| Literature DB >> 27758887 |
Lin Chen1,2, Jie Li1,2, Fei Wang1, Chengliang Dai2, Fan Wu2, Xiaoman Liu2, Taotao Li3, Rainer Glauben4, Yi Zhang1, Guangjun Nie5, Yulong He6, Zhihai Qin7,2.
Abstract
Tumor relapse after chemotherapy is a major hurdle for successful cancer therapy. Chemotherapeutic drugs select for resistant tumor cells and reshape tumor microenvironment, including the blood supply system. Using animal models, we observed on macrophages in tumor tissue a close correlation between upregulated Tie2 expression and tumor relapse upon chemotherapy. Conditional deletion of Tie2 expression in macrophages significantly prohibited blood supply and regrowth of tumors. Tie2+ macrophages were derived from tumor-infiltrating Tie2-CD11b+ cells and hypoxia-induced Tie2 expression on these cells. Mechanistically, expression of Tie2 prevented macrophages from apoptosis in stress conditions via the AKT-dependent signaling pathway. Together, these results demonstrate that Tie2 expression by macrophages is necessary and sufficient to promote the reconstruction of blood vessels after chemotherapy, shedding new light on developing novel strategies to inhibit tumor relapse. Cancer Res; 76(23); 6828-38. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27758887 DOI: 10.1158/0008-5472.CAN-16-1114
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701