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sFas levels increase in response to cisplatin-based chemotherapy in lung cancer patients.

机译:肺癌患者对基于顺铂的化疗反应中sFas水平升高。

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The Fas/Fas Ligand (FasL) system and survivin have counteracting roles in cell survival. Therefore, we explored the role of circulating soluble Fas (sFas) and the tissue levels of Fas and survivin with regard to response to chemotherapy in lung cancer patients. Serum samples from 52 lung cancer patients and 54 control subjects (19 benign lung disease and 35 healthy control subjects) were collected prior to and 24 and 48 h after chemotherapy. sFas was statistically significantly higher in the cancer group than that in the control groups (p < 0.001). Baseline (before chemotherapy) sFas values showed a statistically significant inverse correlation with overall survival (r = -0.599, p < 0.001). There was a significant increase in serum sFas levels 24 h after treatment (p < 0.05). Contrarily, tissue levels of Fas and survivin were not changed following the chemotherapy (p > 0,05). In conclusion, increased sFas may be an indicator of poor outcome in lung cancer patients. However, cisplatin-based chemotherapy may not be effective via neither the Fas/FasL system nor survivin pathway. Indeed, larger sample size is required for further evaluation.
机译:Fas / Fas配体(FasL)系统和survivin在细胞存活中具有抵消作用。因此,我们探讨了循环可溶性Fas(sFas)的作用以及Fas和survivin的组织水平对肺癌患者化疗的反应。在化疗之前,化疗后24小时和48小时后,收集了52名肺癌患者和54名对照受试者(19名良性肺病和35名健康对照受试者)的血清样本。癌症组中的sFas在统计学上显着高于对照组(p <0.001)。基线(化疗前)的sFas值与总体生存率在统计学上呈显着负相关(r = -0.599,p <0.001)。治疗后24小时血清sFas水平显着升高(p <0.05)。相反,化学疗法后Fas和survivin的组织水平没有改变(p> 0.05)。总之,sFas增加可能是肺癌患者预后不良的指标。但是,基于顺铂的化疗可能既不能通过Fas / FasL系统也不能通过survivin途径有效。实际上,需要更大的样本量来进行进一步评估。

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