Expressions of junB and c-fos are enhanced in 4-nitroquinoline 1-oxide-induced rat tongue cancers

被引:11
|
作者
Ohyama, M
Hirayama, Y
Tanuma, J
Hirano, M
Semba, I
Shisa, H
Hiai, H
Sugihara, K
Kitano, M
机构
[1] Kagoshima Univ, Sch Dent, Dept Oral Pathol, Kagoshima 8908544, Japan
[2] Kagoshima Univ, Sch Dent, Dept Oral & Maxillofacial Surg 1, Kagoshima 8908544, Japan
[3] Saitama Canc Ctr, Res Inst, Lab Basic Canc Study, Saitama, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Pathol & Biol Dis, Kyoto, Japan
关键词
4-nitroquinoline 1-oxide (4NQO); c-fos; junB; rat tongue cancer; Tscc1;
D O I
10.1046/j.1440-1827.2003.01587.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Activator protein-1 (AP-1) is a transcription factor activated in many tumors. Using 4-nitroquinoline 1-oxide (4NQO)-induced rat tongue cancers (TC), the present study investigated the expression levels of genes that encode the components of AP-1, the jun gene family (c-jun, junB and junD) and the fos gene family (c-fos, fra-1, fra-2 and fosB). Expression levels of junB and c-fos mRNAs in TC were significantly elevated compared with those in epithelial tissue of control rat tongue, although only c-fos mRNA levels tended to be elevated in dysplastic tongue epithelium. Histologically, all 4NQO-induced rat TC were well-differentiated squamous cell carcinomas. Immunostaining for JunB and c-Fos proteins was positive in the nuclei of tumor cells of all TC. It is noteworthy that JunB was negative, but c-Fos was positive in the dysplastic tongue epithelium of the 4NQO-treated rats. Immunostaining for both proteins was negative in tongue mucosal epithelium of control rats. There were no mutations in the coding regions of either junB or c-fos in all the TC examined. These results suggest the possibility that the expressions of junB and c-fos were enhanced stepwise in 4NQO-induced carcinogenesis of rat tongue, and that the coexpression of JunB and c-Fos might play an important role in the establishment of TC.
引用
收藏
页码:35 / 40
页数:6
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