Miller Geoffrey D, Woessner David W, Sirch Monika J, Lim Carol S
Department of Pharmaceutics and Pharmaceutical Chemistry, ‡Department of Pharmacology and Toxicology, College of Pharmacy, University of Utah , Salt Lake City, Utah 84112, United States.
Mol Pharm. 2013 Sep 3;10(9):3475-83. doi: 10.1021/mp400323c. Epub 2013 Aug 20.
The oncoprotein Bcr-Abl, the causative agent of chronic myeloid leukemia (CML), requires homo-oligomerization via a coiled-coil domain to function [Bartram, C. R.; et al. Nature 1983, 306 (5940), 277-280; and Zhao, X.; et al. Nat. Struct. Biol. 2002, 9(2), 117-120]. While tyrosine kinase inhibitors (TKIs) have shown great efficacy as treatment options for CML, their use may cause an acquisition of mutations in the tyrosine kinase domain, which prevent TKI binding and lead to a loss in activity [Woessner, D. W.; et al. Cancer J. 2011, 17(6), 477-486]. Previously, we have shown that a rationally modified coiled-coil domain (CC(mut3)) can disrupt this oligomerization, inhibit proliferation, and induce apoptosis in CML cells [Dixon, A. S.; et al. Mol. Pharmaceutics 2012, 9(1), 187-195]. Here, we show that using the most recently approved TKI, ponatinib (Iclusig), in combination with CC(mut3) allows a dose reduction of ponatinib and increased therapeutic efficacy in vitro measured by reduction in kinase activity, induction of apoptosis via caspase-3/7 and 7-AAD/Annexin V assays, and reduced transformative ability measured by a colony forming assay. The combination was effective not only in cells containing wild-type Bcr-Abl (K562, Ba/F3-p210) but also cells with Bcr-Abl containing the T315I mutation (Ba/F3-p210-T315I). In addition, we report for the first time the ability of CC(mut3) alone to inhibit the T315I mutant form of Bcr-Abl. This novel combination may prove to be more potent than single agent therapies and should be further explored for clinical use.
致癌蛋白Bcr-Abl是慢性髓性白血病(CML)的致病因子,它需要通过一个卷曲螺旋结构域进行同源寡聚化才能发挥作用[巴特兰,C.R.等人,《自然》,1983年,306(5940),277 - 280页;以及赵,X.等人,《自然结构生物学》,2002年,9(2),117 - 120页]。虽然酪氨酸激酶抑制剂(TKIs)已显示出作为CML治疗选择的巨大疗效,但它们的使用可能会导致酪氨酸激酶结构域发生突变,从而阻止TKI结合并导致活性丧失[沃斯纳,D.W.等人,《癌症杂志》,2011年,17(6),477 - 486页]。此前,我们已经表明,一种经过合理修饰的卷曲螺旋结构域(CC(mut3))可以破坏这种寡聚化,抑制CML细胞的增殖并诱导其凋亡[迪克森,A.S.等人,《分子药剂学》,2012年,9(1),187 - 195页]。在此,我们表明,使用最新批准的TKI波纳替尼(Iclusig)与CC(mut3)联合使用,可以降低波纳替尼的剂量,并通过降低激酶活性、通过caspase - 3/7和7 - AAD/膜联蛋白V检测诱导凋亡以及通过集落形成检测降低转化能力,在体外提高治疗效果。这种联合不仅对含有野生型Bcr - Abl的细胞(K562,Ba/F3 - p210)有效,而且对含有Bcr - Abl T315I突变的细胞(Ba/F3 - p210 - T315I)也有效。此外,我们首次报道了CC(mut3)单独抑制Bcr - Abl的T315I突变体形式的能力。这种新型联合可能比单一药物疗法更有效,应进一步探索其临床应用。