Abstract | OBJECTIVE: To explore the effects of Juglone on proliferation and apoptosis of human cervical cancer Caski cells, and to further study the related mechanism of cell apoptosis. METHODS: Cultured Caski cells were incubated with 20, 40, 60, 80 and 100 μmol/L juglone for 24 h. The proliferation of Caski cells was detected by methyl thiazolyl tetrazolium (MTT) assay. The cell apoptosis were detected by transmission electron microscope. The expression of Bcl-2 and Bax were detected by Western blot. RESULTS: MTT results showed that in different doses of juglone groups, the Caski cell growth was greatly inhibited (P < 0.05, P < 0.01) and showed dose dependent when compared with control group except 20 μmol/L. The IC50 of juglone was 42.4 μmol/L. After treatment on Caski cells with 40 μmol/L juglone, typical apoptosis characteristics was observed by transmission electronmicro scope. The expression of Bcl-2 was decreased while the expression of Bax was increased significantly when compared with control group (P < 0.05). CONCLUSION:
Juglone significantly inhibits the proliferation and induces the apoptosis of Caski cells in vitro.
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Authors | Wei Zhang, Yan Li, Jun Luo, Xingyu Zhao, Junjie Xu, Wenhe Zhu, Yanxia Jiang, Fang Fang |
Journal | Wei sheng yan jiu = Journal of hygiene research
(Wei Sheng Yan Jiu)
Vol. 43
Issue 6
Pg. 959-61, 971
(Nov 2014)
ISSN: 1000-8020 [Print] China |
PMID | 25603606
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- BAX protein, human
- Naphthoquinones
- bcl-2-Associated X Protein
- juglone
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Topics |
- Antineoplastic Agents, Phytogenic
(pharmacology)
- Apoptosis
(drug effects)
- Blotting, Western
- Cell Cycle
(physiology)
- Cell Proliferation
(drug effects)
- Female
- Humans
- Microscopy, Electron, Transmission
- Naphthoquinones
(pharmacology)
- Uterine Cervical Neoplasms
(drug therapy, metabolism)
- bcl-2-Associated X Protein
(metabolism)
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