Pharmacotherapeutic Targeting of G Protein-Coupled Receptors in Oncology: Examples of Approved Therapies and Emerging Concepts

被引:17
|
作者
Lappano, Rosamaria [1 ]
Maggiolini, Marcello [1 ]
机构
[1] Univ Calabria, Dept Pharm Hlth & Nutr Sci, Arcavacata Di Rende, Italy
关键词
GONADOTROPIN-RELEASING-HORMONE; HEDGEHOG PATHWAY INHIBITOR; ANDROGEN DEPRIVATION THERAPY; CELL LEUKEMIA-LYMPHOMA; CXCR4 ANTAGONIST CTCE-9908; ADVANCED PROSTATE-CANCER; PRIMARY TUMOR-GROWTH; EARLY BREAST-CANCER; PHASE-I; CHEMOKINE RECEPTORS;
D O I
10.1007/s40265-017-0738-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G protein-coupled receptors (GPCRs) are involved in numerous physio-pathological processes, including the stimulation of cancer progression. In this regard, it should be mentioned that although GPCRs may represent major pharmaceutical targets, only a few drugs acting as GPCR inhibitors are currently used in anti-tumor therapies. For instance, certain pro-malignancy effects mediated by GPCRs are actually counteracted by the use of small molecules and peptides that function as receptor antagonists or inverse agonists. Recently, humanized monoclonal antibodies targeting GPCRs have also been developed. Here, we review the current GPCR-targeted therapies for cancer treatment, summarizing the clinical studies that led to their official approval. We provide a broad overview of the mechanisms of action of the available anti-cancer drugs targeting gonadotropin-releasing hormone, somatostatin, chemokine, and Smoothened receptors. In addition, we discuss the anti-tumor potential of novel non-approved molecules and antibodies able to target some of the aforementioned GPCRs in different experimental models and clinical trials. Likewise, we focus on the repurposing in cancer patients of non-oncological GPCR-based drugs, elucidating the rationale behind this approach and providing clinical evidence on their safety and efficacy.
引用
收藏
页码:951 / 965
页数:15
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