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Chloroquine Promotes the Anticancer Effect of TACE in a Rabbit VX2 Liver Tumor Model

机译:氯喹促进TACE在兔VX2肝肿瘤模型中的抗癌作用

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Background: To investigate the efficacy of TACE combined with CQ, an autophagic inhibitor, in a rabbit VX2 liver tumor model. Methods: Tumor size was measured. And tumor growth rate was calculated to examine the effect of the combined treatment. Apoptosis was detected by TUNEL assay. Meanwhile, autophagic activity was detected by immunohistochemistry and Western blotting to investigate the mechanism underlying. Liver function was also examined to assess feasibility and safety of the combined therapy. Results: Tumors in the control grew more than 4 times bigger after 14 days, while that in the group of TACE alone just showed mild growth. But a slight shrinkage was shown after the treatment of CQ+TACE. Growth ratio of TACE alone was 96.45% ± 28.958% while that of CQ+TACE was -28.73% ± 12.265%. Compared with TACE alone, necrosis in CQ+TACE showed no significant difference, however, the apoptosis was much higher. There were only 14.8±3.11% apoptotic cells in TACE, but 33±4.18% in CQ+TACE, which suggests the increased apoptosis in CQ+TACE contributed to the decrease of tumor volume. In terms of autophagic activity, the result is negative when we immunostained sections of the control with LC3 antibody, but positive in TACE alone and CQ+TACE. And the result of Western blot showed that there was just a low level of LC3Ⅱexpressed in the control and CQ alone, but higher in TACE, and much higher in CQ+TACE because CQ inhibited its degradation in autophagy. Compared with control, p62 decreased in TACE, but the decrease was partially reversed in CQ+TACE. In addition, toxicity of CQ+TACE was assessed not higher than TACE alone, which supports the safety of CQ+TACE. Conclusion: CQ+TACE works better than TACE alone in rabbit VX2 liver tumor model because CQ inhibits autophagy induced by TACE. The inhibited autophagy loses its resistance to apoptosis that apoptosis increased, which contributes to the inhibition of tumor growth. This study indicates CQ may be a promising adjuvant to promote the effect of TACE.
机译:背景:研究TACE与自噬抑制剂CQ联合在兔VX2肝肿瘤模型中的疗效。方法:测量肿瘤大小。并计算肿瘤生长速率以检查联合治疗的效果。通过TUNEL测定法检测凋亡。同时,通过免疫组织化学和蛋白质印迹检测自噬活性,以研究其潜在机制。还检查了肝功能以评估联合治疗的可行性和安全性。结果:对照组的肿瘤在14天后增长了4倍以上,而仅TACE组的肿瘤仅显示了轻度增长。但是在CQ + TACE处理后显示出轻微的收缩。仅TACE的增长率为96.45%±2​​8.958%,而CQ + TACE的增长率为-28.73%±12.265%。与单独的TACE相比,CQ + TACE的坏死没有显着差异,但是细胞凋亡更高。 TACE中只有14.8±3.11%的凋亡细胞,而CQ + TACE中有33±4.18%的细胞凋亡,提示CQ + TACE中凋亡的增加与肿瘤体积的减小有关。就自噬活性而言,当我们用LC3抗体对对照切片进行免疫染色时,结果为阴性,而在单独的TACE和CQ + TACE中为阳性。 Western印迹的结果表明,仅在对照和CQ中表达的LC3Ⅱ水平较低,而在TACE中表达较高,而在CQ + TACE中表达较高,因为CQ抑制了其在自噬中的降解。与对照相比,p62在TACE中下降,但在CQ + TACE中下降部分逆转。此外,评估的CQ + TACE毒性不高于单独的TACE,这支持了CQ + TACE的安全性。结论:CQ + TACE在兔VX2肝肿瘤模型中比单独使用TACE效果更好,因为CQ抑制TACE诱导的自噬。受抑制的自噬丧失了对细胞凋亡的抵抗力,而细胞凋亡增加了,这有助于抑制肿瘤的生长。这项研究表明CQ可能是一种有希望的佐剂,以促进TACE的作用。

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