Sundaresan V, Forgacs I C, Wight D G, Wilson B, Evan G I, Watson J V
Medical Research Council Clinical Oncology Unit, Medical School, Cambridge.
J Clin Pathol. 1987 Nov;40(11):1274-81. doi: 10.1136/jcp.40.11.1274.
Monoclonal antibodies raised by synthetic peptide immunisation were used to determine the distribution of the protein product of the c-myc gene by immunocytochemical staining of archival wax embedded material from patients with familial adenomatous polyposis. Polyps from 18 cases of familial adenomatous polyposis, 10 of whom had developed malignant change, and 30 normal control colonic biopsy specimens were examined. A consistent staining pattern was observed in normal mucosa; nuclear staining in the basal proliferative zone; mixed nuclear and cytoplasmic staining in the maturation zone; and cytoplasmic localisation in the surface mature zone. In contrast, the polyps and carcinomata showed a mixed pattern of cytoplasmic and nuclear localisation in the basal proliferative zone with nuclear persistence throughout the crypts to the surface mature zone. This abnormal distribution of the c-myc oncogene product may have a role in the evolution of polyps and their subsequent malignant transformation into familial adenomatous polyposis.
通过合成肽免疫产生的单克隆抗体,用于通过对家族性腺瘤性息肉病患者存档蜡块包埋材料进行免疫细胞化学染色,来确定c-myc基因蛋白产物的分布。检查了18例家族性腺瘤性息肉病患者的息肉,其中10例已发生恶变,以及30份正常对照结肠活检标本。在正常黏膜中观察到一致的染色模式:在基底增殖区为核染色;在成熟区为核染色与胞质染色混合;在表面成熟区为胞质定位。相比之下,息肉和癌在基底增殖区显示出胞质和核定位的混合模式,核染色持续存在于整个隐窝直至表面成熟区。c-myc癌基因产物的这种异常分布可能在息肉的演变及其随后向家族性腺瘤性息肉病的恶性转化中起作用。