Department of Neurological Surgery, University of Washington, Seattle, WA 98195-6470, USA.
Int J Cancer. 2011 Nov 15;129(10):2370-9. doi: 10.1002/ijc.25900. Epub 2011 May 5.
Apurinic/apyrimidinic endonuclease (Ap endo) is a key DNA repair activity that confers radiation resistance in human cells. Here we examined the association between Ap endo activity and response to radiotherapy in pediatric ependymomas, tumors for which treatment options are limited and survival rates are only about 50%. We assayed Ap endo activity in 36 ependymomas and expression of Ape1/Ref-1, the predominant Ap endo activity in humans, in 44 tumors by immunostaining. Cox proportional hazards regression models were used to analyze the association of activity or expression with progression-free survival or with overall survival. Activity varied 13-fold and was not associated with tumor or patient characteristics. In univariate models with Ap endo activity entered as a continuous variable, the hazard ratio for progression increased by a factor of 2.18 for every 0.01 unit increase in activity (p ≤ 0.003) in 24 grade II ependymomas. Risk for death increased by a factor of 1.89 (p ≤ 0.02) in the same population. The fraction of Ape1/Ref-1 immunopositive cells varied widely within individual tumors and was not associated with either progression-free or with overall survival. Suppressing Ap endo activity in pediatric ependymoma cells significantly increased radiation sensitivity, suggesting that the association of activity with radiation response reflected, at least in part, repair of radiation-induced DNA lesions. Our data indicate that Ap endo activity is predictive of outcome following radiotherapy, and suggest that Ape1/Ref-1 promotes radiation resistance in pediatric ependymomas. Our findings support the use of inhibitors of Ap endo activity to overcome resistance.
脱嘌呤/脱嘧啶核酸内切酶(Ap endo)是一种关键的 DNA 修复活性酶,可赋予人类细胞辐射抗性。在这里,我们研究了 Ap endo 活性与儿科室管膜瘤放疗反应之间的关系,这些肿瘤的治疗选择有限,生存率仅约为 50%。我们通过免疫染色法检测了 36 例室管膜瘤中的 Ap endo 活性和 44 例肿瘤中的 Ape1/Ref-1(人类中主要的 Ap endo 活性酶)的表达。Cox 比例风险回归模型用于分析活性或表达与无进展生存期或总生存期的关系。活性的变化范围为 13 倍,与肿瘤或患者特征无关。在将 Ap endo 活性作为连续变量纳入的单变量模型中,在 24 例 II 级室管膜瘤中,活性每增加 0.01 个单位,进展的风险比增加 2.18 倍(p ≤ 0.003)。在同一人群中,死亡的风险增加了 1.89 倍(p ≤ 0.02)。单个肿瘤内 Ape1/Ref-1 免疫阳性细胞的比例差异很大,与无进展生存期或总生存期均无关。抑制儿科室管膜瘤细胞中的 Ap endo 活性显著增加了辐射敏感性,这表明活性与辐射反应的关联至少部分反映了修复辐射诱导的 DNA 损伤。我们的数据表明 Ap endo 活性是放疗后预后的预测指标,并表明 Ape1/Ref-1 促进了儿科室管膜瘤的辐射抗性。我们的研究结果支持使用 Ap endo 活性抑制剂来克服耐药性。