PEROXIREDOXIN IV PROTECTS CELLS FROM RADIATION-INDUCED APOPTOSIS IN HEAD-AND-NECK SQUAMOUS CELL CARCINOMA
- Authors
- Park, Jung Je; Chang, Hyo Won; Jeong, Eun-Jeong; Roh, Jong-Lyel; Choi, Seung-Ho; Jeon, Sea-Yuong; Ko, Gyung Hyuck; Kim, Sang Yoon
- Issue Date
- 15-Mar-2009
- Publisher
- ELSEVIER SCIENCE INC
- Keywords
- Peroxiredoxin IV; Radiation seisitivity; Apoptosis; Reactive oxygen species; Head-and-neck cancer
- Citation
- INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, v.73, no.4, pp 1196 - 1202
- Pages
- 7
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
- Volume
- 73
- Number
- 4
- Start Page
- 1196
- End Page
- 1202
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/26365
- DOI
- 10.1016/j.ijrobp.2008.10.070
- ISSN
- 0360-3016
1879-355X
- Abstract
- Purpose: Human peroxiredoxins (Prxs) are known as a family of thiol-specific antioxidant enzymes, among which Prx-I and -II play an important role in protecting cells from irradiation-induced cell death. It is not known whether Prx-IV also protects cells from ionizing radiation (IR). Methods and Materials: To evaluate the protective role of Prx-IV in IR, we transfected full-length Prx-IV cDNA into AMC-HN3 cells, which weakly express endogenous Prx-IV, and knocked down the expression of Prx-IV with siRNA methods using AMC-HN7 cells, which express high levels of endogenous Prx-IV. Radiosensitivity profiles in these cells were evaluated using clonogenic assay, FACS analysis, cell viability, and TUNEL assay. Results: Three Prx-IV expressing clones were isolated. Prx-IV regulated intracellular reactive oxygen species (ROS) levels and made cells more resistant to IR-induced apoptosis. Furthermore, the knockdown of Prx-IV with siRNA made cells more sensitive to IR-induced apoptosis. Conclusion: The results of these studies suggest that Prx-IV may play an important role in protecting cells from IR-induced apoptosis in head-and-neck squamous cell carcinoma. (C) 2009 Elsevier Inc.
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