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Cetuximab inhibits cisplatin-induced activation of EGFR signaling in esophageal squamous cell carcinomaopen access

Authors
Kwon, JunhyeYoon, Hyeon-JoonKim, Ji-HeeLee, Tae SupSong, In HoLee, Hae WonKang, Moon ChulPark, Jong Ho
Issue Date
Sep-2014
Publisher
SPANDIDOS PUBL LTD
Keywords
esophageal squamous cell carcinoma; epidermal growth factor receptor; cisplatin; cetuximab
Citation
ONCOLOGY REPORTS, v.32, no.3, pp 1188 - 1192
Pages
5
Journal Title
ONCOLOGY REPORTS
Volume
32
Number
3
Start Page
1188
End Page
1192
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/10811
DOI
10.3892/or.2014.3302
ISSN
1021-335X
1791-2431
Abstract
A malignant esophageal cancer, squamous cell carcinoma is one of the most prevalent cancers. Despite the use of present surgical techniques combined with various treatment modalities, the overall 5-year survival rate remains at 15-34%. Epidermal growth factor receptor (EGFR) is the most well studied receptor in various cancers and EGFR overexpression is detected in 40% of esophageal squamous cell carcinomas (ESCCs) and ESCC cell lines. To examine the EGFR antibody combination effect, we used treatment with cisplatin and cetuximab in ESCC cell lines, TE-4 and TE-8. Combination of cetuximab and cisplatin resulted in a growth inhibition only in the EGFR overexpressed TE-8 cell line. Furthermore, we confirmed that cisplatin-induced EGFR activation was inhibited by cetuximab in TE-8 but not in TE-4 cells. Our data suggest that cetuximab combined with cisplatin exerts antitumorigenic effects in vitro and in vivo via suppression of EGF signaling, which can be applied toward targeted ESCC treatments.
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