Toll-like Receptor 5 Agonist Protects Mice From Dermatitis and Oral Mucositis Caused by Local Radiation: Implications for Head-and-Neck Cancer Radiotherapy

被引:93
作者
Burdelya, Lyudmila G. [1 ]
Gleiberman, Anatoli S. [2 ]
Toshkov, Ilia [2 ]
Aygun-Sunar, Semra [1 ]
Bapardekar, Meghana [2 ]
Manderscheid-Kern, Patricia [1 ]
Bellnier, David [1 ]
Krivokrysenko, Vadim I. [2 ]
Feinstein, Elena [2 ]
Gudkov, Andrei V. [1 ,2 ]
机构
[1] Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA
[2] Cleveland BioLabs Inc, Buffalo, NY USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2012年 / 83卷 / 01期
基金
美国国家卫生研究院;
关键词
Radiotherapy; Flagellin; Mucositis; Dermatitis; Inflammation; AMIFOSTINE; MOUSE; TOLL-LIKE-RECEPTOR-5; RADIOPROTECTOR; TUMOR; MODEL;
D O I
10.1016/j.ijrobp.2011.05.055
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Development of mucositis is a frequent side effect of radiotherapy of patients with head-and-neck cancer. We have recently reported that bacterial flagellin, an agonist of Toll-like receptor 5 (TLR5), can protect rodents and primates from acute radiation syndrome caused by total body irradiation. Here we analyzed the radioprotective efficacy of TLR5 agonist under conditions of local, single dose or fractionated radiation treatment. Methods and Materials: Mice received either single-dose (10, 15, 20, or 25 Gy) or fractioned irradiation (cumulative dose up to 30 Gy) of the head-and-neck area with or without subcutaneous injection of pharmacologically optimized flagellin, CBLB502, 30 min before irradiation. Results: CBLB502 significantly reduced the severity of dermatitis and mucositis, accelerated tissue recovery, and reduced the extent of radiation induced weight loss in mice after a single dose of 15 or 20 Gy but not 25 Gy of radiation. CBLB502 was also protective from cumulative doses of 25 and 30 Gy delivered in two (10 + 15 Gy) or three (3 x 10 Gy) fractions, respectively. While providing protection to normal epithelia, CBLB502 did not affect the radiosensitivity of syngeneic squamous carcinoma SCCVII grown orthotopically in mice. Use of CBLB502 also elicited a radiation independent growth inhibitory effect upon TLR5-expressing tumors demonstrated in the mouse xenograft model of human lung adenocarcinoma A549. Conclusion: CBLB502 combines properties of supportive care (radiotherapy adjuvant) and anticancer agent, both mediated via activation of TLR5 signaling in the normal tissues or the tumor, respectively. (C) 2012 Elsevier Inc.
引用
收藏
页码:228 / 234
页数:7
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