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蛋白酶体抑制剂——硼替佐米的临床治疗研究进展 被引量:7

Advances in studies on the therapy with proteasome inhibitor Bortezomib
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摘要 泛素-蛋白酶体通路是生物体内进行蛋白质选择性降解的重要途径之一,它参与了细胞内许多重要的生理生化过程。蛋白酶体抑制剂可阻断大量调节蛋白的降解,引起细胞内信号系统的紊乱和超负荷,导致细胞生长的抑制,最终使肿瘤进展过程延缓甚至停滞。硼替佐米作为一种蛋白酶体抑制剂,能抑制多发性骨髓瘤细胞的生长及诱导肿瘤细胞的凋亡,同时对血液系统其它恶性肿瘤具有显著作用,并对某些实体瘤也有良好疗效,克服化疗耐药性。本文就蛋白酶体抑制剂硼替佐米在临床上的治疗的研究进展作一综述。 The ubiquitin-proteasome pathway is one of important pathways during protein selective degradation in organism which participates in many intracellular physiological and biochemical processes. Proteasome inhibitor can block the degradation of quantity of regulatory proteins and induce intraeellular signal pathway disorder and over loading,which will result in cell growth inhibition as well as the delay and even stop of tumor invasion. As a proteasome inhibitor, Bortezomib can inhibit cell growth of multiple myeloma and induce apoptosis of tumor cells. Further more, it has significant effect on other hematological malignancies, as well as other solid tumors. At the same time, Bortezomib can overcome drug resistance in chemotherapy. This article reviewed studies on therapy with proteasome inhibitor Bortezomib.
出处 《国际内科学杂志》 CAS 2008年第11期657-661,671,共6页 International Journal of Internal Medicine
关键词 蛋白酶体抑制剂 治疗 硼替佐米 Proteasome inhihitor Therapy Bortezomib
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参考文献30

  • 1Voorhees PM, Dees EC, O' Neil B, et al. The proteasome as a target for cancer therapy. Clin Cancer Res,2003,9 (17) : 6316-6325.
  • 2Tao GZ, Rott LS, Lowe AW,et al. Hyposmotic stress induces cell growth arrest via proteasome activation and cyclin/cyclin-dependent kinase degradation. J Biol Chem, 2002, 277 ( 22 ) : 19295-19303.
  • 3Aghajanian C, Soigent S, Dizon DS,et al. A phase Ⅰ trial of the novel proteasome inhibitor PS341 in advanced solid tumor malignancies. Clin Cancer Res, 2002, 8 (8) : 2505- 2511.
  • 4Meister S, Schubert U, Neubert K,et al. Extensive immunoglobulin production sensitizes myeloma cells for proteasome inhibition. Cancer Res ,2007,67 (4) : 1783-1792.
  • 5Pelletier N, Casamayor-Palleja M , De Luea K, et al. The endoplasmic reticulum is a key component of the plasma cell death pathway. J Immunol,2006,1 76 ( 3 ) : 1340-1347.
  • 6Davies FE, Wu P, Jenner M, et al. The combination of cyclophosphamide, velcade and dexamethasone induces high response rates with comparable toxicity to velcade alone and velcade plus dexamethasone. Haematologica, 2007,92 ( 8 ) : 1149-1150.
  • 7Mateos MV, Hernandez JM, Henandez MT, et al. Bortezomib plus melphalan and prednisone in olderly untreated patients with multiple myeloma:resuhs a multicenter phase 1/2 study. Blood ,2006,108 (7) :2165-2172.
  • 8Mateos MV, Hemandez JM, Hernandez MT, et al. Bortezomib plus melphalan and prednisone in elderly untreated patients with multiple myeloma: updated time-to- events resuits and prognostic factors for time to progression. Haematologica,2008, Mar 5 [ Epub ahead of print].
  • 9San-Miguel JF, Richardson PG, Sonneveld P, et al. Efficaey and safety of bortezomib in patients with renal impairment: results from the APEX phase 3 study. Leukemia, 2008, Jan 17 [ Epub ahead of print ].
  • 10El-Cheikh J, Michallet M, Arnon Nagler A, et al. High response rate and improved graft-versus-host disease following bortezomib as salvage therapy after reduced intensity conditioning allogeneic stem cell transplantation for multiple myeloma. Haematologica, 93 (3) :455-458.

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