Myricanol 5-fluorobenzyloxy ether regulation of survivin pathway inhibits human lung adenocarcinoma A549 cells growth in vitro.


Journal

BMC complementary medicine and therapies
ISSN: 2662-7671
Titre abrégé: BMC Complement Med Ther
Pays: England
ID NLM: 101761232

Informations de publication

Date de publication:
03 Sep 2020
Historique:
received: 04 03 2020
accepted: 28 08 2020
entrez: 5 9 2020
pubmed: 5 9 2020
medline: 6 5 2021
Statut: epublish

Résumé

This study aimed to explore the growth inhibitory effect of myricanol 5-fluorobenzyloxy ether (5FEM) and its underlying mechanisms in human lung adenocarcinoma A549 cells in vitro. 5FEM was obtained by the chemical modification of myricanol with fluorobenzyloxy ether at the OH(5) position. The cytotoxicity, cell apoptosis, cell cycle, mitochondrial membrane potential (ΔΨm), scratch test, colony formation, and the expression levels of the key survivin pathway-related genes in A549 were evaluated. 5FEM could significantly inhibit A549 cell growth; induce cell apoptosis; increase G0/G1 population; reduce ΔΨm; inhibit cell migration and colony formation; upregulate caspase-9, P21, and Bax expression levels; and downregulate PARP, survivin, and Bcl-2 expression level. These results enhanced our understanding of 5FEM and aid the discovery of novel myricanol derivatives as potential antitumor agents.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to explore the growth inhibitory effect of myricanol 5-fluorobenzyloxy ether (5FEM) and its underlying mechanisms in human lung adenocarcinoma A549 cells in vitro.
METHODS METHODS
5FEM was obtained by the chemical modification of myricanol with fluorobenzyloxy ether at the OH(5) position. The cytotoxicity, cell apoptosis, cell cycle, mitochondrial membrane potential (ΔΨm), scratch test, colony formation, and the expression levels of the key survivin pathway-related genes in A549 were evaluated.
RESULTS RESULTS
5FEM could significantly inhibit A549 cell growth; induce cell apoptosis; increase G0/G1 population; reduce ΔΨm; inhibit cell migration and colony formation; upregulate caspase-9, P21, and Bax expression levels; and downregulate PARP, survivin, and Bcl-2 expression level.
CONCLUSION CONCLUSIONS
These results enhanced our understanding of 5FEM and aid the discovery of novel myricanol derivatives as potential antitumor agents.

Identifiants

pubmed: 32883260
doi: 10.1186/s12906-020-03062-8
pii: 10.1186/s12906-020-03062-8
pmc: PMC7470448
doi:

Substances chimiques

Antineoplastic Agents 0
Diarylheptanoids 0
Survivin 0
myricanol 5-fluorobenzyloxy ether 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

269

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Auteurs

Guan-Hai Dai (GH)

Zhejiang Academy of Traditional Chinese Medicine, Institute of Basic Medicine, Hangzhou, 310007, China. daiguanhai@gmail.com.

Xuan Chen (X)

Zhejiang Academy of Traditional Chinese Medicine, Institute of Basic Medicine, Hangzhou, 310007, China.

Ze-Ming Ren (ZM)

Zhejiang Academy of Traditional Chinese Medicine, Institute of Basic Medicine, Hangzhou, 310007, China.

Chen-Jie Dai (CJ)

Zhejiang University-University of Edinburgh Institute, Zhejiang University, Haining, 314400, China.

Ye-Ling Tong (YL)

Zhejiang Academy of Traditional Chinese Medicine, Institute of Basic Medicine, Hangzhou, 310007, China.

Ke-Qun Chai (KQ)

Oncology Department, Tongde Hospital of Zhejiang Province, Hangzhou, 310012, China. ckq_official@163.com.

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Classifications MeSH