Liu Y I, Liu Zhao, Chen Yuxin, Xu Kesen, Dong Jiahong
Department of Hepatobiliary Surgery, Qilu Hospital, Shandong University, Jinan, Shandong 250012, P.R. China.
Department of Hepatobiliary Surgery, Jinan Central Hospital, Shandong University, Jinan, Shandong 250013, P.R. China.
Exp Ther Med. 2016 Feb;11(2):387-396. doi: 10.3892/etm.2015.2934. Epub 2015 Dec 11.
Ischemia/reperfusion (I/R) injury during liver resection or transplantation for the treatment of hepatocellular carcinoma (HCC) may increase the risk of metastasis. Peroxisome proliferator-activated receptor-γ (PPARγ) activation has been observed to exert a protective effect against hepatic I/R injury. However, whether PPARγ activation exerts a protective effect against I/R-associated liver metastasis remains unknown. Therefore, the present study aimed to investigate the effects of the PPAR agonist rosiglitazone and the specific PPARγ antagonist GW9662 on tumor metastasis following hepatic I/R. An experimental mouse model of hepatic I/R-induced HCC metastasis was designed in order to determine the effects of I/R on tumor metastasis in the liver. Four groups were established: Sham, control (I/R), rosiglitazone (Ro) and rosiglitazone with GW9662 (Ro + GW) groups. In the latter two groups, the treatments were administered intravenously 1 h prior to the induction of ischemia. Tumor load was measured 12 days after the procedure. Furthermore, tissue analyses were conducted to determine the expression levels of alanine aminotransferase, myeloperoxidase (MPO), matrix metalloproteinase (MMP)-9, vascular cell adhesion molecule (VCAM)-1, nuclear factor (NF)-κB and PPARγ. Rosiglitazone pretreatment appeared to significantly mitigate hepatic I/R injury, as indicated by serological and histological analysis. The levels of VCAM-1, MPO and MMP-9 expression in the Ro group were significantly reduced at 8 h following ischemia compared with those in the control and Ro + GW groups. In addition, rosiglitazone inhibited the I/R-induced activation of NF-κB, and GW9662 attenuated the inhibitory effect. To the best of our knowledge, the present study is the first to report on the expression and the functional roles of PPARγ in I/R-associated metastasis. Short-term treatment of mice with rosiglitazone, a potent PPARγ agonist, confers protective effects against hepatic I/R-associated metastasis. Thus, PPARγ may be a potential therapeutic target for the protection of the liver against I/R-associated metastasis.
在肝细胞癌(HCC)肝切除或移植过程中,缺血/再灌注(I/R)损伤可能会增加转移风险。已观察到过氧化物酶体增殖物激活受体γ(PPARγ)激活对肝脏I/R损伤具有保护作用。然而,PPARγ激活是否对I/R相关的肝转移具有保护作用仍不清楚。因此,本研究旨在探讨PPAR激动剂罗格列酮和特异性PPARγ拮抗剂GW9662对肝脏I/R后肿瘤转移的影响。设计了一种肝脏I/R诱导的HCC转移实验小鼠模型,以确定I/R对肝脏肿瘤转移的影响。建立了四组:假手术组、对照组(I/R)、罗格列酮组(Ro)和罗格列酮与GW9662联合组(Ro + GW)。在后两组中,在诱导缺血前1小时静脉给药。术后12天测量肿瘤负荷。此外,进行组织分析以确定丙氨酸转氨酶、髓过氧化物酶(MPO)、基质金属蛋白酶(MMP)-9、血管细胞粘附分子(VCAM)-1、核因子(NF)-κB和PPARγ的表达水平。血清学和组织学分析表明,罗格列酮预处理似乎能显著减轻肝脏I/R损伤。与对照组和Ro + GW组相比,Ro组缺血后8小时VCAM-1、MPO和MMP-9表达水平显著降低。此外,罗格列酮抑制I/R诱导的NF-κB激活,而GW9662减弱了这种抑制作用。据我们所知,本研究首次报道了PPARγ在I/R相关转移中的表达及功能作用。用强效PPARγ激动剂罗格列酮对小鼠进行短期治疗,可对肝脏I/R相关转移产生保护作用。因此,PPARγ可能是保护肝脏免受I/R相关转移的潜在治疗靶点。