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多发性骨髓瘤患者血浆HSP90的表达及其临床意义 被引量:5

Expression and Significance of HSP90 in Plasma of Patients with Multiple Myeloma
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摘要 本研究检测多发性骨髓瘤(MM)患者外周血HSP90的表达情况,探讨其在MM发病中的作用及与疾病治疗、预后转归的关系。收集58例MM患者和20例健康志愿者的外周血,应用双抗体夹心ELISA法检测血浆HSP90的表达水平。结果表明,MM患者外周血HSP90的表达水平明显高于对照组[(325.205±75.942)vs(85.401±11.261)ng/ml](P<0.001)。HSP90表达水平与MM患者的性别、年龄和疾病分型无关(P>0.05),而与疾病国际分期系统(ISS)的分期、疗效、浆细胞百分比和球蛋白、免疫球蛋白、M蛋白、β2-微球蛋白和轻链水平明显相关(P<0.05)。结论:HSP90在MM患者外周血中的过度表达可能参与了MM发病和进展,检测外周血HSP90的表达水平可能对判断MM患者的病情、疗效和预后有一定临床指导意义。 This study was purposed to investigate the expression of heat shock protein 90 (HSP90) in peripheral blood plasma of patients with multipl myeloma(MM),and to explore its possible role in the pathogenesis of MM,and its relationship with treatment,prognosis and the outcome of patients.The peripheral blood samples from 58 patients with MM and 20 healthy volunteers were collected.The plasma concentration of HSP90 in patients and healthy volunteers was measured by ELISA.The results showed that the concentration of HSP90 in peripheral blood of patients with MM was significantly higher than that in the healthy volunteers [(32.398 ± 3.674)vs (25.762 ± 2.916)ng/ml] (P 〈 0.001).The concentration of HSP90 showed positively correlation with International Staging System(ISS) stage,therapeutic response,frequency of plasmocyte,globulin,immune globulin,M-protein,β2 micro-globulin,and light chain of MM patients (P 〈 0.05) ; while it showed little correlation with sex,age and type of MM patients (P 〉 0.05).It is concluded that the HSP90 may be involved in the occurrence and development of MM.Detection of HSP90 in plasma would contribute to judge the clinical course,therapeutic efficacy and prognosis of MM patients.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2014年第5期1326-1330,共5页 Journal of Experimental Hematology
关键词 多发性骨髓瘤 外周血 HSP90 multiple myeloma peripheral blood HSP90
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参考文献14

  • 1Andrulis M,Chatlerjee M,Jain S,et al.Heat shock protein 902/βare overexpressed in multiple myeloma cells and critically contribute to survival.Verh Dtsch Ges Pathol,2007;91(1):330-337.
  • 2Khong T,Spencer A.Targeting HSP 90 induces apoptosis and inhibits critical survival and proliferation pathways in multiple myeloma.Mol Cancer Ther,2011;10(10):1909-1917.
  • 3Giménez Ortiz A,Montalar Salcedo J.Heat shock proteins as targets in oncology.Clin Transl Oncol,2010;12(3):166-173.
  • 4中国多发性骨髓瘤诊治指南(2011年修订)[J].中华内科杂志,2011,50(10):892-896. 被引量:111
  • 5Munshi NC,Anderson KC.New Strategies in the Treatment of Multiple Myeloma.Clin Cancer Res,2013;19(13):3337-3344.
  • 6Ludwig H,Sonneveld P.Disease control in patients with relapsed and/or refractory multiple myeloma:what is the optimal duration of therapy?.Leuk Res,2012;36(Suppl 1):S27-34.
  • 7Li J,Buchner J.Structure,function and regulation of the hsp90machinery.Biomed J,2013;36(3):106-117.
  • 8Duus J,Bahar HI,Venkataraman G,et al.Analysis of expression of heat shock protein-90(HSP90)and the effects of HSP90 inhibitor(17-AAG)in multiple myeloma.Leuk Lymphoma,2006;47(7):1369-1378.
  • 9Mitsiades CS,Mitsiades NS,McMullan CJ,et al.Antimyeloma activity of heat shock protein-90 inhibition.Blood,2006;107(3):1092-1100.
  • 10Richardson PG,Mitsiades CS,Laubach JP,et al.Inhibition of heat shock protein 90(HSP90)as a therapeutic strategy for the treatment of myeloma and other cancers.Br J Haematol,2011;152(4):367-379.

二级参考文献10

  • 1Rousseau S, Houle F, Kotanides H, et al. Vascular endothelial growth factor (VEGF) -driven actin-based motility is mediated by VEGFR2 and requires concerted activation of stress-activated protein kinase 2 ( SAPK2 /p38 ) and geldanamycin-sensitive phosphorylation of focal adhesion kinase. J Biol Chem, 2000; 275 (14) : 10661 - 10672.
  • 2Webb CP, Hose CD, Koochekpour S, et al. The geldanamycins are potent inhibitors of the hepatocyte growth factor/scatter factor- met-urokinase plasminogen activator-plasmin proteolytic network. Cancer Res, 2000;60 (2): 342-349.
  • 3Ferrarini M, Heltai S, Zocchi R, et al. Unusual expression and localization of heat-shock proteins in human tumor cells. Int J Cancer, 1992; 51(4) : 613 -619.
  • 4Ludwig H, Khayat D, Giaccone G, et al. Proteasome inhibition and its clinical prospects in the treatment of hematologic and solid malignancies. Cancer, 2005; 104(9): 1794-1807.
  • 5Jackson G, Einsele H, Moreau P, et al. Bortezomib, a novel proteasomes inhibitor, in the treatment of hematologic malignancies. Cancer Treat Rev, 2005; 31(8) : 591 -602.
  • 6Saunders G. Overview of drug therapy for multiple myeloma. J Oncol Pharm Pract, 2005 ; 11 (3) : 83 - 100.
  • 7Sinha R, Kaufman JL, Lonial S. Novel treatment approaches for patients with multiple myeloma. Clin Lymphoma Myeloma, 2006 ; 6(4) :281 -288.
  • 8Dubois D, Dhawan R, van de Velae H, et al. Descriptive and prognostic value of patients-reported outcomes. The bortezomib experience in relapsed and refractory multiple myeloma. J Clin Ocol,2006; 24(6) : 976 -982.
  • 9Andrulis M, Chatterjee M, Jain S, et al. Heat shock protein 90 alpha and beta are overexpressed in multiple myeloma cells and critically contribute to survival. Verh Dtsch Ges Pathol, 2007 ; 91 (1) :30 -337.
  • 10Spisek R, Charalambous A, Mazumder A, et al. Bortezomib enhances dendritic cell ( DC ) -mediated induction of immunity to human myeloma via exposure of cell surface heat shock protein 90 on dying tumor cells: therapeutic implications. Blood, 2007; 109 ( 11 ) : 4839 - 4845.

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