Liu Xiaojun, Jiang Yingjun, Nowak Billie, Hargis Sarah, Plunkett William
Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mol Cancer Ther. 2016 Oct;15(10):2302-2313. doi: 10.1158/1535-7163.MCT-15-0801. Epub 2016 Jul 29.
CNDAC (2'-C-cyano-2'-deoxy-1-β-d-arabino-pentofuranosyl-cytosine, DFP10917) and its orally bioavailable prodrug, sapacitabine, are undergoing clinical trials for hematologic malignancies and solid tumors. The unique action mechanism of inducing DNA strand breaks distinguishes CNDAC from other deoxycytidine analogs. To optimize the clinical potentials of CNDAC, we explored multiple strategies combining CNDAC with chemotherapeutic agents targeting distinct DNA damage repair pathways that are currently in clinical use. The ability of each agent to decrease proliferative potential, determined by clonogenic assays, was determined in paired cell lines proficient and deficient in certain DNA repair proteins. Subsequently, each agent was used in combination with CNDAC at fixed concentration ratios. The clonogenicity was quantitated by median effect analysis, and a combination index was calculated. The c-Abl kinase inhibitor imatinib had synergy with CNDAC in HCT116 cells, regardless of p53 status. Inhibitors of PARP1 that interfere with homologous recombination (HR) repair or base excision repair (BER) and agents such as temozolomide that cause DNA damage repaired by the BER pathway were also synergistic with CNDAC. The toxicity of the nitrogen mustards bendamustine and cytoxan, or of platinum compounds, which generate DNA adducts repaired by nucleotide excision repair and HR, was additive with CNDAC. An additive cell killing was also achieved by the combination of CNDAC with taxane mitotic inhibitors (paclitaxel and docetaxel). At concentrations that allow survival of the majority of wild-type cells, the synergistic or additive combination effects were selective in HR-deficient cells. This study provides mechanistic rationales for combining CNDAC with other active drugs. Mol Cancer Ther; 15(10); 2302-13. ©2016 AACR.
CNDAC(2'-C-氰基-2'-脱氧-1-β-D-阿拉伯呋喃糖基胞嘧啶,DFP10917)及其口服生物可利用的前体药物沙帕西他滨正在针对血液系统恶性肿瘤和实体瘤进行临床试验。诱导DNA链断裂的独特作用机制使CNDAC有别于其他脱氧胞苷类似物。为了优化CNDAC的临床潜力,我们探索了多种策略,将CNDAC与目前正在临床使用的、针对不同DNA损伤修复途径的化疗药物联合使用。通过克隆形成试验确定每种药物降低增殖潜力的能力,在对某些DNA修复蛋白有缺陷和无缺陷的配对细胞系中进行测定。随后,每种药物以固定浓度比例与CNDAC联合使用。通过中位效应分析对克隆形成能力进行定量,并计算联合指数。无论p53状态如何,c-Abl激酶抑制剂伊马替尼在HCT116细胞中与CNDAC具有协同作用。干扰同源重组(HR)修复或碱基切除修复(BER)的PARP1抑制剂以及通过BER途径修复DNA损伤的药物如替莫唑胺也与CNDAC具有协同作用。氮芥类药物苯达莫司汀和环磷酰胺或铂类化合物的毒性与CNDAC相加,铂类化合物产生的DNA加合物通过核苷酸切除修复和HR进行修复。CNDAC与紫杉烷类有丝分裂抑制剂(紫杉醇和多西他赛)联合使用也实现了相加的细胞杀伤作用。在允许大多数野生型细胞存活的浓度下,协同或相加的联合效应在HR缺陷细胞中具有选择性。本研究为将CNDAC与其他活性药物联合使用提供了机制依据。《分子癌症治疗》;15(10);2302 - 2313。©2016美国癌症研究协会。