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Self-assembly of vascularized tissue to support tumor explants in vitro.
Bazou, Despina; Maimon, Nir; Gruionu, Gabriel; Munn, Lance L.
Afiliación
  • Bazou D; Edwin L. Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, 100 Blossom Street, Boston, Massachusetts 02114, USA. munn@steele.mgh.harvard.edu.
  • Maimon N; Edwin L. Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, 100 Blossom Street, Boston, Massachusetts 02114, USA. munn@steele.mgh.harvard.edu.
  • Gruionu G; Department of Surgery, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, Boston, Massachusetts 02114, USA.
  • Munn LL; Edwin L. Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, 100 Blossom Street, Boston, Massachusetts 02114, USA. munn@steele.mgh.harvard.edu.
Integr Biol (Camb) ; 8(12): 1301-1311, 2016 12 05.
Article en En | MEDLINE | ID: mdl-27787529
ABSTRACT
Testing the efficacy of cancer drugs requires functional assays that recapitulate the cell populations, anatomy and biological responses of human tumors. Although current animal models and in vitro cell culture platforms are informative, they have significant shortcomings. Mouse models can reproduce tissue-level and systemic responses to tumor growth and treatments observed in humans, but xenografts from patients often do not grow, or require months to develop. On the other hand, current in vitro assays are useful for studying the molecular bases of tumorigenesis or drug activity, but often lack the appropriate in vivo cell heterogeneity and natural microenvironment. Therefore, there is a need for novel tools that allow rapid analysis of patient-derived tumors in a robust and representative microenvironment. We have developed methodology for maintaining harvested tumor tissue in vitro by placing them in a support bed with self-assembled stroma and vasculature. The harvested biopsy or tumor explant integrates with the stromal bed and vasculature, providing the correct extracellular matrix (collagen I, IV, fibronectin), associated stromal cells, and a lumenized vessel network. Our system provides a new tool that will allow ex vivo drug-screening and can be adapted for the guidance of patient-specific therapeutic strategies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Técnicas de Cultivo de Tejidos / Microambiente Tumoral / Técnicas de Cultivo Celular por Lotes / Neoplasias Experimentales / Neovascularización Patológica Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Revista: Integr Biol (Camb) Asunto de la revista: BIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Técnicas de Cultivo de Tejidos / Microambiente Tumoral / Técnicas de Cultivo Celular por Lotes / Neoplasias Experimentales / Neovascularización Patológica Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Revista: Integr Biol (Camb) Asunto de la revista: BIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos