Abstract Title:

Inhibition of oral mucosal cell wound healing by bisphosphonates.

Abstract Source:

J Oral Maxillofac Surg. 2008 May;66(5):839-47. PMID: 18423269

Abstract Author(s):

Regina Landesberg, Matthew Cozin, Serge Cremers, Victoria Woo, Stavroula Kousteni, Satrajit Sinha, LeeAnn Garrett-Sinha, Srikala Raghavan

Article Affiliation:

Columbia University, College of Dental Medicine, Division of Oral and Maxillofacial Surgery, New York, NY 10032, USA. rl351@columbia.edu


PURPOSE: Bisphosphonates (BPs) are a widely used class of drugs that are effective in the treatment and prevention of osteoporosis, hypercalcemia of malignancy, and bone metastases associated with multiple myeloma, breast cancer, and other solid tumors. In the past several years there have been numerous reports describing the occurrence of osteonecrosis of the jaws (ONJ) associated with these drugs. Whether the ONJ lesion initiates in the oral mucosa or derives from the underlying bone is not well understood. In this report we describe the effect of pamidronate, a second-generation BP, on oral mucosal cells. MATERIALS AND METHODS: Murine oral keratinocytes were isolated and exposed to pamidronate at a range of clinically relevant doses. Cellular proliferation was measured using a MTS/PMS reagent-based kit and wound healing was examined with a scratch assay. To determine whether oral keratinocytes undergo apoptosis following exposure to pamidronate, TUNEL, caspase-3, and DAPI apoptosis assays were performed. RESULTS: We show that BP pretreatment of oral mucosal cells inhibits proliferation and wound healing at clinically relevant doses, and that this inhibition is not due to cellular apoptosis. CONCLUSIONS: To our knowledge this is the first report investigating the effect of nitrogen-containing BPs on oral mucosal cells. This study suggests that BPs inhibit oral keratinocyte wound healing which may play a significant role in the initiation of ONJ.

Study Type : In Vitro Study

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