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Plasma and urine DNA levels are related to microscopic hematuria in patients with bladder urothelial carcinoma

Authors :
Antonio Carlos Lima Pompeo
Sarah Alves
Flávia de Sousa Gehrke
Marcelo Langer Wroclawski
Eduardo Ferreira Pedroso de Almeida
Ligia Ajaime Azzalis
Fernando Luiz Affonso Fonseca
Pamela de Oliveira Delgado
Marcos Tobias-Machado
Tiago Pedromonico Arrym
Tomás Elias Abdalla
Beatriz da Costa Aguiar Alves
Source :
Clinical Biochemistry. 49:1274-1277
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

a) Objective: An increase in cell-free DNA was observed in the plasma of many cancer patients. This major biomarker can be used to differentiate patients with malignant neoplasms from those with benign neoplasms or healthy patients. Depending on the characteristic of the tumor, there are qualitative variations in the circulating cell-free DNA. Today, studies on the concentration of fragments of circulating cell-free DNA and their respective sizes in patients with bladder cancer are not plentiful in the literature. A 100% effective plasma tumor marker, which would help in the diagnosis and follow-up of bladder cancer, is yet to be developed; therefore, cell-free DNA levels in the plasma may represent a valuable biomarker for the diagnosis, prognosis and follow-up of patients with this type of tumor. b) Design and methods: In this study we analyze the kinetics of plasma and urine DNA concentrations in patients with bladder cancer, relating them to the other clinical laboratory variables. c) Results: Patients with hematuria showed a positive correlation with urine DNA. d) Conclusion: An increase in plasma and urine DNA was unprecedentedly reported over time, a fact that may come in handy in the prognosis of patients. Furthermore, microscopic haematuria is correlated with plasma and urinary DNA levels.

Details

ISSN :
00099120
Volume :
49
Database :
OpenAIRE
Journal :
Clinical Biochemistry
Accession number :
edsair.doi.dedup.....38a4e9c81b7200bf6340809e8a2661d6
Full Text :
https://doi.org/10.1016/j.clinbiochem.2016.08.021