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骨髓微环境与多发性骨髓瘤 被引量:2

Bone marrow microenvironment and multiple myeloma
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摘要 骨髓微环境不仅支持正常造血细胞的生长和分化,而且有助于肿瘤细胞的生长,它在多发性骨髓瘤细胞的增生、分化、凋亡中起重要作用。多发性骨髓瘤(MM)的瘤细胞定居在骨髓很少浸润骨髓以外的器官,与肿瘤细胞所处的骨髓造血微环境密切相关。骨髓瘤细胞与骨髓基质细胞及细胞外基质相互黏附,并产生细胞因子,进而影响肿瘤细胞的存活,而且还影响瘤细胞对治疗的反应。MM是一个进展性、致死性疾病,传统的化疗很易发生耐药。目前随着免疫学、分子生物学的发展及对骨髓微环境的研究,一些新型的以生物学为基础的药物不仅针对瘤细胞本身,而且以骨髓微环境为靶子,通过改变骨髓微环境而达到克服耐药的目的,从而延长骨髓瘤患者的无病生存期。 Bone marrow microenvironment(BMM)not only support hematopoietic cells growth and dif- ferentiation,but also contribute to tumor cells growth.BMM play a critical role in proliferation,differentiation and apoptosis of multiple myeloma(MM)ceils.MM cells predominantly localize in bone marrow and rarely in- vade to other organs,which is closely associated with the bone marrow microenvironment.The MM cells ad- hero to extracetlular matrix proteins and BM stromal ceils,which affect the myleoma cells survial and the ther- aputic reaction through cell adhesion and cytokine-mediated mechanisms.Multiple myeloma is a aggressive and fatal disease.Conventional chemotherapy ultimately develop drug resistance.Nowadays,with the develop- ment of immunology and molecularbiology and approach to the bone marrow micrenviroment,Novel biological- ly-based drugs not only target to myeloma cell not only its BM milieu.These studies have also provided the framework for a new treatment paradigm that disruption of the bone marrow microenviroment overcome the drug resisence and prolong the patient disease-free survial in MM.
出处 《白血病.淋巴瘤》 CAS 2007年第4期317-320,共4页 Journal of Leukemia & Lymphoma
关键词 骨髓瘤 骨髓微环境 基质细胞 细胞因子 黏附 耐药 Multiple myeloma Bone marrow microenvironment Stromal cell Cytokine Adhesion Drug resistence
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参考文献30

  • 1宋伦,黎燕,孙英勋,于鸣,沈倍奋.JAK/STAT信号转导途径活化和Mcl-1表达上调介导IL-6在人骨髓瘤细胞系XG-7上的凋亡抑制效应(英文)[J].癌症,2002,21(2):113-116. 被引量:5
  • 2D. Chauhan,K. C. Anderson.Mechanisms of cell death and survival in multiple myeloma (MM): Therapeutic implications[J]. APOPTOSIS . 2003 (4) 被引量:1
  • 3Mitsiades CS,Mitsiades NS,Munshi NC,et al.The role of the bone microenviwnment in the pathophysiology and therapeutic manage- ment of multiple myeloma:interplay of growth factors,their recep- tors and stromal interactions. European Journal of Cancer . 2006 被引量:1
  • 4Tricot G.New insights into role of microenvironment in multiple myeloma. International Journal of Hematology . 2002 被引量:1
  • 5Damiano JS,Cress AE,Hazlehurst LA,et al.Cell adhesion mediat- ed drug resistence(CAM-DR):role of integrins and resistance to apoptosis in human myeloma cell lines. Blood . 1999 被引量:1
  • 6Jourdan M,Mahtouk K,Veyrune JL,et al.Delineation of the roles of paracrine and autocrine interleukin-6(IL-6)in myeloma cell lines in survival versus cell cycle.A possible model for the cooper- ation of myeloma cell growth factors. European Cytokine Network . 2005 被引量:1
  • 7Chauhan D,Pandey P,Hideshima T,et al.SHP2 mediates the pro- tective effect of interleukin-6 against dexamethasone-induced apoptosis in multiple myeloma cells. Journal of Biological Chemistry . 2000 被引量:1
  • 8Hideshima T,Chanhan D,Schlossman R,et al.The role of tumor necrosis factor in the pathophysiology of human multiple myeloma: therapeutic applications. Oncegene . 2001 被引量:1
  • 9De Raeve HR,,Vanderkerken K.The role of the bone marrow mi- croenvironment in multiple myeloma. Histology and Histopathology . 2005 被引量:1
  • 10Choi SJ,Cruz Craig F,et al.Macrophage inflammary protein 1-α(MIP-1α)is a potential osteoclast stimulatory factor in multiple myeloma. Blood . 2000 被引量:1

二级参考文献4

  • 1HeinrichPC,BehrmannI,Muller-NewenG,etal.IL-6-typecytokinesignallingthroughgp130/JAK/STATpathway[].Biochemistry.1998 被引量:1
  • 2AdamJCorryS.TheBcl-2proteinfamily:arbitersofcellsurvival[].Science.1998 被引量:1
  • 3PuthierD,DerenneS,BarilleS,etal.Mcl-1andBcl-xLareco-regulatedbyIL-6inhumanmyelomacells[].British Journal of Haematology.1999 被引量:1
  • 4HalekM,BergsagelPL,AudersonKC.Multiplemyeloma:increasingevidenceforamultisteptransformationprocess[].Blood.1998 被引量:1

共引文献4

同被引文献19

  • 1冯继良,姚焕玲,吴强,马传侠.耐药基因检测及体外药敏试验在卵巢癌个体化治疗中的价值[J].肿瘤研究与临床,2008,20(8):529-531. 被引量:3
  • 2Zhang X, Liu Y, Si YJ, et al. Effect of Cx43 gene-modified leukemic bone marrow stromal cells on the regulation of Jurkat cell line in vitro. Leuk Res, 2012, 36:198-204. 被引量:1
  • 3Li J,Wood WH,Becker KG,et al.Gene expression response to cisplatin treatment in drug-sensitive and drug-resistant ovarian cancer ceils. Oncogene, 2007, 26:2860 -2872. 被引量:1
  • 4Chang LT,Sun CK,Sheu JJ,et al.Cilostazol therapy attenuates monocrotaline induced pulmonary arterial hypertension in rat model. Circ J, 2005, 72:825-831. 被引量:1
  • 5张之南,沈悌.血液病诊断及疗效标准3版.北京:科学出版社,2007:103-105,1131-1134. 被引量:1
  • 6SOez JC,Viviana MB,Maria CB. Plasma membrane channels formed by connexins:their regulation and functions.Physiol Rev, 2003, 83:1359- 1400. 被引量:1
  • 7Holder JW, Elmor EE,Barrett J. Gap junction function and cancer. Cancer Res, 1993, 53:3475-3485. 被引量:1
  • 8Hazlehurst LA, Landowski TH, Dalton WS.Role of the tumor microenvironment in mediating de novo resistance to drugs and physiological mediators of cell death. Oncogene, 2003, 22:7396-7402. 被引量:1
  • 9Sato H, Iwata H, TakanoY, et al. Enhanced effect of connexin 43 on cisplatininduced cytotoxieity in mesothelioma cells. J Pharmacol Sei, 2009,110:466-475. 被引量:1
  • 10Benko G,Spajie B,Demirovie A, et al. Prognostic value of eonnexin43 expression in patients with clinically localized prostate cancer. Prostate Cancer Prostatic Dis, 2010,14:90-95. 被引量:1

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