Abstract | BACKGROUND:
Ovarian cancer is the first leading cause of death among gynecologic malignancies worldwide. Discovery of new chemotherapeutic drugs is still imperative for the improvement of the survival rate. PURPOSE: METHODS: MTT assay was performed to evaluate cell viability after treatment with AB23, along with flow cytometry for apoptosis and cell cycle analysis. Western blotting was conducted to determine the relative protein level. Wound healing and transwell assays were performed to investigate the effect of AB23 on cell migration and invasion. RESULTS: AB23 obviously inhibited proliferation of the three ovarian cancer cell lines, down-regulated the protein levels of CDK4, CDK6, and cyclin D1, and blocked the cell cycle progressions in G1 phase. Meanwhile, AB23 induced accumulation of the sub-G1 phase in the three cell lines in a concentration dependent manner. The protein levels of cleaved poly ADP-ribose polymerase (PARP) and the ratio of Bax/Bcl-2 were up-regulated after treatment with AB23. Further study showed that AB23 induced endoplasmic reticulum stress through IRE1 signaling pathway and silencing of IRE1α partially enhanced AB23-induced apoptosis. Wound healing and transwell assays showed that AB23 could also suppress the migration and invasion of HEY cells. Moreover, it down-regulated the protein levels of matrix metalloproteinases MMP-2 and MMP-9. CONCLUSION: AB23 possessed anti-proliferation, anti-migration and anti-invasion activities as a single agent on ovarian cancer cells.
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Authors | Le-Le Zhang, Yu-Lian Xu, Zheng-Hai Tang, Xiao-Huang Xu, Xin Chen, Ting Li, Chun-Yong Ding, Ming-Qing Huang, Xiu-Ping Chen, Yi-Tao Wang, Xiao-Feng Yuan, Jin-Jian Lu |
Journal | Phytomedicine : international journal of phytotherapy and phytopharmacology
(Phytomedicine)
Vol. 23
Issue 8
Pg. 800-9
(Jul 15 2016)
ISSN: 1618-095X [Electronic] Germany |
PMID | 27288915
(Publication Type: Journal Article)
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Copyright | Copyright © 2016 Elsevier GmbH. All rights reserved. |
Chemical References |
- Antineoplastic Agents, Phytogenic
- Cholestenones
- Neoplasm Proteins
- alisol B 23-acetate
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Topics |
- Antineoplastic Agents, Phytogenic
(pharmacology)
- Apoptosis
(drug effects)
- Cell Cycle Checkpoints
(drug effects)
- Cell Line, Tumor
- Cell Movement
(drug effects)
- Cholestenones
(pharmacology)
- Drug Resistance, Neoplasm
- Female
- G1 Phase
(drug effects)
- Humans
- Neoplasm Invasiveness
- Neoplasm Proteins
(antagonists & inhibitors, biosynthesis)
- Ovarian Neoplasms
(drug therapy, pathology)
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