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抑制p38α丝裂原活化蛋白激酶可通过在体外调节热休克蛋白27(Hsp27)、Bcl-XL、髓细胞白血病-1(Mcl-1)和p53水平来增强蛋白酶体抑制剂诱导的骨髓瘤细胞凋亡,并在体内抑制肿瘤生长。

Inhibition of p38alpha MAPK enhances proteasome inhibitor-induced apoptosis of myeloma cells by modulating Hsp27, Bcl-X(L), Mcl-1 and p53 levels in vitro and inhibits tumor growth in vivo.

作者信息

Navas T A, Nguyen A N, Hideshima T, Reddy M, Ma J Y, Haghnazari E, Henson M, Stebbins E G, Kerr I, O'Young G, Kapoun A M, Chakravarty S, Mavunkel B, Perumattam J, Luedtke G, Dugar S, Medicherla S, Protter A A, Schreiner G F, Anderson K C, Higgins L S

机构信息

Scios, Inc., Fremont, CA, USA.

出版信息

Leukemia. 2006 Jun;20(6):1017-27. doi: 10.1038/sj.leu.2404200.

Abstract

Inhibition of p38 kinase blocks the production of tumor-promoting factors in the multiple myeloma (MM) bone marrow microenvironment. Proteasome inhibitors MG132 and bortezomib have been shown to have direct cytotoxic effects on MM cells. We show that a selective inhibitor of p38alpha, SCIO-469, enhances the ability of MG132 and bortezomib to induce the apoptosis of MM cells. Previously, we showed that p38 inhibition with SCIO-469 enhances MM cytotoxicity of bortezomib by inhibiting the transient expression and phosphorylation of Hsp27, a downstream target of p38. Here we show that continued treatment of MM cells with bortezomib leads to a SCIO-469-enhanced downregulation of Hsp27 and to increased MM apoptosis. Furthermore, we show that p38 inhibition enhances the bortezomib-induced MM apoptosis by upregulation of p53 and downregulation of Bcl-X(L) and Mcl-1. In a mouse xenograft plasmacytoma model of MM, we found that inhibiting p38 augments the effects of bortezomib in decreasing MM tumor growth in vivo. Thus, in addition to its role in suppressing an activated MM microenvironment, co-treatment with a p38 inhibitor, such as SCIO-469, may enhance the cytotoxicity of bortezomib by modulating pro-apoptotic and anti-apoptotic factors in MM cells, suggesting great potential for co-therapy.

摘要

抑制p38激酶可阻断多发性骨髓瘤(MM)骨髓微环境中肿瘤促进因子的产生。蛋白酶体抑制剂MG132和硼替佐米已被证明对MM细胞具有直接细胞毒性作用。我们发现,p38α的选择性抑制剂SCIO-469可增强MG132和硼替佐米诱导MM细胞凋亡的能力。此前,我们表明,用SCIO-469抑制p38可通过抑制p38的下游靶点Hsp27的瞬时表达和磷酸化来增强硼替佐米对MM的细胞毒性。在此我们表明,用硼替佐米持续处理MM细胞会导致SCIO-469增强Hsp27的下调并增加MM细胞凋亡。此外,我们表明,抑制p38可通过上调p53以及下调Bcl-X(L)和Mcl-1来增强硼替佐米诱导的MM细胞凋亡。在MM的小鼠异种移植浆细胞瘤模型中,我们发现抑制p38可增强硼替佐米在体内减少MM肿瘤生长的作用。因此,除了其在抑制活化的MM微环境中的作用外,与p38抑制剂(如SCIO-469)联合治疗可能通过调节MM细胞中的促凋亡和抗凋亡因子来增强硼替佐米的细胞毒性,这表明联合治疗具有巨大潜力。

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