Evaluation of Plasma Circulating Cell Free DNA Concentration and Integrity in Patients with Prostate Cancer in Jamaica: A Preliminary Study.

cancer cell free circulating DNA integrity prostate

Journal

Diseases (Basel, Switzerland)
ISSN: 2079-9721
Titre abrégé: Diseases
Pays: Switzerland
ID NLM: 101636232

Informations de publication

Date de publication:
07 Sep 2020
Historique:
received: 04 08 2020
revised: 04 09 2020
accepted: 05 09 2020
entrez: 10 9 2020
pubmed: 11 9 2020
medline: 11 9 2020
Statut: epublish

Résumé

Cell free circulating DNA (cfcDNA) is a promising diagnostic tool for prostate cancer (PCa). This study aimed to measure the cfcDNA concentration and integrity in PCa patients using quantitative polymerase chain reaction (qPCR) analysis. This study also assessed the correlation between these molecular biomarkers with total prostate-specific antigen (PSA), Gleason score, prostate volume, and age. Eleven PCa patients and 9 persons with benign prostatic hyperplasia (BPH) were recruited. Blood samples were collected before prostate biopsy and plasma quantified by qPCR amplification of the ALU 115 DNA sequence, with the ratio of ALU 247 to ALU 115 reflecting cfcDNA integrity. There were no significant differences in median, interquartile range (IQR) cfcDNA concentration or cfcDNA integrity between the patients with PCa (47.9 (214.93) ng/mL; 0.61 (0.49)) and persons with BPH (41.5 (55.13) ng/mL, cfcDNA concentration was relatively nonsignificantly higher in PCa patients in comparison to persons with BPH, whereas cfcDNA integrity was similar in both groups. Though limited in sample size, this study shows that cfcDNA concentration may be a potentially valuable noninvasive biomarker for the diagnosis of PCa.

Sections du résumé

BACKGROUND BACKGROUND
Cell free circulating DNA (cfcDNA) is a promising diagnostic tool for prostate cancer (PCa). This study aimed to measure the cfcDNA concentration and integrity in PCa patients using quantitative polymerase chain reaction (qPCR) analysis. This study also assessed the correlation between these molecular biomarkers with total prostate-specific antigen (PSA), Gleason score, prostate volume, and age.
METHODS METHODS
Eleven PCa patients and 9 persons with benign prostatic hyperplasia (BPH) were recruited. Blood samples were collected before prostate biopsy and plasma quantified by qPCR amplification of the ALU 115 DNA sequence, with the ratio of ALU 247 to ALU 115 reflecting cfcDNA integrity.
RESULTS RESULTS
There were no significant differences in median, interquartile range (IQR) cfcDNA concentration or cfcDNA integrity between the patients with PCa (47.9 (214.93) ng/mL; 0.61 (0.49)) and persons with BPH (41.5 (55.13) ng/mL,
CONCLUSION CONCLUSIONS
cfcDNA concentration was relatively nonsignificantly higher in PCa patients in comparison to persons with BPH, whereas cfcDNA integrity was similar in both groups. Though limited in sample size, this study shows that cfcDNA concentration may be a potentially valuable noninvasive biomarker for the diagnosis of PCa.

Identifiants

pubmed: 32906694
pii: diseases8030034
doi: 10.3390/diseases8030034
pmc: PMC7564624
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Andrew Condappa (A)

Department of Basic Medical Sciences (Pharmacology Section), Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica.

Donovan McGrowder (D)

Department of Pathology, Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica.

William Aiken (W)

Department of Surgery, Radiology, Anaesthesia and Intensive Care, Section of Surgery, Urology Division, Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica.

Wayne McLaughlin (W)

Department of Basic Medical Sciences (Molecular Biology Section), Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica.

Maxine Gossell-Williams (M)

Department of Basic Medical Sciences (Pharmacology Section), Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica.

Classifications MeSH