Siddappa Gangotri, Kulsum Safeena, Ravindra Doddathimmasandra Ramanjanappa, Kumar Vinay V, Raju Nalini, Raghavan Nisheena, Sudheendra Holalugunda Vittalamurthy, Sharma Anupam, Sunny Sumsum P, Jacob Tina, Kuruvilla Binu T, Benny Merina, Antony Benny, Seshadri Mukund, Lakshminarayan Padma, Hicks Wesley, Suresh Amritha, Kuriakose Moni A
Integrated Head and Neck Oncology Research Program, DSRG-5, Mazumdar Shaw Centre for Translational Research, Mazumdar Shaw Medical Centre, Narayana Health, Bangalore, Karnataka, India.
Head and Neck Oncology, Mazumdar Shaw Medical Centre, Narayana Health, Bangalore, Karnataka, India.
Mol Carcinog. 2017 Nov;56(11):2446-2460. doi: 10.1002/mc.22692. Epub 2017 Jul 13.
Effective chemoprevention is critical for improving outcomes of oral cancer. As single agents, curcumin and metformin are reported to exhibit chemopreventive properties, in vitro as well as in patients with oral cancer. In this study, the chemopreventive efficacy of this drug combination was tested in a 4-nitro quinoline-1-oxide (4NQO) induced mice oral carcinogenesis model. Molecular analysis revealed a cancer stem cell (CSC)-driven oral carcinogenic progression in this model, wherein a progressive increase in the expression of CSC-specific markers (CD44 and CD133) was observed from 8th to 25th week, at transcript (40-100-fold) and protein levels (P ≤ 0.0001). Chemopreventive treatment of the animals at 17th week with curcumin and metformin indicated that the combination regimen decreased tumor volume when compared to the control arm (0.69+0.03 vs 6.66+2.4 mm ; P = 0.04) and improved overall survival of the animals (P = 0.03). Assessment of the molecular status showed an overall downregulation of CSC markers in the treatment arms as compared to the untreated control. Further, in vitro assessment of the treatment on the primary cells generated from progressive stages of 4NQO-induced mice tissue showed a concordant and consistent downregulation of the CSC markers following combination treatment (P < 0.05). The treatment also inhibited the migratory and self-renewal properties of these cells; the effect of which was prominent in the cultures of early dysplastic tissue (P < 0.002). Collectively, our observations suggest that the combination of curcumin and metformin may improve chemopreventive efficacy against oral squamous cell carcinoma through a CSC-associated mechanism.
有效的化学预防对于改善口腔癌的治疗效果至关重要。据报道,姜黄素和二甲双胍作为单一药物,在体外以及口腔癌患者中均表现出化学预防特性。在本研究中,在4-硝基喹啉-1-氧化物(4NQO)诱导的小鼠口腔致癌模型中测试了这种药物组合的化学预防效果。分子分析揭示了该模型中癌症干细胞(CSC)驱动的口腔致癌进展,其中从第8周到第25周,在转录水平(40 - 100倍)和蛋白质水平(P≤0.0001)观察到CSC特异性标志物(CD44和CD133)的表达逐渐增加。在第17周用姜黄素和二甲双胍对动物进行化学预防治疗表明,与对照组相比,联合治疗方案可减小肿瘤体积(0.69 + 0.03 vs 6.66 + 2.4 mm;P = 0.04)并提高动物的总体生存率(P = 0.03)。分子状态评估显示,与未治疗的对照组相比,治疗组中CSC标志物总体下调。此外,对4NQO诱导的小鼠组织进展阶段产生的原代细胞进行的体外治疗评估显示,联合治疗后CSC标志物一致且持续下调(P < 0.05)。该治疗还抑制了这些细胞的迁移和自我更新特性;这种作用在早期发育异常组织的培养物中尤为突出(P < 0.002)。总体而言,我们的观察结果表明,姜黄素和二甲双胍的组合可能通过与CSC相关的机制提高对口腔鳞状细胞癌的化学预防效果。