Abstract | OBJECTIVE: METHODS: The mRNA expression levels of STAT3, cyclin D1 and p42/44MAPK were detected in a human epidermal carcinoma cell line A431 by RT-PCR. Their expressions at protein level were studied by Western blot. The expression levels were studied in cells treated with or without 10(-5) mol/L acitretin at different time intervals. RESULTS: (1) Acitretin could significantly inhibit the expression of STAT3 and cyclin D1 mRNA in a time-dependent manner (P < 0.05). The STAT3 and cyclin D1 protein expression levels were down-regulated. Acitretin could also down-regulate the p42/4MAPK mRNA expression. (2) After incubation with acitretin, the mRNA level of cyclin D1 cells was positively correlated with that of STAT3 (P < 0.05). The cyclin D1 protein level was also positively correlated with that of STAT3 (P < 0.05). However there was no correlation of mRNA levels between cyclin D1 and p42/44MAPK. CONCLUSION: Regulation of the Jak/STAT3 signaling pathway may play an important role in the effect of acitretin on epidermal squamous-cell carcinoma cells. The abnormal expression of STAT3 can be regarded as a prerequisite for acitretin treatment effect.
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Authors | Sui-qing Cai, Li-rong Chen, Min Zheng |
Journal | Zhonghua zhong liu za zhi [Chinese journal of oncology]
(Zhonghua Zhong Liu Za Zhi)
Vol. 28
Issue 1
Pg. 21-4
(Jan 2006)
ISSN: 0253-3766 [Print] China |
PMID | 16737614
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- RNA, Messenger
- STAT3 Transcription Factor
- STAT3 protein, human
- Cyclin D1
- Mitogen-Activated Protein Kinase 1
- Mitogen-Activated Protein Kinase 3
- Acitretin
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Topics |
- Acitretin
(pharmacology)
- Antineoplastic Agents
(pharmacology)
- Carcinoma, Squamous Cell
(metabolism, pathology)
- Cell Line, Tumor
- Cyclin D1
(biosynthesis, genetics)
- Down-Regulation
- Gene Expression Regulation, Neoplastic
- Humans
- Mitogen-Activated Protein Kinase 1
(biosynthesis, genetics)
- Mitogen-Activated Protein Kinase 3
(biosynthesis, genetics)
- RNA, Messenger
(biosynthesis, genetics)
- STAT3 Transcription Factor
(biosynthesis, genetics)
- Signal Transduction
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