Abstract |
The objective of this study was to investigate the impact of human beta-defensins (hBDs) on oral squamous cell carcinoma (OSCC) proliferation and hBD expression in vitro. BHY-OSCC cell lines were stimulated with hBD-1, -2, and -3. Proliferation of BHY cells was ascertained and hBD- mRNA expression was evaluated by real-time PCR. Proliferation of BHY cells decreased by 25% in response to hBD-1 stimulation but increased after stimulation with hBD-2 and -3. HBD-1 stimulation enhanced hBD-3 expression, whereas HBD-2 stimulation decreased early hBD-3 expression. HBD-3 stimulation enhanced hBD-1 expression. HBDs profoundly impact on OSCC proliferation and hBD expression in vitro. Therefore, hBD-1 might function as a tumor suppressor gene in OSCCs, while hBD-2 and -3 might be protooncogenes.
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Authors | Jochen Winter, Annette Pantelis, Rudolf Reich, Markus Martini, Dominik Kraus, Soeren Jepsen, Jean-Pierre Allam, Natalija Novak, Matthias Wenghoefer |
Journal | Cancer investigation
(Cancer Invest)
Vol. 29
Issue 3
Pg. 196-201
(Mar 2011)
ISSN: 1532-4192 [Electronic] England |
PMID | 21280982
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DEFB1 protein, human
- DEFB103A protein, human
- DEFB4A protein, human
- RNA, Messenger
- beta-Defensins
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Topics |
- Carcinoma, Squamous Cell
(genetics, metabolism, pathology)
- Cell Line, Tumor
- Cell Proliferation
- Humans
- Mouth Neoplasms
(genetics, metabolism, pathology)
- RNA, Messenger
(analysis)
- Reverse Transcriptase Polymerase Chain Reaction
- beta-Defensins
(metabolism)
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