Mishra Pradyumna Kumar, Bhargava Arpit, Raghuram Gorantla Venkata, Jatawa Suresh Kumar, Akhtar Nabila, Khan Saba, Tiwari Archana, Maudar Kewal Krishan
Bhopal Memorial Hospital & Research Centre, Bhopal, India.
Cell Biol Int. 2009 Jun;33(6):675-83. doi: 10.1016/j.cellbi.2009.03.008. Epub 2009 Apr 17.
The toxic response of cultured human colon epithelial-FHC cells to methyl isocyanate was investigated with regard to genomic instability. Qualitative and quantitative assessments of the extent of phosphorylation of DNA damage signaling factors such as ATM, gammaH2AX and p53, was increased in treated cells compared to controls. At the same time, many treated cells were arrested at the G2/M phase of the cell cycle, and had an elevated apoptotic index and increased inflammatory cytokine levels. Cytogenetic analyses revealed varied chromosomal anomalies, with abnormal expression of pericentrin protein. Analysis through ISSR PCR demonstrated increased microsatellite instability. The results imply that isocyanates can cause genomic instability in colonocytes.
研究了培养的人结肠上皮-FHC细胞对异氰酸甲酯的毒性反应与基因组不稳定性的关系。与对照组相比,处理后的细胞中DNA损伤信号因子如ATM、γH2AX和p53的磷酸化程度在定性和定量评估中均有所增加。同时,许多处理后的细胞停滞在细胞周期的G2/M期,凋亡指数升高,炎性细胞因子水平增加。细胞遗传学分析显示出各种染色体异常,伴有中心粒蛋白的异常表达。通过ISSR PCR分析表明微卫星不稳定性增加。结果表明异氰酸酯可导致结肠细胞基因组不稳定。