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Advances in Anti-Tumor Treatments Targeting the CD47/SIRPα Axis

期刊

FRONTIERS IN IMMUNOLOGY
卷 11, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2020.00018

关键词

CD47; CD47; SIRPa axis; immunotherapy; phagocytosis; signal-regulatory protein alpha (SIRP alpha)

资金

  1. Science and Technology Project of Guangdong Province [2017A010103019]
  2. National Natural Science Foundation of China [81572184, 81801649]
  3. China Postdoctoral Science Foundation [2018M631026]
  4. Special Funds for the Cultivation of Guangdong College Students' Scientific and Technological Innovation (Climbing Program Special Funds) [pdjh2019b0224]
  5. Ph.D early development program of Guangdong Medical University [B2019012]
  6. Grouptype Special Supporting Project for Educational Talents in Universities [4SG19057G]
  7. American Heart Association Career Development Award [19CDA34500000]

向作者/读者索取更多资源

CD47 is an immunoglobulin that is overexpressed on the surface of many types of cancer cells. CD47 forms a signaling complex with signal-regulatory protein alpha (SIRP alpha), enabling the escape of these cancer cells from macrophage-mediated phagocytosis. In recent years, CD47 has been shown to be highly expressed by various types of solid tumors and to be associated with poor patient prognosis in various types of cancer. A growing number of studies have since demonstrated that inhibiting the CD47-SIRP alpha signaling pathway promotes the adaptive immune response and enhances the phagocytosis of tumor cells by macrophages. Improved understanding in this field of research could lead to the development of novel and effective anti-tumor treatments that act through the inhibition of CD47 signaling in cancer cells. In this review, we describe the structure and function of CD47, provide an overview of studies that have aimed to inhibit CD47-dependent avoidance of macrophage-mediated phagocytosis by tumor cells, and assess the potential and challenges for targeting the CD47-SIRP alpha signaling pathway in anti-cancer therapy.

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