Expression of 70-kDa heat shock protein in oral lesions: marker of biological stress or pathogenicity

Citation
J. Kaur et al., Expression of 70-kDa heat shock protein in oral lesions: marker of biological stress or pathogenicity, ORAL ONCOL, 34(6), 1998, pp. 496-501
Citations number
18
Categorie Soggetti
Oncology
Journal title
ORAL ONCOLOGY
ISSN journal
13688375 → ACNP
Volume
34
Issue
6
Year of publication
1998
Pages
496 - 501
Database
ISI
SICI code
1368-8375(199811)34:6<496:EO7HSP>2.0.ZU;2-R
Abstract
We showed differential expression of HSP70 during oral tumorigenesis. The p recise functional role of HSP70 overexpression in the pathogenesis of betel and tobacco related oral cancer remains to be determined, To evaluate the utility of HSP70 as an indicator of the biological stress experienced by tu mour cells or the malignant potential of oral epithelial lesions and predic ting clinical outcome, its expression was assessed in different stages of o ral carcinogenesis by immunohistochemical analysis and correlated with clin icopathological parameters. Overexpression of HSP70 protein was observed in 38 of 64 (59%) dysplastic lesions and 92 of 125 (74%) oral squamous cell c arcinomas (SCCs) which included 76 of 105 cases (72%) of primary oral SCCs and 16 of 20 (80%) of recurrent oral SCCs. A significant correlation of HSP 70 expression was observed with severity of dysplasia (P = 0.0006767), poor histological differentiation of primary tumours (P = 0.0184348), increase primary tumour size (P = 0.0221103) and consumption of betel and tobacco (P < 0.01). Follow-up studies showed that in patients with premalignant lesio ns the median transition time (premalignancy to malignancy) was significant ly shorter in HSP70 overexpressing cases than those showing basal level of HSP70 (P = 0.012). Oral cancer patients with elevated levels of HSP70 showe d decreased median disease-free survival time (no recurrence/ metastasis) t han those showing basal HSP70 immunoreactivity (P = 0.0246). The results su ggest that HSP70 expression may not be a mere marker of biological stress b ut may also be implicated in the pathogenesis of oral cancer. (C) 1998 Else vier Science Ltd. All rights reserved.