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Updated: Jun 3, 2026

Simultaneous Imaging and Flow-Cytometry-based Detection of Multiple Fluorescent Senescence Markers in Therapy-Induced Senescent Cancer Cells
Published on: July 12, 2022
Monoamine Oxidase A-Activatable Theranostic Probe for Image-Guided Photodynamic Elimination of Senescent Tumor Cells
Sudong Wang1, Ran Ji1, Yu Zeng1
1Department of Radiology, Nanjing Drum Tower Hospital, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, Jiangsu Key Laboratory of Micro Nano Sensing and Separation Science for Analytical Chemistry, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.
Abstract:
Cellular senescence contributes to tumor recurrence by fostering a pro-tumorigenic microenvironment after therapy. While SA-β-gal serves as a widely adopted biomarker of senescence, its inadequate specificity impedes the precision with which senolytic therapies can be directed. Here, we designed and developed a theranostic probe named DMTP-1 to target monoamine oxidase A (MAO-A), an enzyme that is upregulated in senescent tumor cells. Upon MAO-A activation, DMTP-1 is converted to a cationic product, ADMTP-1, which exhibits aggregation-induced emission (AIE) for imaging and generates reactive oxygen species (ROS) under light for photodynamic therapy (PDT). Cellular studies demonstrate that the fluorescence signal and PDT efficacy of DMTP-1 are markedly enhanced in MAO-A-overexpressing senescent tumor cells, enabling image-guided elimination of these cells. Moreover, DMTP-1 shows potent photodynamic activity in 3D multicellular tumor spheroids and enables clear visualization of senescence-associated MAO-A upregulation in a zebrafish senescence model. This MAO-A-activated probe enables specific detection and eradication of therapy-induced senescent tumor cells, offering a targeted strategy for senolytic intervention.
