Induction of apoptosis by Xiakemycin A in human hepatoma HepG2 cells.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
Apr 2020
Historique:
entrez: 26 4 2020
pubmed: 26 4 2020
medline: 10 5 2020
Statut: ppublish

Résumé

Xiakemycin A (XKA), a new antibiotic in the pyranonaphthoquinone family, shows antitumor activity. However, the type of cell death induced by XKA remains elusive. In this study, we aim to investigate the type of death induced by XKA in hepatic cancer.The apoptotic features, such as chromatic agglutination, reactive oxygen species generation and membrane potential of mitochondria, in HepG2 cells treated by XKA were measured by Hoechst 33342 staining and flow cytometry. Apoptosis of HepG2 cells treated with XKA was determined by Annexin V-FITC/propidium iodide double staining and Western blot analysis, respectively.XKA had a significant dose-dependent elevation of chromatic agglutination, reactive oxygen species generation, Annexin V and propidium iodide staining, decrease of membrane potential. Meanwhile, in apoptotic HepG2 cells induced by XKA, robust increment was noticed in p53 expression, cleavage of PARP, caspase-3, and caspase-9.XKA showed potent inhibitory effects on the proliferation of HepG2 cells. Such phenomenon may be related to activation of the apoptotic pathway.

Identifiants

pubmed: 32332640
doi: 10.1097/MD.0000000000019848
pii: 00005792-202004240-00051
pmc: PMC7220762
doi:

Substances chimiques

Annexin A5 0
Antineoplastic Agents 0
Naphthoquinones 0
Reactive Oxygen Species 0
xiakemycin A 0
Propidium 36015-30-2
PARP1 protein, human EC 2.4.2.30
Poly (ADP-Ribose) Polymerase-1 EC 2.4.2.30
CASP3 protein, human EC 3.4.22.-
CASP9 protein, human EC 3.4.22.-
Caspase 3 EC 3.4.22.-
Caspase 9 EC 3.4.22.-

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e19848

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Auteurs

Chuan Chen (C)

Faculty of Basic Medical Sciences, Jiujiang University, Jiujiang.

Zhu Han (Z)

Department of Biological and Chemical Engineering, Jingdezhen University, Jingdezhen.

Minjie Yang (M)

Faculty of Nursing, Jiujiang University, Jiujiang.

Zhongke Jiang (Z)

Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, and Chinese Academy of Medical Sciences.

Xiuyuan Ou (X)

Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

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Classifications MeSH