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DNA Methylation Screening of Primary Prostate Tumors Identifies SRD5A2 and CYP11A1 as Candidate Markers for Assessing Risk of Biochemical Recurrence

Horning, A. M. (författare)
University of Texas Health Science Center, San Antonio, USA
Awe, Julius Adebayo (författare)
Högskolan i Skövde,Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,Institutionen för biovetenskap,Forskningscentrum för Systembiologi,Manitoba Institute of Cell Biology, University of Manitoba, Winnipeg, Manitoba, Canada / Department of Clinical Genetics, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden,Tumörbiologi, Tumor Biology
Wang, C. M. (författare)
University of Texas Health Science Center, San Antonio, USA
visa fler...
Liu, J. (författare)
University of Texas Health Science Center, San Antonio, USA
Lai, Z. (författare)
University of Texas Health Science Center, San Antonio, USA
Wang, V. Y. (författare)
University of Texas Health Science Center, San Antonio, USA
Jadhav, R. R. (författare)
University of Texas Health Science Center, San Antonio, USA
Louie, A. D. (författare)
University of Texas Health Science Center, San Antonio, USA,University of Manitoba, Winnipeg, Canada
Lin, C. L. (författare)
University of Texas Health Science Center, San Antonio, USA
Kroczak, T. (författare)
University of Manitoba, Winnipeg, Manitoba, Canada
Chen, Y. D. (författare)
University of Texas Health Science Center, San Antonio, USA
Jin, V. X. (författare)
University of Texas Health Science Center, San Antonio, USA
Abboud-Werner, S. L. (författare)
University of Texas Health Science Center, San Antonio, USA
Leach, R. J. (författare)
Hernandez, J. (författare)
University of Texas Health Science Center, San Antonio, USA
Thompson, I. M. (författare)
University of Texas Health Science Center, San Antonio, USA
Saranchuk, J. (författare)
University of Manitoba, Winnipeg, Canada
Drachenberg, D. (författare)
Chen, C. L. (författare)
University of Texas Health Science Center, San Antonio, USA
Mai, S. (författare)
University of Manitoba, Winnipeg, Canada
Huang, T. H. M. (författare)
University of Texas Health Science Center, San Antonio, USA
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 (creator_code:org_t)
2015-09-01
2015
Engelska.
Ingår i: Prostate. - : Wiley. - 0270-4137 .- 1097-0045. ; 75:15, s. 1790-1801
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND. Altered DNA methylation in CpG islands of gene promoters has been implicated in prostate cancer (PCa) progression and can be used to predict disease outcome. In this study, we determine whether methylation changes of androgen biosynthesis pathway (ABP)-related genes in patients' plasma cell-free DNA (cfDNA) can serve as prognostic markers for biochemical recurrence (BCR). METHODS. Methyl-binding domain capture sequencing (MBDCap-seq) was used to identify differentially methylated regions (DMRs) in primary tumors of patients who subsequently developed BCR or not, respectively. Methylation pyrosequencing of candidate loci was validated in cfDNA samples of 86 PCa patients taken at and/or post-radical prostatectomy (RP) using univariate and multivariate prediction analyses. RESULTS. Putative DMRs in 13 of 30 ABP-related genes were found between tumors of BCR (n = 12) versus no evidence of disease (NED) (n = 15). In silico analysis of The Cancer Genome Atlas data confirmed increased DNA methylation of two loci-SRD5A2 and CYP11A1, which also correlated with their decreased expression, in tumors with subsequent BCR development. Their aberrant cfDNA methylation was also associated with detectable levels of PSA taken after patients' post-RP. Multivariate analysis of the change in cfDNA methylation at all of CpG sites measured along with patient's treatment history predicted if a patient will develop BCR with 77.5% overall accuracy. CONCLUSIONS. Overall, increased DNA methylation of SRD5A2 and CYP11A1 related to androgen biosynthesis functions may play a role in BCR after patients' RP. The correlation between aberrant cfDNA methylation and detectable PSA in post-RP further suggests their utility as predictive markers for PCa recurrence. (C) 2015 Wiley Periodicals, Inc.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

prostate cancer
DNA methylation
plasma
biochemical recurrence
GENE-EXPRESSION
RADICAL PROSTATECTOMY
CANCER PROGRESSION
CIRCULATING
DNA
ANTIGEN
PLASMA
GROWTH
SERUM
TESTOSTERONE
FINASTERIDE
Endocrinology & Metabolism
Urology & Nephrology
ATES OF AMERICA
V108
P13728
prostate cancer

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