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PMID: 26569345 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Diagnostic and prognostic potential of circulating cell-free genomic and mitochondrial DNA fragments in clear cell renal cell carcinoma patients.

Lu H, Busch J, Jung M, Rabenhorst S, Ralla B, Kilic E, Mergemeier S, Budach N, Fendler A, Jung K

Abstract

There is inconsistent information about the clinical usefulness of circulating cell-free DNA (cfDNA) in plasma from clear cell renal cell cancer (RCC) patients. This is attributed to preanalytical, analytical, and clinical factors that were considered as far as possible in this study. cfDNA was extracted from EDTA plasma of healthy people (n=40), non-metastatic (n=145) and metastatic (n=84) RCC patients using the QIAamp Circulating Nucleic Acid Kit. Genomic and mitochondrial cfDNA concentrations were determined using qPCR of different cfDNA fragments (67-306bp). Their diagnostic and prognostic potential was estimated using receiver operating characteristics (ROC) and Cox regression analyses. The 67bp and 180bp genomic cfDNA fragments did not differ between the three study groups while the 306bp fragment was lower in RCC patients than in controls. The mitochondrial cfDNA was higher in metastatic than in non-metastatic patients and controls. The cfDNA integrity indices decreased from controls to metastatic patients. Models built by logistic regression and Cox regression resulted in area under the ROC curves >0.75 and concordance indices of >0.800 in predicting recurrence-free survival and overall survival. The study suggests that combinations of cfDNA markers have promising diagnostic and prognostic potential in RCC patients and are worth for further validation in future prospective multicenter studies.

Keywords
Circulating cell-free DNA Clear cell renal cell carcinoma Diagnostic Metastasis Predictive models Prognostic markers
MeSH Terms
Aged Carcinoma, Renal Cell/blood,diagnosis,genetics Cell Nucleus/genetics DNA, Mitochondrial/blood,genetics Female Humans Kidney Neoplasms/blood,diagnosis,genetics Male Middle Aged Prognosis Real-Time Polymerase Chain Reaction Regression Analysis
Chemicals
DNA, Mitochondrial
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Lu Hongbiao
Department of Urology, University Hospital Charité, Berlin, Germany; Berlin Institute for Urological Research, Berlin, Germany; Department of Urology, Changzhou No.2 People's Hospital, Jiangsu, China.
Busch Jonas
Department of Urology, University Hospital Charité, Berlin, Germany.
Jung Monika
Department of Urology, University Hospital Charité, Berlin, Germany.
Rabenhorst Silke
Department of Urology, University Hospital Charité, Berlin, Germany.
Ralla Bernhard
Department of Urology, University Hospital Charité, Berlin, Germany.
Kilic Ergin
Institute of Pathology, University Hospital Charité, Berlin, Germany.
Mergemeier Steffen
CONGEN Biotechnologie GmbH, Berlin, Germany.
Budach Nils
Department of Radiology, University Hospital Charité, Berlin, Germany.
Fendler Annika
Department of Urology, University Hospital Charité, Berlin, Germany; Berlin Institute for Urological Research, Berlin, Germany; Department of Signal Transduction, Invasion and Metastasis of Epithelial Cells, Max Delbrück Center of Molecular Medicine, Berlin, Germany.
Jung Klaus
Department of Urology, University Hospital Charité, Berlin, Germany; Berlin Institute for Urological Research, Berlin, Germany. Electronic address: klaus.jung@charite.de.
Article Info
Journal
Clinica chimica acta; international journal of clinical chemistry
Abbr.
Clin Chim Acta
ISSN
1873-3492
Published
2016-01-15
Epub
2015-00-10
Pages
109-19
Language
English
Region
Netherlands
NLM ID
1302422
Subset
IM
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