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Elevation of circulating branched-chain amino acids is an early event in human pancreatic adenocarcinoma development.
Mayers, Jared R; Wu, Chen; Clish, Clary B; Kraft, Peter; Torrence, Margaret E; Fiske, Brian P; Yuan, Chen; Bao, Ying; Townsend, Mary K; Tworoger, Shelley S; Davidson, Shawn M; Papagiannakopoulos, Thales; Yang, Annan; Dayton, Talya L; Ogino, Shuji; Stampfer, Meir J; Giovannucci, Edward L; Qian, Zhi Rong; Rubinson, Douglas A; Ma, Jing; Sesso, Howard D; Gaziano, John Michael; Cochrane, Barbara B; Liu, Simin; Wactawski-Wende, Jean; Manson, JoAnn E; Pollak, Michael N; Kimmelman, Alec C; Souza, Amanda; Pierce, Kerry; Wang, Thomas J; Gerszten, Robert E; Fuchs, Charles S; Vander Heiden, Matthew G; Wolpin, Brian M.
Afiliação
  • Mayers JR; Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA.
  • Wu C; Department of Etiology and Carcinogenesis, Cancer Institute and Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
  • Clish CB; Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
  • Kraft P; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Torrence ME; Broad Institute of MIT and Harvard University, Cambridge, MA.
  • Fiske BP; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Yuan C; Department of Biostatistics, Harvard School of Public Health, Boston, MA.
  • Bao Y; Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA.
  • Townsend MK; Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA.
  • Tworoger SS; Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
  • Davidson SM; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Papagiannakopoulos T; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Yang A; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Dayton TL; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Ogino S; Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA.
  • Stampfer MJ; Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA.
  • Giovannucci EL; Division of Genomic Stability and DNA repair, Department of Radiation Oncology, Dana- Farber Cancer Institute, Boston, MA 02215.
  • Qian ZR; Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA.
  • Rubinson DA; Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
  • Ma J; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Sesso HD; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Gaziano JM; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Cochrane BB; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Liu S; Department of Nutrition, Harvard School of Public Health, Boston, MA.
  • Wactawski-Wende J; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Manson JE; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Pollak MN; Department of Nutrition, Harvard School of Public Health, Boston, MA.
  • Kimmelman AC; Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
  • Souza A; Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
  • Pierce K; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Wang TJ; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
  • Gerszten RE; Department of Epidemiology, Harvard School of Public Health, Boston, MA.
  • Fuchs CS; Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA.
  • Vander Heiden MG; Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA.
  • Wolpin BM; Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC), VA Boston Healthcare System.
Nat Med ; 20(10): 1193-1198, 2014 10.
Article em En | MEDLINE | ID: mdl-25261994
ABSTRACT
Most patients with pancreatic ductal adenocarcinoma (PDAC) are diagnosed with advanced disease and survive less than 12 months. PDAC has been linked with obesity and glucose intolerance, but whether changes in circulating metabolites are associated with early cancer progression is unknown. To better understand metabolic derangements associated with early disease, we profiled metabolites in prediagnostic plasma from individuals with pancreatic cancer (cases) and matched controls from four prospective cohort studies. We find that elevated plasma levels of branched-chain amino acids (BCAAs) are associated with a greater than twofold increased risk of future pancreatic cancer diagnosis. This elevated risk was independent of known predisposing factors, with the strongest association observed among subjects with samples collected 2 to 5 years before diagnosis, when occult disease is probably present. We show that plasma BCAAs are also elevated in mice with early-stage pancreatic cancers driven by mutant Kras expression but not in mice with Kras-driven tumors in other tissues, and that breakdown of tissue protein accounts for the increase in plasma BCAAs that accompanies early-stage disease. Together, these findings suggest that increased whole-body protein breakdown is an early event in development of PDAC.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Aminoácidos de Cadeia Ramificada Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Animals / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Aminoácidos de Cadeia Ramificada Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Animals / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article