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Common mitochondrial polymorphisms as risk factor for endometrial cancer
Endometrial carcinoma is the most commonly diagnosed gynaecological cancer in developed countries. Although the molecular genetics of this disease has been in the focus of many research laboratories for the last 20 years, relevant prognostic and diagnostic markers are still missing. At the same time...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775024/ https://www.ncbi.nlm.nih.gov/pubmed/19863780 http://dx.doi.org/10.1186/1755-7682-2-33 |
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author | Czarnecka, Anna M Klemba, Aleksandra Semczuk, Andrzej Plak, Katarzyna Marzec, Barbara Krawczyk, Tomasz Kofler, Barbara Golik, Pawel Bartnik, Ewa |
author_facet | Czarnecka, Anna M Klemba, Aleksandra Semczuk, Andrzej Plak, Katarzyna Marzec, Barbara Krawczyk, Tomasz Kofler, Barbara Golik, Pawel Bartnik, Ewa |
author_sort | Czarnecka, Anna M |
collection | PubMed |
description | Endometrial carcinoma is the most commonly diagnosed gynaecological cancer in developed countries. Although the molecular genetics of this disease has been in the focus of many research laboratories for the last 20 years, relevant prognostic and diagnostic markers are still missing. At the same time mitochondrial DNA mutations have been reported in many types of cancer during the last two decades. It is therefore very likely that the mitochondrial genotype is one of the cancer susceptibility factors. To investigate the presence of mtDNA somatic mutations and distribution of inherited polymorphisms in endometrial adenocarcinoma patients we analyzed the D-loop sequence of cancer samples and their corresponding normal tissues and moreover performed mitochondrial haplogroup analysis. We detected 2 somatic mutation and increased incidence of mtDNA polymorphisms, in particular 16223C (80% patients, p = 0.005), 16126C (23%, p = 0.025) and 207A (19%, p = 0.027). Subsequent statistical analysis revealed that endometrial carcinoma population haplogroup distribution differs from the Polish population and that haplogroup H (with its defining polymorphism - C7028T) is strongly underrepresented (p = 0.003), therefore might be a cancer-protective factor. Our report supports the notion that mtDNA polymorphisms establish a specific genetic background for endometrial adenocarcinoma development and that mtDNA analysis may result in the development of new molecular tool for cancer detection. |
format | Text |
id | pubmed-2775024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27750242009-11-10 Common mitochondrial polymorphisms as risk factor for endometrial cancer Czarnecka, Anna M Klemba, Aleksandra Semczuk, Andrzej Plak, Katarzyna Marzec, Barbara Krawczyk, Tomasz Kofler, Barbara Golik, Pawel Bartnik, Ewa Int Arch Med Original Research Endometrial carcinoma is the most commonly diagnosed gynaecological cancer in developed countries. Although the molecular genetics of this disease has been in the focus of many research laboratories for the last 20 years, relevant prognostic and diagnostic markers are still missing. At the same time mitochondrial DNA mutations have been reported in many types of cancer during the last two decades. It is therefore very likely that the mitochondrial genotype is one of the cancer susceptibility factors. To investigate the presence of mtDNA somatic mutations and distribution of inherited polymorphisms in endometrial adenocarcinoma patients we analyzed the D-loop sequence of cancer samples and their corresponding normal tissues and moreover performed mitochondrial haplogroup analysis. We detected 2 somatic mutation and increased incidence of mtDNA polymorphisms, in particular 16223C (80% patients, p = 0.005), 16126C (23%, p = 0.025) and 207A (19%, p = 0.027). Subsequent statistical analysis revealed that endometrial carcinoma population haplogroup distribution differs from the Polish population and that haplogroup H (with its defining polymorphism - C7028T) is strongly underrepresented (p = 0.003), therefore might be a cancer-protective factor. Our report supports the notion that mtDNA polymorphisms establish a specific genetic background for endometrial adenocarcinoma development and that mtDNA analysis may result in the development of new molecular tool for cancer detection. BioMed Central 2009-10-28 /pmc/articles/PMC2775024/ /pubmed/19863780 http://dx.doi.org/10.1186/1755-7682-2-33 Text en Copyright © 2009 Czarnecka 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 | Original Research Czarnecka, Anna M Klemba, Aleksandra Semczuk, Andrzej Plak, Katarzyna Marzec, Barbara Krawczyk, Tomasz Kofler, Barbara Golik, Pawel Bartnik, Ewa Common mitochondrial polymorphisms as risk factor for endometrial cancer |
title | Common mitochondrial polymorphisms as risk factor for endometrial cancer |
title_full | Common mitochondrial polymorphisms as risk factor for endometrial cancer |
title_fullStr | Common mitochondrial polymorphisms as risk factor for endometrial cancer |
title_full_unstemmed | Common mitochondrial polymorphisms as risk factor for endometrial cancer |
title_short | Common mitochondrial polymorphisms as risk factor for endometrial cancer |
title_sort | common mitochondrial polymorphisms as risk factor for endometrial cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775024/ https://www.ncbi.nlm.nih.gov/pubmed/19863780 http://dx.doi.org/10.1186/1755-7682-2-33 |
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