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A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma

BACKGROUND: Low mitochondrial DNA (mtDNA) copy number is a common feature of renal cell carcinoma (RCC), and may influence tumor development. Results from a recent case-control study suggest that low mtDNA copy number in peripheral blood may be a marker for increased RCC risk. In an attempt to repli...

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Autores principales: Purdue, Mark P., Hofmann, Jonathan N., Colt, Joanne S., Hoxha, Mirjam, Ruterbusch, Julie J., Davis, Faith G., Rothman, Nathaniel, Wacholder, Sholom, Schwartz, Kendra L., Baccarelli, Andrea, Chow, Wong-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427307/
https://www.ncbi.nlm.nih.gov/pubmed/22937019
http://dx.doi.org/10.1371/journal.pone.0043149
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author Purdue, Mark P.
Hofmann, Jonathan N.
Colt, Joanne S.
Hoxha, Mirjam
Ruterbusch, Julie J.
Davis, Faith G.
Rothman, Nathaniel
Wacholder, Sholom
Schwartz, Kendra L.
Baccarelli, Andrea
Chow, Wong-Ho
author_facet Purdue, Mark P.
Hofmann, Jonathan N.
Colt, Joanne S.
Hoxha, Mirjam
Ruterbusch, Julie J.
Davis, Faith G.
Rothman, Nathaniel
Wacholder, Sholom
Schwartz, Kendra L.
Baccarelli, Andrea
Chow, Wong-Ho
author_sort Purdue, Mark P.
collection PubMed
description BACKGROUND: Low mitochondrial DNA (mtDNA) copy number is a common feature of renal cell carcinoma (RCC), and may influence tumor development. Results from a recent case-control study suggest that low mtDNA copy number in peripheral blood may be a marker for increased RCC risk. In an attempt to replicate that finding, we measured mtDNA copy number in peripheral blood DNA from a U.S. population-based case-control study of RCC. METHODOLOGY/PRINCIPAL FINDINGS: Relative mtDNA copy number was measured in triplicate by a quantitative real-time PCR assay using DNA extracted from peripheral whole blood. Cases (n = 603) had significantly lower mtDNA copy number than controls (n = 603; medians 0.85, 0.91 respectively; P = 0.0001). In multiple logistic regression analyses, the lowest quartile of mtDNA copy number was associated with a 60% increase in RCC risk relative to the highest quartile (OR = 1.6, 95% CI = 1.1–2.2; P (trend) = 0.009). This association remained in analyses restricted to cases treated by surgery alone (OR (Q1) = 1.4, 95% CI = 1.0–2.1) and to localized tumors (2.0, 1.3–2.8). CONCLUSIONS/SIGNIFICANCE: Our findings from this investigation, to our knowledge the largest of its kind, offer important confirmatory evidence that low mtDNA copy number is associated with increased RCC risk. Additional research is needed to assess whether the association is replicable in prospective studies.
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spelling pubmed-34273072012-08-30 A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma Purdue, Mark P. Hofmann, Jonathan N. Colt, Joanne S. Hoxha, Mirjam Ruterbusch, Julie J. Davis, Faith G. Rothman, Nathaniel Wacholder, Sholom Schwartz, Kendra L. Baccarelli, Andrea Chow, Wong-Ho PLoS One Research Article BACKGROUND: Low mitochondrial DNA (mtDNA) copy number is a common feature of renal cell carcinoma (RCC), and may influence tumor development. Results from a recent case-control study suggest that low mtDNA copy number in peripheral blood may be a marker for increased RCC risk. In an attempt to replicate that finding, we measured mtDNA copy number in peripheral blood DNA from a U.S. population-based case-control study of RCC. METHODOLOGY/PRINCIPAL FINDINGS: Relative mtDNA copy number was measured in triplicate by a quantitative real-time PCR assay using DNA extracted from peripheral whole blood. Cases (n = 603) had significantly lower mtDNA copy number than controls (n = 603; medians 0.85, 0.91 respectively; P = 0.0001). In multiple logistic regression analyses, the lowest quartile of mtDNA copy number was associated with a 60% increase in RCC risk relative to the highest quartile (OR = 1.6, 95% CI = 1.1–2.2; P (trend) = 0.009). This association remained in analyses restricted to cases treated by surgery alone (OR (Q1) = 1.4, 95% CI = 1.0–2.1) and to localized tumors (2.0, 1.3–2.8). CONCLUSIONS/SIGNIFICANCE: Our findings from this investigation, to our knowledge the largest of its kind, offer important confirmatory evidence that low mtDNA copy number is associated with increased RCC risk. Additional research is needed to assess whether the association is replicable in prospective studies. Public Library of Science 2012-08-24 /pmc/articles/PMC3427307/ /pubmed/22937019 http://dx.doi.org/10.1371/journal.pone.0043149 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Purdue, Mark P.
Hofmann, Jonathan N.
Colt, Joanne S.
Hoxha, Mirjam
Ruterbusch, Julie J.
Davis, Faith G.
Rothman, Nathaniel
Wacholder, Sholom
Schwartz, Kendra L.
Baccarelli, Andrea
Chow, Wong-Ho
A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma
title A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma
title_full A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma
title_fullStr A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma
title_full_unstemmed A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma
title_short A Case-Control Study of Peripheral Blood Mitochondrial DNA Copy Number and Risk of Renal Cell Carcinoma
title_sort case-control study of peripheral blood mitochondrial dna copy number and risk of renal cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427307/
https://www.ncbi.nlm.nih.gov/pubmed/22937019
http://dx.doi.org/10.1371/journal.pone.0043149
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