Casticin inhibits stemness of hepatocellular carcinoma cells via disrupting the reciprocal negative regulation between DNMT1 and miR-148a-3p.


Journal

Toxicology and applied pharmacology
ISSN: 1096-0333
Titre abrégé: Toxicol Appl Pharmacol
Pays: United States
ID NLM: 0416575

Informations de publication

Date de publication:
01 06 2020
Historique:
received: 17 11 2019
revised: 21 03 2020
accepted: 04 04 2020
pubmed: 9 4 2020
medline: 21 8 2020
entrez: 9 4 2020
Statut: ppublish

Résumé

Casticin (CAS) is a polymethyl flavonoid from Fructus viticis and has multiple pharmacological activities, including anticancer. However, whether the molecular mechanism underlying CAS represses stemness characteristics in hepatocellular carcinoma (HCC) cells involves intervention in the reciprocal negative regulation between DNA methyltransferase 1 (DNMT1) and miR-148a-3p has not yet been reported. In this study, the effect of CAS on stemness characteristics of HCC cells and its mechanism were investigated. Results showed that CAS selectively reduced the viabilities of HCC cells but not L02 cells, as determined by CCK-8 assay. Importantly, the sub-cytotoxic concentrations of CAS could inhibit the stemness characteristics in HCC cells, as demonstrated by the expression of stemness biomarkers (CD44, EpCAM, Bmi1, Nanog, and Oct4), sphere forming assay, RT-qPCR, and Western blotting. In addition, CAS repressed DNMT1 activity and expression and increased miR-148a-3p. The effect of CAS on stemness characteristics was abolished by stable DNMT1 overexpression. MiR-148a-3p overexpression enhanced the reduction of CAS on stemness characteristics. DNMT1 overexpression promoted miR-148a-3p promoter hypermethylation as detected by methylation-specific PCR (MSP), which repressed its expression. Conversely, miR-148a-3p repressed DNMT1 expression by specific site binding to 3'-UTR of DNMT1 mRNA, as determined by luciferase assay. Moreover, the combination of CAS and agomir-148a-3p had robust effects on tumor suppression as compared to the sole activity of either molecule in nude mouse xenograft experiments in vivo. The findings suggested that CAS could inhibit stemness characteristics in HCC cells by interruption of the reciprocal negative regulation between DNMT1 and miR-148a-3p.

Identifiants

pubmed: 32268151
pii: S0041-008X(20)30122-8
doi: 10.1016/j.taap.2020.114998
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Flavonoids 0
MIRN148 microRNA, human 0
MicroRNAs 0
casticin 753GT729OU
DNA (Cytosine-5-)-Methyltransferase 1 EC 2.1.1.37
DNMT1 protein, human EC 2.1.1.37

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

114998

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no competing interests.

Auteurs

Xiang Li (X)

Department of Preclinical Medicine, Medical College, Hunan Normal University, Changsha 410013, China. Electronic address: lx58616@163.com.

Lianghou Wang (L)

Department of Preclinical Medicine, Medical College, Hunan Normal University, Changsha 410013, China.

Xiaocheng Cao (X)

Department of Pharmaceutical Science, Medical College, Hunan Normal University, Changsha 410013, China; Key Laboratory of Study and Discover of Small Targeted Molecules of Hunan Province, Medical College, Hunan Normal University, Changsha 410013, China.

Lingli Zhou (L)

Department of Preclinical Medicine, Medical College, Hunan Normal University, Changsha 410013, China.

Chang Xu (C)

Department of Pharmaceutical Science, Medical College, Hunan Normal University, Changsha 410013, China; Key Laboratory of Study and Discover of Small Targeted Molecules of Hunan Province, Medical College, Hunan Normal University, Changsha 410013, China.

Yinghong Cui (Y)

Department of Preclinical Medicine, Medical College, Hunan Normal University, Changsha 410013, China.

Yebei Qiu (Y)

Department of Pharmaceutical Science, Medical College, Hunan Normal University, Changsha 410013, China; Key Laboratory of Study and Discover of Small Targeted Molecules of Hunan Province, Medical College, Hunan Normal University, Changsha 410013, China.

Jianguo Cao (J)

Department of Pharmaceutical Science, Medical College, Hunan Normal University, Changsha 410013, China; Key Laboratory of Study and Discover of Small Targeted Molecules of Hunan Province, Medical College, Hunan Normal University, Changsha 410013, China. Electronic address: caojianguo2005@126.com.

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Classifications MeSH