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抗癌药物与冷冻在诱导肝癌细胞凋亡方面具有协同作用。

Anticancer drugs are synergistic with freezing in induction of apoptosis in HCC cells.

作者信息

Yuan FangJun, Zhou Wenbo, Zhang Jifa, Zhang Zhiyun, Zou Can, Huang Ling, Zhang YouShun, Dai Zongqing

机构信息

Institute of Liver Surgery, DongFeng Hospital, YunYang Medical College, 10# Daling Road, Shiyan, Hubei 442008, China.

出版信息

Cryobiology. 2008 Aug;57(1):60-5. doi: 10.1016/j.cryobiol.2008.06.001. Epub 2008 Jun 11.

Abstract

Cryotherapy has been shown to be an important therapeutic alternative to surgery in the treatment of hepatocellular carcinoma (HCC). Here, the influence of cryo-chemotherapy on HCC was examined in vitro using the human HCC cell line Bel-7402, a drug-resistant HCC cell line originating from Bel-7402 cells (Bel-7402/R), as well as two control cell lines, the HCC cell line SMMC-7721 and a colorectal tumor cell line HIC-251. Cells were treated with either exposure to different freezing temperatures (ranging from -15 to -80 degrees C for 20 min), exposure to sub-lethal concentrations of anticancer chemotherapy drugs or a combination of cryotherapy and chemotherapy. Cell viability and apoptosis under each condition were investigated. We found that the combined treatment resulted in increases in both cell death and apoptosis compared to either treatment alone. The increased level of apoptosis observed in Bel-7402 cells after cryo-chemotherapy was inhibited in the presence of caspase inhibitors. Furthermore, Bax expression was increased 2- to 3-fold in cells exposed to the combination treatment compared with cells treated by freezing or drugs alone. In contrast, Bcl-2 levels remained constant. Although Bel-7402/R cells originated from the Bel-7402 cell line, they were more sensitive to the freezing procedure than the parental cell line. The level of Bax expression in Bel-7402/R cells was also higher than that observed in the parental cell line. In addition, we found that Bel-7402/R cells had lower levels of survivin mRNA than the parental Bel-7402 cells, in both untreated and treated cells. In conclusion, our data show that in HCC cells, apoptosis induced by cryotherapy can be synergistically enhanced using anticancer drugs.

摘要

冷冻疗法已被证明是治疗肝细胞癌(HCC)时一种重要的替代手术的治疗方法。在此,我们使用人肝癌细胞系Bel-7402、源自Bel-7402细胞的耐药肝癌细胞系(Bel-7402/R)以及两种对照细胞系——肝癌细胞系SMMC-7721和结肠直肠肿瘤细胞系HIC-251,在体外研究了冷冻化疗对肝癌的影响。细胞分别接受不同冷冻温度(-15至-80摄氏度,持续20分钟)、亚致死浓度的抗癌化疗药物或冷冻疗法与化疗的联合处理。研究了每种条件下的细胞活力和凋亡情况。我们发现,与单独的任何一种治疗相比,联合治疗导致细胞死亡和凋亡均增加。在存在半胱天冬酶抑制剂的情况下,冷冻化疗后Bel-7402细胞中观察到的凋亡增加水平受到抑制。此外,与单独接受冷冻或药物处理的细胞相比,联合处理的细胞中Bax表达增加了2至3倍。相比之下,Bcl-2水平保持不变。尽管Bel-7402/R细胞源自Bel-7402细胞系,但它们对冷冻程序比亲代细胞系更敏感。Bel-7402/R细胞中Bax表达水平也高于亲代细胞系。此外,我们发现,在未处理和处理的细胞中,Bel-7402/R细胞中生存素mRNA水平均低于亲代Bel-7402细胞。总之,我们的数据表明,在肝癌细胞中,使用抗癌药物可协同增强冷冻疗法诱导的凋亡。

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