Combinatorial photochemotherapy on liver cancer stem cells with organoplatinum(ii) metallacage-based nanoparticles.
Animals
Antineoplastic Agents
/ chemistry
Apoptosis
/ drug effects
Cell Line, Tumor
Coordination Complexes
/ chemistry
Humans
Infrared Rays
Liver
/ pathology
Liver Neoplasms
/ drug therapy
Male
Membrane Potential, Mitochondrial
/ drug effects
Metal Nanoparticles
/ chemistry
Mice, Nude
Neoplastic Stem Cells
/ drug effects
Photochemotherapy
Photosensitizing Agents
/ chemistry
Platinum
/ chemistry
Porphyrins
/ chemistry
Reactive Oxygen Species
/ metabolism
Spheroids, Cellular
/ drug effects
Xenograft Model Antitumor Assays
Journal
Journal of materials chemistry. B
ISSN: 2050-7518
Titre abrégé: J Mater Chem B
Pays: England
ID NLM: 101598493
Informations de publication
Date de publication:
14 11 2019
14 11 2019
Historique:
pubmed:
30
8
2019
medline:
23
9
2020
entrez:
30
8
2019
Statut:
ppublish
Résumé
Liver cancer is a kind of lethal and aggressive malignant neoplasm with a high rate of relapse and metastasis after therapy. An important cause for the relapse and metastasis is the existence of liver cancer stem cells (CSCs), which have high resistance to chemotherapy and high tumorigenic potential. Therefore, it is crucial to develop new methods to eradicate CSCs in tumors. Herein, we develop a photodynamic therapy (PDT) that features bimodal metallacage-loaded nanoparticles (MNPs) for integrated chemotherapy. This platform achieves chemo-photodynamic combinational therapy. Organoplatinum(ii) metallacage-loaded nanoparticles show excellent ability to kill liver CSCs, decreasing their mobility and sphenoid formation ability under near-infrared laser irradiation. Importantly, MNPs can successfully penetrate into 3D tumor spheroids, which display higher drug resistance compared to traditional 2D cultured cells. This destroys CSCs and prevents subsequent tumor formation in vivo. With the excellent combinational therapeutic results in hand, the working mechanisms of MNPs were then studied. MNPs under NIR light irradiation can generate reactive oxygen species (ROS), resulting in damage of mitochondrial membrane and subsequent cell apoptosis with chemotherapeutic platinum. This study proves the great potential of MNPs for combinational cancer therapy, providing a new insight for the next generation of nanomedicines.
Substances chimiques
5,10,15,20-tetra(4-pyridyl)porphyrin
0
Antineoplastic Agents
0
Coordination Complexes
0
Photosensitizing Agents
0
Porphyrins
0
Reactive Oxygen Species
0
Platinum
49DFR088MY
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM