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作 者:陈献国[1] 余国伟[2] 郑昭璟[3] 施亚明[1] 周志有[1]
机构地区:[1]金华市中心医院胸外科,浙江金华321000 [2]浙江大学医学院附属第一医院胸外科,浙江杭州310003 [3]金华市中心医院流式细胞实验室,浙江金华321000
出 处:《中华肿瘤防治杂志》2009年第10期758-760,共3页Chinese Journal of Cancer Prevention and Treatment
基 金:浙江省金华市科学技术基金(2006-3-038)
摘 要:目的:探讨通过流式细胞术进行食管脱落细胞DNA分析,在食管癌诊断中的价值。方法:用食管拉网法获得61例食管癌和31例非食管癌患者食管脱落细胞,记录和计算DNA指数(DI)、G2/G1、S期比率(SPF)和细胞增殖活性指数(PI)等,同时结合肿瘤的临床病理学特征,并与脱落细胞常规细胞学检查进行对比。结果:食管癌组DI为1.31±0.23,对照组为1.00±0.03;异倍体(An)出现率为70.7%,高于对照组4.8%;食管癌组G2/G1为2.071±0.153,对照组为1.996±0.099;并且SPF和PI两组指标的差异均有统计学意义,P<0.05。结论:食管脱落细胞DNA增殖活性指标对食管癌普查及提高早期诊断率具有一定的应用价值。OBJECTIVE: To evaluate the clinical significance of DNA analysis of extoliated esophageal cells in early diagnosis of esophageal carcinoma. METHODS: The exfoliated cells were obtained by the esophagus fleece-pulling. The single-cell suspension was made by mechanical decentralization and then detected by the flow cytometry for DNA analysis. DNA index (DI), G2/G1, S-phase fraction (SPF), proliferation index (PI), etc were recorded and calculated. The clinical evaluation was made by comparing with the routine cytology examination. RESULTS: The DI of esophageal carcinoma group and the control group was 1.31±0.23 and 1.00±0.03. The Aneuploid rate of esophageal carcinoma group was 70. 7%, while that of control group was 4.8%. The G2/G1 for esophageal carcinoma group was 2. 071 ± 0. 153 and that for control group was 1. 996±0. 099. There was significant difference between two groups (P 〈 0. 05) in SPF and PI. CONCLUSION: DNA analysis of exfoliated esophageal cells can raise the early diagnostic rate of esophageal carcinoma.
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