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A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer

机译:碳酸酐酶IX和组蛋白脱乙酰酶抑制剂对癌症的增强合作

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The emergence of tumour recurrence and resistance limits the survival rate for most tumour-bearing patients. Only, combination therapies targeting pathways involved in the induction and in the maintenance of cancer growth and progression might potentially result in an enhanced therapeutic efficacy. Herein, we provided a prospective combination treatment that includes suberoylanilide hydroxamic acid (SAHA), a well-known inhibitor of histone deacetylases (HDACs), and SLC-0111, a novel inhibitor of carbonic anhydrase (CA) IX. We proved that HDAC inhibition with SAHA in combination with SLC-0111 affects cell viability and colony forming capability to greater extent than either treatment alone of breast, colorectal and melanoma cancer cells. At the molecular level, this therapeutic regimen resulted in a synergistically increase of histone H4 and p53 acetylation in all tested cell lines. Overall, our findings showed that SAHA and SLC-0111 can be regarded as very attractive combination providing a potential therapeutic strategy against different cancer models.
机译:肿瘤复发和阻力的出现限制了大多数肿瘤患者的存活率。仅,诱导诱导和维持癌症生长和进展中涉及涉及的途径的组合疗法可能导致增强的治疗效果。在此,我们提供了一种预期组合处理,其包括Suberoylanilide羟胺酸(Saha),可公知的组蛋白脱乙酰酶(HDACs)和SLC-0111,碳酸酐酶(CA)IX的新型抑制剂。我们证明,与SLC-0111组合的HDAC抑制与SLC-0111的组合影响细胞活力和菌落形成能力比单独的乳腺,结直肠和黑素瘤癌细胞的治疗更大程度地影响。在分子水平下,这种治疗方案导致组蛋白H4和P53乙酰化在所有测试细胞系中的协同增加。总体而言,我们的研究结果表明,萨哈和SLC-0111可以被视为非常有吸引力的组合,为不同癌症模型提供潜在的治疗策略。

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