Increased leukocyte mitochondrial DNA copy number is associated with oral premalignant lesions: An epidemiology study

Yonggang He, Yilei Gong, Jian Gu, J. Jack Lee, Scott M. Lippman, Xifeng Wu

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Although changes in the mitochondrial DNA (mtDNA) copy number in peripheral blood leukocytes (PBLs) have been linked to increased susceptibility to several cancers, the relationship between the mtDNA copy number in PBLs and the risk of cancer precursors has not been investigated. In this study, we measured the relative mtDNA copy number in PBLs of 143 patients with histologically confirmed oral premalignant lesions (OPLs) and of 357 healthy controls that were frequency-matched to patients according to age, sex and race. OPL patients had a significantly higher mtDNA copy number than the controls (1.36 ± 0.74 versus 1.11 ± 0.32; P <0.001). In analyses stratified by sex, race, alcohol consumption and smoking status, the mtDNA copy number was higher in the OPL patients than in the controls in all the strata. Using the median mtDNA copy number in the control group as a cutoff, we found that individuals with a high mtDNA copy number had significantly higher risk of having OPLs than individuals with a low mtDNA copy number (adjusted odds ratio, 1.93; 95% confidence interval, 1.23-3.05, P = 0.004). Analysis of the joint effect of alcohol consumption and smoking revealed even greater risk for OPLs. Our results suggest that high mtDNA copy number in PBLs is significantly associated with having OPLs. To our knowledge, this is the first epidemiologic study to show that the mtDNA copy number may indicate the risk of cancer precursors.

Original languageEnglish (US)
Pages (from-to)1760-1764
Number of pages5
JournalCarcinogenesis
Volume35
Issue number8
DOIs
StatePublished - Aug 2014

Keywords

  • Mitochondrial DNA copy number
  • Oral premalignant lesions

ASJC Scopus subject areas

  • Cancer Research

MD Anderson CCSG core facilities

  • Biostatistics Resource Group
  • Clinical Trials Office

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