrial
Colorectal Neoplasms
Electron Transport Complex I
MT-ND1 Protein
Human
Oxidative Phosphorylation
Reactive Oxygen Species
author_facet Mansoureh Akouchekian
Massoud Houshmand
Mohammad Hassan Hosseini Akbari
Behnam Kamalidehghan
Masoumeh Dehghan
author_sort Mansoureh Akouchekian
title Analysis of mitochondrial ND1 gene in human colorectal cancer
title_short Analysis of mitochondrial ND1 gene in human colorectal cancer
title_full Analysis of mitochondrial ND1 gene in human colorectal cancer
title_fullStr Analysis of mitochondrial ND1 gene in human colorectal cancer
title_full_unstemmed Analysis of mitochondrial ND1 gene in human colorectal cancer
title_sort analysis of mitochondrial nd1 gene in human colorectal cancer
publisher Wolters Kluwer Medknow Publications
series Journal of Research in Medical Sciences
issn 1735-1995
1735-7136
publishDate 2011-01-01
description Background: Colorectal cancer as a mortal disease affected both sexes of all ethnic and racial human groups. Former studies have indicated some mutations in the mitochondrial DNA (mtDNA) in different human cancers. Complex I NADH has the most subunits encoded by mtDNA. For a better understanding of the mtDNA abnormality in colorectal cancer some genes of this complex is screened for existence of mutations. Methods: One of the main regions of the mtDNA encoding protein was screened by PCR-RFLP followed by DNA sequencing. The obtained sequences were aligned with the revised Cambridge Reference Sequence (rCRS). Each altera-tion recorded as single nucleotide polymorphisms (SNPs), deletions or insertions. Results: Eight mutations were found in 15 samples out of 30 studied populations and no mutation detected in other 15 samples. Among these 15 mutated samples, 7 different mutations were found in 7 patients, that means one mutation per patient and the 8th mutation (T4216C) was common in the rest of 8 samples; in other words T4216C mutation in 27% of tested samples was identified (8 patients out of 30 patients). The existence of T4216C mutation was found to be sig-nificantly different (p ≤ 0.05) between tumoral patient′s tissue and adjacent normal tissue. Conclusions: Results showed that a high frequency of somatic alterations of mtDNA occurs during the carcinogenesis and/or the progression of colorectal cancer. Based on the mtDNA mutation pattern observed in this study and other pre-viously studies it is believed that looking for somatic mutations in mtDNA would be one of the diagnostic values in early detection of cancer.
topic DNA
Mitochondrial
Colorectal Neoplasms
Electron Transport Complex I
MT-ND1 Protein
Human
Oxidative Phosphorylation
Reactive Oxygen Species
url http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2011;volume=16;issue=1;spage=50;epage=55;aulast=Akouchekian
work_keys_str_mv AT mansourehakouchekian analysisofmitochondrialnd1geneinhumancolorectalcancer
AT massoudhoushmand analysisofmitochondrialnd1geneinhumancolorectalcancer
AT mohammadhassanhosseiniakbari analysisofmitochondrialnd1geneinhumancolorectalcancer
AT behnamkamalidehghan analysisofmitochondrialnd1geneinhumancolorectalcancer
AT masoumehdehghan analysisofmitochondrialnd1geneinhumancolorectalcancer
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