Cimigenoside functions as a novel γ-secretase inhibitor and inhibits the proliferation or metastasis of human breast cancer cells by γ-secretase/Notch axis. (July 2021)
- Record Type:
- Journal Article
- Title:
- Cimigenoside functions as a novel γ-secretase inhibitor and inhibits the proliferation or metastasis of human breast cancer cells by γ-secretase/Notch axis. (July 2021)
- Main Title:
- Cimigenoside functions as a novel γ-secretase inhibitor and inhibits the proliferation or metastasis of human breast cancer cells by γ-secretase/Notch axis
- Authors:
- Jia, Hui
Liu, Mingyue
Wang, Xinying
Jiang, Qiyu
Wang, Shu
Santhanam, Ramesh Kumar
Lv, Chongning
Zhao, Qingchun
Lu, Jincai - Abstract:
- Abstract: Breast cancer (BC) occurrence and development tremendously affect female health. Currently breast cancer targeted drugs are still scarce. Natural products have become the main source of targeted drug for breast cancer due to low toxicity and high efficiency. Cimigenoside, natural compound isolated and purified from Cimicifuga dahurica (Turcz.) Maxim has been suggested to utilize for breast cancer treatment, however the mechanism of action has not been elucidated yet. In this article, the antitumor potential of Cimigenoside against breast cancer in vitro and in vivo study. Moreover, we further predicted the possible binding mode of Cimigenoside with γ-secretase through molecular docking studies. The results show that Cimigenoside has a significant inhibitory effect towards the proliferation or metastasis of breast cancer cells via suppressing the Notch signaling pathway-mediated mitochondrial apoptosis and EMT (epithelial mesenchymal transition). In terms of mechanism, Cimigenoside could inhibit the activation of PSEN-1, the catalytic subunit of γ-secretase, and also by cleaving the Notch protein mediated by PSEN-1. Overall, our findings provide scientific support to utilize Cimigenoside as an effective targeted drug for clinical treatment of BC. Graphical Abstract: ga1 Highlights: ● Cimigenoside inhibits the growth of human breast cancer in vivo and in vitro. ● Cimigenoside exerts anti-tumor activity by blocking Notch signaling pathway. ● Cimigenoside inhibits theAbstract: Breast cancer (BC) occurrence and development tremendously affect female health. Currently breast cancer targeted drugs are still scarce. Natural products have become the main source of targeted drug for breast cancer due to low toxicity and high efficiency. Cimigenoside, natural compound isolated and purified from Cimicifuga dahurica (Turcz.) Maxim has been suggested to utilize for breast cancer treatment, however the mechanism of action has not been elucidated yet. In this article, the antitumor potential of Cimigenoside against breast cancer in vitro and in vivo study. Moreover, we further predicted the possible binding mode of Cimigenoside with γ-secretase through molecular docking studies. The results show that Cimigenoside has a significant inhibitory effect towards the proliferation or metastasis of breast cancer cells via suppressing the Notch signaling pathway-mediated mitochondrial apoptosis and EMT (epithelial mesenchymal transition). In terms of mechanism, Cimigenoside could inhibit the activation of PSEN-1, the catalytic subunit of γ-secretase, and also by cleaving the Notch protein mediated by PSEN-1. Overall, our findings provide scientific support to utilize Cimigenoside as an effective targeted drug for clinical treatment of BC. Graphical Abstract: ga1 Highlights: ● Cimigenoside inhibits the growth of human breast cancer in vivo and in vitro. ● Cimigenoside exerts anti-tumor activity by blocking Notch signaling pathway. ● Cimigenoside inhibits the activation of the catalytic subunit PSEN-1 of γ-secretase. ● Cimigenoside is expected to become a potential therapeutic drug for breast cancer. … (more)
- Is Part Of:
- Pharmacological research. Volume 169(2021)
- Journal:
- Pharmacological research
- Issue:
- Volume 169(2021)
- Issue Display:
- Volume 169, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 169
- Issue:
- 2021
- Issue Sort Value:
- 2021-0169-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-07
- Subjects:
- Breast cancer -- Notch -- γ-secretase -- Apoptosis -- EMT -- PSEN-1
Pharmacology -- Periodicals
Pharmacology -- Periodicals
Research -- Periodicals
Médicaments -- Recherche -- Périodiques
Pharmacologie -- Périodiques
615.105 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10436618 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phrs.2021.105686 ↗
- Languages:
- English
- ISSNs:
- 1043-6618
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6446.550000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17248.xml