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In Vitro Radiosensitization of Esophageal Cancer Cells with the Aminopeptidase Inhibitor CHR-2797

机译:氨基肽酶抑制剂CHR-2797对食管癌细胞的体外放射增敏作用

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With the increased incidence of esophageal cancer, chemoradiotherapy continues to play an important role in the management of this disease. Developing potent radiosensitizers is therefore critical for improving outcomes. The use of drugs that have already undergone clinical testing is an appealing approach once the side effects and tolerated doses are established. Here, we demonstrate that the aminopeptidase inhibitor, CHR-2797/tosedostat, increases the radiosensitivity of esophageal cancer cell lines (FLO-1 and OE21) in vitro in both normoxic and physiologically relevant low oxygen conditions. To our knowledge, the effective combination of CHR-2797 with radiation exposure has not been reported previously in any cancer cell type. The mechanism of increased radiosensitivity was not dependent on the induction of DNA damage or DNA repair kinetics. Our data support the need for further preclinical testing of CHR-2797 in combination with radiotherapy for the treatment of esophageal cancer. (C) 2015 by Radiation Research Society
机译:随着食管癌的发病率增加,放化疗在该疾病的治疗中继续发挥重要作用。因此,开发有效的放射增敏剂对于改善治疗效果至关重要。一旦确定了副作用和耐受剂量,使用经过临床测试的药物将是一种有吸引力的方法。在这里,我们证明了氨基肽酶抑制剂CHR-2797 / tosedostat在常氧和生理相关的低氧条件下均可提高食管癌细胞系(FLO-1和OE21)的放射敏感性。据我们所知,CHR-2797与放射线的有效结合以前尚未在任何癌细胞类型中报道。放射敏感性增加的机制并不依赖于DNA损伤的诱导或DNA修复动力学。我们的数据支持需要对CHR-2797进行进一步的临床前测试,并结合放射疗法治疗食道癌。 (C)辐射研究学会2015年

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