Beeharry Neil, Banina Eugenia, Hittle James, Skobeleva Natalia, Khazak Vladimir, Deacon Sean, Andrake Mark, Egleston Brian L, Peterson Jeffrey R, Astsaturov Igor, Yen Timothy J
Cancer Biology Program; Fox Chase Cancer Center; Philadelphia, PA USA.
Program in Developmental Therapeutics; Fox Chase Cancer Center; Philadelphia, PA USA.
Cell Cycle. 2014;13(14):2172-91. doi: 10.4161/cc.29214. Epub 2014 Jun 23.
Inhibitors of the DNA damage checkpoint kinase, Chk1, are highly effective as chemo- and radio-sensitizers in preclinical studies but are not well-tolerated by patients. We exploited the promiscuous nature of kinase inhibitors to screen 9 clinically relevant kinase inhibitors for their ability to sensitize pancreatic cancer cells to a sub-lethal concentration of gemcitabine. Bosutinib, dovitinib, and BEZ-235 were identified as sensitizers that abrogated the DNA damage checkpoint. We further characterized bosutinib, an FDA-approved Src/Abl inhibitor approved for chronic myelogenous leukemia. Unbeknownst to us, we used an isomer (Bos-I) that was unknowingly synthesized and sold to the research community as "authentic" bosutinib. In vitro and cell-based assays showed that both the authentic bosutinib and Bos-I inhibited DNA damage checkpoint kinases Chk1 and Wee1, with Bos-I showing greater potency. Imaging data showed that Bos-I forced cells to override gemcitabine-induced DNA damage checkpoint arrest and destabilized stalled replication forks. These inhibitors enhanced sensitivity to the DNA damaging agents' gemcitabine, cisplatin, and doxorubicin in pancreatic cancer cell lines. The in vivo efficacy of Bos-I was validated using cells derived directly from a pancreatic cancer patient's tumor. Notably, the xenograft studies showed that the combination of gemcitabine and Bos-I was significantly more effective in suppressing tumor growth than either agent alone. Finally, we show that the gatekeeper residue in Wee1 dictates its sensitivity to the 2 compounds. Our strategy to screen clinically relevant kinase inhibitors for off-target effects on cell cycle checkpoints is a promising approach to re-purpose drugs as chemosensitizers.
DNA损伤检查点激酶Chk1的抑制剂在临床前研究中作为化疗和放疗增敏剂非常有效,但患者对其耐受性不佳。我们利用激酶抑制剂的多效性,筛选了9种临床相关激酶抑制剂,以研究它们使胰腺癌细胞对亚致死浓度吉西他滨敏感的能力。博舒替尼、多韦替尼和BEZ - 235被鉴定为能消除DNA损伤检查点的增敏剂。我们进一步对博舒替尼进行了表征,它是一种已获美国食品药品监督管理局(FDA)批准用于慢性粒细胞白血病的Src/Abl抑制剂。我们当时并不知晓,我们使用的是一种异构体(Bos - I),它在不知情的情况下被合成并作为“正宗”博舒替尼出售给了科研界。体外和基于细胞的试验表明,正宗博舒替尼和Bos - I均能抑制DNA损伤检查点激酶Chk1和Wee1,其中Bos - I的效力更强。成像数据显示,Bos - I迫使细胞越过吉西他滨诱导的DNA损伤检查点停滞,并使停滞的复制叉不稳定。这些抑制剂增强了胰腺癌细胞系对DNA损伤剂吉西他滨、顺铂和阿霉素的敏感性。Bos - I的体内疗效在直接来源于一名胰腺癌患者肿瘤的细胞中得到了验证。值得注意的是,异种移植研究表明,吉西他滨和Bos - I联合使用在抑制肿瘤生长方面比单独使用任何一种药物都显著更有效。最后,我们表明Wee1中的守门残基决定了其对这两种化合物的敏感性。我们筛选临床相关激酶抑制剂对细胞周期检查点的脱靶效应的策略,是一种将药物重新用作化学增敏剂的有前景的方法。