Shimada Mai, Kitagawa Kyoko, Dobashi Yoh, Isobe Tomoyasu, Hattori Takayuki, Uchida Chiharu, Abe Kenji, Kotake Yojiro, Oda Toshiaki, Suzuki Hiroyuki, Hashimoto Kenji, Kitagawa Masatoshi
Department of Biochemistry 1, Hamamatsu University School of Medicine, Higashi-ku, Hamamatsu, Shizuoka, Japan.
Cancer Sci. 2009 May;100(5):866-72. doi: 10.1111/j.1349-7006.2009.01122.x.
Downregulation of the cyclin-dependent kinase inhibitory protein p27 is frequently observed in various cancers due to enhancement of its degradation. We recently reported that p53-inducible protein with RING-H2 domain (Pirh2) is a novel ubiquitin ligase for p27, required for the ubiquitylation and consequent degradation of p27 protein. However, there is no reports about the involvement of Pirh2 in both p27 downregulation and pathogenesis in human cancers. In the present study, we investigated them using cultured cell lines and surgical specimens derived from human head and neck squamous cell carcinoma (HNSCC). Depletion of Pirh2 by short interfering RNA induced accumulation of p27 and inhibited the growth of cultured HNSCC cells. By immunohistochemical analysis in 57 cases of HNSCC specimens, higher levels of Pirh2 expression (labeling index > or = 60%) were found in 61.4% of HNSCC in comparison with 0% of normal mucosa. In addition, 83.3% of HNSCC with lower p27 expression (labeling index < 20%) displayed high Pirh2 levels. Therefore, Pirh2 expression was inversely correlated with p27 expression. Finally, Pirh2 expression was well correlated with poor prognosis. These findings suggest that Pirh2 overexpression may have an important role in the development and maintenance of HNSCC at least partially through p27 degradation, and that Pirh2 may be a potential molecular target for human HNSCC.
细胞周期蛋白依赖性激酶抑制蛋白p27的下调在各种癌症中经常可见,这是由于其降解增强所致。我们最近报道,含RING-H2结构域的p53诱导蛋白(Pirh2)是p27的一种新型泛素连接酶,是p27蛋白泛素化及随后降解所必需的。然而,尚无关于Pirh2参与人类癌症中p27下调和发病机制的报道。在本研究中,我们使用源自人头颈部鳞状细胞癌(HNSCC)的培养细胞系和手术标本对它们进行了研究。通过短发夹RNA使Pirh2缺失可诱导p27蓄积,并抑制培养的HNSCC细胞生长。通过对57例HNSCC标本进行免疫组织化学分析,发现61.4%的HNSCC中Pirh2表达水平较高(标记指数≥60%),而正常黏膜中这一比例为0%。此外,83.3%的p27表达较低(标记指数<20%)的HNSCC显示Pirh2水平较高。因此,Pirh2表达与p27表达呈负相关。最后,Pirh2表达与预后不良密切相关。这些发现表明,Pirh2过表达可能至少部分通过p27降解在HNSCC的发生和维持中起重要作用,并且Pirh2可能是人类HNSCC的一个潜在分子靶点。