摘要
目的探讨流式细胞术双标记法检测恶性实体肿瘤细胞DNA含量、细胞周期和Ki67表达和组织学分级之间的关系。方法利用流式细胞术Ki67/DNA双标记法同时检测87例新鲜恶性实体肿瘤的DNA含量、细胞周期和增殖核抗原Ki67的表达。结果异倍体发生率为40.2%,其中高分化肿瘤为11.l%,中分化肿瘤为37.5%,低分化肿瘤为 46. 3%。 Ki67阳性细胞为 0. 5%~87%(17. 36%士16. 6%)。 S期细胞百分比为 0~24%(5 28%±4. 85%)。高分化肿瘤 S期细胞百分比及增殖核抗原 Ki67的表达明显低于中分化和低分化肿瘤,统计学上有显著性差异(P<0.01)。中分化和低分化肿瘤之间则差异无显著性(P>0.05)。异倍体肿瘤S期细胞百分比高于二倍体肿瘤,差异有显著性(P<0.01),而Ki67的表达在两者之间无显著性差异。结论流式细胞术Ki67/DNA双标记法可同时检测实体恶性肿瘤细胞的DNA含量、细胞周期和增殖核抗原Ki67的表达,并能进一步阐明这些参数与组织学分级的关系。方法简便、快速,有利于对肿瘤生物学特性的了解。
Objective To study the relationship between DNA content,S phase,Ki67 expression and histological grade of solid tumors by bivariate flow cytometry. Methods Ki67/DNA bivariate flow cytometry was used to detect DNA ploidy, cell cycle and Ki67 expression on 87 cases of malignant solid tumor. Results Aneuploidy was 40. 23% in all tumors,including 11. 1% on grade I, 37. 5% on grade Ⅱ and 46. 3% on grade Ⅲ. Ki67 possive cells varied from 0. 5%- 87% (17. 36 ± 16. 6% ). Cells on S phase ranged from 0-24% (5. 28±4. 85% ). S phase cells and Ki67 expression on grade I were significantly lower than those on grade Ⅱ and grade Ⅲ. No difference between those on grade Ⅱ and grade Ⅲ. S phase cells on aneuploid tumor were higher than on diploid tumor. There was no difference between aneuploid and diploid tumor on Ki67 expression. Conclusion Ki67/DNA bivariate flow cytometry can simultaneously detect DNA content, cell cycle and Ki67 expression on tumor cells. It is a valuable method for clinical application.
出处
《实用肿瘤杂志》
CAS
北大核心
2000年第6期385-387,393,共4页
Journal of Practical Oncology
关键词
实体肿瘤
生物学行为
Ki67/DNA双标记法
neoplasma/pathology
Ki67
cell cycle
Proliferation PCNA antigen
flow cytometry