Positive association of glucose-regulated protein 78 during oral cancer progression and the prognostic value in oral precancerous lesions

Background. Our aim was to examine the potential role of glucose‐regulated protein (GRP)78 during oral cancer progression and the prognostic value in oral precancerous lesions. Methods. A total of 204 patients with oral cancer and 86 with precancerous lesions were investigated. GRP78 expression was...

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Published inHead & neck Vol. 32; no. 8; pp. 1028 - 1039
Main Authors Lin, Chien-Yu, Chen, Wen-Ho, Liao, Chun-Ta, Chen, I-How, Chiu, Ching-Chi, Wang, Hung-Ming, Yen, Tzu-Chen, Lee, Li-Yu, Chang, Joseph Tung-Chieh, Cheng, Ann-Joy
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2010
Wiley
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Summary:Background. Our aim was to examine the potential role of glucose‐regulated protein (GRP)78 during oral cancer progression and the prognostic value in oral precancerous lesions. Methods. A total of 204 patients with oral cancer and 86 with precancerous lesions were investigated. GRP78 expression was determined in the lesion tissues by Western blot analysis. Association of GRP78 with clinicopathology or disease prognosis was examined using Fisher's exact, Kaplan–Meier, or Cox regression method. Results. Hyperexpression of GRP78 was found to be correlated with increasing malignant potential of oral lesions, with 14% in leukoplakia, 27% in erythroplakia, 50% in verrucous lesion, and 74% in oral cancer (p < .0001), suggesting this molecule plays a crucial role in the early steps of oral oncogenesis. In patients with precancerous lesions of the oral cavity, GRP78 expression predicts poorer same‐site premalignancy‐free survival (p = .002) and malignancy‐free survival rates (p = .002). Conclusion. Determination of GRP78 expression levels might enable a better risk stratification for patients with oral premalignant lesions. © 2009 Wiley Periodicals, Inc. Head Neck, 2010
Bibliography:Chang Gung Memorial Hospital - No. CMRPD160021
ArticleID:HED21287
ark:/67375/WNG-5W2KM1ZB-3
National Science Research Grant of Taiwan - No. NSC 95- 2314-B-182A-017; No. 96-2628-B-182A-099-MY2
istex:A93E326EBCFB0B9A1E06F3AF3076E3A09206C7C2
Chien‐Yu Lin and Wen‐Ho Chen contributed equally to this work.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1043-3074
1097-0347
DOI:10.1002/hed.21287