Xue Q, Sano T, Kashiwabara K, Oyama T, Nakajima T
Second Department of Pathology, Gunma University School of Medicine, aebashi, Gunma 371-8511, Japan.
Jpn J Cancer Res. 2001 Mar;92(3):285-92. doi: 10.1111/j.1349-7006.2001.tb01093.x.
Expression of cell cycle regulatory proteins in both the RB and p53 pathways was investigated in 50 cases of squamous cell carcinoma (SCC) of the lung using immunohistochemical techniques. Abnormality of pRb and p16 expression was seen at the frequencies of 16% and 78%, respectively, and appeared to be in a reciprocal relationship. On the other hand, strong and diffuse p53 immunoreactivity was seen in 60% of SCCs. MDM2 and p14ARF expressions were each observed in about half of the cases of SCC and were not significantly associated with strong p53 immunoreactivity. Statistical analysis revealed that p14ARF expression was significantly correlated with both p16 and MDM2 expression. Moreover, strong p53 expression was not correlated with the expression of p21. In comparing clinicopathological status with the immunohistochemical results, lack of p16 immunoreactivity was observed in the elderly group (over 65 years) as compared with the younger group (less than 65 years). Strong p53 expression was frequently observed in higher stages of SCC, with the developing tumor located in the central field of the lung. Similarly, the frequency of p14ARF expression was high in centrally developed SCC, but low in SCC developed in the periphery. These results suggest that disruption of the RB and p53 pathways is a frequent event in SCC, and that abnormal expression of p16 and p53 plays a more critical role than that of pRB, p14ARF and MDM2 in the development of SCC of the lung.
采用免疫组化技术研究了50例肺鳞状细胞癌(SCC)中RB和p53通路中细胞周期调节蛋白的表达情况。pRb和p16表达异常的频率分别为16%和78%,且呈负相关关系。另一方面,60%的SCC中可见强烈弥漫性的p53免疫反应性。MDM2和p14ARF的表达在约半数SCC病例中均可观察到,且与强烈的p53免疫反应性无显著相关性。统计分析显示,p14ARF表达与p16和MDM2表达均显著相关。此外,强烈的p53表达与p21的表达无关。在比较临床病理状态与免疫组化结果时,与年轻组(小于65岁)相比,老年组(大于65岁)中观察到p16免疫反应性缺失。强烈的p53表达在SCC的较高分期中经常观察到,肿瘤位于肺中央区域。同样,p14ARF表达频率在中央型SCC中较高,而在周围型SCC中较低。这些结果表明,RB和p53通路的破坏在SCC中是常见事件,并且p16和p53的异常表达在肺SCC的发生发展中比pRB、p14ARF和MDM2发挥更关键的作用。