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Evaluation of two mitochondrial DNA biomarkers for prostate cancer detection.
Maragh, Samantha; Veltri, Robert W; Lund, Steven P; Mangold, Leslie; Isharwal, Sumit; Christudass, Christhunesa S; Partin, Alan W; Humphreys, Elizabeth B; Sorbara, Lynn; Srivastava, Sudhir; Wagner, Paul D.
Afiliação
  • Maragh S; Biosystems and Biomaterials Division, National Institute of Standards and Technology, Gaithersburg, MD, USA.
  • Veltri RW; Department of Urology, Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Lund SP; Statistical Engineering Division, National Institute of Standards and Technology, Gaithersburg, MD, USA.
  • Mangold L; Department of Urology, Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Isharwal S; Department of Urology, Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Christudass CS; Department of Neurological Sciences, Christian Medical College, Vellore, Tamilnadu, India.
  • Partin AW; Department of Urology, Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Humphreys EB; Department of Urology, Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Sorbara L; Division of Cancer Prevention, National Cancer Institute, Rockville, MD, USA.
  • Srivastava S; Division of Cancer Prevention, National Cancer Institute, Rockville, MD, USA.
  • Wagner PD; Division of Cancer Prevention, National Cancer Institute, Rockville, MD, USA.
Cancer Biomark ; 15(6): 763-73, 2015.
Article em En | MEDLINE | ID: mdl-26406418
ABSTRACT

BACKGROUND:

A 3.4kb deletion (3.4kbΔ ) in mitochondrial DNA (mtDNA) found in histologically normal prostate biopsy specimens has been reported to be a biomarker for the increased probability of prostate cancer. Increased mtDNA copy number is also reported as associated with cancer.

OBJECTIVE:

Independent evaluation of these two potential prostate cancer biomarkers using formalin-fixed paraffin-embedded (FFPE) prostate tissue and matched urine and serum from a high risk cohort of men with and without prostate cancer.

METHODS:

Biomarker levels were detected via qPCR.

RESULTS:

Both 3.4kbΔ and mtDNA levels were significantly higher in cancer patient FFPE cores (p= 0.045 and p= 0.070 respectively at > 90% confidence). Urine from cancer patients contained significantly higher levels of mtDNA (p= 0.006, 64.3% sensitivity, 86.7% specificity). Combining the 3.4kbΔ and mtDNA gave better performance of detecting prostate cancer than either biomarker alone (FFPE 73.7% sensitivity, 65% specificity; urine 64.3% sensitivity, 100% specificity). In serum, there was no difference for any of the biomarkers.

CONCLUSIONS:

This is the first report on detecting the 3.4kbΔ in urine and evaluating mtDNA levels as a prostate cancer biomarker. A confirmation study with increased sample size and possibly with additional biomarkers would need to be conducted to corroborate and extend these observations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Próstata / Neoplasias da Próstata / DNA Mitocondrial / Marcadores Genéticos Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Próstata / Neoplasias da Próstata / DNA Mitocondrial / Marcadores Genéticos Idioma: En Ano de publicação: 2015 Tipo de documento: Article