C
Cai-Ping Tan
Researcher at Sun Yat-sen University
Publications - 82
Citations - 5111
Cai-Ping Tan is an academic researcher from Sun Yat-sen University. The author has contributed to research in topics: Apoptosis & Autophagy. The author has an hindex of 38, co-authored 80 publications receiving 3891 citations.
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Cyclometalated iridium(III) complexes as lysosome-targeted photodynamic anticancer and real-time tracking agents
TL;DR: In this article, four cyclometalated iridium(III)-β-carboline complexes with pH-responsive singlet oxygen (1O2) production and lysosome-specific imaging properties have been designed and synthesized.
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Nuclear Permeable Ruthenium(II) β-Carboline Complexes Induce Autophagy To Antagonize Mitochondrial-Mediated Apoptosis
Cai-Ping Tan,Sensen Lai,Shouhai Wu,Sheng Hu,Lingjun Zhou,Yu Chen,Minxu Wang,Yiping Zhu,Wu Lian,Wenlie Peng,Liang-Nian Ji,Anlong Xu +11 more
TL;DR: It is demonstrated that a series of ruthenium(II) complexes containing a β-carboline alkaloid as ligand can simultaneously induce autophagy and apoptosis in tumor cells, and suppression ofautophagy using pharmacological inhibitors enhances apoptotic cell death.
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Phosphorescent iridium(III)-bis-N-heterocyclic carbene complexes as mitochondria-targeted theranostic and photodynamic anticancer agents.
TL;DR: Mechanism studies show that these complexes exert their anticancer efficacy by initiating a cascade of events related to mitochondrial dysfunction, and display up to 3 orders of magnitude higher cytotoxicity upon irradiation at 365 nm, which is so far the highest photocytotoxic responses reported for iridium complexes.
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Synthesis, structural characteristics, DNA binding properties and cytotoxicity studies of a series of Ru(III) complexes.
TL;DR: It has been found that the extension of the N-N ligands can increase the stability of the complexes and the in vitro anticancer activities of these compounds are moderate on the five human cancer cell lines screened.
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Multifunctional QD-based co-delivery of siRNA and doxorubicin to HeLa cells for reversal of multidrug resistance and real-time tracking.
Jin-Ming Li,Yuan-Yuan Wang,Yuan-Yuan Wang,Mei-Xia Zhao,Cai-Ping Tan,Yi-Qun Li,Xue-Yi Le,Liang-Nian Ji,Zong-Wan Mao,Zong-Wan Mao +9 more
TL;DR: Two CdSe/ZnSe QDs modified with β-CD coupled to L-Arg or L-His were used to simultaneously deliver doxorubicin (Dox) and siRNA targeting the MDR1 gene to reverse the multidrug resistance of HeLa cells.