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Cited 14 time in webofscience Cited 17 time in scopus
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Therapeutic Effects of Recombinant Human Epidermal Growth Factor (rhEGF) in a Murine Model of Concurrent Chemo- and Radiotherapy-Induced Oral Mucositisopen access

Authors
Ryu, Seung-HeeKang, Ki MunMoon, Soo YoungChai, Gyu YoungHong, Joon PioCho, Kyoung-OhKang, Mun-IlChoi, Eun KyungLee, Sang-Wook
Issue Date
Sep-2010
Publisher
OXFORD UNIV PRESS
Keywords
Recombinant human epidermal growth factor (rhEGF); Mucositis; Concurrent chemo-and radiotherapy (CCRT); Ki-67; BALB; c mice
Citation
JOURNAL OF RADIATION RESEARCH, v.51, no.5, pp 595 - 601
Pages
7
Indexed
SCI
SCIE
SCOPUS
Journal Title
JOURNAL OF RADIATION RESEARCH
Volume
51
Number
5
Start Page
595
End Page
601
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/24964
DOI
10.1269/jrr.10069
ISSN
0449-3060
1349-9157
Abstract
Concurrent chemotherapy with radiotherapy (CCRT) has been applied for the treatment of advanced stage of head and neck cancer patients. However CCRT is associated with several complications including mucositis, dermatitis, stornatitis, etc. This study was conducted to evaluate the therapeutic effect of systemically administrated recombinant human epidermal growth factor (rhEGF) in CCRT-induced oral mucositis in a mouse model. Oral mucositis was induced in male BALB/c mice through combination treatment with cisplatin (11 mg/kg, i.p.) and irradiation (17 Gy) of the head and neck area. rhEGF (1.0 mg/kg/day for consecutive 3 days) was administered systemically, and the therapeutic effect was determined by histological evaluation of the oral mucosa. To elucidate optimal dose of rhEGF on CCRT-induced mucositis, various concentrations (0.04-3 mg/kg) of rhEGF were injected for 3 clays. Systemic rhEGF administration accelerated the recovery of body weight. Histologically, rhEGF-treated mice showed significantly increased epithelial cell layer thickness, basal cell number, and expression of -Ki-67 compared to control mice. Most effective dose was I mg/kg among other doses tested. Systemic administration of 1 mg/kg of rhEGF reduces the severity of oral mucositis induced by CCRT in a mouse model, suggesting that rhEGF can be used for treating CCRT-induced mucositis during the cancer treatment.
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