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Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress.
- Source :
-
Toxicology letters [Toxicol Lett] 2016 Sep 06; Vol. 258, pp. 227-236. Date of Electronic Publication: 2016 Jul 05. - Publication Year :
- 2016
-
Abstract
- Application of cisplatin (DDP) for treating lung cancer is restricted due to its toxicity and lung cancer's drug resistance. In this study, we examined the effect of Jinfukang (JFK), an effective herbal medicine against lung cancer, on DDP-induced cytotoxicity in lung cancer cells. Morphologically, we observed that JFK increases DDP-induced pro-apoptosis in A549 cells in a synergistic manner. Transcriptome profiling analysis indicated that the combination of JFK and DDP regulates genes involved in apoptosis-related signaling pathways. Moreover, we found that the combination of JFK and DDP produces synergistic pro-apoptosis effect in other lung cancer cell lines, such as NCI-H1975, NCI-H1650, and NCI-H2228. Particularly, we demonstrated that AIFM2 is activated by the combined treatment of JFK and DDP and partially mediates the synergistic pro-apoptosis effect. Collectively, this study not only offered the first evidence that JFK promotes DDP-induced cytotoxicity, and activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress, but also provided a novel insight for improving cytotoxicity by combining JFK with DDP to treat lung cancer cells.<br /> (Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.)
- Subjects :
- A549 Cells
Adenocarcinoma, Bronchiolo-Alveolar drug therapy
Adenocarcinoma, Bronchiolo-Alveolar metabolism
Antineoplastic Agents pharmacology
Apoptosis Regulatory Proteins antagonists & inhibitors
Apoptosis Regulatory Proteins genetics
Apoptosis Regulatory Proteins metabolism
Cell Line, Tumor
Cisplatin pharmacology
Drug Resistance, Neoplasm
Drug Synergism
Gene Expression Profiling
Gene Expression Regulation, Neoplastic drug effects
Gene Regulatory Networks drug effects
Humans
Lung Neoplasms metabolism
Mitochondrial Proteins antagonists & inhibitors
Mitochondrial Proteins genetics
Mitochondrial Proteins metabolism
Neoplasm Proteins antagonists & inhibitors
Neoplasm Proteins genetics
Neoplasm Proteins metabolism
RNA Interference
RNA, Small Interfering
Antineoplastic Agents, Phytogenic pharmacology
Antineoplastic Combined Chemotherapy Protocols pharmacology
Apoptosis drug effects
Apoptosis Regulatory Proteins agonists
Drugs, Chinese Herbal pharmacology
Lung Neoplasms drug therapy
Mitochondrial Proteins agonists
Neoplasm Proteins agonists
Subjects
Details
- Language :
- English
- ISSN :
- 1879-3169
- Volume :
- 258
- Database :
- MEDLINE
- Journal :
- Toxicology letters
- Publication Type :
- Academic Journal
- Accession number :
- 27392435
- Full Text :
- https://doi.org/10.1016/j.toxlet.2016.07.002