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选择性抑制髓系Src 家族激酶 Fgr 可强力抑制 AML 细胞的体外和体内生长。

Selective Inhibition of the Myeloid Src-Family Kinase Fgr Potently Suppresses AML Cell Growth in Vitro and in Vivo.

机构信息

Department of Microbiology and Molecular Genetics , University of Pittsburgh School of Medicine , Pittsburgh , Pennsylvania , United States.

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and Department of Cancer Biology , Dana-Farber Cancer Institute , 250 Longwood Avenue , Boston , Massachusetts 02115 , United States.

出版信息

ACS Chem Biol. 2018 Jun 15;13(6):1551-1559. doi: 10.1021/acschembio.8b00154. Epub 2018 May 30.

Abstract

Acute myelogenous leukemia (AML) is the most common hematologic malignancy in adults and is often associated with constitutive tyrosine kinase signaling. These pathways involve the nonreceptor tyrosine kinases Fes, Syk, and the three Src-family kinases expressed in myeloid cells (Fgr, Hck, and Lyn). In this study, we report remarkable anti-AML efficacy of an N-phenylbenzamide kinase inhibitor, TL02-59. This compound potently suppressed the proliferation of bone marrow samples from 20 of 26 AML patients, with a striking correlation between inhibitor sensitivity and expression levels of the myeloid Src family kinases Fgr, Hck, and Lyn. No correlation was observed with Flt3 expression or mutational status, with the four most sensitive patient samples being wild-type for Flt3. Kinome-wide target specificity profiling coupled with in vitro kinase assays demonstrated a narrow overall target specificity profile for TL02-59, with picomolar potency against the myeloid Src-family member Fgr. In a mouse xenograft model of AML, oral administration of TL02-59 for 3 weeks at 10 mg/kg completely eliminated leukemic cells from the spleen and peripheral blood while significantly reducing bone marrow engraftment. These results identify Fgr as a previously unrecognized kinase inhibitor target in AML and TL02-59 as a possible lead compound for clinical development in AML cases that overexpress this kinase independent of Flt3 mutations.

摘要

急性髓细胞白血病 (AML) 是成年人中最常见的血液系统恶性肿瘤,通常与组成性酪氨酸激酶信号有关。这些途径涉及非受体酪氨酸激酶 Fes、Syk 和在髓样细胞中表达的三个Src 家族激酶 (Fgr、Hck 和 Lyn)。在这项研究中,我们报告了 N- 苯基苯甲酰胺激酶抑制剂 TL02-59 对 AML 的显著疗效。该化合物强烈抑制了 26 例 AML 患者中的 20 例骨髓样本的增殖,与抑制剂敏感性和髓样 Src 家族激酶 Fgr、Hck 和 Lyn 的表达水平之间存在显著相关性。与 Flt3 的表达或突变状态没有相关性,四个最敏感的患者样本为 Flt3 野生型。激酶组广泛的靶特异性分析结合体外激酶测定表明,TL02-59 的靶特异性谱较窄,对髓样 Src 家族成员 Fgr 的抑制作用为皮摩尔级。在 AML 的小鼠异种移植模型中,口服 TL02-59 3 周,剂量为 10mg/kg,可完全消除脾脏和外周血中的白血病细胞,同时显著减少骨髓植入。这些结果表明 Fgr 是 AML 中以前未被识别的激酶抑制剂靶标,TL02-59 可能是 AML 临床开发的潜在先导化合物,这些 AML 病例独立于 Flt3 突变过度表达这种激酶。

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