强效基于ATP的致癌蛋白激酶抑制剂AP23464对野生型和突变型Bcr-Abl的抑制作用:对慢性粒细胞白血病的意义
Inhibition of wild-type and mutant Bcr-Abl by AP23464, a potent ATP-based oncogenic protein kinase inhibitor: implications for CML.
作者信息
O'Hare Thomas, Pollock Roy, Stoffregen Eric P, Keats Jeffrey A, Abdullah Omar M, Moseson Erika M, Rivera Victor M, Tang Hao, Metcalf Chester A, Bohacek Regine S, Wang Yihan, Sundaramoorthi Raji, Shakespeare William C, Dalgarno David, Clackson Tim, Sawyer Tomi K, Deininger Michael W, Druker Brian J
机构信息
Howard Hughes Medical Institute, Oregon Health and Science University, L592, 3181 SW Sam Jackson Park Rd, Portland, OR 97239, USA.
出版信息
Blood. 2004 Oct 15;104(8):2532-9. doi: 10.1182/blood-2004-05-1851. Epub 2004 Jul 15.
The deregulated, oncogenic tyrosine kinase Bcr-Abl causes chronic myeloid leukemia (CML). Imatinib mesylate (Gleevec, STI571), a Bcr-Abl kinase inhibitor, selectively inhibits proliferation and promotes apoptosis of CML cells. Despite the success of imatinib mesylate in the treatment of CML, resistance is observed, particularly in advanced disease. The most common imatinib mesylate resistance mechanism involves Bcr-Abl kinase domain mutations that impart varying degrees of drug insensitivity. AP23464, a potent adenosine 5'-triphosphate (ATP)-based inhibitor of Src and Abl kinases, displays antiproliferative activity against a human CML cell line and Bcr-Abl-transduced Ba/F3 cells (IC(50) = 14 nM; imatinib mesylate IC(50) = 350 nM). AP23464 ablates Bcr-Abl tyrosine phosphorylation, blocks cell cycle progression, and promotes apoptosis of Bcr-Abl-expressing cells. Biochemical assays with purified glutathione S transferase (GST)-Abl kinase domain confirmed that AP23464 directly inhibits Abl activity. Importantly, the low nanomolar cellular and biochemical inhibitory properties of AP23464 extend to frequently observed imatinib mesylate-resistant Bcr-Abl mutants, including nucleotide binding P-loop mutants Q252H, Y253F, E255K, C-terminal loop mutant M351T, and activation loop mutant H396P. AP23464 was ineffective against mutant T315I, an imatinib mesylate contact residue. The potency of AP23464 against imatinib mesylate-refractory Bcr-Abl and its distinct binding mode relative to imatinib mesylate warrant further investigation of AP23464 for the treatment of CML.
失调的致癌性酪氨酸激酶Bcr-Abl会引发慢性髓性白血病(CML)。甲磺酸伊马替尼(格列卫,STI571),一种Bcr-Abl激酶抑制剂,可选择性抑制CML细胞的增殖并促进其凋亡。尽管甲磺酸伊马替尼在治疗CML方面取得了成功,但仍观察到耐药性,尤其是在晚期疾病中。最常见的甲磺酸伊马替尼耐药机制涉及Bcr-Abl激酶结构域突变,这些突变赋予不同程度的药物不敏感性。AP23464,一种基于三磷酸腺苷(ATP)的强效Src和Abl激酶抑制剂,对人CML细胞系和Bcr-Abl转导的Ba/F3细胞具有抗增殖活性(IC(50)=14 nM;甲磺酸伊马替尼IC(50)=350 nM)。AP23464消除Bcr-Abl酪氨酸磷酸化,阻断细胞周期进程,并促进表达Bcr-Abl的细胞凋亡。用纯化的谷胱甘肽S转移酶(GST)-Abl激酶结构域进行的生化分析证实AP23464直接抑制Abl活性。重要的是,AP23464的低纳摩尔细胞和生化抑制特性扩展到经常观察到的对甲磺酸伊马替尼耐药的Bcr-Abl突变体,包括核苷酸结合P环突变体Q252H、Y253F、E255K、C末端环突变体M351T和激活环突变体H396P。AP23464对突变体T315I无效,T315I是甲磺酸伊马替尼的接触残基。AP23464对甲磺酸伊马替尼难治性Bcr-Abl的效力及其相对于甲磺酸伊马替尼的独特结合模式值得进一步研究其用于治疗CML的可能性。