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硼替佐米单用或联合三氧化二砷对Jurkat细胞凋亡和Livin mRNA表达的影响

Effects of Bortezomib Alone or Combined with Arsenic Trioxide on the Apoptosis of Jurkat Cells and Expression of Livin mRNA
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摘要 本研究旨在探讨硼替佐米单用或联合三氧化二砷对Jurkat细胞凋亡的影响。用不同浓度硼替佐米、三氧化二砷处理细胞24小时,采用MTT比色法检测细胞增殖活性,流式细胞术检测细胞凋亡,RT-PCR法检测Livin mRNA的表达。结果表明,5-25 nmol/L硼替佐米对Jurkat细胞增殖均有一定抑制作用,随着浓度增加抑制作用逐渐增强。硼替佐米和三氧化二砷联合处理组对细胞的抑制作用比同剂量两药中任一种单独使用时都显著增强(p<0.05)。硼替佐米能促使Jurkat细胞凋亡,且随浓度增加而凋亡增多,联合处理组对细胞的凋亡作用比同剂量单药作用时显著增强(p<0.01)。硼替佐米能下调Jurkat细胞Livin mRNA的表达,且随着药物浓度增加,表达逐渐降低,联合处理组比同剂量单药组更显著下调LivinmRNA的表达(p<0.05)。结论:硼替佐米或联合三氧化二砷可以下调Jurkat细胞中Livin mRNA的表达,并可能通过此机制诱导K562细胞凋亡,两药具有协同作用。 This study was aimed to investigate the effect of bortezomib alone or combined with arsenic trioxide on the apoptosis of Jurkat cells and expressiom of livin mRNA. The Jurkat cells were cultured and treated with different concentrations of bortezomib, arsenic trioxide or their combination for 24 hours. Then, the expression of livin mRNA was detected by RT-PCR, the cell proliferation was analyzed with MTT assay and flow cytometry. The results showed that 5 - 25 nmol/L bortezomib could effectively inhibit Jurkat cells in a dose-dependent manner, the group of bortezomib combined with arsenic trioxide showed more inhibitory effect on Jurkat cells than the effect of bortezomib alone or arsenic trioxide alone on Jurkat cells. The expression of livin mRNA in Jurkat cells decreased in a dose-dependent manner after treated with bortezomib, which was downregulated significantly after combined treatment. It is concluded that bortezomib and arsenic trioxide can induce apoptosis by inhibiting the expression of livin mRNA in Jurkat cells. The combination of bortezomib with arsenic trioxide displays a synergistic effect.
出处 《中国实验血液学杂志》 CAS CSCD 2011年第4期898-901,共4页 Journal of Experimental Hematology
关键词 硼替佐米 三氧化二砷 凋亡 LIVIN mRNA bortezomib arsenic trioxide apoptosis Livin mRNA
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参考文献7

  • 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.
  • 2Gatto S scappini B, Pham L,et al. The proteasome inhibitor PS-341 inhibits growth and induces apoptosis in Bcr/Abl-positive cell lines sensitive and resistant to imatinib mesylate. Haematologica,2003 ;88 (8) :853 -863.
  • 3Lin JH, Dell G, Huang Q, et al. KIAP, a novel member of the inhibitor of apoptosis protein family . Biochem Biophys Res Commun, 2000 ;279 (3) :820 - 831.
  • 4Kasof GM, Comes BC. Livin, a novel inhibitor of apoptosis protein family member . J Biol Chem,2001 ;276(5 ) :3238 -3246.
  • 5Vucic D. Stennicke HR,Pisabarre MT,et al. ML-IAP,a novel inhibitor of apeptosis that is preferentially expressed in human melanomas. Curt Biol,2000 ; 10 ( 21 ) : 1359 - 1366.
  • 6Ashhab Y, Allan A, Polliack A, et al. Two splicing variants of a new inhibitor of apoptosis gene with different biological properties andtissue distribution pattern. FEBS Lett,2001 ;495( 1 -2) :56 -60.
  • 7Du C, Fang M, Li Y, et al. Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition. Cell ,2000 ;102( 1 ) :33 -42.

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