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Transforming growth factor-β3 mediated modulation of cell cycling and attenuation of 5-fluorouracil induced oral mucositis

  • S. T. Sonis
  • , A. G. Van Vugt
  • , J. P.O. Brien
  • , A. D. Muska
  • , A. M. Bruskin
  • , A. Rose
  • , J. D. Haley
  • Brigham and Women’s Hospital
  • Oncogene Science, Inc.

Research output: Contribution to journalArticlepeer-review

90 Scopus citations

Abstract

Mucositis is a common, dose-limiting complication in patients receiving cancer chemotherapy, which derives from damage to the epithelial cell layer. We have shown that transforming growth factor-β3 (TGF-β3) negatively regulates epithelial cell proliferation and reduces the incidence of oral mucositis. Here, we report the findings of a large study examining the effects of TGF-β3 administration in a hamster model on oral epithelial cell cycling in vivo, on oral mucositis, on weight retention and on survival. Topical application of TGF-β3 to the buccal mucosa significantly reduced basal cell proliferation, as measured by proliferating cell nuclear antigen (PCNA) immunohistochemistry and DNA ploidy. Administration of topical TGF-β3 prior to chemotherapy with 5-fluorouracil (5-FU) significantly reduced the severity of mucositis with respect to time, reduced chemotherapy-associated weight loss and increased survival.

Original languageEnglish
Pages (from-to)47-54
Number of pages8
JournalEuropean Journal of Cancer Part B: Oral Oncology
Volume33
Issue number1
DOIs
StatePublished - Jan 1997

Keywords

  • Chemoprotection
  • DNA ploidy
  • Epithelial cell proliferation
  • Oral mucositis
  • PCNA
  • Transformi8ng growth factor-beta

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