中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Emerging roles of class I PI3K inhibitors in modulating tumor microenvironment and immunity

文献类型:期刊论文

作者Sun, Pu1,2; Meng, Ling-hua1,2
刊名ACTA PHARMACOLOGICA SINICA
出版日期2020-09-16
页码8
关键词phosphoinositide 3-kinase (PI3K) PI3K inhibitors tumor microenvironment immune cells immunotherapy
ISSN号1671-4083
DOI10.1038/s41401-020-00500-8
通讯作者Meng, Ling-hua(lhmeng@simm.ac.cn)
英文摘要Immune system-mediated tumor killing has revolutionized anti-tumor therapies, providing long-term and durable responses in some patients. The phosphoinositide 3-kinase (PI3K) pathway controls multiple biological processes and is frequently dysregulated in malignancies. Enormous efforts have been made to develop inhibitors against class I PI3K. Notably, with the increasing understanding of PI3K, it has been widely accepted that PI3K inhibition not only restrains tumor progression, but also reshapes the immunosuppressive tumor microenvironment. In this review, we focus on the pivotal roles of class I PI3Ks in adaptive and innate immune cells, as well as other stromal components. We discuss the modulation by PI3K inhibitors of the tumor-supportive microenvironment, including eliminating the regulatory immune cells, restoring cytotoxic cells or regulating angiogenesis. The potential combinations of PI3K inhibitors with other therapies to enhance the anti-tumor immunity are also described.
WOS关键词PHOSPHATIDYLINOSITOL 3-KINASE-AKT PATHWAY ; ENDOTHELIAL GROWTH-FACTOR ; REGULATORY T-CELLS ; IMPAIRED B-CELL ; MATRIX METALLOPROTEINASES ; P110-GAMMA ISOFORM ; SUPPRESSOR-CELLS ; BETA-SELECTION ; P110-DELTA ; PI3K-GAMMA
资助项目Personalized Medicines-Molecular Signature-based Drug Discovery and Development, Strategic Priority Research Program of the Chinese Academy of Sciences[XDA12020111] ; Personalized Medicines-Molecular Signature-based Drug Discovery and Development, Strategic Priority Research Program of the Chinese Academy of Sciences[XDA12020235] ; Personalized Medicines-Molecular Signature-based Drug Discovery and Development, Strategic Priority Research Program of the Chinese Academy of Sciences[XDA12050407] ; National Science and Technology Major Project Key New Drug Creation and Manufacturing Program[2018ZX09711002-011-014] ; National Science and Technology Major Project Key New Drug Creation and Manufacturing Program[2018ZX09711002-004-004] ; National Natural Science Foundation of China[81773760] ; National Natural Science Foundation of China[81973345] ; Fudan-SIMM Joint Research Fund[FU-SIMM20172005]
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000570042600003
出版者NATURE PUBLISHING GROUP
源URL[http://119.78.100.183/handle/2S10ELR8/291138]  
专题中国科学院上海药物研究所
通讯作者Meng, Ling-hua
作者单位1.Chinese Acad Sci, Shanghai Inst Materia Med, Div Antitumor Pharmacol, 501 Haike Rd, Shanghai 201203, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
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Sun, Pu,Meng, Ling-hua. Emerging roles of class I PI3K inhibitors in modulating tumor microenvironment and immunity[J]. ACTA PHARMACOLOGICA SINICA,2020:8.
APA Sun, Pu,&Meng, Ling-hua.(2020).Emerging roles of class I PI3K inhibitors in modulating tumor microenvironment and immunity.ACTA PHARMACOLOGICA SINICA,8.
MLA Sun, Pu,et al."Emerging roles of class I PI3K inhibitors in modulating tumor microenvironment and immunity".ACTA PHARMACOLOGICA SINICA (2020):8.

入库方式: OAI收割

来源:上海药物研究所

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