G protein-coupled receptor-targeting antibody-drug conjugates: Current status and future directions

被引:8
作者
High, Peyton [1 ,2 ]
Carmon, Kendra S. [1 ,3 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Brown Fdn, Inst Mol Med, Ctr Translat Canc Res, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr UTHealth Houston, Grad Sch Biomed Sci, Houston, TX 77030 USA
[3] Univ Texas Hlth Sci Ctr Houston, Ctr Translat Canc Res, Brown Fdn, Inst Mol Med, 1825 Pressler St,Rm 330G, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Antibody; Drug conjugate; G protein -coupled receptor; Linker; Payload; GASTROINTESTINAL STROMAL TUMORS; MONOMETHYL AURISTATIN E; STEM-CELLS; INTRACELLULAR TRAFFICKING; MONOCLONAL-ANTIBODY; CHEMOKINE RECEPTORS; COLON; LGR5; INTERNALIZATION; CALCITONIN;
D O I
10.1016/j.canlet.2023.216191
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, antibody-drug conjugates (ADCs) have emerged as promising anti-cancer therapeutic agents with several having already received market approval for the treatment of solid tumor and hematological malig-nancies. As ADC technology continues to improve and the range of indications treatable by ADCs increases, the repertoire of target antigens has expanded and will undoubtedly continue to grow. G protein-coupled receptors (GPCRs) are well-characterized therapeutic targets implicated in many human pathologies, including cancer, and represent a promising emerging target of ADCs. In this review, we will discuss the past and present therapeutic targeting of GPCRs and describe ADCs as therapeutic modalities. Moreover, we will summarize the status of existing preclinical and clinical GPCR-targeted ADCs and address the potential of GPCRs as novel targets for future ADC development.
引用
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页数:10
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