scispace - formally typeset
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.

Papers
More filters
Journal ArticleDOI

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.
Journal ArticleDOI

Nuclear Permeable Ruthenium(II) β-Carboline Complexes Induce Autophagy To Antagonize Mitochondrial-Mediated Apoptosis

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.
Journal ArticleDOI

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.
Journal ArticleDOI

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.
Journal ArticleDOI

Multifunctional QD-based co-delivery of siRNA and doxorubicin to HeLa cells for reversal of multidrug resistance and real-time tracking.

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.