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作 者:Pengcheng Zhao Longyan Xie Lei Yu Ping Wang
机构地区:[1]School of Life Sciences and Medicine,Shandong University of Technology,Zibo,Shandong 255000,China [2]Tongji University Cancer Center,Shanghai Tenth People's Hospital,School of Medicine,Tongji University,Shanghai 200092,China
出 处:《Genes & Diseases》2024年第1期205-217,共13页基因与疾病(英文)
基 金:supported by the National Key Research and Development Program of China(No.2020YFA0803201);the National Natural Science Foundation of China(No.31830053,31920103007,22207084);the Fundamental ResearchFunds fortheCornellUniversity(No.22120220463).
摘 要:The interaction between cluster of differentiation 47(CD47)and signal regulatory proteinα(SiRPa)protects healthy cells from macrophage attack,which is crucial for maintain-ing immune homeostasis.Overexpression of CD47 occurs widely across various tumor cell types and transmits the"don't eat me"signal to macrophages to avoid phagocytosis through binding to SIRPa.Blockade of the CD47-SIRPa axis is therefore a promising approach for cancer treat-ment.Lymphoma is the most common hematological malignancy and is an area of unmet clin-ical need.This review mainly described the current strategies targeting the CD47-SIRPa axis,including antibodies,SiRPaFc fusion proteins,small molecule inhibitors,and peptides both in preclinical studies and clinical trials with Hodgkin lymphoma and non-Hodgkin lymphoma.
关 键 词:Cancer treatment CD47-SIRPαaxis Hodgkin lymphoma IMMUNOTHERAPY Non-Hodgkin lymphoma
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