| Literature DB >> 29183891 |
Tiara T Byrd1,2,3, Kristen Fousek4,2,3, Antonella Pignata2,3, Christopher Szot5, Heba Samaha2,3,6, Steven Seaman5, Lacey Dobrolecki7, Vita S Salsman2,3, Htoo Zarni Oo8, Kevin Bielamowicz2,3, Daniel Landi2,3, Nino Rainusso2,3, John Hicks9, Suzanne Powell10, Matthew L Baker11, Winfried S Wels12, Joachim Koch12,13, Poul H Sorensen14,15, Benjamin Deneen4,2,16, Matthew J Ellis7, Michael T Lewis7, Meenakshi Hegde2,3, Bradley S Fletcher17, Brad St Croix5, Nabil Ahmed1,2,3.
Abstract
Triple-negative breast cancer (TNBC) is an aggressive disease lacking targeted therapy. In this study, we developed a CAR T cell-based immunotherapeutic strategy to target TEM8, a marker initially defined on endothelial cells in colon tumors that was discovered recently to be upregulated in TNBC. CAR T cells were developed that upon specific recognition of TEM8 secreted immunostimulatory cytokines and killed tumor endothelial cells as well as TEM8-positive TNBC cells. Notably, the TEM8 CAR T cells targeted breast cancer stem-like cells, offsetting the formation of mammospheres relative to nontransduced T cells. Adoptive transfer of TEM8 CAR T cells induced regression of established, localized patient-derived xenograft tumors, as well as lung metastatic TNBC cell line-derived xenograft tumors, by both killing TEM8+ TNBC tumor cells and targeting the tumor endothelium to block tumor neovascularization. Our findings offer a preclinical proof of concept for immunotherapeutic targeting of TEM8 as a strategy to treat TNBC.Significance: These findings offer a preclinical proof of concept for immunotherapeutic targeting of an endothelial antigen that is overexpressed in triple-negative breast cancer and the associated tumor vasculature. Cancer Res; 78(2); 489-500. ©2017 AACR. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 29183891 PMCID: PMC5771806 DOI: 10.1158/0008-5472.CAN-16-1911
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701