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在费城染色体阳性的ABL酪氨酸激酶抑制剂耐药细胞中对极光激酶A进行治疗性靶向作用。

Therapeutic targeting of Aurora A kinase in Philadelphia chromosome-positive ABL tyrosine kinase inhibitor-resistant cells.

作者信息

Okabe Seiichi, Tauchi Tetsuzo, Tanaka Yuko, Ohyashiki Kazuma

机构信息

Department of Hematology, Tokyo Medical University, Tokyo, Japan.

出版信息

Oncotarget. 2018 Aug 21;9(65):32496-32506. doi: 10.18632/oncotarget.25985.

Abstract

Abelson murine leukemia viral oncogene homolog (ABL) tyrosine kinase inhibitors (TKIs) have been shown to be effective for treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia patients. However, resistance to ABL TKIs can develop as a result of breakpoint cluster region-ABL point mutations. Aurora kinases regulate many processes associated with mitosis. In this study, we investigated whether inhibiting Aurora kinase can reduce the viability of Ph+ leukemia cells. Treatment with the Aurora kinase A inhibitor alisertib blocked Ph+ leukemia cell proliferation and Aurora kinase A phosphorylation; it also induced G2/M-phase arrest and increased the intracellular levels of reactive oxygen species. Combined treatment of Ph+ cells with ABL TKIs and alisertib was cytotoxic, with the fraction of senescent cells increasing in a time- and dose-dependent manner. Aurora A gene silencing suppressed cell proliferation and enhanced ABL TKI efficacy. In a mouse xenograft model, co-administration of ponatinib and alisertib enhanced survival and reduced tumor size; moreover, the treatments were well tolerated by the animals. These results indicate that inhibiting Aurora kinase can enhance the cytotoxic effects of ABL TKIs and is, therefore, an effective therapeutic strategy against ABL TKI-resistant cells, including those with the T315I mutation.

摘要

阿贝尔逊鼠白血病病毒癌基因同源物(ABL)酪氨酸激酶抑制剂(TKIs)已被证明对治疗慢性髓性白血病(CML)和费城染色体阳性(Ph+)急性淋巴细胞白血病患者有效。然而,由于断裂点簇集区-ABL点突变,可能会产生对ABL TKIs的耐药性。极光激酶调节许多与有丝分裂相关的过程。在本研究中,我们调查了抑制极光激酶是否能降低Ph+白血病细胞的活力。用极光激酶A抑制剂阿利西替尼治疗可阻断Ph+白血病细胞增殖和极光激酶A磷酸化;还可诱导G2/M期阻滞并增加细胞内活性氧水平。用ABL TKIs和阿利西替尼联合治疗Ph+细胞具有细胞毒性,衰老细胞比例呈时间和剂量依赖性增加。极光A基因沉默可抑制细胞增殖并增强ABL TKI疗效。在小鼠异种移植模型中,泊那替尼和阿利西替尼联合给药可提高生存率并减小肿瘤大小;此外,动物对这些治疗耐受性良好。这些结果表明,抑制极光激酶可增强ABL TKIs的细胞毒性作用,因此是针对ABL TKI耐药细胞(包括携带T315I突变的细胞)的一种有效治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d8c/6126699/1279f92d9005/oncotarget-09-32496-g001.jpg

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