Abstract | OBJECTIVE: METHODS: PEO4 cells were maintained in DMEM medium with 10% neonatal bovine serum. Five days before the beginning of experiments, the cells were seeded in phenol red-free DMEM medium containing 5% charcoal dextran-treated FBS. The cells were harvested and seeded in 6-well culture plates or in 75ml flacks. After various concentration of NP, BisA and DBP treatment for 72h, the cells were harvested and detected mRNA and protein expression of PCNA, bcl-2 and bax by reverse transcription-polymerase chain reaction and immunohistochemistry, respectively. RESULTS: 32 x 10(-7) mol/L NP and 32 x 10(-7) mol/L BisA could significantly up-regulate PCNA and bcl-2 mRNA expression and down-regulate the bax mRNA expression, and 32 x 10(-6) mol/L DBP could up-regulate PCNA mRNA expression, but had no effect on bax and bcl-2 mRNA expression. These results were further confirmed by following immunohistochemistry. CONCLUSION:
PCNA, bcl-2 and bax pathway might involve in cell proliferation and apoptosis events by environmental estrogens in ovarian cancer PEO4 cells.
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Authors | Zengli Yu, Lishi Zhang, Desheng Wu |
Journal | Wei sheng yan jiu = Journal of hygiene research
(Wei Sheng Yan Jiu)
Vol. 33
Issue 4
Pg. 404-6
(Jul 2004)
ISSN: 1000-8020 [Print] China |
PMID | 15461258
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Benzhydryl Compounds
- Estrogens, Non-Steroidal
- Phenols
- Proliferating Cell Nuclear Antigen
- Proto-Oncogene Proteins c-bcl-2
- RNA, Messenger
- bcl-2-Associated X Protein
- Dibutyl Phthalate
- nonylphenol
- bisphenol A
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Topics |
- Apoptosis
(drug effects)
- Benzhydryl Compounds
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Dibutyl Phthalate
(pharmacology)
- Estrogens, Non-Steroidal
(pharmacology)
- Female
- Humans
- Ovarian Neoplasms
(metabolism, pathology)
- Phenols
(pharmacology)
- Proliferating Cell Nuclear Antigen
(genetics, metabolism)
- Proto-Oncogene Proteins c-bcl-2
(genetics, metabolism)
- RNA, Messenger
(genetics)
- bcl-2-Associated X Protein
(genetics, metabolism)
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