Bispecific radioligands targeting prostate-specific membrane antigen and gastrin-releasing peptide receptors on the surface of prostate cancer cells

被引:15
|
作者
Liolios, Christos [1 ]
Sachpekidis, Christos [2 ]
Schaefer, Martin [1 ]
Kopka, Klaus [1 ,3 ]
机构
[1] German Canc Res Ctr, Div Radiopharmaceut Chem, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[2] German Canc Res Ctr, Clin Cooperat Unit Nucl Med, Heidelberg, Germany
[3] German Canc Res Ctr, German Canc Consortium DKTK, Heidelberg, Germany
关键词
GRPr; heterodimers; molecular imaging; prostate cancer; PSMA; PRECLINICAL EVALUATION; BIOLOGICAL EVALUATION; INCREASED SURVIVAL; IN-VITRO; PSMA; PET; EXPRESSION; GRPR; TOMOGRAPHY; THERAPY;
D O I
10.1002/jlcr.3749
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metastases of prostate cancer usually show highly heterogeneous or partly lost prostate-specific membrane antigen (PSMA) expression. In order to image and treat both PSMA positive and negative tissues, the extension of PSMA tracer specificity to other receptors, also highly expressed on the surface of prostate cancer cells, has been suggested. Prostate cancer cells usually express both PSMA and gastrin-releasing peptide (GRP) receptors; thus, bispecific heterodimeric molecules, addressing both targets at the same time, may significantly improve prostate cancer imaging and therapy. This article summarizes preclinical data regarding low-molecular weight molecules targeting PSMA and GRP receptors.
引用
收藏
页码:510 / 522
页数:13
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