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Cell fusion potentiates tumor heterogeneity and reveals circulating hybrid cells that correlate with stage and survival.
Gast, Charles E; Silk, Alain D; Zarour, Luai; Riegler, Lara; Burkhart, Joshua G; Gustafson, Kyle T; Parappilly, Michael S; Roh-Johnson, Minna; Goodman, James R; Olson, Brennan; Schmidt, Mark; Swain, John R; Davies, Paige S; Shasthri, Vidya; Iizuka, Shinji; Flynn, Patrick; Watson, Spencer; Korkola, James; Courtneidge, Sara A; Fischer, Jared M; Jaboin, Jerry; Billingsley, Kevin G; Lopez, Charles D; Burchard, Julja; Gray, Joe; Coussens, Lisa M; Sheppard, Brett C; Wong, Melissa H.
  • Gast CE; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Silk AD; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Zarour L; Department of Surgery, Oregon Health & Science University, Portland, OR 97239, USA.
  • Riegler L; Department of Medicine, Oregon Health & Science University, Portland, OR 97239, USA.
  • Burkhart JG; Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Gustafson KT; Center for Early Detection Advanced Research, Oregon Health & Science University, Portland, OR 97239, USA.
  • Parappilly MS; Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
  • Roh-Johnson M; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Goodman JR; Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, WA 98109, USA.
  • Olson B; Department of Physiology and Pharmacology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Schmidt M; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Swain JR; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Davies PS; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Shasthri V; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Iizuka S; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Flynn P; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Watson S; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Korkola J; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Courtneidge SA; Department of Medicine, Oregon Health & Science University, Portland, OR 97239, USA.
  • Fischer JM; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA.
  • Jaboin J; Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
  • Billingsley KG; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA.
  • Lopez CD; Center for Early Detection Advanced Research, Oregon Health & Science University, Portland, OR 97239, USA.
  • Burchard J; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA.
  • Gray J; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR 97239, USA.
  • Coussens LM; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA.
  • Sheppard BC; Department of Radiation Medicine, Oregon Health & Science University, Portland, OR 97239, USA.
  • Wong MH; Department of Surgery, Oregon Health & Science University, Portland, OR 97239, USA.
Sci Adv ; 4(9): eaat7828, 2018 09.
Article en En | MEDLINE | ID: mdl-30214939
ABSTRACT
High lethality rates associated with metastatic cancer highlight an urgent medical need for improved understanding of biologic mechanisms driving metastatic spread and identification of biomarkers predicting late-stage progression. Numerous neoplastic cell intrinsic and extrinsic mechanisms fuel tumor progression; however, mechanisms driving heterogeneity of neoplastic cells in solid tumors remain obscure. Increased mutational rates of neoplastic cells in stressed environments are implicated but cannot explain all aspects of tumor heterogeneity. We present evidence that fusion of neoplastic cells with leukocytes (for example, macrophages) contributes to tumor heterogeneity, resulting in cells exhibiting increased metastatic behavior. Fusion hybrids (cells harboring hematopoietic and epithelial properties) are readily detectible in cell culture and tumor-bearing mice. Further, hybrids enumerated in peripheral blood of human cancer patients correlate with disease stage and predict overall survival. This unique population of neoplastic cells provides a novel biomarker for tumor staging, as well as a potential therapeutic target for intervention.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Células Neoplásicas Circulantes Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Células Neoplásicas Circulantes Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article