Identification of A2BAR as a potential target in colorectal cancer using novel fluorescent GPCR ligands

被引:4
作者
Barbazan, Jorge [1 ]
Majellaro, Maria [2 ]
Martinez, Anton L. [3 ]
Brea, Jose M. [3 ]
Sotelo, Eddy [4 ,5 ]
Abal, Miguel [1 ,6 ]
机构
[1] Univ Hosp Santiago de Compostela SERGAS, Hlth Res Inst Santiago de Compostela IDIS, Translat Med Oncol Grp ONCOMET, Trav Choupana S-N, Santiago De Compostela 15706, Spain
[2] Celtarys Res SL, Santiago De Compostela 15706, Spain
[3] Univ Santiago de Compostela, Ctr Singular Invest Med Mol & Enfermedades Cron C, Santiago De Compostela 15782, Spain
[4] Univ Santiago de Compostela, Ctr Singular Invest Quim Biol & Mat Mol CiQUS, Santiago De Compostela 15782, Spain
[5] Univ Santiago de Compostela, Dept Quim Organ, Santiago De Compostela 15782, Spain
[6] Ctr Invest Biomed Red Canc CIBERONC, Monforte de Lemos 3-5, Madrid 28029, Spain
关键词
Colorectal cancer; GPCRs; Adenosine receptors; Tumor microenvironment; Fluorescent ligands; Drug screening; ADENOSINE RECEPTOR; 3,4-DIHYDROPYRIMIDIN-2(1H)-ONES; DISCOVERY;
D O I
10.1016/j.biopha.2022.113408
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
G-protein coupled receptors (GPCRs) have been largely targeted in a wide range of diseases, but few therapies have been directed against GPCRs in the field of cancer, partly because of the lack of effective target identification strategies. Here, using colorectal cancer (CRC) as a model, we explored the gene expression of a panel of GPCRs in tumor and stromal cells, identifying specific gene sets defining each cellular compartment. We selected the adenosine receptor 2B (A(2B)AR), specifically expressed in cancer cell lines compared with stromal cells, to explore the use of fluorescent ligands that can be used for target visualization. Fluorescent probes allowed semi-quantitative receptor mapping in living cells and validated the specific expression of A(2B)AR in CRC cell lines. As well, fluorescent ligands were effective at monitoring real-time A(2B)AR receptor labeling using live-imaging modalities, and displayed high efficiency when used to label complex 3D cellular systems such as tumor spheroids. Finally, we validated A(2B)AR as a potential pharmacological tool in CRC, using selective antagonists, finding a reduction in tumor cell proliferation. This proof-of-concept study suggests the use of fluorescent ligands for GPCR characterization through imaging, and as possible new tools used for target validation in drug screening methodologies.
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页数:9
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