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Fusobacterium nucleatum and Clinicopathologic Features of Colorectal Cancer: Results From the ColoCare Study.
Eisele, Yannick; Mallea, Patrick M; Gigic, Biljana; Stephens, W Zac; Warby, Christy A; Buhrke, Kate; Lin, Tengda; Boehm, Juergen; Schrotz-King, Petra; Hardikar, Sheetal; Huang, Lyen C; Pickron, T Bartley; Scaife, Courtney L; Viskochil, Richard; Koelsch, Torsten; Peoples, Anita R; Pletneva, Maria A; Bronner, Mary; Schneider, Martin; Ulrich, Alexis B; Swanson, Eric A; Toriola, Adetunji T; Shibata, David; Li, Christopher I; Siegel, Erin M; Figueiredo, Jane; Janssen, Klaus-Peter; Hauner, Hans; Round, June; Ulrich, Cornelia M; Holowatyj, Andreana N; Ose, Jennifer.
Afiliação
  • Eisele Y; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT; Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany; Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Mallea PM; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Gigic B; Department of General, Visceral and Transplantation Surgery, University Hospital of Heidelberg, Heidelberg, Germany.
  • Stephens WZ; Department of Pathology, University of Utah, Salt Lake City, UT.
  • Warby CA; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Buhrke K; Department of Pathology, University of Utah, Salt Lake City, UT.
  • Lin T; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Boehm J; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Schrotz-King P; Division of Preventive Oncology, National Center for Tumor Diseases, German Cancer Research Center, Heidelberg, Germany.
  • Hardikar S; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Huang LC; Division of General Surgery, Department of Surgery, School of Medicine, University of Utah, Salt Lake City, UT.
  • Pickron TB; Division of General Surgery, Department of Surgery, School of Medicine, University of Utah, Salt Lake City, UT.
  • Scaife CL; Division of General Surgery, Department of Surgery, School of Medicine, University of Utah, Salt Lake City, UT.
  • Viskochil R; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Koelsch T; Department of General, Visceral and Transplantation Surgery, University Hospital of Heidelberg, Heidelberg, Germany.
  • Peoples AR; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Pletneva MA; Huntsman Cancer Institute, Salt Lake City, UT; Department of Pathology, University of Utah, Salt Lake City, UT.
  • Bronner M; Huntsman Cancer Institute, Salt Lake City, UT; Department of Pathology, University of Utah, Salt Lake City, UT.
  • Schneider M; Department of General, Visceral and Transplantation Surgery, University Hospital of Heidelberg, Heidelberg, Germany.
  • Ulrich AB; Department of General, Visceral and Transplantation Surgery, University Hospital of Heidelberg, Heidelberg, Germany.
  • Swanson EA; Department of Pathology, University of Utah, Salt Lake City, UT.
  • Toriola AT; Washington University in St. Louis, St. Louis, MO.
  • Shibata D; Department of Surgery, University of Tennessee Health Science Center, Memphis, TN.
  • Li CI; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Siegel EM; Cancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
  • Figueiredo J; Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA.
  • Janssen KP; Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany; Department of Surgery, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
  • Hauner H; Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany; Else Kröner-Fresenius-Centre for Nutritional Medicine, School of Life Sciences, Technical University of Munich, Munich, Germany.
  • Round J; Department of Pathology, University of Utah, Salt Lake City, UT.
  • Ulrich CM; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT.
  • Holowatyj AN; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN; Vanderbilt-Ingram Cancer Center, Nashville, TN. Electronic address: andreana.holowatyj@vumc.or
  • Ose J; Huntsman Cancer Institute, Salt Lake City, UT; Department of Population Health Sciences, University of Utah, Salt Lake City, UT. Electronic address: jennifer.ose@hci.utah.edu.
Clin Colorectal Cancer ; 20(3): e165-e172, 2021 09.
Article em En | MEDLINE | ID: mdl-33935016
ABSTRACT

BACKGROUND:

Fusobacterium nucleatum (Fn), a bacterium associated with a wide spectrum of infections, has emerged as a key microbe in colorectal carcinogenesis. However, the underlying mechanisms and clinical relevance of Fn in colorectal cancer (CRC) remain incompletely understood. PATIENTS AND

METHODS:

We examined associations between Fn abundance and clinicopathologic characteristics among 105 treatment-naïve CRC patients enrolled in the international, prospective ColoCare Study. Electronic medical charts, including pathological reports, were reviewed to document clinicopathologic features. Quantitative real-time polymerase chain reaction (PCR) was used to amplify/detect Fn DNA in preoperative fecal samples. Multinomial logistic regression was used to analyze associations between Fn abundance and patient sex, age, tumor stage, grade, site, microsatellite instability, body mass index (BMI), alcohol consumption, and smoking history. Cox proportional hazards models were used to investigate associations of Fn abundance with overall survival in adjusted models.

RESULTS:

Compared to patients with undetectable or low Fn abundance, patients with high Fn abundance (n = 22) were 3-fold more likely to be diagnosed with rectal versus colon cancer (odds ratio [OR] = 3.01; 95% confidence interval [CI], 1.06-8.57; P = .04) after adjustment for patient sex, age, BMI, and study site. Patients with high Fn abundance also had a 5-fold increased risk of being diagnosed with rectal cancer versus right-sided colon cancer (OR = 5.32; 95% CI, 1.23-22.98; P = .03). There was no statistically significant association between Fn abundance and overall survival.

CONCLUSION:

Our findings suggest that Fn abundance in fecal samples collected prior to surgery varies by tumor site among treatment-naïve CRC patients. Overall, fecal Fn abundance may have diagnostic and prognostic significance in the clinical management of CRC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Fusobacterium nucleatum Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Colorectal Cancer Assunto da revista: GASTROENTEROLOGIA / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Fusobacterium nucleatum Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Colorectal Cancer Assunto da revista: GASTROENTEROLOGIA / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article