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Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion.
Kim, Jong Hyuk; Schulte, Ashley J; Sarver, Aaron L; Lee, Donghee; Angelos, Mathew G; Frantz, Aric M; Forster, Colleen L; O'Brien, Timothy D; Cornax, Ingrid; O'Sullivan, M Gerard; Cheng, Nuojin; Lewellen, Mitzi; Oseth, LeAnn; Kumar, Sunil; Bullman, Susan; Pedamallu, Chandra Sekhar; Goyal, Sagar M; Meyerson, Matthew; Lund, Troy C; Breen, Matthew; Lindblad-Toh, Kerstin; Dickerson, Erin B; Kaufman, Dan S; Modiano, Jaime F.
Afiliação
  • Kim JH; Animal Cancer Care and Research Program, University of Minnesota, St Paul, Minnesota.
  • Schulte AJ; Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St Paul, Minnesota.
  • Sarver AL; Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
  • Lee D; Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, Florida.
  • Angelos MG; University of Florida Health Cancer Center, University of Florida, Gainesville, Florida.
  • Frantz AM; Intelligent Critical Care Center, University of Florida, Gainesville, Florida.
  • Forster CL; Artificial Intelligence Academic Initiative (AI2) Center, University of Florida, Gainesville, Florida.
  • O'Brien TD; Animal Cancer Care and Research Program, University of Minnesota, St Paul, Minnesota.
  • Cornax I; Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St Paul, Minnesota.
  • O'Sullivan MG; Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
  • Cheng N; Animal Cancer Care and Research Program, University of Minnesota, St Paul, Minnesota.
  • Lewellen M; Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
  • Oseth L; Institute for Health Informatics, University of Minnesota, Minneapolis, Minnesota.
  • Kumar S; Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, Florida.
  • Bullman S; Stem Cell Institute, University of Minnesota, Minneapolis, Minnesota.
  • Pedamallu CS; Department of Medicine (Division of Hematology, Oncology, and Transplantation), Medical School, University of Minnesota, Minneapolis, Minnesota.
  • Goyal SM; Microbiology, Immunology and Cancer Biology (MICaB) Graduate Program, University of Minnesota, Minneapolis, Minnesota.
  • Meyerson M; Department of Medicine, Division of Hematology and Oncology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Lund TC; Animal Cancer Care and Research Program, University of Minnesota, St Paul, Minnesota.
  • Breen M; Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St Paul, Minnesota.
  • Lindblad-Toh K; Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
  • Dickerson EB; Capstan Therapeutics, San Diego, California.
  • Kaufman DS; The University of Minnesota Biological Materials Procurement Network (BioNet), University of Minnesota, Minneapolis, Minnesota.
  • Modiano JF; Animal Cancer Care and Research Program, University of Minnesota, St Paul, Minnesota.
Cancer Res Commun ; 4(6): 1467-1480, 2024 Jun 11.
Article em En | MEDLINE | ID: mdl-38757809
ABSTRACT
Hemangiosarcoma and angiosarcoma are soft-tissue sarcomas of blood vessel-forming cells in dogs and humans, respectively. These vasoformative sarcomas are aggressive and highly metastatic, with disorganized, irregular blood-filled vascular spaces. Our objective was to define molecular programs which support the niche that enables progression of canine hemangiosarcoma and human angiosarcoma. Dog-in-mouse hemangiosarcoma xenografts recapitulated the vasoformative and highly angiogenic morphology and molecular characteristics of primary tumors. Blood vessels in the tumors were complex and disorganized, and they were lined by both donor and host cells. In a series of xenografts, we observed that the transplanted hemangiosarcoma cells created exuberant myeloid hyperplasia and gave rise to lymphoproliferative tumors of mouse origin. Our functional analyses indicate that hemangiosarcoma cells generate a microenvironment that supports expansion and differentiation of hematopoietic progenitor populations. Furthermore, gene expression profiling data revealed hemangiosarcoma cells expressed a repertoire of hematopoietic cytokines capable of regulating the surrounding stromal cells. We conclude that canine hemangiosarcomas, and possibly human angiosarcomas, maintain molecular properties that provide hematopoietic support and facilitate stromal reactions, suggesting their potential involvement in promoting the growth of hematopoietic tumors.

SIGNIFICANCE:

We demonstrate that hemangiosarcomas regulate molecular programs supporting hematopoietic expansion and differentiation, providing insights into their potential roles in creating a permissive stromal-immune environment for tumor progression.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemangiossarcoma Limite: Animals / Humans Idioma: En Revista: Cancer Res Commun Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemangiossarcoma Limite: Animals / Humans Idioma: En Revista: Cancer Res Commun Ano de publicação: 2024 Tipo de documento: Article