A Bivalent Activatable Fluorescent Probe for Screening and Intravital Imaging of Chemotherapy-Induced Cancer Cell Death

被引:1
|
作者
Barth, Nicole D. [1 ]
Mendive-Tapia, Lorena [1 ]
Subiros-Funosas, Ramon [1 ]
Ghashghaei, Ouldouz [2 ,3 ]
Lavilla, Rodolfo [2 ,3 ]
Maiorino, Laura [4 ]
He, Xue-Yan [4 ]
Dransfield, Ian [1 ]
Egeblad, Mikala [4 ]
Vendrell, Marc [1 ]
机构
[1] Univ Edinburgh, Ctr Inflammat Res, Edinburgh, Midlothian, Scotland
[2] Univ Barcelona, Fac Pharm, Lab Med Chem, Barcelona, Spain
[3] Univ Barcelona, Inst Biomed IBUB, Barcelona, Spain
[4] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
基金
英国工程与自然科学研究理事会; 英国惠康基金;
关键词
apoptosis; breast cancer; chemotherapy; fluorogenic probes; peptides; IN-VIVO; ANNEXIN-V; ANTICANCER THERAPY; CYCLIC PEPTIDE; APOPTOSIS; PHOSPHATIDYLSERINE; MICROENVIRONMENT; STAUROSPORINE; RECOGNITION; EXPRESSION;
D O I
10.1002/anie.202113020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The detection and quantification of apoptotic cells is a key process in cancer research, particularly during the screening of anticancer therapeutics and in mechanistic studies using preclinical models. Intravital optical imaging enables high-resolution visualisation of cellular events in live organisms; however, there are few fluorescent probes that can reliably provide functional readouts in situ without interference from tissue autofluorescence. We report the design and optimisation of the fluorogenic probe Apotracker Red for real-time detection of cancer cell death. The strong fluorogenic behaviour, high selectivity, and excellent stability of Apotracker Red make it a reliable optical reporter for the characterisation of the effects of anticancer drugs in cells in vitro and for direct imaging of chemotherapy-induced apoptosis in vivo in mouse models of breast cancer.
引用
收藏
页数:8
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