J Korean Assoc Maxillofac Plast Reconstr Surg.  1998 Nov;20(4):362-372.

A immunohistochemical study on heat shock protein in oral carcinogenesis in hamster

Affiliations
  • 1Department of Oral and Maxillofacial Surgery, School of Dentistry, Wonkwang University.

Abstract

Heat shock protein (HSP) expression is unregulated in tumor cells and, HSP expression is likely marker of the malignant potential of oral epithelial lesion. Furthermore, the 70kDa HSP is implicated in the degree of tumor differentiation, the rate of tumor proliferation and the magnitude of the anti-tumor immune response. Accordingly, the distribution and intensity of HSP 70 and HSP 47 expression was assessed in the DMBA induced oral carcinogenesis in hamster. Golden Syrian hamsters which were 3 months-age and 90-120g were collected. 9,10-dimethyl -1,2-benzanthracene (DMBA) in a 0.5% solution in mineral oil was painted on the buccal pouch mucosa 3 times per week in the study group. In each control and experimental groups of 6, 8, 10, 12, 14, 16, 18, 20 weeks, specimen were sectioned for immunohistochemical study with anti-HSP47 and anti-HSP70 antibody. The following results were obtained. 1. HSP47 positive cells were rare or negative of normal oral mucosa, increased mildly in basal and suprabasal basal layer, and spinous cell layer after experimental 6 weeks (dysplastic or CIS stage). In CIS stage, HSP47 expression is prominent in dysplastic free or normal adjacent epithelium. 2. HSP 47 positive cells in connective tissue were mainly inflammatory cells, which is gradually increased from control to precancerous and cancer stage. But HSP47 positive cells after 14 weeks were decreased , especially normal and cancer adjacent epithelium. 3. The positive staining cells of HSP70 in control, dysplastic, and CIS stage were not seen. But they were mild findings in basal layer and moderate findings in spinous layer after experimental 14 weeks (cancer stage). 4. HSP70 positive cells were increased in precancerous and cancer stage than control group in connective tissue. After experimental 16 weeks, we could not find the HSP expression in cancer cells according to cancer differentiation or cancer stage. It is concluded that HSP70 or HSP47 expression is not a definitive marker of oral malignancy or malignant potential. However, with further development, HSP immunoreactivity may be valuable as an adjunct to conventional histology for assessing the malignant potential of oral mucosal lesions.

Keyword

Oral carcinogenesis; epithelial dysplasia; squamous cell carcinoma; heat shock protein

MeSH Terms

9,10-Dimethyl-1,2-benzanthracene
Animals
Carcinogenesis*
Carcinoma, Squamous Cell
Connective Tissue
Cricetinae*
Epithelium
Heat-Shock Proteins*
Hot Temperature*
Mesocricetus
Mineral Oil
Mouth Mucosa
Mucous Membrane
Paint
9,10-Dimethyl-1,2-benzanthracene
Heat-Shock Proteins
Mineral Oil
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