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Advanced glycation end products are elevated in estrogen receptor-positive breast cancer patients, alter response to therapy, and can be targeted by lifestyle intervention

  1. Author:
    Walter, Katherine R
    Ford, Marvella E
    Gregoski, Mathew J
    Kramer, Rita M
    Knight, Kendrea D
    Spruill, Laura
    Nogueira, Lourdes M
    Krisanits, Bradley A
    Phan, Van
    La Rue, Amanda C
    Lilly, Michael B
    Ambs, Stefan
    Chan,King
    Turner, Tonya F
    Varner, Heidi
    Singh, Shweta
    Uribarri, Jaime
    Garrett-Mayer, Elizabeth
    Armeson, Kent E
    Hilton, Ebony J
    Clair, Mark J
    Taylor, Marian H
    Abbott, Andrea M
    Findlay, Victoria J
    Peterson, Lindsay L
    Magwood, Gayenell
    Turner, David P [ORCID]
  2. Author Address

    Department of Pathology & Laboratory Medicine, Medical University of South Carolina (MUSC), Charleston, SC, USA., Department of Public Health Sciences, MUSC, Charleston, SC, USA. fordmar@musc.edu., Hollings Cancer Center, MUSC, Charleston, SC, USA. fordmar@musc.edu., James E. Clyburn Research Center Medical University of South Carolina, Charleston, SC, 29425, USA. fordmar@musc.edu., Department of Exercise Science, College of Arts and Sciences, Campbell University, Buies Creek, NC, USA., Ralph H. Johnson Veterans Affairs Medical Center, Charleston, SC, USA., Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Cancer Research Technology Program, Leidos Biomedical Research, Frederick National Laboratory, Frederick, MD, USA., Dietetic Services, MUSC, Charleston, SC, USA., Department of Medicine/Renal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA., Department of Anesthesia and Perioperative Medicine, MUSC, Charleston, SC, USA., Department of Medicine, Division of Cardiology, MUSC, Charleston, SC, USA., Department of Surgery, MUSC, Charleston, SC, USA., Washington University School of Medicine, St. Louis, MO, USA., College of Nursing, MUSC, Charleston, SC, USA., Department of Pathology & Laboratory Medicine, Medical University of South Carolina (MUSC), Charleston, SC, USA. turnerda@musc.edu., Department of Public Health Sciences, MUSC, Charleston, SC, USA. turnerda@musc.edu., James E. Clyburn Research Center Medical University of South Carolina, Charleston, SC, 29425, USA. turnerda@musc.edu.,
    1. Year: 2019
    2. Date: Feb
    3. Epub Date: 2018 10 27
  1. Journal: Breast cancer research and treatment
    1. 173
    2. 3
    3. Pages: 559-571
  2. Type of Article: Article
  1. Abstract:

    Lifestyle factors associated with personal behavior can alter tumor-associated biological pathways and thereby increase cancer risk, growth, and disease recurrence. Advanced glycation end products (AGEs) are reactive metabolites produced endogenously as a by-product of normal metabolism. A Western lifestyle also promotes AGE accumulation in the body which is associated with disease phenotypes through modification of the genome, protein crosslinking/dysfunction, and aberrant cell signaling. Given the links between lifestyle, AGEs, and disease, we examined the association between dietary-AGEs and breast cancer. We evaluated AGE levels in bio-specimens from estrogen receptor-positive (ER+) and estrogen receptor-negative (ER-) breast cancer patients, examined their role in therapy resistance, and assessed the ability of lifestyle intervention to reduce circulating AGE levels in ER+ breast cancer survivors. An association between ER status and AGE levels was observed in tumor and serum samples. AGE treatment of ER+ breast cancer cells altered ERa phosphorylation and promoted resistance to tamoxifen therapy. In a proof of concept study, physical activity and dietary intervention was shown to be viable options for reducing circulating AGE levels in breast cancer survivors. There is a potential prognostic and therapeutic role for lifestyle derived AGEs in breast cancer. Given the potential benefits of lifestyle intervention on incidence and mortality, opportunities exist for the development of community health and nutritional programs aimed at reducing AGE exposure in order to improve breast cancer prevention and treatment outcomes.

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External Sources

  1. DOI: 10.1007/s10549-018-4992-7
  2. PMID: 30368741
  3. PMCID: PMC6394600
  4. PII : 10.1007/s10549-018-4992-7

Library Notes

  1. Fiscal Year: FY2018-2019
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