Takahashi Masamitsu, Araki Takuya, Yashima Hideaki, Nagamine Ayumu, Nagano Daisuke, Yamamoto Koujirou
Department of Clinical Pharmacology and Therapeutics, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.
Department of Pharmacy, Gunma University Hospital, Maebashi, Gunma 371-8511, Japan.
Oncol Lett. 2023 Oct 25;26(6):529. doi: 10.3892/ol.2023.14116. eCollection 2023 Dec.
Lenvatinib, a multi-kinase inhibitor, serves a crucial role in the treatment of unresectable hepatocellular carcinoma (HCC). However, >50% of patients receiving lenvatinib therapy experience tumor growth or metastasis within 1 year, highlighting the need to address acquired resistance as a critical clinical challenge. To elucidate the factors associated with acquired resistance to lenvatinib, a lenvatinib-resistant HCC cell line (JHH-7_LR) was established by exposing a lenvatinib-sensitive HCC cell line, JHH-7, to lenvatinib. The changes in protein expression associated with the development of resistance were analyzed using a proteomic approach, detecting 1,321 proteins and significant changes in the expression of 267 proteins. Using Ingenuity Pathway Analysis bioinformatics software, it was revealed that the activity of multiple signaling pathways varied alongside the changes in expression of these proteins, and c-SRC was identified as a protein involved in a number of these signaling pathways, with its activity varying markedly upon the acquisition of resistance. When co-administering dasatinib, a c-SRC inhibitor, the partial restoration of lenvatinib sensitivity in the JHH-7_LR cell line was observed. The present study demonstrated that increased c-SRC expression was partially associated with HCC resistance to lenvatinib, suggesting that c-SRC inhibition could reduce the resistance of HCC to lenvatinib.
仑伐替尼是一种多激酶抑制剂,在不可切除肝细胞癌(HCC)的治疗中发挥着关键作用。然而,超过50%接受仑伐替尼治疗的患者在1年内出现肿瘤生长或转移,这凸显了将克服获得性耐药作为一项关键临床挑战加以应对的必要性。为了阐明与仑伐替尼获得性耐药相关的因素,通过将对仑伐替尼敏感的HCC细胞系JHH-7暴露于仑伐替尼,建立了一种对仑伐替尼耐药的HCC细胞系(JHH-7_LR)。采用蛋白质组学方法分析与耐药发展相关的蛋白质表达变化,检测到1321种蛋白质,其中267种蛋白质的表达有显著变化。使用Ingenuity Pathway Analysis生物信息学软件发现,多个信号通路的活性随着这些蛋白质表达的变化而改变,并且c-SRC被鉴定为参与许多这些信号通路的一种蛋白质,其活性在获得耐药性时显著变化。当联合给予c-SRC抑制剂达沙替尼时,观察到JHH-7_LR细胞系中仑伐替尼敏感性部分恢复。本研究表明,c-SRC表达增加与HCC对仑伐替尼的耐药性部分相关,提示抑制c-SRC可降低HCC对仑伐替尼的耐药性。