Fan Guo-Kang, Imanaka Masashi, Yang Beibei, Takenaka Hiroshi
Department of Otorhinolaryngology, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, Jie-fang Road 88, Hanghzhou, Zhejiang 310009, China.
Am J Rhinol. 2006 May-Jun;20(3):360-3. doi: 10.2500/ajr.2006.20.2851.
In nasal inverted papilloma (IP) and its malignant transformation process, abnormal cell growth has been regarded as a altered proliferation of the epithelial cells, while the role of programmed cell death in this process remains to be determined.
An apoptotic index was calculated, and the proliferation ability by using Ki67 as a marker was evaluated in the study subjects, which consisted of 15 cases of nasal chronic sinusitis, 23 cases of nasal IP, 9 cases of nasal IP with dysplasia, 8 cases of nasal IP with squamous cell carcinoma (SCC), and 21 cases of primary SCC. In addition, expressions of apoptosis-related molecules p53, Bcl-2, Bax, and Fas were investigated also.
The result showed that the Ki67 index increased in IP and IP with dysplasia. The Ki67 value was further enhanced in SCC within IP and primary SCC. The apoptotic index was low in IP with dysplasia, IP with SCC, and primary SCC. Concerning the expression of apoptosis-related proteins, p53 protein accumulated in IP with dysplasia, IP with SCC, and primary SCC. The p53 overexpression was directly correlated with the Ki67 index in IP and primary SCC diseases. No remarkable differences were found regarding expression of Bcl-2 and Fas productions among these diseases, and Bax protein was decreased only in primary SCC.
We concluded that inhibition of apoptosis could be an early sign of IP undergoing malignant transformation. A high proliferative rate was a characteristic of IP-associated malignant diseases.
在鼻腔内翻性乳头状瘤(IP)及其恶变过程中,异常细胞生长一直被认为是上皮细胞增殖改变,而程序性细胞死亡在此过程中的作用仍有待确定。
计算凋亡指数,并以Ki67为标志物评估研究对象的增殖能力,研究对象包括15例鼻慢性鼻窦炎、23例鼻腔IP、9例伴发育异常的鼻腔IP、8例伴鳞状细胞癌(SCC)的鼻腔IP以及21例原发性SCC。此外,还研究了凋亡相关分子p53、Bcl-2、Bax和Fas的表达。
结果显示,IP及伴发育异常的IP中Ki67指数升高。IP内的SCC及原发性SCC中Ki67值进一步升高。伴发育异常的IP、伴SCC的IP及原发性SCC的凋亡指数较低。关于凋亡相关蛋白的表达,p53蛋白在伴发育异常的IP、伴SCC的IP及原发性SCC中积聚。在IP和原发性SCC疾病中,p53过表达与Ki67指数直接相关。这些疾病中Bcl-2和Fas产物的表达未发现显著差异,仅原发性SCC中Bax蛋白减少。
我们得出结论,凋亡抑制可能是IP发生恶变的早期迹象。高增殖率是IP相关恶性疾病的一个特征。