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多发性骨髓瘤患者原代细胞与U266细胞株zeste基因增强子同源物2表达升高的初步研究 被引量:2

Expression of enhancer of zeste homolog 2 in U266 cell line and bone marrow mononuclear cells of multiple myeloma patients
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摘要 目的探讨多发性骨髓瘤(MM)U266细胞株和MM患者的骨髓单个核细胞(BMMNC)中DNA甲基化相关蛋白zeste基因增强子同源物2(EZH2)的表达,分析DNA甲基化与MM的关系。方法选取MMU266细胞株及10例MM患者BMMNC(MM—BMMNC),同时选取10名健康人骨髓提取的单个核细胞(N—BMMNC)。用Westernblot法测定细胞EZH2的含量,以目的蛋白EZH2与内参照8一actin表达量的比值作为EZH2蛋白相对表达水平。结果与10例N—BMMNC(0.2277±0.1306)比较,EZH2在U266细胞(0.9730±0.1029)和10例MM—BMMNC(0.9220±0.1301)中表达明显升高,差异有统计学意义(P〈0.05)。结论EZH2在MMU266细胞株及MM—BMMNC中含量明显增多,EZH2与MM的发生和发展机制可能有密切联系。 Objective To investigate the expression of DNA methylation related protein enhancer of zeste homolog 2 (EZH2) in multiple myeloma (MM) cell line U266 and enriched MM cells (MM-BMMNC) from 10 patients, and analyze the potential role of DNA methylation in the occurrence and development of MM. Methods Human MM cell line U266 and MM cells from l0 MM patients were studied. Enriched bone marrow mononuclear cells (N-BMMNC) from 10 healthy persons were used as the control. The expression of EZH2 were determined by Western blot using the ratio of target protein EZH2 and the internal reference β-actin expression as the final results. Results The preliminary in vitro results showed that EZH2 expression was higher in MM cell line U266 and patient MM-BMMNC (N-BMMNC 0.2277±0.1306, MM-BMMNC 0.9220±0.1301, U266 0.9730±0.1029), with statistically significant differences (P 〈 0.05). Conclusion EZH2 is enriched in U266 and MM-BMMNC. DNA methylation may have a close correlation with the occurrence and development of MM.
出处 《白血病.淋巴瘤》 CAS 2013年第5期284-285,293,共3页 Journal of Leukemia & Lymphoma
基金 山西省留学人员科研资助项目(200810-99)
关键词 多发性骨髓瘤 DNA甲基化 zeste基因增强子同源物2 Multiple myeloma DNA methylation Enhancer of zeste homolog 2
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  • 1Kalushkova A, Fryknas M, Lemaire M, et al. Polycomb target genes are silenced in multiple myeloma. PLoS One, 2010, 5: e1 1483.
  • 2Simon ]A, Lange CA. Rnles of the EZH2 histone methyltransferase in cancer epigenetics. Mutation Res, 2008, 647: 21-29.
  • 3Huang W, Zhu C, Wang H, et al. The interferon consensus sequence- binding protein (1C SBP/IRF8) represses PTPN13 gene transcription in differentiating myeloid ceils. J Biol Chem, 2008, 283: 7921-7935.
  • 4Yang DF, Thangaraju M, Greenehch K, et al. Repression of IFN regulatory factor 8 by DNA methylation is a molecular determinant of apoptotic resistance and metastatic phenotype in metastatic tumor cells. Cancer Res, 2007, 67: 3301-3309.
  • 5Tshuikina M, Jernberg-Wiklund H, Nilsson K, et al. Epigenetic silencing of the interferon regulatory factor IC SBP/IRF8 in human multiple myeloma. Exp Hematol, 2008, 36: 1673-1681.
  • 6Sharma A, Heuck C J, Fazzari MJ. et al. DNA methylation alterations in multiple myeloma as a model for epigenetic changes in cancer. Wiley Interdiscip Rev Syst Biol Med, 2010, 2: 654-669.
  • 7Croonquist PA, Van Ness B. The polycomb group protein enhancer of zeste homolog 2 (EZH2) is an oncogene that inuences myeIoma cell growth and the mutant ras phenotype. Oncogene, 2005, 24: 6269- 6280.
  • 8McCabe MT, Brandes JC, Vertino PM. Cancer DNA methylation: molecular mechanisms and clinical implications. Clin Cancer Res, 2009, 15: 3927-3937.
  • 9Peng B, Hurt EM, Hodge DR, et al. DNA hypermethylation and partial gene silencing of human thymine-DNA glycosylase in multiple myeloma cell lines. Epigenetics, 2006, 1: 138-145.
  • 10王艺华,马艳萍.马钱子碱对多发性骨髓瘤骨病骨代谢影响的体外研究[J].白血病.淋巴瘤,2011,20(11):659-662. 被引量:1

二级参考文献29

  • 1王春红,王秀丽,范哲,顾莲芝,李广生.骨保护素和破骨细胞分化因子在多发性骨髓瘤患者骨髓中的表达[J].临床血液学杂志,2005,18(3):181-183. 被引量:5
  • 2张建华,傅晋翔,张晓慧,孙谕.破骨细胞在多发性骨髓瘤发病中的作用[J].中华血液学杂志,2007,28(5):323-326. 被引量:9
  • 3Kumar SK, Rajkumar SV, Dispenzieri A, et al. Improved survival in multiple myeloma and the impact of novel therapies. Blood, 2008, 111: 2516 -2520.
  • 4Pineda-Roman M, Zangari M, Hssler J, et al. Sustained complete remissions in multiple myeloma linked to bortezomib in total therapy 3: comparison with total therapy 2. Br J Haematol, 2008, 140: 625- 634.
  • 5Cavo M, Patriarca F, Tacchetti P. Superior complete response rate and progression-free survival after autologous transplantation with up-front velcade-thalidomide-dexamethasone compared with thalidomide- dexamethasone in newly diagnosed multiple myeloma [abstract]. Blood, 2008, i12: 158.
  • 6Attal M, Haroussean JL, Stoppa AM, et al. A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in muhiple myeloma. Intergroupe Francais du Myelome. N Engl J Med, 1996, 335: 91-97.
  • 7Barlogie B, Kyle RA, Anderson KC, et al. Standard chemotherapy compared with high-dose chemoradiotherapy for multiple myeloma: final results of phase ]II US Intergroup Trial $9321. J Clin Oncol, 2006, 24: 929-936.
  • 8Spencer A, Prince HM, Roberts AW, et al. Consolidation therapy with low-dose thalidomide and prednisolone prolongs the survival of multiple myeloma patients undergoing a single autologous stem-cell transplantation procedure. J Clin Oncol, 2009, 27: 1788-1793.
  • 9Gulbrandsen N, Waage A, Gimsing P, et al. A randomised placebo controlled study with melphalan/ prednisone vs melphalan/prednisone/tbalidomide:quality of life and toxicity [abstract]. Haematologica, 2008, 93: 0209.
  • 10Kyle RA, Rajkumar SV. Criteria for diagnosis, staging, risk stratification and response assessment of multiple myeloma. Leukemia,2009, 23: 3-9.

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