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.
Original language | English (US) |
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Pages (from-to) | 763-773 |
Number of pages | 11 |
Journal | Cancer Biomarkers |
Volume | 15 |
Issue number | 6 |
DOIs | |
State | Published - Nov 24 2015 |
Keywords
- 3.4kb deletion
- EDRN
- FFPE
- NIST
- Prostate
- biomarker
- cancer
- mitochondrial DNA
- serum
- urine
ASJC Scopus subject areas
- Oncology
- Genetics
- Cancer Research