期刊文献+

CyclinE阈值降低促进细胞增殖 被引量:2

Promotive Effect of Decreased Cyclin E Threshold on Cell Proliferation
下载PDF
导出
摘要 背景与目的:许多研究表明高表达CyclinE使细胞增殖能力增加,也有研究报道CyclinE表达较低而细胞增殖并未降低,而在我们对临床肿瘤样本进行研究时发现大量低Cyclin表达(包括CyclinE)的细胞具有旺盛的增殖能力。为了解释这一现象,本研究旨在探讨MOLT-4细胞中CyclinE阈值下降后细胞进入S期的增殖状况。方法:以低浓度咖啡因处理MOLT-4细胞2h、4h,构建CyclinE阈值降低模型,采用流式细胞术分析增殖细胞核抗原(proliferationcellnuclearantigen,PCNA)、增生抗原Ki67和光裂解诱导的选择性DNA断裂链(DNAstrandbreakinductionbphotolysis,SBIP)阳性细胞数。结果:低浓度咖啡因处理MOLT-4细胞2h、4h后,CyclinE阈值明显下降,PCNA、Ki67和SBIP阳性细胞数增加,并以咖啡因处理2h时变化最为明显。结论:CyclinE阈值由高水平迅速降低后细胞增殖陡然增加,CyclinE阈值在较低水平时细胞仍然可增殖。 BACKGROUND &OBJECTIVE: Many studies showed that high expression of Cyclin E promotes cell proliferation, but contrary data was also reported that cell proliferation didnt decrease with low expression of Cyclin E. In addition, we observed that many tumor cells have strong capability of proliferation with low expression of Cyclins, including Cyclin E. This study was to analyze effect of reduced Cyclin E threshold on proliferation of acute lymphocyte leukemia cell line MOLT 4 to explain the above phenomena. METHODS: We have established the model of decreased Cyclin E threshold in MOLT 4 cells by treating cells with low concentration (5 mmol/L)of caffeine for 2, and 4 h. The positive rates of proliferation cell nuclear antigen (PCNA), Ki67, and DNA strand break induction by photolysis (SBIP) were analyzed by flow cytometry. RESULTS: MOLT 4 cells presented sharply decrease of Cyclin E threshold, and increase of positive rates of PCNA, Ki67, and SBIP after treated with caffeine, especially at 2 h point. CONCLUSIONS: Decrease of Cyclin E threshold was accompanied by increase of cell proliferation. MOLT 4 cells may remain high proliferation capability with low level of Cyclin expression.
出处 《癌症》 SCIE CAS CSCD 北大核心 2004年第11期1244-1248,共5页 Chinese Journal of Cancer
基金 国家自然科学基金(No.39670265 39730270 39725027) 973肿瘤计划(No.G1998051212) 卫生部临床重点学科(No.20012537)~~
关键词 细胞周期 细胞周期蛋白 阈值 流式细胞术 细胞增殖 Cell cycle Cyclin Threshold Flow cytometry Cell proliferation
  • 相关文献

参考文献16

  • 1Darzynkiewicz Z,Gong JP,Juan G,et al.Cytometry of cyclin proteins [J].Cytometry,1996,25(1):1-13. 被引量:1
  • 2Dosaka Akita H,Hommura F,Mishina T,et al.A risk stratification model of non small cell lung cancers using cyclin E,Ki 67,and ras p21:different roles of G1 cyclins in cell proliferation and prognosis [J].Cancer Res,2001,61(6):2500-2504. 被引量:1
  • 3Dulic V,Drullinger LF,Lees E,et al.Altered regulation of G1 cyclins in senescent human diploid fibroblasts: accumulation of inactive cyclin E Cdk2 and cyclin D1 Cdk2 complexes [J].Proc Natl Acad Sci USA,1993,90(23):11034-11038. 被引量:1
  • 4Sgambato A,Han EK,Zhou P,et al.Overexpression of Cyclin E in the HC11 mouse mammary epithelial cell line is associated with growth inhibition and increased expression of p27Kipl [J].Cancer Res,1996,56(6):1389-1399. 被引量:1
  • 5Keyomarsi K,Herliczek TW.The role of cyclin E in cell proliferation,development and cancer [J].Prog Cell Cycle Res,1997,3:171-191. 被引量:1
  • 6Dutta A,Chandra R,Leiter LM.Cyclins as markers of tumor proliferation:immunocytochemical studies in breast cancer [J].Proc Natl Acad Sci USA,1995,92(12):5386-5390. 被引量:1
  • 7Nielsen NH,Arnerlov C,Cajander S.Cyclin E expression and proliferation in breast cancer [J].Anal Cell Pathol,1998,17(3):177-188. 被引量:1
  • 8Gong J,Traganos F,Darzynkiewicz Z.Threshold expression of cyclin E but not D type cyclins characterizes normal and tumour cells entering S phase[J].Cell Prolif,1995,28(6):337-46. 被引量:1
  • 9Li X,Traganos F,Melamed MR,et al.Single step procedure for labeling DNA strand breaks with fluorescein or BODIPY conjugated deoxynucleotides: detection of apoptosis and bromodeoxyuridine incorporation [J].Cytometry,1995,20(2):172-80. 被引量:1
  • 10谢大兴,吴剑宏,余源,龚建平.细胞周期素E表达阈值的定量分析[J].癌症,2002,21(7):705-709. 被引量:3

二级参考文献1

共引文献2

同被引文献9

引证文献2

二级引证文献22

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