Translocator protein (TSPO)-Targeted agents for photodynamic therapy of cancer

被引:6
|
作者
Xie, Qing [1 ]
Su, Meng [1 ]
Liu, Yang [1 ]
Zhang, Dawei [1 ,2 ]
Li, Zhen [1 ,3 ]
Bai, Mingfeng [1 ,4 ,5 ]
机构
[1] Vanderbilt Univ, Inst Imaging Sci, Med Ctr, 1161 21st Ave South, Nashville, TN 37232 USA
[2] Guangzhou Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 2, 250 East Changgang Rd, Guangzhou 510260, Peoples R China
[3] China Med Univ, Dept Gen Surg, Affiliated Hosp 4, 4 Chongshan East Rd, Shenyang 110032, Peoples R China
[4] Vanderbilt Univ, Dept Radiol & Radiol Sci, Med Ctr, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Vanderbilt Ingram Canc Ctr, Med Ctr, Nashville, TN 37232 USA
关键词
Translocator protein; Cancer therapy; Photodynamic therapy; Agent development; Fluorescence microscopy; PERIPHERAL BENZODIAZEPINE-RECEPTOR; BREAST-CANCER; BIOLOGICAL EVALUATION; EXPRESSION; LIGAND; PBR; PROLIFERATION; TARGET;
D O I
10.1016/j.pdpdt.2021.102209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Photodynamic therapy (PDT) is a clinically approved therapeutic strategy that combines a specific wavelength of light and light-activated photosensitizers (PSs). The usage of PDT for cancer treatment is often hampered by the lack of tumor selectivity of PSs, which may cause photodamage to surrounding normal tissues. Recently, translocator protein (TSPO) has attracted great interest as a tumor biomarker, whose expression correlates with tumor aggressiveness. In this study, we report the development of a series of novel TSPO-PSs based on quinazoline, pyrazolopyrimidine, and tetrahydrocarbazole structures. These TSPO-PSs bind to TSPO with nanomolar affinities and demonstrated efficient and target-specific PDT effect upon light irradiation. Therefore, they may have great potential in the treatment of tumors associated with high-TSPO expression.
引用
收藏
页数:13
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