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盐酸普鲁卡因对人结肠癌HT-29细胞的作用及其机制 被引量:2

Effects and Its Mechanism of Procaine Hydrochloride on Human Colon Cancer HT-29 Cells
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摘要 目的探讨盐酸普鲁卡因对人结肠癌HT-29细胞生长的抑制作用及其机制。方法应用不同浓度(0-10mmol/L)盐酸普鲁卡因处理HT-29细胞,通过倒置显微镜观察细胞形态学改变、四甲基偶氮唑盐比色法(MTT)检测细胞存活率、流式细胞术(FCM)观察细胞周期变化。结果倒置显微镜观察盐酸普鲁卡因处理后的HT-29细胞呈现缩小、皱缩、空泡、脱壁等增殖变慢的形态学特征;MTT结果分析表明盐酸普鲁卡因能显著抑制HT-29细胞增殖,其抑制率呈药物浓度及时间依赖性;FCM结果显示盐酸普鲁卡因可以使HT-29细胞的G0/G1期延长,S期缩短。结论盐酸普鲁卡因能够使HT-29细胞的生长阻滞在G0/G1期,从而显著抑制HT-29细胞的增殖,并且具有剂量、时间依赖效应。 Objective To investigate the influence of Procaine hydrochloride(PCA) on human colon cancer HT-29 cells proliferation and explore its mechanism.Methods HT-29 cells were treated with 0~10mmol/L of PCA,cell morphology changes were observed under contrast microscope.Cell proliferation was detected by MTT assay and cell cycle was detected by fIow cytometry(FCM).Results With different concentrations of PCA being used to dispose cancer cells separately,growth inhibition taking the form of cell's decreased size,shrinkage,vacuoles,cells abscised from the inner surface of the bottle became increasing obvious under contrast microscope.With the rise of the PCA concentration,HT-29 cells has a presentation of negative acceleration in the proliferation by MTT.The analysis of the result indicated that PCA can inhibit the cell proliferation significantly whose effect was replying on the dosage and time.The result by FCM shows that PCA can lengthen the G0/G1 phase and shorten the S phase in HT-29 cells.Conclusion PCA can make the growth of the HT-29 cells blocked in G0/G1 phase,thus inhibiting the cell multiplication significantly,whose effect was relying on the dosage and time.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2011年第2期137-140,共4页 Cancer Research on Prevention and Treatment
基金 三峡大学研究生科研创新基金资助项目(2009-35)
关键词 盐酸普鲁卡因 HT-29细胞 细胞增殖 Procaine hydrochloride HT-29 cells Proliferation
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  • 1张新宇,高燕宁.PCR引物设计及软件使用技巧[J].生物信息学,2004,2(4):15-18. 被引量:102
  • 2邓惠华,胡新荣,唐慰萍.人低分化鼻咽癌细胞克隆亚系的分离及生长特性观察[J].广东医学院学报,1994,12(2):99-101. 被引量:14
  • 3聂思槐,曾广华,王立伟,陈丽新,钟平,吴枫,胡新荣,唐慰萍.高、低分化的鼻咽癌细胞膜电位比较[J].中国病理生理杂志,1995,11(3):246-250. 被引量:5
  • 4付志婕,潘新良,雷大鹏,刘大昱,刘文君,刘春喜,王荣,叶萍.细胞周期素D1和p16在下咽癌中的表达及临床意义[J].临床耳鼻咽喉头颈外科杂志,2007,21(9):406-409. 被引量:10
  • 5王立伟,Pflugers Arch,1995年,430卷,4期,R30页
  • 6隋志仁,放射损伤学,1985年
  • 7Ai ZW, Zha XL, Chen HL. Effect of retinic acid on hepato-carcinoma cell line[ J ]. J Tumor Marker Oncol, 1990,26 (5): 59-64.
  • 8Bruno S, Darzynkiewicz Z. Cell cycle dep pression and stability of the nuclear protein detected by Ki-67 antibody in HL-60 cell[J].Cell Prolif, 1992,25 ( 1 ): 31-40.
  • 9Masood R, Cai J, Zheng T, et al. Vascular endothelial growth factor/vascular permeability factor is an autocine growth factor for AIDS-Kaposi sarcoma[J]. Proc Natl Acad Sci USA, 1997, 94(3) :979-984.
  • 10Zhang W, Ran S, Sambade M, et al. A monoclonal antibody that blocks VEGF binding to VEGFR2 (KDR/FLK- 1 ) inhibits vascular expression of FLK-1 and tumor growth in an orthotopic human breast cancer model[J]. Angiogenesis, 2002, 5(1-2) :35-44.

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  • 1Sakamoto J, Fujiya M, Okamoto K, et al. Immunoprecipitation of nucleosomal DNA is a novel procedure to improve the sensitivity of serum screening for the p16 hypermethylation associated with colon Caneer[J]. Cancer Epidemiol,2010,34(2) :194-199.
  • 2Bohze C. Loss of maspin is a helpful prognosticator in colorectal Cancer:a tissue microarray analysis [ J]. Pathol Res Pract, 2005, 200(11/12) :783-790.
  • 3Bondurant AE, Huang Z, Whitaker RS, et al. Quantitative detection of RASSF1A DNA promoter methylation in tumors and serum of patients with serous epithelial ovarian cancer [ J ]. Gynecol Oncol, 2011,123(3) :581-587.
  • 4Pehlivan S,Artac M, Sever T, et al. Gene methylation of SFRP2, PI6,DAPK1 ,HICI, and MGMT and KRAS mutations in sporadic colorectal cancer[ J ]. Cancer Genet Cytogenet ,2010,201 ( 2 ) : 128- 132.
  • 5Dobrovic A, Kristensen LS. DNA methylation, epimutations andcancer predisposition[ J]. Int J Biochem Cell Biol,2009,41 ( 1 ) : 34-59.
  • 6Espada J, Esteller M. DNA methylation and the functional organiza- tion of the nuclear compartment[ J]. Semin Cell Dev Biol,2010,21 (2) :238-246.
  • 7Gravina GL, Marampon F, Piccolella M, et al. Hormonal therapy promotes Hormone-Resistant phenotype by increasing DNMT activ- ity and expression in prostate cancer models [ J ]. Endocrinology, 2011,152 (12) :4550-4561.
  • 8Tittle RK, Sze R, Ng A, et al. Uhrfl and Dnmtl are required for de- velopment and maintenance of the zebrafish lens [ J ]. Dev Biol, 2011,350( 1 ) :50-63.
  • 9Lee ME, Rha SY, Jeung HC, et al. Subtelomeric DNA methylation and telomere length in human cancer ceils[ J ]. Cancer Lett ,2009, 281(1) :82-91.
  • 10Przybylski M, Koztowska A, Pietkiewicz PP, et al. Increased CX- CR4 expression in AsPC1 pancreatic carcinoma ceils with RNA in- terference-mediated knockdown of DNMT1 and DNM33B [ J ]. Bi- omed Pharmaeoth,2010,64(4) :254-258.

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