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本文引用的文献

1
Hepatocellular carcinoma.肝细胞癌。
Nat Rev Dis Primers. 2021 Jan 21;7(1):6. doi: 10.1038/s41572-020-00240-3.
2
Targeted therapy for hepatocellular carcinoma.肝细胞癌的靶向治疗。
Signal Transduct Target Ther. 2020 Aug 11;5(1):146. doi: 10.1038/s41392-020-00264-x.
3
Quantitation of the ROS production in plasma and radiation treatments of biotargets.定量检测生物靶区的血浆和辐射处理中的 ROS 产生。
Sci Rep. 2019 Dec 27;9(1):19837. doi: 10.1038/s41598-019-56160-0.
4
Tumour Treating Fields in combination with pemetrexed and cisplatin or carboplatin as first-line treatment for unresectable malignant pleural mesothelioma (STELLAR): a multicentre, single-arm phase 2 trial.肿瘤电场治疗联合培美曲塞和顺铂或卡铂作为不可切除恶性胸膜间皮瘤的一线治疗(STELLAR):一项多中心、单臂、Ⅱ期临床试验。
Lancet Oncol. 2019 Dec;20(12):1702-1709. doi: 10.1016/S1470-2045(19)30532-7. Epub 2019 Oct 15.
5
Tumour treating fields in a combinational therapeutic approach.组合治疗方法中的肿瘤治疗电场
Oncotarget. 2018 Nov 27;9(93):36631-36644. doi: 10.18632/oncotarget.26344.
6
Functional Biological Activity of Sorafenib as a Tumor-Treating Field Sensitizer for Glioblastoma Therapy.索拉非尼作为一种肿瘤治疗电场增敏剂的功能生物学活性用于治疗脑胶质瘤。
Int J Mol Sci. 2018 Nov 21;19(11):3684. doi: 10.3390/ijms19113684.
7
Tumor treating fields in combination with gemcitabine or gemcitabine plus nab-paclitaxel in pancreatic cancer: Results of the PANOVA phase 2 study.肿瘤电场治疗联合吉西他滨或吉西他滨联合白蛋白紫杉醇治疗胰腺癌:PANOVA 期 2 研究结果。
Pancreatology. 2019 Jan;19(1):64-72. doi: 10.1016/j.pan.2018.10.004. Epub 2018 Oct 17.
8
Selective toxicity of tumor treating fields to melanoma: an in vitro and in vivo study.肿瘤治疗电场对黑色素瘤的选择性毒性:一项体外和体内研究。
Cell Death Discov. 2018 Oct 3;4:46. doi: 10.1038/s41420-018-0106-x. eCollection 2018.
9
Tumor Treating Fields Technology: Alternating Electric Field Therapy for the Treatment of Solid Tumors.肿瘤治疗电场技术:用于实体瘤治疗的交变电场疗法
Semin Oncol Nurs. 2018 May;34(2):137-150. doi: 10.1016/j.soncn.2018.03.005. Epub 2018 Apr 6.
10
Tumor treating fields (TTFields) delay DNA damage repair following radiation treatment of glioma cells.肿瘤治疗电场(TTFields)会延迟胶质细胞瘤细胞放射治疗后 DNA 损伤的修复。
Radiat Oncol. 2017 Dec 29;12(1):206. doi: 10.1186/s13014-017-0941-6.

肿瘤治疗电场联合索拉非尼可抑制肝癌增殖。

Tumor-treating fields in combination with sorafenib restrain the proliferation of liver cancer .

作者信息

Jang Yoonjung, Lee Won Seok, Sai Sei, Kim Jeong Yub, Kim Jong-Ki, Kim Eun Ho

机构信息

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.

出版信息

Oncol Lett. 2022 Aug 11;24(4):338. doi: 10.3892/ol.2022.13458. eCollection 2022 Oct.

DOI:10.3892/ol.2022.13458
PMID:36039063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9404698/
Abstract

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.

摘要

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。