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首页> 外文期刊>Biochemical and Biophysical Research Communications >Adiponectin signals through Adiponectin Receptor 1 to reverse imatinib resistance in K562 human chronic myeloid leukemia cells
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Adiponectin signals through Adiponectin Receptor 1 to reverse imatinib resistance in K562 human chronic myeloid leukemia cells

机译:脂联素通过脂联素受体1信号逆转K562人慢性髓性白血病细胞中的伊马替尼耐药性

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Adiponectin, a member of adipokines, is a functional ligand for Adiponectin Receptor-1 (AdipoR1) and Adiponectin Receptor-2 (AdipoR2), and has been found to be linked to the risk of CML. Imatinib has undoubtedly revolutionised the management and outcome of chronic myeloid leukemia (CML), however imatinib resistance has been recognized as a major problem in CML therapy. In this study, we first established imatinib-resistant K562 CML cells, and then evaluated the effect of Adiponectin in reversing imatinib resistance. The data presented here demonstrated that Adiponectin was able to reverse 1(562 resistance to imatinib in vitro and in vivo. Additional data with molecular approaches suggested that the reversion of Adiponectin in imatinib resistance signals through AdipoR1 but not AdipoR2 to downregulate Bcr-Abl expression and effect in imatinib-resistant K562 CML cells. Taken together, our data showed that Adiponectin can reverse imatinib resistance in CML, and to a certain extent elucidate the mechanism of Adiponectin reversing imatinib resistance that may provide a new and promising approach in imatinib resistance management in CML therapy. (C) 2014 Elsevier Inc. All rights reserved.
机译:脂联素是脂联素的成员,是脂联素受体1(AdipoR1)和脂联素受体2(AdipoR2)的功能性配体,已发现与CML的风险有关。伊马替尼无疑已经改变了慢性粒细胞白血病(CML)的治疗和治疗结果,但是伊马替尼耐药性已被认为是CML治疗中的主要问题。在这项研究中,我们首先建立了对伊马替尼耐药的K562 CML细胞,然后评估了脂联素在逆转伊马替尼耐药中的作用。此处提供的数据表明脂联素在体内外均可逆转1(562对伊马替尼的耐药性。分子方法的其他数据表明,伊马替尼耐药信号中的脂联素通过AdipoR1而不是AdipoR2的逆转来下调Bcr-Abl表达和综上所述,我们的数据显示脂联素可以逆转CML中的伊马替尼耐药性,并在一定程度上阐明了脂联素逆转伊马替尼耐药性的机制,这可能为伊马替尼耐药管理提供一种新的有希望的方法(C)2014 Elsevier Inc.保留所有权利。

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