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Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer

BACKGROUND: Mitochondrial DNA (mtDNA) haplogroups and single nucleotide polymorphisms (mtSNP) have been shown to play a role in various human conditions including aging and some neurodegenerative diseases, metabolic diseases and cancer. METHODS: To investigate whether mtDNA haplogroups contribute to...

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Autores principales: Fang, Hezhi, Shen, Lijun, Chen, Tao, He, Jing, Ding, Zhinan, Wei, Jia, Qu, Jianchun, Chen, Guorong, Lu, Jianxin, Bai, Yidong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933623/
https://www.ncbi.nlm.nih.gov/pubmed/20704735
http://dx.doi.org/10.1186/1471-2407-10-421
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author Fang, Hezhi
Shen, Lijun
Chen, Tao
He, Jing
Ding, Zhinan
Wei, Jia
Qu, Jianchun
Chen, Guorong
Lu, Jianxin
Bai, Yidong
author_facet Fang, Hezhi
Shen, Lijun
Chen, Tao
He, Jing
Ding, Zhinan
Wei, Jia
Qu, Jianchun
Chen, Guorong
Lu, Jianxin
Bai, Yidong
author_sort Fang, Hezhi
collection PubMed
description BACKGROUND: Mitochondrial DNA (mtDNA) haplogroups and single nucleotide polymorphisms (mtSNP) have been shown to play a role in various human conditions including aging and some neurodegenerative diseases, metabolic diseases and cancer. METHODS: To investigate whether mtDNA haplogroups contribute to the occurrence of cancer in a specific Chinese population, we have carried out a comprehensive case-control study of mtDNA from large cohorts of patients with three common cancer types, namely, colorectal cancer (n = 108), thyroid cancer (n = 100) and breast cancer (n = 104), in Wenzhou, a southern Chinese city in the Zhejiang Province. RESULTS: We found that patients with mtDNA haplogroup M exhibited an increased risk of breast cancer occurrence [OR = 1.77; 95% CI (1.03-3.07); P = 0.040], and that this risk was even more pronounced in a sub-haplogroup of M, D5 [OR = 3.11; 95%CI (1.07-9.06); p = 0.030]. In spite of this, in patients with breast cancer, haplogroup M was decreased in the metastatic group. On the other hand, our results also showed that haplogroup D4a was associated with an increased risk of thyroid cancer [OR = 3.00; 95%CI (1.09-8.29); p = 0.028]. However, no significant correlation has been detected between any mtDNA haplogroups and colorectal cancer occurrence. CONCLUSION: Our investigation indicates that mitochondrial haplogroups could have a tissue-specific, population-specific and stage-specific role in modulating cancer development.
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spelling pubmed-29336232010-09-07 Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer Fang, Hezhi Shen, Lijun Chen, Tao He, Jing Ding, Zhinan Wei, Jia Qu, Jianchun Chen, Guorong Lu, Jianxin Bai, Yidong BMC Cancer Research Article BACKGROUND: Mitochondrial DNA (mtDNA) haplogroups and single nucleotide polymorphisms (mtSNP) have been shown to play a role in various human conditions including aging and some neurodegenerative diseases, metabolic diseases and cancer. METHODS: To investigate whether mtDNA haplogroups contribute to the occurrence of cancer in a specific Chinese population, we have carried out a comprehensive case-control study of mtDNA from large cohorts of patients with three common cancer types, namely, colorectal cancer (n = 108), thyroid cancer (n = 100) and breast cancer (n = 104), in Wenzhou, a southern Chinese city in the Zhejiang Province. RESULTS: We found that patients with mtDNA haplogroup M exhibited an increased risk of breast cancer occurrence [OR = 1.77; 95% CI (1.03-3.07); P = 0.040], and that this risk was even more pronounced in a sub-haplogroup of M, D5 [OR = 3.11; 95%CI (1.07-9.06); p = 0.030]. In spite of this, in patients with breast cancer, haplogroup M was decreased in the metastatic group. On the other hand, our results also showed that haplogroup D4a was associated with an increased risk of thyroid cancer [OR = 3.00; 95%CI (1.09-8.29); p = 0.028]. However, no significant correlation has been detected between any mtDNA haplogroups and colorectal cancer occurrence. CONCLUSION: Our investigation indicates that mitochondrial haplogroups could have a tissue-specific, population-specific and stage-specific role in modulating cancer development. BioMed Central 2010-08-12 /pmc/articles/PMC2933623/ /pubmed/20704735 http://dx.doi.org/10.1186/1471-2407-10-421 Text en Copyright ©2010 Fang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Fang, Hezhi
Shen, Lijun
Chen, Tao
He, Jing
Ding, Zhinan
Wei, Jia
Qu, Jianchun
Chen, Guorong
Lu, Jianxin
Bai, Yidong
Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
title Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
title_full Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
title_fullStr Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
title_full_unstemmed Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
title_short Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
title_sort cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933623/
https://www.ncbi.nlm.nih.gov/pubmed/20704735
http://dx.doi.org/10.1186/1471-2407-10-421
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