Tollenaar R A, van Krieken J H, van Slooten H J, Bruinvels D J, Nelemans K M, van den Broek L J, Hermans J, van Dierendonck J H
Department of Surgery, Leiden University Medical Center, The Netherlands.
Br J Cancer. 1998 Jun;77(11):1842-7. doi: 10.1038/bjc.1998.306.
To evaluate the prognostic significance of immunohistochemically detected p53 and Bcl-2 proteins in colorectal cancer, tissue sections from 238 paraffin-embedded colorectal carcinomas were immunostained for p53 (MAb DO-7 and CM-1 antiserum) and Bcl-2 (MAb Bcl-2:124). Staining patterns were assessed semiquantitatively and correlated with each other and with sex, age, tumour site, Dukes' classification, tumour differentiation, mucinous characteristics, lymphocyte and eosinophilic granulocyte infiltration, and patient survival. In our series, 35% of carcinomas showed no nuclear staining and 34% (DO-7) to 40% (CM-1) showed staining in over 30% of tumour cell nuclei. A majority of carcinomas that had been immunostained with CM-1 showed cytoplasmic staining, but this was not observed with DO-7. With respect to Bcl-2, 51% of tumours were completely negative, 32% displayed weak and 15% moderate staining; only 3% showed strong positive staining. No evidence was found for reciprocity between Bcl-2 expression and nuclear p53 accumulation. From 13 cases containing tumour-associated adenoma, four were Bcl-2 negative in premalignant and malignant cells, in another four cases these cells showed similar staining intensities and in the remaining cases only the malignant colorectal cells were Bcl-2 negative. Therefore, our data indicate that Bcl-2 is dispensable in the progression towards carcinoma. Except for an association between nuclear p53 accumulation and mucinous tumours (P = 0.01), no significant correlation was found between the clinicopathological parameters mentioned above and immunostaining pattern of (nuclear or cytoplasmic) p53 or Bcl-2.
为评估免疫组化检测的p53和Bcl-2蛋白在结直肠癌中的预后意义,对238例石蜡包埋的结直肠癌组织切片进行p53(单克隆抗体DO-7和CM-1抗血清)和Bcl-2(单克隆抗体Bcl-2:124)免疫染色。对染色模式进行半定量评估,并相互关联,同时与性别、年龄、肿瘤部位、Dukes分期、肿瘤分化、黏液特征、淋巴细胞和嗜酸性粒细胞浸润以及患者生存率进行关联分析。在我们的研究系列中,35%的癌组织未显示核染色,34%(DO-7)至40%(CM-1)显示超过30%的肿瘤细胞核染色。大多数用CM-1免疫染色的癌组织显示胞质染色,但DO-7未观察到这种情况。关于Bcl-2,51%的肿瘤完全阴性,32%显示弱阳性,15%显示中度染色;仅3%显示强阳性染色。未发现Bcl-2表达与核p53积累之间存在相互关系。在13例含有肿瘤相关腺瘤的病例中,4例在癌前和恶性细胞中Bcl-2阴性,另外4例这些细胞显示相似的染色强度,其余病例中仅恶性结直肠细胞Bcl-2阴性。因此,我们的数据表明Bcl-2在癌进展过程中并非必需。除了核p53积累与黏液性肿瘤之间存在关联(P = 0.01)外,未发现上述临床病理参数与(核或胞质)p53或Bcl-2的免疫染色模式之间存在显著相关性。