Peptide-Based Radiopharmaceuticals for Molecular Imaging of Prostate Cancer

被引:8
作者
Reynolds, Tamila J. Stott [1 ]
Smith, Charles J. [2 ]
Lewis, Michael R. [3 ]
机构
[1] Univ Texas El Paso, Lab Anim Resources Ctr, El Paso, TX 79968 USA
[2] Univ Missouri, Dept Radiol, Columbia, MO USA
[3] Univ Missouri, Dept Vet Med & Surg, Columbia, MO 65211 USA
来源
MOLECULAR & DIAGNOSTIC IMAGING IN PROSTATE CANCER: CLINICAL APPLICATIONS AND TREATMENT STRATEGIES | 2019年 / 1126卷
关键词
Peptides; Radiopharmaceuticals; PET; SPECT; Gastrin-releasing peptide receptor; alpha(v)beta(3) integrin; GASTRIN-RELEASING-PEPTIDE; POSITRON-EMISSION-TOMOGRAPHY; MEMBRANE ANTIGEN-EXPRESSION; SKELETAL-RELATED EVENTS; AGENTS TARGETING PSMA; STEM-CELL ANTIGEN; GRP-RECEPTOR; RGD-PEPTIDE; INTEGRIN ALPHA-V-BETA-3; BIOLOGICAL EVALUATION;
D O I
10.1007/978-3-319-99286-0_8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Given the high incidence of prostate cancer, there is a continuing need for advances in early detection and in effective treatments. Over the last several years, radiolabeled peptides have been developed, which can target receptors on prostate tumors with high affinity and specificity. These peptides are eliminated from normal tissues rapidly, producing high contrast for PET and SPECT imaging. Receptors of interest for tumor imaging include prostate specific membrane antigen (PSMA), gastrin-releasing peptide receptor (GRPR), and alpha(v)beta(3) integrin. Because radiolabeled peptides afford high tumor-to-normal tissue uptake ratios, the potential of peptide-based targeted radiotherapy of prostate cancer is being explored. In addition, targeting either of two receptors with one peptide may allow more tumors to be detected and aid in the delineation of early versus advanced disease. Taken together, all these developments in peptide-based imaging and therapy of prostate cancer offer the promise of personalized, molecular medicine for individual patients.
引用
收藏
页码:135 / 158
页数:24
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