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Blf-ADT对HeLa细胞的抑制作用及其机制的研究

Study on Anti-Tumor Activity and Mechanisms of Blf-ADT
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摘要 研究Blf-ADT(布洛芬硫化氢供体物)的抗肿瘤作用,并对其机制作初步探讨.通过形态学观察、噻唑蓝(MTT)比色实验、集落形成实验测定He La细胞的增殖能力;细胞划痕实验测定He La细胞的迁移能力;Annexin VFITC/PI双染流式细胞仪测定He La细胞的凋亡率;Western blotting检测细胞凋亡相关蛋白(Bcl-2、Bax、Erk、P38和Procaspase-3等)的表达.结果显示,Blf-ADT能呈浓度或时间依赖性抑制细胞增殖、减少细胞集落的形成,降低细胞的迁移能力,同时能显著提高He La细胞的凋亡率,影响细胞凋亡相关蛋白(Bcl-2、Bax、Erk、P38和Procaspase-3等)的表达.Blf-ADT对人宫颈癌He La细胞的生长有显著的抑制作用,对治疗宫颈癌具有潜在的临床应用价值. The purpose of this study was to observe the activity and mechanisms of a new compound Blf-ADT on He La cells. The effects of Blf-ADT on Hela cells was investigated by morphological observation,MTT assay and colony formation assay,respectively. Wound healing assay was used to detect the effect of Blf-ADT on the migration of He La cells.Meanwhile,the activities of Blf-ADT on apoptosis was measured by Flow cytometry. Furthermore,Western blot was performed to investigate the expressions of related proteins in He La cell line treated with Blf-ADT. As a result,we found that Blf-ADT could inhibit cell proliferation and reduce cell migration in a dose-and time-dependent manner. In addition,Blf-ADT could significantly increase the rate of apoptosis and affect the expression of apoptosis-related proteins.Taken together,the data indicate that Blf-ADT can significantly inhibit the growth of He La cells and have potential clinical value for treatment of cervical cancer.
出处 《南京师大学报(自然科学版)》 CAS CSCD 北大核心 2016年第1期67-72,共6页 Journal of Nanjing Normal University(Natural Science Edition)
基金 教育部留学回国人员科研启动基金资助项目(教外司留[2015]311号) 南京师范大学留学回国人员启动基金项目
关键词 HELA Blf-ADT 细胞增殖 细胞凋亡 抗肿瘤作用 HeLa Blf-ADT cell proliferation cell apoptosis anti-tumor effect
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参考文献10

  • 1LI X Y,WANG X. The role of human cervical cancer oncogene in cancer progression[J].Int J Clin Exp Med,2015,15:8 363-8 368.
  • 2卢秀娥.宫颈癌及癌前病变筛查现状及其研究进展[J].中国社区医师(医学专业),2013,15(10):9-9. 被引量:4
  • 3SAMBROOK J. Molecular cloning:a laboratory manual[M].Beijing:Science Press,2008.
  • 4SCHIFFMAN M H,BRINTON L A. The epidemiology of cervical carcinogenesis[J].Cancer,2006,76:1 888-1 901.
  • 5PANKIN D M,PISAN I P,FERLAY J. Estinates of the worldwide incidence of 25 major cancers[J].Int Cancer,2007,80:827-841.
  • 6ABBOTT R G,FORREST S,PIENTA K J. Simulating the hallmarks of cancer[J].Artif Life,2006,12:617-634.
  • 7ADAMS J M,CORY S. The Bcl-2 protein family:arbiters of cell survival[J].Science,1998,281(5 381):1 322-1 326.
  • 8徐美华,张桂英,谢兆霞,何春梅.吲哚美辛对结肠癌细胞CDK_2、CDK_4、p21^(WAF1/CIP1)、Bcl-2及Bax蛋白表达的影响[J].中华消化杂志,2002,22(10):605-607. 被引量:15
  • 9DEVERAUX Q L,REED J C. IAP family proteins-suppressors of apoptosis[J].Genes Dev,1999,13:239-252.
  • 10UEHLING D E,HARRIS P A. Recent progress on MAP kinase pathway inhibitors[J].Bioorg Med Chem Lett,2015,25:4?047-4056.

二级参考文献16

  • 1Shiff SJ, Qiao, Tsai LL, et al.Sulindac sulfide, an aspirin-likecompound, inhibits prolifcration, causes cell cyclcquiescence, andinduces apoptosis in HT-29 colon adenocarcinoma cells. J Clin Invest, 1995,96:491-503.
  • 2Shiff SJ, Koutsos MI, Qiao L, et al. Nonsteroidal antiinflammatory drugs inhibitthe proliferation of colon adenocarcinoma cells:effects on cell cycle and apoptosis. ExpCell Res, 1996, 222:179-188.
  • 3Lonnroth C, Andersson M, Lundholm K. Indomethacin andtelomerase activity in tumorgrowth retardation. Int J Oncol,2001, 18:929-937.
  • 4Li Y, Bhuiyan M, Mohammad RM, et al. Induction of apoptosisin breast cancer cellsby TPA. Oncogene, 1998, 17: 2915-2920.
  • 5Zhang G, Tu C, Zhang G, et al. Indomethacin induces apoptosisand inhibitsproliferation in chronic myeloid lenk cells. Leuk Res,2000, 24: 385-392.
  • 6Brown J M, Wouters BG. Apoptosis, p53, and tumor cell sensitivity to anticanceragents. Cancer Res, 1999, 59:1391-1399.
  • 7Koshiji M, Adachi Y, Sogom S, et al. Apoptosis of colorectal adenocarcinoma(COLO-201) by tumour necrosis factor-alpha (TNFα) and/or interferon-gamma (IFN-γ),resulting from down-modulation of Bcl-2 expression. Clin Exp Immunol, 1998, 111:211-218.
  • 8Sandfi MT, Lentati P, Benini E, et al. Compari- son of the Digene HC2 As - say and the Roche AMPLICOR [ J ]. J Clin Microbiol, 2006,44 : 2141 -2146.
  • 9张桂英,段朝军,施家琦,冷爱民.消炎痛抗肿瘤作用及体外增敏作用的研究[J].湖南医科大学学报,1997,22(6):478-482. 被引量:15
  • 10李震乾,林爱珍,崔金环,罗红涛.HPV-DNA检测与TCT检查在宫颈癌前病变筛查中的相关性[J].现代医院,2010,10(1):28-30. 被引量:14

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