Effect of selective inhibitors of inflammation on oral mucositis: Preclinical studies

被引:39
作者
Haagen, Julia [1 ]
Krohn, Hanna [1 ]
Roellig, Sophie [1 ]
Schmidt, Margret [1 ]
Wolfram, Kathrin [1 ]
Doerr, Wolfgang [1 ,2 ]
机构
[1] Tech Univ Dresden, Med Fac Carl Gustav Carus, Dept Radiotherapy & Radiat Oncol, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Med Fac Carl Gustav Carus, Expt Ctr, D-01307 Dresden, Germany
关键词
Oral mucositis; Fractionated irradiation; Animal model; Anti-inflammation; Tumor necrosis factor-alpha; Cyclooxygenase-2; BONE-MARROW-TRANSPLANTATION; NECK-CANCER; RADIATION; HEAD; PENTOXIFYLLINE; INDOMETHACIN; RADIOTHERAPY; ESOPHAGITIS; TOXICITIES; ACTIVATION;
D O I
10.1016/j.radonc.2009.06.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Oral mucositis is a severe, dose-limiting side effect of radio(chemo)therapy for head and neck tumors. The epithelial radiation response (ulceration) is accompanied by inflammatory changes. Their interaction with the epithelial processes remains unclear. The present study was initiated to determine the effect of inhibition of TNF-alpha or COX-2 on the epithelial radiation response in the mouse tongue model. Methods: Daily fractionated irradiation was given with 5 x 3 Gy/week over one (days 0-4) or two weeks (days 0-4, 7-11). Each protocol was terminated by graded test doses (5 dose groups, 10 animals each) to a defined area of the lower tongue surface to generate full dose-effect curves for mucosal ulceration. A TNF-alpha inhibiting antibody (Infliximab) or a COX-2 inhibitor (Celecoxib) was administered. Results: No effect of Infliximab or Celecoxib was found in any of the protocols. Isoeffective doses for ulcer induction were unchanged. Also, the time course of the response was largely unaffected. Conclusions: Inhibition of TNF-alpha or COX-2, two dominating inflammatory pathways, did not result in modulation of the response of oral epithelium during fractionated irradiation. This suggests that the inflammatory changes mediated through TNF-alpha or COX-2 are not relevant for the epithelial radiation response of oral mucosa. (C) 2009 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 92 (2009) 472-476
引用
收藏
页码:472 / 476
页数:5
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