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淋巴瘤患者血浆中miR-21、miR-155、miR-210的表达及临床意义 被引量:16

Expressions of miR-21,miR-155 and miR-210 in Plasma of Patients withLymphoma and Its Clinical Significance
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摘要 本研究旨在检测淋巴瘤患者血浆中miR-21、miR-155、miR-210的表达,分析其与临床特征的相关性并探讨其在淋巴瘤诊断、评价疗效及预后方面的作用。运用RT-PCR方法检测淋巴瘤患者(55例)、淋巴结炎性肿大患者(10例)和正常对照(27名)血浆中miR-21、miR-155、miR-210的表达。结果表明,淋巴瘤患者血浆中miR-21、miR-155、miR-210的表达量均明显高于正常对照及淋巴结炎性肿大患者(P<0.05),淋巴结炎性肿大患者血浆中miR-21、miR-210的表达量与正常对照无显著差异。淋巴瘤患者血浆中miR-21的表达随血清乳酸脱氢酶水平增高而增高。初治淋巴瘤患者血浆中miR-21、miR-210的表达量明显高于6个疗程以上患者的表达量(P<0.05)。miR-21、miR-155、miR-210用于淋巴瘤的诊断准确度分别可达56.4%、65.3%、47.6%,三者联合诊断率可达82.7%。结论:淋巴瘤血浆中miR-21、miR-155、miR-210的表达量增高,检测三者在血浆中的表达量有助于临床淋巴瘤的诊断及疗效、预后的判断。 This study was purposed to investigate the expressions of miR-21,miR-155 and miR-210 in plasma of patients with lymphoma,and explore their role played in diagnosis,evaluation of chemotherapy effect and prognosis of lymphoma.The expressions of miR-21,miR-155 and miR-210 were assayed by RT-PCR in plasma of 54 cases of lymphoma,10 cases of lymphonode inflammation and 27 cases of normal controls.The results indicated that the expressions of miR-21,miR-155 and miR-210 in plasma of lymphoma patients were higher than those of control group and lymphonode inflammation group(P0.05).The expressions of miR-21 and miR-210 in plasma of control group and lymphonode inflammation group had no significant differences(P 0.05).The expression of miR-21 in plasma of lymphoma patient group significantly correlated with their serum LDH level.The expressions of miR-21 and miR-210 in plasma of previously untreated lymphoma patient group were higher than those of the patients treated for 6 or more courses(P0.05).The diagnostic accuracy of miR-21,miR-155 and miR-210 used for lymphoma patients was 56%,65%,48% respectively,and reached to 83% when combined three of them.It is concluded that the expressions of miR-21,miR-155 and miR-210 in plasma of lymphoma patients were significantly higher.Detection of these 3 miRNA in plasma of patients can contribute to the clinical diagnosis,treatment and prognosis evaluation of lymphoma.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2012年第2期305-309,共5页 Journal of Experimental Hematology
基金 国家自然科学基金(编号81170472) "十一五"国家科技支撑计划(编号2008BA161B00) 高等学校博士学科点专项科研基金(编号200800620004) 卫生行业科研专项项目(编号201002024) 天津市自然科学基金(编号09JCYBJC11200) 天津市科技支撑计划重点项目重大疾病防治专项基金(编号07ZCGYSF00600) 天津医科大学重点学科基金(编号2009xk51) 天津医科大学基金(编号2006KY31)
关键词 淋巴瘤 血浆 MIRNA MIR-21 MIR-155 MIR-210 lymphoma plasma miRNA miR-21 miR-155 miR-210
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  • 1Duffy MJ. Clinical uses of tumor markers: a critical review. Crit Rev Clin Lab Sci 2001; 38:225-262.
  • 2Thomas CM, Sweep CG. Serum tumor markers: past, state of the art, and future, lnt J Biol Markers 2001; 16:73-86.
  • 3Duffy MJ. Role of tumor markers in patients with solid cancers: a critical review. Eur J lntern Med 2007; 18:175-184.
  • 4Roulston JE. Limitations of tumour markers in screening. Br J Surg 1990; 77:961-962.
  • 5Esquela-Kerscher A, Slack FJ. Oncomirs - microRNAs with a role in cancer. Nat Rev Cancer 2006; 6:259-269.
  • 6Calin GA, Croce CM. MicroRNA signatures in human cancers. Nat Rev Cancer 2006; 6:857-866.
  • 7Chen C, Ridzon DA, Broomer A J, et al. Real-time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res 2005; 33:e179.
  • 8Tang F, Hajkova P, Barton SC, Lao K, Surani MA. MicroRNA expression profiling of single whole embryonic stem cells. Nucleic Acids Res 2006; 34:e9.
  • 9Hafner M, Landgraf P, Ludwig J, et al. Identification of microRNAs and other small regulatory RNAs using cDNA library sequencing. Methods 2008; 44:3-12.
  • 10Volinia S, Calin GA, Liu CG, et al. A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 2006; 103:2257-2261.

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  • 1王晓薇.肿瘤细胞微环境对癌症转移力的影响[J].中州大学学报,2010,27(1):120-123. 被引量:1
  • 2苏剑东,吴灵飞.NF-kB与细胞凋亡[J].世界华人消化杂志,2007,15(12):1411-1416. 被引量:51
  • 3徐卫,李建勇,沈秋丹,李丽,于慧.套层细胞淋巴瘤细胞系中染色体13q31-q32上miR-17-92基因簇的DNA序列研究[J].中国实验血液学杂志,2007,15(5):986-988. 被引量:1
  • 4张晋琳.中枢神经系统淋巴瘤研究进展[J].实用医院临床杂志,2007,4(6):25-28. 被引量:4
  • 5Sandhu SK, Croce CM, Garzon R, et al. Micro-RNA Expression and Function in Lymphomas. Adv Hematol, 2011 ;2011 : 1 - 12.
  • 6Zhang T, Nie K, Tam W. BIC is processed efficiently to microRNA- 155 in Burkitt lymphoma ceils. Leukemia, 2008; 22(9): 1795 - 1797.
  • 7Babar IA, Cheng C J, Booth C J, et al. Nanoparticle-based therapy in an in vivo microRNA-155 (miR-155)-dependent mouse model of lymphoma. Proceedings of the National Academy of Sciences of the United States of America, 2012; 109(26) : 1695 - 1704.
  • 8Kubiczkova L, Sedlarikova L, Hajek R, et al. TGF-β - an excel- lent servant but a bad master. J Transl Med, 2012; 10( 1 ) : 183 - 207.
  • 9Connolly EC, Freimuth J, Akhurst RJ. Complexities of TGF-β Tar- geted Cancer Therapy. Inter J Biol Sci, 2012; 8(7): 964-978.
  • 10Bakkebo M, Huse K, Hilden VI, et al. TGF-β-induced growth inhi- bition in B-cell lymphoma correlates with Smadl/5 signalling and constitutively active p38 MAPK. BMC Immunol, 2010; 11 ( 1 ) : 57 - 67.

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