The p27 Kip1 protein is a negative regulator of the cell cycle and a potential tumor suppressor gene. Reduced expression of the p27 Kip1 protein has been reported in several human tumors and has been associated with higher tumor grade and increased mortality in breast, lung, colon, prostate, bladder
Reduced expression of cyclin-dependent kinase inhibitor p27Kip1 is an indicator of malignant behavior in oral squamous cell carcinoma
β Scribed by Yasusei Kudo; Takashi Takata; Wataru Yasui; Ikuko Ogawa; Mutsumi Miyauchi; Toshitsugu Takekoshi; Eiichi Tahara; Hiromasa Nikai
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 199 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
Reduced expression of the cyclin-dependent kinase inhibitor p27 Kip1 has been reported to correlate with poor survival in cohorts of breast and colorectal carcinoma patients. Posttranslational ubiquitin-mediated proteasomal proteolysis is related to p27 Kip1 protein levels. However, to the authors' knowledge, no previous study has examined the expression of p27 Kip1 in oral squamous cell carcinoma (OSCC).
METHODS.
To examine the expression of p27 Kip1 and its clinicopathologic roles in OSCC, the authors studied the expression of p27 Kip1 protein by immunohistochemistry in deparaffinized tissue sections of 20 normal oral mucosa specimens, 22 epithelial dysplasia specimens, and 70 OSCCs, and analyzed its correlation with clinicopathologic parameters. They also studied the expression of p27 Kip1 mRNA and protein in six OSCC cell lines by Northern blot and Western blot analysis. To examine the mechanism of reduced expression of p27 Kip1 , OSCC cell lines were treated with the proteasome inhibitor LLnV.
RESULTS.
All the normal oral mucosa specimens and 73% (16 of 22) of the oral epithelial dysplasia specimens expressed p27 Kip1 at high levels, whereas 87% of the OSCCs (61 of 70) showed reduced expression of p27 Kip1 . Furthermore, the levels of expression of this protein were significantly lower in carcinomas with metastasis than those without metastasis. Although OSCC cell lines expressed p27 Kip1 mRNA at various levels, most of them expressed p27 Kip1 protein at lower or undetectable levels. LLnV induced the expression of p27 Kip1 protein in HSC2 cells, in which p27 Kip1 protein was originally undetectable.
CONCLUSIONS. These findings suggest that 1) reduced expression of p27 Kip1 may correlate with the development and progression of OSCC and can be an indicator of malignant behavior of this neoplasm, and 2) increased proteasome-mediated degradation may play an important role in the reduction of p27 Kip1 protein expression.
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