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首页> 外文期刊>Cancer radiotherapie: journal de la Soci閠?fran鏰ise de radiotherapie oncologique >In vitro oxygen-dependent survival of 2 human cell lines after radiation combined with tirapazamine (SR-4233) and cisplatin
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In vitro oxygen-dependent survival of 2 human cell lines after radiation combined with tirapazamine (SR-4233) and cisplatin

机译:联合替拉帕明(SR-4233)和顺铂联合放射后2种人类细胞系的体外氧依赖性存活

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Recent data have shown that the in vitro and in vivo cytotoxicity of bioreductive drugs could be significantly increased by combination with ionising radiation or chemotherapy. Various parameters such as oxygen tension and timing of administration of the drugs could play a crucial role in the efficacy of combined treatment modalities. The aim of this study was to define the oxygen dependency of cell survival after in vitro irradiation and incubation with tirapazamine, a bioreductive drug, and cisplatin given alone or simultaneously. Two human cell lines were studied: one cell line sensitive to tirapazamine, Na11+, a pigmented melanoma with a high percentage of hypoxic cells, and a less sensitive cell line to tirapazamine, HRT18, a rectal adenocarcinoma. Gas changes were made to study cell survival at four different oxygen concentrations (pO2): air (20.9% O2), 10.2 and 0.2% O2. Cells were incubated with tirapazamine and cisplatin alone or combined for one hour at 37 degrees C, then irradiated and cultured. For Na11+, cell survival after irradiation was comparable in air and at 10% oxygen with the two drugs given alone or combined. At 2 and 0.2% oxygen, cell killing was largely increased by tirapazamine and was not modified by the addition of cisplatin. For HRT18, cell survival was not modified when cisplatin was added to radiation, whatever the oxygen partial pressure. At low pO2 (2 and 0.2%) the cytotoxic effect of tirapazamine was not significantly decreased by the addition of cisplatin. When cytotoxic and bioreductive drugs are combined to radiation, the magnitude of the observed effect is highly dependent on the partial oxygen pressure and on the sensitivity of the cell line to the individual drugs. This has very important implications for clinical strategies based on combined chemo-radiotherapy.
机译:最近的数据表明,通过与电离辐射或化学疗法相结合,可以大大提高生物还原药物的体外和体内细胞毒性。各种参数,例如氧气张力和药物的给药时间可能在联合治疗方式的功效中起关键作用。这项研究的目的是确定在体外照射并与单独或同时给予的替拉帕明(一种生物还原性药物和顺铂)孵育后细胞存活的氧依赖性。研究了两种人类细胞系:一种对替拉帕明(Na11 +)敏感的细胞系,一种色素沉着的黑色素瘤,缺氧细胞比例高,而另一种对替拉帕明(HRT18)敏感性较低的细胞系,一种直肠腺癌。进行气体变化以研究在四种不同氧气浓度(pO2):空气(20.9%O2),10.2和0.2%O2下的细胞存活率。将细胞单独与替拉帕明和顺铂一起孵育,或在37摄氏度下合并1小时,然后进行辐射和培养。对于Na11 +,单独或联合使用两种药物,在空气中和10%氧气条件下,辐射后的细胞存活率相当。在氧浓度为2%和0.2%的条件下,替拉帕明大大增强了细胞杀伤力,但未通过添加顺铂来改变细胞杀伤力。对于HRT18,无论氧分压如何,将顺铂加入放射线均不会改变细胞存活率。在低pO2(2%和0.2%)下,通过加入顺铂并没有显着降低替拉帕明的细胞毒性作用。当细胞毒性和生物还原性药物与放射线结合使用时,所观察到的效应的程度高度取决于氧分压以及细胞系对单个药物的敏感性。这对于基于联合化学放射疗法的临床策略具有非常重要的意义。

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