中华肝胆外科杂志
中華肝膽外科雜誌
중화간담외과잡지
CHINESE JOURNAL OF HEPATOBILIARY SURGERY
2011年
11期
919-923
,共5页
王育和%李非%刘爽%孙海晨%崔叶青
王育和%李非%劉爽%孫海晨%崔葉青
왕육화%리비%류상%손해신%최협청
胰腺癌%干细胞%耐药性
胰腺癌%榦細胞%耐藥性
이선암%간세포%내약성
Pancreatic carcinoma%Stem cell%Drug resistance
目的 探讨胰腺癌肿瘤干细胞对抗肿瘤药物的敏感性.方法 FACS技术分选人胰腺癌PANC-1细胞;RT-PCR技术检测分选PANC-1细胞中CD133、ABCG2、Notch1的表达情况;MTT法检测分选细胞对抗肿瘤药物5-氟尿嘧啶和吉西他滨的耐药性.建立分选细胞的移植瘤模型,随机分为吉西他滨治疗组(n=3)和对照组(n=3),观察肿瘤生长情况,作CD133免疫组化染色.结果PANC-1细胞中含有SP亚群.SP细胞CD133、ABCG2、Notch1的mRNA的表达明显上调,non-SP细胞的表达量显著低于前者.在吉西他滨的干预下,SP细胞和non-SP细胞的OD值差异有统计学意义.而5-氟尿嘧啶的干预(10 μg/ml和100 μg/ml)则没有显著差异.移植肿瘤治疗组中CD133阳性细胞明显多于对照组(P=0.001).结论胰腺癌中存在SP亚群细胞.胰腺癌PANC-1的成瘤能力是由其中的SP亚群细胞决定的,而并非所有胰腺癌PANC-1细胞.胰腺癌肿瘤干细胞对抗肿瘤药吉西他滨具有较高耐药性.
目的 探討胰腺癌腫瘤榦細胞對抗腫瘤藥物的敏感性.方法 FACS技術分選人胰腺癌PANC-1細胞;RT-PCR技術檢測分選PANC-1細胞中CD133、ABCG2、Notch1的錶達情況;MTT法檢測分選細胞對抗腫瘤藥物5-氟尿嘧啶和吉西他濱的耐藥性.建立分選細胞的移植瘤模型,隨機分為吉西他濱治療組(n=3)和對照組(n=3),觀察腫瘤生長情況,作CD133免疫組化染色.結果PANC-1細胞中含有SP亞群.SP細胞CD133、ABCG2、Notch1的mRNA的錶達明顯上調,non-SP細胞的錶達量顯著低于前者.在吉西他濱的榦預下,SP細胞和non-SP細胞的OD值差異有統計學意義.而5-氟尿嘧啶的榦預(10 μg/ml和100 μg/ml)則沒有顯著差異.移植腫瘤治療組中CD133暘性細胞明顯多于對照組(P=0.001).結論胰腺癌中存在SP亞群細胞.胰腺癌PANC-1的成瘤能力是由其中的SP亞群細胞決定的,而併非所有胰腺癌PANC-1細胞.胰腺癌腫瘤榦細胞對抗腫瘤藥吉西他濱具有較高耐藥性.
목적 탐토이선암종류간세포대항종류약물적민감성.방법 FACS기술분선인이선암PANC-1세포;RT-PCR기술검측분선PANC-1세포중CD133、ABCG2、Notch1적표체정황;MTT법검측분선세포대항종류약물5-불뇨밀정화길서타빈적내약성.건립분선세포적이식류모형,수궤분위길서타빈치료조(n=3)화대조조(n=3),관찰종류생장정황,작CD133면역조화염색.결과PANC-1세포중함유SP아군.SP세포CD133、ABCG2、Notch1적mRNA적표체명현상조,non-SP세포적표체량현저저우전자.재길서타빈적간예하,SP세포화non-SP세포적OD치차이유통계학의의.이5-불뇨밀정적간예(10 μg/ml화100 μg/ml)칙몰유현저차이.이식종류치료조중CD133양성세포명현다우대조조(P=0.001).결론이선암중존재SP아군세포.이선암PANC-1적성류능력시유기중적SP아군세포결정적,이병비소유이선암PANC-1세포.이선암종류간세포대항종류약길서타빈구유교고내약성.
Objective To explore the sensitivity of cancer stem cells to chemotherapy in human pancreatic carcinoma.Methods PANC-1 ceils were cultured in an incubator filled with 5% CO2 at a temperature of 37℃,and were labeled with Hoechst 33342.The SP analysis and sorting were performed using a FACSVantage SE.RT-PCR was performed to detect the expression of human CD133 ABCG2 and Notch1.SP and non-SP cells from the PANC-1 cell line were treated with 5-fluorouracil (5-FU; 1,10,or 100 μg/ml) or gemcitabine (10,100,or 1000μg/ml),and the cell viability was determined using the MTT assay.The sensitivity of sorted tumor cells to chemotherapeutics was determined in NOD/SCID mice model.Results SP cells were found to have higher drug-resistance both in vivo and in vitro and higher levels of mRNA expression for CD133,ABCG2 and Notch1,when compared to non-SP ceils.The xenografted tumors derived from injected SP cells and treated with gemcitabine had more CD133± cells than the untreated group.Conclusions The SP of PANC-1 pancreatic carcinoma cells are enriched with highly gemcitabine-resistant CSCs and determine the carcinogenesis of the PANC-1 pancreatic carcinoma cells.