Rikkunshito attenuates induction of epithelial-mesenchymal switch via activation of Sirtuin1 in ovarian cancer cells.


Journal

Endocrine journal
ISSN: 1348-4540
Titre abrégé: Endocr J
Pays: Japan
ID NLM: 9313485

Informations de publication

Date de publication:
28 Apr 2020
Historique:
pubmed: 17 12 2019
medline: 9 3 2021
entrez: 17 12 2019
Statut: ppublish

Résumé

Rikkunshito, a traditional Japanese herbal medicine, improves appetite via activation of gastrointestinal hormone ghrelin pathway. The function of ghrelin is mediated by growth hormone secretagogue receptor (GHSR1a), and ghrelin has been known to possess diverse physiological functions including growth suppression of some cancer cells. Considering that increased ghrelin signaling by Rikkunshito could enhance sirtuin1 (SIRT1) activity in nervous system, we aimed to investigate the effect of Rikkunshito in ovarian cancer cells. Ovarian cancer cell lines were treated with Rikkunshito, and cellular viability, gene expressions and epithelial-mesenchymal transition (EMT) status were investigated. To investigate the involvement of SIRT1 by Rikkunshito in SKOV3 cancer cells, endogenous expression of SIRT1 was depleted using small interfering RNA (siRNA). Treatment with Rikkunshito elevated ghrelin, GHSR1a and SIRT1, while cellular viability was decreased. The treatment of Rikkunshito also inhibited cellular migration and invasion status in a dose-dependent manner, and these effects were translated to the enhanced EMT status, although the role of SIRT1 was not determined. Our study revealed a novel function of Rikkunshito in enhancing EMT status of ovarian cancer cells. Therefore, we would like to propose that Rikkunshito may be used as a novel adjunctive therapy in chemotherapy of ovarian cancer because platinum-based chemotherapy frequently used for the treatment of ovarian cancer inevitably impairs appetite.

Identifiants

pubmed: 31839623
doi: 10.1507/endocrj.EJ19-0368
doi:

Substances chimiques

Antigens, CD 0
CDH2 protein, human 0
Cadherins 0
Drugs, Chinese Herbal 0
Ghrelin 0
Ghsr1a protein, human 0
Receptors, Ghrelin 0
VIM protein, human 0
Vimentin 0
liu-jun-zi-tang 0
SIRT1 protein, human EC 3.5.1.-
Sirtuin 1 EC 3.5.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

379-386

Auteurs

Ranka Kanda (R)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

Yuko Miyagawa (Y)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

Osamu Wada-Hiraike (O)

Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.

Haruko Hiraike (H)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

Shiho Fukui (S)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

Kazunori Nagasaka (K)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

Eiji Ryo (E)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

Tomoyuki Fujii (T)

Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.

Yutaka Osuga (Y)

Department of Obstetrics and Gynecology, The University of Tokyo, Tokyo, Japan.

Takuya Ayabe (T)

Department of Obstetrics and Gynecology, Teikyo University School of Medicine, Tokyo, Japan.

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Classifications MeSH