Jang Yoonjung, Lee Won Seok, Sai Sei, Kim Jeong Yub, Kim Jong-Ki, Kim Eun Ho
Department of Biochemistry, School of Medicine, Daegu Catholic University, Daegu, North Gyeongsang 42471, Republic of Korea.
Department of Basic Medical Sciences for Radiation Damage, National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology, Chiba 263-8555, Japan.
Oncol Lett. 2022 Aug 11;24(4):338. doi: 10.3892/ol.2022.13458. eCollection 2022 Oct.
Liver cancer is a common malignancy worldwide, with a poor prognosis and a high recurrence rate despite the available treatment methodologies. Tumor-treating fields (TTFields) have shown good preclinical and clinical results for improving the prognosis of patients with glioblastoma and malignant pleural mesothelioma. However, there is minimal evidence for the effect of TTFields on other cancer types. Thus, the present study aimed to investigate the therapeutic efficacy of TTFields in an model, and to further elucidate the underlying mechanisms. In the present study, two hepatocellular carcinoma (HCC) cell lines (Hep3B and HepG2) were treated with TTFields (intensity, 1.0 V/cm; frequency, 150 kHz) in order to determine the potential antitumor effects of this approach. TTFields significantly inhibited the proliferation and viability of HCC cell lines, as measured using Trypan blue and MTT assays, as well as colony formation in three-dimensional cultures. The TTFields also significantly inhibited the migration and invasion of HCC cells in Transwell chamber and wound-healing assays. Moreover, TTFields enhanced the production of reactive oxygen species in the cells and increased the proportion of apoptotic cells, as evidenced by increased caspase-3 activity, as well as PARP cleavage in western blotting experiments. All of these effects were increased following the application of TTFields in combination with the multi-kinase inhibitor sorafenib, which demonstrated a synergistic effect. Thus, to the best of our knowledge, these results demonstrate for the first time the potential of TTFields in improving the sensitivity of HCC cells to sorafenib, which may lay the foundation for future clinical trials for this combination treatment strategy.
肝癌是全球常见的恶性肿瘤,尽管有现有的治疗方法,但预后较差且复发率高。肿瘤治疗电场(TTFields)在改善胶质母细胞瘤和恶性胸膜间皮瘤患者的预后方面已显示出良好的临床前和临床结果。然而,关于TTFields对其他癌症类型影响的证据很少。因此,本研究旨在探讨TTFields在一个模型中的治疗效果,并进一步阐明其潜在机制。在本研究中,为了确定这种方法的潜在抗肿瘤作用,用TTFields(强度,1.0 V/cm;频率,150 kHz)处理了两种肝癌(HCC)细胞系(Hep3B和HepG2)。通过台盼蓝和MTT测定以及三维培养中的集落形成来测量,TTFields显著抑制了HCC细胞系的增殖和活力。在Transwell小室和伤口愈合试验中,TTFields也显著抑制了HCC细胞的迁移和侵袭。此外,TTFields增强了细胞中活性氧的产生并增加了凋亡细胞的比例,这在蛋白质印迹实验中通过caspase-3活性增加以及PARP裂解得到证明。在将TTFields与多激酶抑制剂索拉非尼联合应用后,所有这些作用都增强了,这表明了协同作用。因此,据我们所知,这些结果首次证明了TTFields在提高HCC细胞对索拉非尼敏感性方面的潜力,这可能为这种联合治疗策略的未来临床试验奠定基础。