Emig R, Magener A, Ehemann V, Meyer A, Stilgenbauer F, Volkmann M, Wallwiener D, Sinn H P
Frauenklinik, Tübingen, Germany.
Br J Cancer. 1998 Dec;78(12):1661-8. doi: 10.1038/bjc.1998.739.
The p16 protein plays an important role in the transition of cells into the G1 phase of the cell cycle. We have studied the prevalence of p16 protein expression in breast carcinomas in a prospective series of 368 invasive and 52 non-invasive malignancies, as well as in 88 locally recurring tumours and three tumour cell lines. p16 protein expression was evaluated immunohistochemically on paraffin sections using monoclonal and polyclonal anti-p16 antibodies, and by immunoblotting of tumour cell suspensions. Tumour cell lines were also subjected to polymerase chain reaction-single strand polymorphism (PCR-SSCP) analysis and direct DNA sequencing. The results were compared with established prognostic parameters, DNA flow cytometry and p53 protein expression. In 33 (9%) invasive and two (4%) intraductal carcinomas, a cytoplasmic accumulation of the p16 protein was seen. These cases were characterized by poor histological grade of differentiation, loss of of oestrogen receptors and progesterone receptors and frequent overexpression of the p53 protein. In addition, breast carcinomas with aberrant p16 expression demonstrated a high proliferative activity, with median S-phase fractions 74% higher than in the control group and the median Ki67 fractions elevated to 75%. A genetic alteration of the p16 gene was not detectable in three analysed cell lines with cytoplasmic p16 expression applying PCR-SSCP and direct DNA sequencing. These results indicate that cytoplasmic accumulation of the p16 protein identifies a subset of highly malignant breast carcinomas with accelerated tumour proliferation and other unfavourable parameters in breast cancer. The described protein accumulation is apparently not caused by an alteration of the p16 gene.
p16蛋白在细胞进入细胞周期G1期的转变过程中发挥着重要作用。我们在一个前瞻性系列研究中,对368例浸润性和52例非浸润性恶性肿瘤、88例局部复发性肿瘤以及三种肿瘤细胞系中的乳腺癌p16蛋白表达情况进行了研究。使用单克隆和多克隆抗p16抗体,通过免疫组织化学方法在石蜡切片上评估p16蛋白表达,并通过对肿瘤细胞悬液进行免疫印迹分析。对肿瘤细胞系还进行了聚合酶链反应-单链多态性(PCR-SSCP)分析和直接DNA测序。将结果与既定的预后参数、DNA流式细胞术和p53蛋白表达进行比较。在33例(9%)浸润性癌和2例(4%)导管内癌中,可见p16蛋白的细胞质积聚。这些病例的特征为组织学分化程度差、雌激素受体和孕激素受体缺失以及p53蛋白频繁过度表达。此外,p16表达异常的乳腺癌表现出高增殖活性,S期分数中位数比对照组高74%,Ki67分数中位数升高至75%。应用PCR-SSCP和直接DNA测序,在三个具有细胞质p16表达的分析细胞系中未检测到p16基因的遗传改变。这些结果表明,p16蛋白的细胞质积聚可识别出一部分具有加速肿瘤增殖及其他乳腺癌不良参数的高恶性乳腺癌。所述的蛋白积聚显然不是由p16基因改变引起的。