Miyake Makito, Anai Satoshi, Fujimoto Kiyohide, Ohnishi Sayuri, Kuwada Masaomi, Nakai Yasushi, Inoue Takeshi, Tomioka Atsushi, Tanaka Nobumichi, Hirao Yoshihiko
Department of Urology, Nara Medical University, Nara 634-8522, Japan.
Oncol Lett. 2012 Jun;3(6):1195-1202. doi: 10.3892/ol.2012.662. Epub 2012 Mar 29.
Sorafenib and sunitinib are multi-kinase inhibitors with antitumor activity in patients with advanced renal cell carcinoma (RCC). Several studies have evaluated the effect of sorafenib/sunitinib in combination with chemotherapeutic agents in different types of tumor. However, few studies have addressed the activity of fluorinated pyrimidine in combination with sorafenib/sunitinib. In this study, we examined the potential of combination therapy with 5FU and sorafenib/sunitinib in human RCC cell lines. Three human RCC cell lines, ACHN, Caki-1 and Caki-2, were used to assess sensitivity to 5-fluorouracil (5FU), sorafenib and sunitinib alone or in combination using an in vitro cell survival assay. Caki-2 cells demonstrated significantly higher resistance to 5FU and sorafenib as compared to ACHN and Caki-1. Additive antitumor effects of the combination therapy were observed in the in vitro study. There was a tendency for a positive correlation between the sensitivity to sunitinib and platelet-derived growth factor β (PDGFR-β) expression levels, which were examined by reverse transcription polymerase chain reaction. Caki-1 xenograft models were prepared by inoculating cells subcutaneously into nude mice, which were divided randomly into six groups: control, 5FU (8 mg/kg/day, intraperitoneally), sorafenib (15 mg/kg/day, orally), sunitinib (20 mg/kg/day, orally), and 5FU with sorafenib or sunitinib. The treatments were administered on 5 days each week, and tumor growth was monitored for 42 days following inoculation of cells. Synergistic antitumor effects of the combination therapy were observed in an in vivo study. The resected tumors were evaluated using the Ki-67 labeling index and microvessel density. Both the Ki-67 labeling index and microvessel density were decreased in tumors treated with the combination therapy compared to those treated with sorafenib/sunitinib alone. These findings suggest that the combination therapy of 5FU with sorafenib/sunitinib may be an effective therapeutic modality for advanced RCC patients.
索拉非尼和舒尼替尼是多激酶抑制剂,对晚期肾细胞癌(RCC)患者具有抗肿瘤活性。多项研究评估了索拉非尼/舒尼替尼与化疗药物联合应用于不同类型肿瘤的效果。然而,很少有研究探讨氟嘧啶与索拉非尼/舒尼替尼联合应用的活性。在本研究中,我们检测了5-氟尿嘧啶(5FU)与索拉非尼/舒尼替尼联合治疗在人RCC细胞系中的潜力。使用三种人RCC细胞系ACHN、Caki-1和Caki-2,通过体外细胞存活试验评估其对单独或联合使用的5-氟尿嘧啶(5FU)、索拉非尼和舒尼替尼的敏感性。与ACHN和Caki-1相比,Caki-2细胞对5FU和索拉非尼表现出明显更高的耐药性。在体外研究中观察到联合治疗具有相加的抗肿瘤作用。通过逆转录聚合酶链反应检测发现,对舒尼替尼的敏感性与血小板衍生生长因子β(PDGFR-β)表达水平之间存在正相关趋势。通过将细胞皮下接种到裸鼠体内制备Caki-1异种移植模型,将裸鼠随机分为六组:对照组、5FU(8 mg/kg/天,腹腔注射)、索拉非尼(15 mg/kg/天,口服)、舒尼替尼(20 mg/kg/天,口服)以及5FU与索拉非尼或舒尼替尼联合组。每周给药5天,接种细胞后监测肿瘤生长42天。在体内研究中观察到联合治疗具有协同抗肿瘤作用。使用Ki-67标记指数和微血管密度对切除的肿瘤进行评估。与单独使用索拉非尼/舒尼替尼治疗的肿瘤相比,联合治疗的肿瘤中Ki-67标记指数和微血管密度均降低。这些发现表明,5FU与索拉非尼/舒尼替尼联合治疗可能是晚期RCC患者的一种有效治疗方式。