Stephenson T J, Royds J, Silcocks P B, Bleehen S S
Department of Pathology, University of Sheffield Medical School, U.K.
Br J Dermatol. 1992 Dec;127(6):566-70. doi: 10.1111/j.1365-2133.1992.tb14866.x.
The tumour suppressor gene p53, located on the short arm of chromosome 17, encodes for a nuclear protein which regulates cell proliferation by inhibiting cells entering S-phase. p53 mutations are alleged to be the commonest genetic abnormality in human cancer. We studied mutant p53 oncoprotein expression, using PAb1801 monoclonal antibody immunohistochemistry, in 25 'ideal' keratoacanthomas and 26 well-, 19 moderately and 18 poorly differentiated squamous cell carcinomas of the skin. While there was a highly significant trend in the proportion of p53 oncoprotein-positive lesions from keratoacanthomas to poorly differentiated squamous cell carcinomas (chi 2 = 17.13, df = 1, exact P = 0.00003), p53 expression was inadequate for distinguishing keratoacanthoma from well-differentiated squamous cell carcinoma (chi 2 = 2.55, df = 1, exact P = 0.18; corresponding to a sensitivity of 0.84 and a specificity of only 0.36).
肿瘤抑制基因p53位于17号染色体短臂,编码一种核蛋白,该蛋白通过抑制细胞进入S期来调节细胞增殖。p53突变被认为是人类癌症中最常见的基因异常。我们使用PAb1801单克隆抗体免疫组织化学方法,研究了25例“典型”角化棘皮瘤以及26例高分化、19例中分化和18例低分化皮肤鳞状细胞癌中的突变型p53癌蛋白表达情况。虽然从角化棘皮瘤到低分化鳞状细胞癌,p53癌蛋白阳性病变的比例存在极显著趋势(卡方检验χ² = 17.13,自由度df = 1,确切P值 = 0.00003),但p53表达不足以区分角化棘皮瘤与高分化鳞状细胞癌(卡方检验χ² = 2.55,自由度df = 1,确切P值 = 0.18;相应的敏感度为0.84,特异度仅为0.36)。