期刊文献+

食管癌前病变与食管腺癌细胞DNA倍体变化分析 被引量:3

Precancerous Lesion of Esophagus and Analysis on Ploidy Changes for Cell DNA of Esophageal Adenocarcinoma
下载PDF
导出
摘要 目的探讨慢性炎症-癌前病变-食管腺癌不同阶段的食管黏膜细胞DNA含量及倍体变化,从细胞代谢水平揭示食管癌的发展过程.方法用流式细胞术对15例检查未见器质性病变者的正常组织,27例胃食管反流病患者(GERD)、25例Barrett食管患者和31例食管腺癌患者的病变组织细胞DNA含量进行了检测,并对四组的DNA倍体类型、DNA指数(DI)、G2/G1、增殖活性(SPF)和细胞增殖活性指数(PI)做了对比分析.结果食管腺癌22例DNA含量全部为非整倍体变化(DNA指数DI>1.1),Barrett食管25例中仅6例为非整倍体DNA含量,胃食管反流病和健康者无1例为非整倍体DNA含量;食管腺癌组G2/G1、SPF、PI较正常组织和胃食管反流病组均有明显升高(P<0.05),Barrett食管组介于胃食管反流病与食管腺癌之间,并且G2/G1、SPF和PI指标差异均有统计学意义(P<0.05).流式细胞术诊断阳性率差异显著.结论食管癌的发展是一个渐进的过程,各阶段之间密切相关. Objective To investigate the esophageal nuclear DNA content and ploidy changes of chronic inflammation-precancerous lesion-esophageal adenocarcinoma at different stages,and reveal that the development of esophageal cancer is a progressive process from view of cell metabolism. Methods For 15 patients without evidence of organic lesions in normal tissue,27 cases with gastroesophageal reflux(GERD), 25 cases with Barrett and 31 cases with esophageal adenocarcinoma, flow cytometry was used to test cell DNA content, and for DNA ploidy, DNA index(DI), G2/G1 , proliferative activity(SPF) and proliferation index(PI)of four groups,comparative analysis was done. Results For 22 cases with esophageal adenocarcinoma, all aneuploid changes happened on DNA content (DNA index DI〉1. 1). But for Barrett esophagus, only six of 25 cases had aneuploid DNA content. In the end, for gastroesophageal reflux disease and healthy objects,no aneuploid DNA content happened. Compared with that of normal tissue and gastroesophageal reflux disease groups, index of G2/G1, SPF, PI for esophageal adenocarcinoma group were significantly higher( P 〈0.05) ;while the index of Barrett esophagus group were between that of gastroesophageal reflux disease esophageal adenocarcinoma groups,G2/G1 ,SPF and PI indices were significant different, P 〈0. 05; flow cytometry diagnostic produced significant differences. Conclusion Esophageal cancer development is a progressive process,and there is a strong correlation between the various stages.
出处 《河北北方学院学报(自然科学版)》 2011年第6期59-61,69,共4页 Journal of Hebei North University:Natural Science Edition
基金 河北省科学技术研究发展与指导计划项目(编号:072761678)
关键词 食管腺癌 癌前病变 DNA含量 倍体变化 esophageal adenocareinoma precancerous lesions DNA content ploidy changes
  • 相关文献

参考文献11

  • 1Salud A, Porcel JM, Raikundalia B, et al. Prognostic significance of DNA ploidy, S-phase fraction, and P-glycopro tein expression in colorectal cancer [J]. J Surg Oncol, 1999, 72 (3): 167-174.
  • 2Molnar B, Karman J, Nemeth A, et al. Detection of aneuploidy from gastrointestinal biopsysamples [J]. Orv Hetil, 2000, 141 (15): 789-792.
  • 3Zarbo RJ, Nakhleh RE, Brown RD, et al. Prognostic significance of DNA ploidy and proliferation in 309 colorectal carcinomas as determined by two-color multiparametric DNA flow cytometry [J]. Cancer, 1997, 79 (11): 2073-2086.
  • 4邵宏涛,孙丽华,谷伟,王书奎.DNA倍体分析在恶性胸腔积液诊断中的应用[J].医学研究生学报,2000,13(6):369-370. 被引量:5
  • 5周振英,朱月清,吴晓柳,沈宗丽,王亚平.恶性肿瘤DNA倍体分类与临床生物学行为的关系分析[J].肿瘤研究与临床,2000,12(4):230-232. 被引量:15
  • 6原志庆,姜红光,许春雷,千新来,杨万才,王凤荣.食管鳞状细胞癌DNA倍体异质性研究及其临床病理学意义[J].中华病理学杂志,1996,25(3):159-161. 被引量:14
  • 7Kelein FA. Detection and follow-up of carcinoma of urinary bladder by flow cytometry [J]. Cancer, 1982, 50 (3) : 389.
  • 8Devesa SS, Blot WJ, Fraumeni JF Jr, et al. Changing patterns in the incidence of esophageal and gastric carcinoma in the UnitedStates [J]. Cancer, 1998, 83 (10): 2049-2053.
  • 9Noguchi T, Takeno S, Takahashi Y, et al. Primary adenocarcinoma of the cervical esophagus arising from heterotopic gastric mucosa [J]. J Gastroenterol, 2001, 36 (10): 704-709.
  • 10Reid BJ, aggitt RC, Rubin CE, et al. Barrett' s esophagus: Correlation between flow cytometry and histology in detection of patients at risk for adenocarcinoma[J]. Gastroenterology, 1993, 93 (1): 1-11.

二级参考文献10

  • 1周振英,周鑫官,张军妮,蒋明,高萍.食管癌手术上下切缘及癌灶细胞DNA含量的流式细胞术分析[J].实用癌症杂志,1994,9(2):85-87. 被引量:8
  • 2[1] Kiein FA,Herr HW,Sogani PC,et al.Detection and follow-up of carcinoma of the urinary bladder by flow cytometry[J].Cancer,1982,50:389.
  • 3[2] Joseph E,Fuhr JE,Anthony A,et al.Flow cytometric analysis of pulmonary fluids and cells for the detection of maliganancies[J].AM J Pathol,1992,141(1):211.
  • 4[3] Bartal AH,Gazitt Zidan G,Vermeuben B,et al.Clinical and flow cytometry characteristics of malignant pleural effusions in patients after intracavitary administration of methyprednisolone acetate[J].Cancer,1991,67(10):3136-3140.
  • 5[4] Merkel DE,Mc Guire WL.Ploidy proliferative activity and prognosis DNA flow cytometry of solid tumor[J].Cancer,1990,65(4):1194-1205.
  • 6[5] Alaner KA,Klemi PJ,Kujari H,et al.Comparion of fresh ethanol preserved and paraffin embedded samples in DNA flow cytometry[J].Gytometry,1989,10(1):81-85.
  • 7[6] Yoss EB,David Berd,Jone R,et al.Flow Cytometric evaluation of bronchoscopic washings and lavage fluid for DNA aneuploidy as an adjunct in the dignosis of lung cancer and tumors metastatic to the lung[J].Chest,1989,96:54-59.
  • 8[7] Joseph E,Fuhr JE,Anthony A,et al.Flow Cytometric analysis of pulmonary fluids and cells for the detection of malignancies[J].American Journal of Pathology,1992,141(1):211-215.
  • 92000-11-01
  • 10原志庆,肿瘤防治研究,1994年,21卷,86页

共引文献30

同被引文献48

引证文献3

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部