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作 者:李伟[2] 陈政[2] 宗洋[2] 龚斐然[1] 朱毅[2] 殷红[1] 徐泽宽[2] 陶敏[1] 苗毅[2]
机构地区:[1]苏州大学附属第一医院肿瘤科,苏州215006 [2]南京医科大学第一附属医院普外科
出 处:《中华胰腺病杂志》2011年第4期255-258,共4页Chinese Journal of Pancreatology
基 金:国家自然科学基金(30872509);江苏省“六大人才高峰”项目[2007200(E107)]
摘 要:目的研究斑蝥素对胰腺癌细胞系PANCl、CFPAC-1的凋亡诱导作用及机制。方法用斑蝥素处理PANCl、CFPAC-1细胞。四甲基偶氮唑蓝(MTF)法检测细胞增殖;流式细胞术检测细胞凋亡;酶化学法检测caspase活性;RT—PCR及蛋白质印迹法检测凋亡相关基因的表达。结果斑蝥素呈剂量依赖性明显抑制胰腺癌细胞系PANCl、CFPAC-1增殖及诱导细胞凋亡。10μmol/L斑蝥素处理细胞72h,PANCl、CFPAC-1细胞的增殖抑制率最高,分别达(52.95±6.34)%和(71.21±6.30)%。处理24h,PANCI细胞的早期和晚期凋亡细胞分别从7.35%增加到24.89%、6.36%增加到17.73%;CFPAC-1细胞从6.39%增加到24.70%、9.21%增加到12.58%(P值均〈0.01)。PANCl细胞的caspase8和caspase9活性分别为对照组的(155.84-11.5)%和(194.64-14.7)%;CFPAC-1细胞分别为对照组的(182.54±24.3)%和(215.84±12.2)%(P值均〈0.01)。促凋亡基因TNF-α、TRAILRI、TRAILR2、Bad、Bak和Bid表达增加,抗凋亡基因Bcl-2表达减少。结论斑蝥素通过激活Caspase、上调促凋亡基因及下调抗凋亡基因的表达从而诱导胰腺癌细胞凋亡。Objective To investigate the apoptosis induction effect of Cantharidin on pancreatic cancer cell line PANC1 and CFPAC-1 and possible mechanism. Methods PANC1 and CFPAC-1 was treated with Cantharidin. Cell growth was determined by MTI'. Apoptosis was measured by flow cytometry. Caspase activity was measured by using enzyme chemical method. Apoptosis-related gene expressions were determined by using RT-PCR and Western blotting. Results Cantharidin significantly inhibited the growth of pancreatic cancer cells PANC1, CFPAC-1 and induced apoptosis in a dose-dependent manner. Seventy-two hours after 10 μmol/L Cantharidin treatment, the inhibitory rates of PANC1, CFPAC-1 were (52.95 ± 6.34)% and (71.21± 6.30)%. Twenty-four hours after treatment, the early and later period apoptotic cell of PANC1 was increased from 7.35% to 24.89%, from 6.36% to 17.73%. The early and later period apoptotic cell of CFPAC was increased from 6.39% to 24.70%, from 9.21% to 12.58% (P 〈0.01). Activity of caspase 8 and caspase 9 in PANC1 cells was ( 155.8 ± 11.5 ) % and ( 194.6 ± 14.7 ) % when compared with that of control group. Activity of caspase 8 and easpase 9 in CFPAC-1 was ( 182.5 ± 24.3 ) % and (215.8 ± 12.2) % when compared with that of control group ( P 〈 0.01 ). The expression of pro-apoptotic genes, TNF-α, TRAILR1, TRAILR2, Bad, Bak and Bid was elevated, the expression of anti-apoptotic Bcl-2 gene was decreased. Conclusions Cantharidin can induce apoptosis in pancreatic cancer cell lines by activating caspase,up-regulating the expression of pro-apoptotic genes and down-regulating the expression of anti-apoptotic genes.
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