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DNA methylation patterns in bladder tumors of African American patients point to distinct alterations in xenobiotic metabolism

  • Venkatrao Vantaku
    ,
  • Chandra Sekhar Amara
    ,
  • Danthasinghe Waduge Badrajee Piyarathna
    ,
  • Sri Ramya Donepudi
    ,
  • Chandrashekar R. Ambati
    ,
  • Vasanta Putluri
*Corresponding author for this work
  • Baylor College of Medicine
    ,
  • National Institutes of Health
    ,
  • University of Texas MD Anderson Cancer Center
    ,
  • Medical College of Georgia
    ,
  • Department of Veterans Affairs
    ,
  • University of Texas Medical Branch at Galveston
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Racial/ethnic disparities have a significant impact on bladder cancer outcomes with African American patients demonstrating inferior survival over European-American patients. We hypothesized that epigenetic difference in methylation of tumor DNA is an underlying cause of this survival health disparity. We analyzed bladder tumors from African American and European-American patients using reduced representation bisulfite sequencing (RRBS) to annotate differentially methylated DNA regions. Liquid chromatography-mass spectrometry (LC-MS/MS) based metabolomics and flux studies were performed to examine metabolic pathways that showed significant association to the discovered DNA methylation patterns. RRBS analysis showed frequent hypermethylated CpG islands in African American patients. Further analysis showed that these hypermethylated CpG islands in patients are commonly located in the promoter regions of xenobiotic enzymes that are involved in bladder cancer progression. On follow-up, LC-MS/MS revealed accumulation of glucuronic acid, S-adenosylhomocysteine, and a decrease in S-adenosylmethionine, corroborating findings from the RRBS and mRNA expression analysis indicating increased glucuronidation and methylation capacities in African American patients. Flux analysis experiments with 13C-labeled glucose in cultured African American bladder cancer cells confirmed these findings. Collectively, our studies revealed robust differences in methylation-related metabolism and expression of enzymes regulating xenobiotic metabolism in African American patients indicate that race/ethnic differences in tumor biology may exist in bladder cancer.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1332-1340 (9 pages)

Journal (Volume, Issue Number)

Carcinogenesis (Volume 40, Issue 11)

Publication milestones

  • Published - 11/25/2019

Publication status

Published - 11/25/2019

ISSN

0143-3334

Publication IDs

  • Scopus: 85075814409
  • PubMed: 31284295

Publication metrics

Metrics

Fractional count
2
Fractional count
0.10
Fractional count
19
Fractional count
0.90
Fractional count
2
Fractional count
1
SciVal
Author count
21
SciVal
Paper percentile
33
Scopus
citations

PlumX, opens in new tab

Citation count
11
Captures
23

Funding Details

This research was supported by American Cancer Society (ACS) Award (127430-RSG-15-105-01-CNE to N.P., NIH/NCI R01CA220297 to N.P., NIH/NCI R01CA216426 to N.P. and NIH/NCI U01 CA167234 to A.S.K.). This project was also supported by the Agilent Technologies Center of Excellence (COE) and National Institute of Health (NIH) (P30 CA125123), CPRIT Proteomics and Metabolomics Core Facility (RP170005 to N.P.), and Dan L.  Duncan Cancer Center. P.D.C. and M.M.I., were supported by Human Tissue Acquisition and Pathology at Baylor College of Medicine with funding from National Cancer Institute (NCI) (P30 CA125123). The Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health (NIH) (P30 CA142543 09). 1Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA, 2Dan L. Duncan Cancer Center, Advanced Technology Core, Alkek Center for Molecular Discovery, Baylor College of Medicine, Houston, TX, USA, 3Laboratory of Human Carcinogenesis, Center for Cancer Research (CCR), National Cancer Institute (NCI), National Institutes of Health, Bethesda, MD, USA, 4Center for Cancer Epigenetics, Department of Epigenetics and Molecular Carcinogenesis, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA, 5Department of Surgery: Urology, Augusta University, Augusta, GA, USA, 6Human tissue acquisition and pathology shared source, Baylor College of Medicine, Houston, TX, USA, 7Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, USA, 8Michael E. DeBakey Department of Veterans Affairs Medical Center, Houston, TX, USA, 9Division of Urology, Department of Surgery, The University of Texas Medical Branch, Galveston, TX, USA, 10Scott Department of Urology, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA, 11Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, USA, 12Department of Pathology, Augusta University, Augusta, GA, USA, 13Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA, and 14Department of Urology, University of Texas Southwestern, Dallas, TX, USA
FundersFunding numbers
5Department of Surgery
-
CPRIT Proteomics and Metabolomics Core Facility
RP170005
Center for Cancer Research
CCR
Dan L. Duncan Cancer Center
-
Dan L. Duncan Cancer Center
-
Department of Surgery (Division of Urologic Surgery)
-
M.M.I.
-
Mahatma Gandhi Arts, Science & Late N.P. Commerce College
-
NCI, NIH
R01CA216426, U01 CA167234, R01CA220297
Aarhus University
-
NIH
P30 CA125123
FNIH
P30 CA142543 09
ACS
ACS, 127430-RSG-15-105-01-CNE
NCI
-
Agilent Technologies
COE
CORE
-
CIH, VA
-
UTMB
-
The University of Texas Southwestern Medical Center
-
BCM
-Augusta University-
SOM, JHU
-