Lialiaris Theodore, Polyzou Aggeliki, Mpountoukas Panagiotis, Tsiggene Anthi, Kouskoukis Alexandros, Pouliliou Stamatia, Paraskakis Emmanouil, Tentes Ioannis, Trypsianis Grigorios, Chatzimichail Athanasios
Department of Genetics, Demokrition University of Thrace, Alexandroupolis, Greece.
J Asthma. 2009 Oct;46(8):841-4.
Asthma is a complex disease with multiple interactions between genetic and environmental factors.
The aim of our study was to investigate the possible genetic instability in asthmatic patients (AP) with asthma in human cultured peripheral blood lymphocytes. Furthermore, the presence of either cytostaticity or cytotoxicity was demonstrated.
Human peripheral blood lymphocytes were cultured from 18 admitted children to the Pediatric Clinic of the University Hospital of Alexandroupolis (average age 7.2 years), and 9 healthy blood donors were used as control subjects (average age 6.5 years), none of whom was receiving drugs for medical or other reasons.
A significant (p < 0.05) increase in spontaneous sister chromatid exchanges (SCEs) frequency in asthmatic patients compared with control subjects was observed. No statistically significant modification in the spontaneous proliferation rate index (PRI) in AP compared with the controls was demonstrated. Finally, MMC induced a statistically significant increase in SCEs frequency both to controls and to AP, with the MMC-induced SCEs rates in AP being statistically (p < 0.01) higher compared to the MMC-induced SCEs in controls.
We try to improve a new diagnostic process of possible genetic instability by a combination of genotoxic, cytostatic and cytotoxic effects of asthma on human peripheral lymphocytes.
哮喘是一种复杂的疾病,遗传因素和环境因素之间存在多种相互作用。
我们研究的目的是调查哮喘患者(AP)人类培养外周血淋巴细胞中可能存在的基因不稳定性。此外,还证实了是否存在细胞生长抑制或细胞毒性。
从亚历山德鲁波利斯大学医院儿科诊所收治的18名儿童(平均年龄7.2岁)中培养人类外周血淋巴细胞,并以9名健康献血者作为对照(平均年龄6.5岁),他们均未因医疗或其他原因接受药物治疗。
与对照相比,哮喘患者自发姐妹染色单体交换(SCE)频率显著增加(p < 0.05)。与对照组相比,AP组的自发增殖率指数(PRI)无统计学意义的改变。最后,丝裂霉素C(MMC)使对照组和AP组的SCE频率均有统计学意义的增加,AP组MMC诱导的SCE率与对照组相比有统计学意义的升高(p < 0.01)。
我们试图通过哮喘对人外周淋巴细胞的遗传毒性、细胞生长抑制和细胞毒性作用的组合,改进一种可能的基因不稳定性的新诊断方法。