CAJ | 학술논문

目的：探讨姜黄素对直肠癌CD133＋肿瘤干细胞样细胞群放疗敏感性的影响。方法应用免疫磁珠分选器、阳性分离柱分选出直肠癌CD133＋肿瘤干细胞，随机分成姜黄素组、姜黄素联合放疗组、放疗组，应用四甲基偶氮唑蓝比色（ MTT）法检测24、48、72 h各组细胞生长抑制情况；膜联蛋白V－异硫氨基荧光素／碘化丙啶（ Annexin V－FITC／PI）双染色检测细胞凋亡率。结果姜黄素组随着时间变化肿瘤细胞抑制率变化不大（ P＞0．05）；放疗组和姜黄素联合放疗组24、48、72 h细胞生长抑制率逐渐升高（P＜0．05）；同期三组细胞生长抑制率均有统计学意义（P＜0．05），两两比较24 h细胞生长抑制率，姜黄素组与姜黄素联合放疗组和放疗组之间差异有统计学意义（ P＜0．05），姜黄素联合放疗组与放疗组之间差异无统计学意义（P＞0．05）；48、72 h抑制率两两之间差异均有统计学意义（P＜0．05）；姜黄素组48 h与72 h之间细胞凋亡率差异无统计学意义（P＞0．05），姜黄素联合放疗组和放疗组48 h与72 h之间细胞凋亡率之间差异具有统计学意义（ P＜0．05）。同期内不同组细胞凋亡率之间的差异有统计学意义（ P＜0．05），两两比较细胞凋亡率之间差异具有统计学意义（P＜0．05）。结论姜黄素可以增加直肠癌 CD133＋肿瘤干细胞样细胞群放疗敏感性，抑制肿瘤细胞生长促进细胞凋亡。
목적：탐토강황소대직장암CD133＋종류간세포양세포군방료민감성적영향。방법응용면역자주분선기、양성분리주분선출직장암CD133＋종류간세포，수궤분성강황소조、강황소연합방료조、방료조，응용사갑기우담서람비색（ MTT）법검측24、48、72 h각조세포생장억제정황；막련단백V－이류안기형광소／전화병정（ Annexin V－FITC／PI）쌍염색검측세포조망솔。결과강황소조수착시간변화종류세포억제솔변화불대（ P＞0．05）；방료조화강황소연합방료조24、48、72 h세포생장억제솔축점승고（P＜0．05）；동기삼조세포생장억제솔균유통계학의의（P＜0．05），량량비교24 h세포생장억제솔，강황소조여강황소연합방료조화방료조지간차이유통계학의의（ P＜0．05），강황소연합방료조여방료조지간차이무통계학의의（P＞0．05）；48、72 h억제솔량량지간차이균유통계학의의（P＜0．05）；강황소조48 h여72 h지간세포조망솔차이무통계학의의（P＞0．05），강황소연합방료조화방료조48 h여72 h지간세포조망솔지간차이구유통계학의의（ P＜0．05）。동기내불동조세포조망솔지간적차이유통계학의의（ P＜0．05），량량비교세포조망솔지간차이구유통계학의의（P＜0．05）。결론강황소가이증가직장암 CD133＋종류간세포양세포군방료민감성，억제종류세포생장촉진세포조망。
Objective To investigate the influence of radiotherapy sensitivity of curcumin on CD 133+tumor stem cell-like cell popu-lations in rectal carcinoma .Methods The CD133+cancer stem cells in rectal cancer were separated by immunomagnetic beads sorting de -vice and the positive column , and then randomly divided into curcumin , curcumin combined with radiation , radiotherapy groups .The cell growth inhibition were detected in 24 h, 48 h and 72 h by MTT method,and the cell apoptosis rate was detected by Annexin V-FITC/PI double staining.Results The tumor cell inhibition rate of curcumin group was changed little along with the time (P>0.05),the cell growth inhibition rates of radiotherapy group and curcumin combined with radiation group were gradually increased in 24 h, 48 h and 72 h ( P<0.05);the cell growth inhibition rate between three groups was statistically significant over the same period (P<0.05),the difference of cell apoptosis rate was no statistical difference in curcumin group in 48 h and 72 h(P>0.05), while it was significantly different when curcumin combined with radiotherapy group compared with radiotherapy group (P<0.05);the cell apoptosis rate was different in different groups of the same period(P<0.05),and also was significantly different between any two groups (P<0.05).Conclusions Curcumin could increase the radiation sensitivity of CD133+tumor stem cell-like cell populations in rectal carcinoma , restrain tumor cell growth and promote cell apoptosis.