Raaphorst G P, Li L F, Yang D P, LeBlanc J-M
Medical Physics Department, The Ottawa Hospital Regional Cancer Centre, 503 Smyth Road, Ottawa, Ontario K1H 1C7, Canada.
Oncol Rep. 2005 Jul;14(1):281-5.
The effect of mild hyperthermia on cisplatin sensitization was examined in two cell line pairs, CHO parental AA8 and irsISF, an XRCC3 mutant (deficient in homologous recombination repair), and mouse parental MEF and knockout Ku80 mutants (deficient in non-homologous endjoining repair). The results showed that mild hyperthermia 40, 41 and 42 degrees C given concurrently with cisplatin treatment caused significant sensitization. The degree of sensitization was comparable for the parental and mutant lines, indicating that these repair pathways were likely not involved in cisplatin thermal sensitization. The shorter concurrent treatments cause a larger sensitization than the longer treatments. The reasons for this are not clear, but thermotolerance may be a factor.
在两对细胞系中检测了轻度热疗对顺铂增敏的影响,即中国仓鼠卵巢细胞亲本AA8和irsISF(一种XRCC3突变体,缺乏同源重组修复功能),以及小鼠亲本成纤维细胞和敲除Ku80突变体(缺乏非同源末端连接修复功能)。结果表明,与顺铂治疗同时进行的40、41和42摄氏度的轻度热疗会引起显著的增敏作用。亲本系和突变体系的增敏程度相当,这表明这些修复途径可能不参与顺铂热增敏。较短的同时治疗比较长的治疗引起更大的增敏作用。其原因尚不清楚,但热耐受性可能是一个因素。