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Human beta-defensin-1, -2, and -3 exhibit opposite effects on oral squamous cell carcinoma cell proliferation.

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.
AuthorsJochen Winter, Annette Pantelis, Rudolf Reich, Markus Martini, Dominik Kraus, Soeren Jepsen, Jean-Pierre Allam, Natalija Novak, Matthias Wenghoefer
JournalCancer investigation (Cancer Invest) Vol. 29 Issue 3 Pg. 196-201 (Mar 2011) ISSN: 1532-4192 [Electronic] England
PMID21280982 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DEFB1 protein, human
  • DEFB103A protein, human
  • DEFB4A protein, human
  • RNA, Messenger
  • beta-Defensins
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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