齐齐哈尔医学院学报
齊齊哈爾醫學院學報
제제합이의학원학보
JOURNAL OF QIQIHAR MEDICAL COLLEGE
2015年
4期
477-478
,共2页
肝癌%HepG2细胞系%顺铂%耐药性
肝癌%HepG2細胞繫%順鉑%耐藥性
간암%HepG2세포계%순박%내약성
Hepatoma%HepG2 cell line%Cisplatin%Drug-resistance
目的:体外建立顺铂( DDP)诱导的人肝癌耐药细胞株( HepG2/DDP),研究其生物学特性。方法以采用药物大剂量冲击结合低剂量持续诱导方法诱导HepG2细胞株,建立人肝癌顺铂耐药细胞株HepG2/DDP;MTT法检测顺铂对HepG2和HepG2/DDP的半数抑制浓度(IC50)和耐药系数(RI),绘制细胞生长曲线及计算细胞倍增时间,并用流式细胞仪( FCM )检测细胞周期。结果历时5个月成功建成HepG2/DDP细胞株,MTT法检测DDP对HepG2的IC50为1.35μg/ml,HepG2/DDP的IC50为23.35μg/ml,RI达17生长曲线表明其增殖速度明显低于亲本HepG2人肝癌细胞,且倍增时间增加;细胞周期分析发现相对于亲本HepG2细胞,G0/G1期细胞减少、S期与G2/M期细胞增多。结论成功建立稳定耐药细胞株HepG2/DDP。
目的:體外建立順鉑( DDP)誘導的人肝癌耐藥細胞株( HepG2/DDP),研究其生物學特性。方法以採用藥物大劑量遲擊結閤低劑量持續誘導方法誘導HepG2細胞株,建立人肝癌順鉑耐藥細胞株HepG2/DDP;MTT法檢測順鉑對HepG2和HepG2/DDP的半數抑製濃度(IC50)和耐藥繫數(RI),繪製細胞生長麯線及計算細胞倍增時間,併用流式細胞儀( FCM )檢測細胞週期。結果歷時5箇月成功建成HepG2/DDP細胞株,MTT法檢測DDP對HepG2的IC50為1.35μg/ml,HepG2/DDP的IC50為23.35μg/ml,RI達17生長麯線錶明其增殖速度明顯低于親本HepG2人肝癌細胞,且倍增時間增加;細胞週期分析髮現相對于親本HepG2細胞,G0/G1期細胞減少、S期與G2/M期細胞增多。結論成功建立穩定耐藥細胞株HepG2/DDP。
목적:체외건립순박( DDP)유도적인간암내약세포주( HepG2/DDP),연구기생물학특성。방법이채용약물대제량충격결합저제량지속유도방법유도HepG2세포주,건립인간암순박내약세포주HepG2/DDP;MTT법검측순박대HepG2화HepG2/DDP적반수억제농도(IC50)화내약계수(RI),회제세포생장곡선급계산세포배증시간,병용류식세포의( FCM )검측세포주기。결과력시5개월성공건성HepG2/DDP세포주,MTT법검측DDP대HepG2적IC50위1.35μg/ml,HepG2/DDP적IC50위23.35μg/ml,RI체17생장곡선표명기증식속도명현저우친본HepG2인간암세포,차배증시간증가;세포주기분석발현상대우친본HepG2세포,G0/G1기세포감소、S기여G2/M기세포증다。결론성공건립은정내약세포주HepG2/DDP。
Objective To establish a drug-resistant hepatocellular carcinoma cell line and observe its biological characters .Methods The drug-resistant cell line HepG2 was induced using a concentration gradient of cisplatin (DDP) with exposed to intermittently.Drug sensitivity of HepG2 and HepG2/DDP were detected by MTT assay.The resistance index of the resistant cell line to DDP was determined by the methyl thiazolyl tetrazoliumassay ( MTT ) .Cell growth curve was painted by cell counting assay and the doubling time was accounted.Cycle distribution were measured by flow cytometry .Results The DDP-resistant cell line HepG2/DDP was established after 5 months and indicated drug-resistance to DDP, the drug resistance index being 17 respectively.The growing rate of resistant cells was obviously slower than that of the parental cells .The distributing proportion of HepG 2/DDP cells in G0/G1 phase was less than that of the parental cells , whereas the percentages of cells in G 2/M and S phase were significantly increased in HepG 2/DDP in comparison with those in HepG2.Conclusions A reliable drug-resistant human hepatoma cell line HepG 2/DDP is successfully established.