| Literature DB >> 32795895 |
Xiaomin Cai1, Bin Wei1, Lele Li1, Xiaofeng Chen1, Wen Liu2, Jian Cui2, Yumeng Lin2, Yang Sun2, Qiang Xu3, Wenjie Guo4, Yanhong Gu5.
Abstract
Increasing studies confirm that anti-angiogenesis can increase the effectiveness of immunotherapy. In this study, we found that an angiogenesis inhibitor apatinib enhanced anti-PD-1 therapy for colon cancer in mice via promoting PD-L1 expression. Apatinib treatment upregulated PD-L1 expression in various colon cancer cells both at the mRNA and protein levels. Further, apatinib-treated cancer cells hampered activation and IFN-γ secretion of T cells in the co-culture system, which was reversed by the anti-PD-1 antibody. Based on this, the combination of apatinib with anti-PD-1 on colon cancer growth in mice was examined. The combination treatment showed more significant inhibition on the growth of transplanted tumors in mice than single-drug treatment. Overall, our study here showed the enhancement of anti-PD-1 antitumor efficacy in a syngeneic mouse model (CT-26 cells in Balb/c) by the angiogenesis inhibitor apatinib via upregulating PD-L1 expression as well as angiogenesis inhibition, which may provide a rationale for the combination of apatinib and anti-PD-1 antibody for colorectal cancer treatment in the clinic.Entities:
Keywords: Angiogenesis; Apatinib; Immunotherapy; PD-L1; T cell
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Year: 2020 PMID: 32795895 DOI: 10.1016/j.intimp.2020.106858
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932