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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...

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Autores principales: Czarnecka, Anna M, Klemba, Aleksandra, Semczuk, Andrzej, Plak, Katarzyna, Marzec, Barbara, Krawczyk, Tomasz, Kofler, Barbara, Golik, Pawel, Bartnik, Ewa
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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.
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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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