| Literature DB >> 29054784 |
Matthew T Basel1, Sanjeev Narayanan2, Chanran Ganta3, Tej B Shreshta4, Alejandro Marquez5, Marla Pyle6, Jennifer Hill7, Stefan H Bossmann8, Deryl L Troyer9.
Abstract
Animal models are essential to cancer research, but current xenograft models are limited in their utility especially due to the lack of an immune system. Here we demonstrate that a xenograft tumor model can be developed in immunocompetent mice by tolerizing murine fetuses to human tumor cells. A375 human melanoma cells were injected into day E14 fetuses and after birth mice were challenged with A375 cells to determine their ability to develop tumors. Intravenous injections of cells resulted in metastatic-like lung tumors, which were verified to be human in origin by immunohistochemistry and PCR. These results were replicated with several other human tumor types: BxPC3 (human pancreatic adenocarcinoma), MDA-MB-231 (human breast adenocarcinoma), M21 (human melanoma), and HeLa (human cervical adenocarcinoma). Development of an immunocompetent xenograft tumor model would allow the further elucidation of the interaction of the immune system with therapy in both preclinical research and patient derived xenografts.Entities:
Keywords: Fetal surgery; Immunocompetent; Model; Tolerization; Xenograft
Mesh:
Year: 2017 PMID: 29054784 DOI: 10.1016/j.canlet.2017.10.009
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679