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Effect of Rice Cell-Derived Human Granulocyte-Macrophage Colony-Stimulating Factor on 5-Fluorouracil-Induced Mucositis in Hamsters

Authors
Won, Jong HoonJi, Jung EunAhn, Kyong HoonKim, Seok KyunChoi, Jong MinHa, Hae ChanKim, Hye MiYun, Chang KooHan, KyuboemKim, Dae Kyong
Issue Date
Mar-2013
Publisher
PHARMACEUTICAL SOC JAPAN
Keywords
granulocyte-macrophage colony-stimulating factor; mucositis; wound healing; hamster buccal pouch; plant-based expression system
Citation
BIOLOGICAL & PHARMACEUTICAL BULLETIN, v.36, no.3, pp 425 - 431
Pages
7
Journal Title
BIOLOGICAL & PHARMACEUTICAL BULLETIN
Volume
36
Number
3
Start Page
425
End Page
431
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/14800
DOI
10.1248/bpb.b12-00869
ISSN
0918-6158
1347-5215
Abstract
Granulocyte-macrophage colony-stimulating factor (GM-CSF) is an important regulator of the maturation and function of cells in the granulocyte and macrophage lineages, and also plays a significant role in wound healing. In a previous study, we expressed human GM-CSF in rice cells (rice cell-derived human GM-CSF; rhGM-CSF). The purpose of the present study was to evaluate its effect on wound healing in oral mucositis. Oral mucositis was induced in Syrian hamster cheek pouches by 5-fluorouracil treatment and mechanical scratching. Ulcerated areas were treated from days 3 to 14 with an application of 200 mu L saline, or of the same volume of a solution containing 0.04, 0.2, or 1 mu g/mL rhGM-CSF. Treatment of hamsters with rhGM-CSF reduced the ulcerated areas of the oral mucosa, compared with the control. Early in the healing process, the mucositis tissue layer of the rhGM-CSF-treated group showed significantly decreased myeloper-oxidase activity and increased numbers of proliferating cell nuclear antigen (PCNA)-positive cells. Treatment with rhGM-CSF also affected expression of inflammatory cytokines in the ulcerative mucosal tissue. These results demonstrate the efficacy of plant-produced rhGM-CSF in wound healing and have significant implications for the development of rhGM-CSF as a therapeutic agent for ulcerative oral mucositis.
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