RETRACTED: Ferruginol exhibits anticancer effects in OVCAR-3 human ovary cancer cells by inducing apoptosis, inhibition of cancer cell migration and G2/M phase cell cycle arrest (Retracted article. See vol. 23, 2021)

被引:22
作者
Xiong, Wen-Dong [1 ]
Gong, Jian [2 ,3 ]
Xing, Chao [2 ,3 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Obstet & Gynecol, Wenzhou 325027, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 2, Dept Clin Lab, 109 Xuyuan West Rd, Wenzhou 325027, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Yuying Childrens Hosp, 109 Xuyuan West Rd, Wenzhou 325027, Zhejiang, Peoples R China
关键词
ferruginol; cell cycle; apoptosis; ovarian cancer; cell migration; RESISTANCE;
D O I
10.3892/mmr.2017.7484
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The primary aim of the current study was to investigate the antitumor effects of ferruginol in OVCAR-3 human ovary cancer cells. The effects of ferruginol on cell apoptosis, cell migration and cell cycle phase distribution were also evaluated. Cell cytotoxicity induced by ferruginol was determined by an MTT assay, while fluorescence microscopy and transmission electron microscopy (TEM) were performed to investigate apoptotic effects. Flow cytometry was employed to determine the effects of ferruginol on the cell cycle and an in vitro wound healing assay was performed to investigate effects on cancer cell migration. The results indicated that ferruginol inhibited the growth rate of OVACR-3 cells in a dose-and time-dependent manner. When cells were treated with 20, 80 and 300 mu M ferruginol, cells began to exhibit yellow fluorescence, which indicated the onset of apoptosis. TEM results demonstrated that untreated control cells exhibited intact nuclei and nucleolus. However, on treating cells with various doses of ferruginol, chromatin condensation occurred and disappearance of the nuclear envelope and formation of apoptotic bodies were also observed. The percentage of migrated cells, determined by the wound healing assay, decreased from 98.7% in control to 68.2% and 45.3 in 80 and 300 mu M ferruginol-treated cells, respectively. Flow cytometry results demonstrated that ferruginol induced G2/M cell cycle arrest in OVCAR-3 cells. In conclusion, ferruginol may exhibit anticancer effects in OVCAR-3 human ovary cancer cells by inducing apoptosis, inhibiting cancer cell migration and inducing G2/M cell and may therefore prove beneficial in the treatment and management of ovarian cancer.
引用
收藏
页码:7013 / 7017
页数:5
相关论文
共 20 条
[1]   Ovarian cancer: Strategies for overcoming resistance to chemotherapy [J].
Agarwal, R ;
Kaye, SB .
NATURE REVIEWS CANCER, 2003, 3 (07) :502-516
[2]  
[Anonymous], KARAM JER TSONG HSIE
[3]   Gastroprotective activity of ferruginol in mice and rats:: effects on gastric secretion, endogenous prostaglandins and non-protein sulfhydryls [J].
Areche, Carlos ;
Theoduloz, Cristina ;
Yanez, Tania ;
Souza-Brito, Alba R. M. ;
Barbastefano, Victor ;
de Paula, Debora ;
Ferreira, Anderson L. ;
Schmeda-Hirschmann, Guillermo ;
Rodriguez, Jaime A. .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2008, 60 (02) :245-251
[4]   Cytotoxic Anticancer Candidates from Terrestrial Plants [J].
Chin, Young-Won ;
Yoon, Kee Dong ;
Kim, Jinwoong .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2009, 9 (08) :913-942
[5]   APOPTOSIS AND A REINVESTIGATION OF THE BIOLOGIC BASIS FOR CANCER-THERAPY [J].
DAMICO, AV ;
MCKENNA, WG .
RADIOTHERAPY AND ONCOLOGY, 1994, 33 (01) :3-10
[6]   Targeting apoptosis pathways in cancer therapy [J].
Fulda, S ;
Klaus-Michael, D .
CURRENT CANCER DRUG TARGETS, 2004, 4 (07) :569-576
[7]  
Green D.R., 2011, MEANS END APOPTOSIS
[8]   Anticancer drugs induce mdr1 gene expression in recurrent ovarian cancer [J].
Hille, Stephanie ;
Rein, Daniel T. ;
Riffelmann, Marion ;
Neumann, Rainer ;
Sartorius, Judith ;
Pfuetzner, Andreas ;
Kurbacher, Christian M. ;
Schoendorf, Thomas ;
Breidenbach, Martina .
ANTI-CANCER DRUGS, 2006, 17 (09) :1041-1044
[9]   Ferruginol Inhibits Non-Small Cell Lung Cancer Growth by Inducing Caspase-Associated Apoptosis [J].
Ho, Shang-Tse ;
Tung, Yu-Tang ;
Kuo, Yueh-Hsiung ;
Lin, Chi-Chen ;
Wu, Jyh-Horng .
INTEGRATIVE CANCER THERAPIES, 2015, 14 (01) :86-97
[10]  
JACKSON RC, 1989, ADV ENZYME REGUL, V29, P27, DOI 10.1016/0065-2571(89)90092-7