Engineered Bifunctional Proteins for Targeted Cancer Therapy: Prospects and Challenges

被引:11
|
作者
Du, Yue [1 ]
Xu, Jian [2 ,3 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Pharm, Zhengzhou 450052, Henan, Peoples R China
[2] Natl Inst Hlth, Ctr Canc Res, Mol Biol Lab, Bethesda, MD 20892 USA
[3] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
基金
中国国家自然科学基金;
关键词
bifunctional proteins; classifications; clinical applications; effector molecules; targeted deliveries; T-CELL ENGAGER; ANTI-CD20 X ANTI-CD3; PHASE-I TRIAL; GROWTH-FACTOR RECEPTOR; ACUTE LYMPHOBLASTIC-LEUKEMIA; CHAIN ANTIBODY CONSTRUCTS; COLONY-STIMULATING FACTOR; BISPECIFIC ANTIBODY; FUSION PROTEIN; RECOMBINANT IMMUNOTOXIN;
D O I
10.1002/adma.202103114
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bifunctional proteins (BFPs) are a class of therapeutic agents produced through genetic engineering and protein engineering, and are increasingly used to treat various human diseases, including cancer. These proteins usually have two or more biological functions-specifically recognizing different molecular targets to regulate the related signaling pathways, or mediating effector molecules/cells to kill tumor cells. Unlike conventional small-molecule or single-target drugs, BFPs possess stronger biological activity but lower systemic toxicity. Hence, BFPs are considered to offer many benefits for the treatment of heterogeneous tumors. In this review, the authors briefly describe the unique structural feature of BFP molecules and innovatively divide them into bispecific antibodies, cytokine-based BFPs (immunocytokines), and protein toxin-based BFPs (immunotoxins) according to their mode of action. In addition, the latest advances in the development of BFPs are discussed and the potential limitations or problems in clinical applications are outlined. Taken together, future studies need to be centered on understanding the characteristics of BFPs for optimizing and designing more effective such drugs.
引用
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页数:32
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