Kurokawa Tomohiro, Murata Soichiro, Zheng Yun-Wen, Iwasaki Kenichi, Kohno Keisuke, Fukunaga Kiyoshi, Ohkohchi Nobuhiro
Department of Surgery, Division of Gastroenterological and Hepatobiliary Surgery, and Organ Transplantation, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
Int J Oncol. 2015 Nov;47(5):1696-702. doi: 10.3892/ijo.2015.3180. Epub 2015 Sep 23.
Currently, sorafenib is the only available chemotherapeutic agent for advanced hepatocellular carcinoma (HCC), but it cannot be used in patients with liver cirrhosis (LC) or thrombocytopenia. In these cases, sorafenib is likely effective if given in combination with treatments that increase the number of platelets, such as thrombopoietin (TPO) receptor agonists. Increasing the platelet count via TPO treatment resulted in reduction of LC. Eltrombopag (EP), a TPO receptor agonist, has been reported to have antitumor effects against certain cancers, despite their lack of TPO receptor expression. We hypothesized that EP may possess antitumor activity against HCC in addition to its ability to suppress hepatic fibrosis by increasing the platelet count. In the present study, the antitumor activity of EP was examined by assessing the inhibition of cell proliferation and then ascertaining the ability of iron supplementation to reverse these effects in HepG2, Hep3B and Huh7 cells. In addition, a cell cycle assay was performed using flow cytometry, and signal transduction was evaluated by analyzing cell cycle-related protein expression. The results of EP were compared with those of the most common iron chelator, deferoxamine (DFO). The combined effect of EP and sorafenib was also assessed. The results revealed that EP exerts antitumor activity in HCC that is mediated by the modulation of intracellular iron content. EP suppressed the expression of the cell cycle-related protein cyclin D1 and elicited cell cycle arrest in the G0/G1 phase. The activity of EP was comparable to that of DFO in HCC, and EP did not compete with sorafenib at low concentrations. In conclusion, our findings suggest that EP is a good candidate chemotherapeutic agent for the treatment of HCC in patients with LC and thrombocytopenia.
目前,索拉非尼是唯一可用于晚期肝细胞癌(HCC)的化疗药物,但它不能用于肝硬化(LC)或血小板减少症患者。在这些情况下,如果与增加血小板数量的治疗方法(如血小板生成素(TPO)受体激动剂)联合使用,索拉非尼可能有效。通过TPO治疗增加血小板计数可导致LC减轻。艾曲泊帕(EP)是一种TPO受体激动剂,据报道,尽管某些癌症缺乏TPO受体表达,但它对这些癌症具有抗肿瘤作用。我们假设,EP除了通过增加血小板计数来抑制肝纤维化外,可能还具有抗HCC的肿瘤活性。在本研究中,通过评估细胞增殖抑制情况,然后确定补充铁剂逆转这些作用的能力,来检测EP在HepG2、Hep3B和Huh7细胞中的抗肿瘤活性。此外,使用流式细胞术进行细胞周期分析,并通过分析细胞周期相关蛋白表达来评估信号转导。将EP的结果与最常用的铁螯合剂去铁胺(DFO)的结果进行比较。还评估了EP与索拉非尼的联合作用。结果显示,EP通过调节细胞内铁含量在HCC中发挥抗肿瘤活性。EP抑制细胞周期相关蛋白细胞周期蛋白D1的表达,并使细胞周期停滞在G0/G1期。在HCC中,EP的活性与DFO相当,且在低浓度下EP不与索拉非尼竞争。总之,我们的研究结果表明,EP是治疗LC和血小板减少症患者HCC的良好候选化疗药物。