Preclinical testing of an Atr inhibitor demonstrates improved response to standard therapies for esophageal cancer

被引:37
作者
Leszczynska, Katarzyna B.
Dobrynin, Greg
Leslie, Rhea E.
Ient, Jonathan
Boumelha, Adam J.
Senra, Joana M.
Hawkins, Maria A.
Maughan, Tim
Mukherjee, Somnath
Hammond, Ester M. [1 ,2 ]
机构
[1] Univ Oxford, Canc Res UK, Oxford OX3 7DQ, England
[2] Univ Oxford, MRC, Oxford Inst Radiat Oncol, Dept Oncol, Oxford OX3 7DQ, England
基金
英国医学研究理事会;
关键词
ATR; Esophageal cancer; Radiation; Hypoxia; SQUAMOUS-CELL CARCINOMA; TARGETING ATR; HYPOXIA; EXPRESSION; ADENOCARCINOMA; PROGNOSIS; RADIATION; KINASE;
D O I
10.1016/j.radonc.2016.10.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Esophageal cancer has a persistently low 5-year survival rate and has recently been classified as a cancer of unmet need by Cancer Research UK. Consequently, new approaches to therapy are urgently required. Here, we tested the hypothesis that an ATR inhibitor, VX-970, used in combination with standard therapies for esophageal cancer could improve treatment outcome. Material and methods: Using esophageal cancer cell lines we evaluated the efficacy of combining VX-970 with cisplatin and carboplatin in vitro and with radiation in vitro and in vivo. Radiation experiments were also carried out in hypoxic conditions to mimic the tumor microenvironment. Results: Combining VX-970 with cisplatin, carboplatin and radiation increased tumor cell kill in vitro. A significant tumor growth delay was observed when VX-970 was combined with radiotherapy in vivo. Conclusions: VX-970 is an effective chemo/radiosensitizer which could be readily integrated in the current treatment paradigm to improve the treatment response in esophageal cancer and we plan to test it prospectively in the forthcoming phase I dose escalation safety study combining the ATR inhibitor VX-970 with chemoradiotherapy in esophageal cancer (EudraCT number: 2015-003965-27). (C) 2016 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:232 / 238
页数:7
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