Xie Rui, Xu Tongying, Zhu Jiuxin, Wei Xiaoli, Zhu Wenting, Li Longmin, Wang Yufeng, Han Yu, Zhou Jianhua, Bai Yuxian
Department of Digestive Internal Medicine & Photodynamic Therapy Center, Harbin Medical University Cancer Hospital, Harbin, China.
Department of Pharmacology (the State-Province Key Laboratories of Biomedicine-Pharmaceutics of China, Key Laboratory of Cardiovascular Research, Ministry of Education), Harbin Medical University, Harbin, China.
Ultrasound Med Biol. 2017 Nov;43(11):2640-2650. doi: 10.1016/j.ultrasmedbio.2017.06.031. Epub 2017 Aug 23.
Sonodynamic therapy (SDT) overcomes the shortcoming of photodynamic therapy in the treatment of cancer. Previous studies indicated that the glycolysis inhibitor 2-deoxyglucose (2-DG) potentiated photodynamic therapy induced tumor cell death and microbubbles (MBs) improved the SDT performance. We hypothesized that the combination of 2-DG and MBs will increase the effect of 5-aminolevulinic acid (ALA)-SDT in HepG2 liver cancer cells. When cells were treated with 5-min ALA-SDT and 2-mmol/L 2-DG, the cell survival rate decreased to 73.0 ± 7.1% and 75.2 ± 7.9%, respectively. Furthermore, 2 mmol/L 2-DG increased 5-min ALA-SDT induced growth inhibition and augmented ALA-SDT induced cell apoptotic rate from 9.8 ± 0.7% to 17.4 ± 2.2%. In the combination group (2-DG and ALA-SDT group), HepG2 cells possessed typical apoptotic characters. 2-DG also increased ALA-SDT associated intracellular reactive oxygen species generation and loss of mitochondrial membrane potential. Moreover, SonoVue MBs had stimulatory function on cell viability inhibition, apoptosis, reactive oxygen species production and mitochondrial membrane potential loss for combination treatment. This study suggests a promising therapeutic strategy using a combination of 2-DG, MBs and ALA-SDT for treating liver cancer.
声动力疗法(SDT)克服了光动力疗法在癌症治疗中的缺点。先前的研究表明,糖酵解抑制剂2-脱氧葡萄糖(2-DG)可增强光动力疗法诱导的肿瘤细胞死亡,而微泡(MBs)可改善声动力疗法的性能。我们推测,2-DG与MBs联合使用将增强5-氨基酮戊酸(ALA)-声动力疗法对肝癌细胞HepG2的治疗效果。当细胞接受5分钟的ALA-声动力疗法和2 mmol/L的2-DG处理时,细胞存活率分别降至73.0±7.1%和75.2±7.9%。此外,2 mmol/L的2-DG增强了5分钟ALA-声动力疗法诱导的生长抑制作用,并使ALA-声动力疗法诱导的细胞凋亡率从9.8±0.7%提高到17.4±2.2%。在联合治疗组(2-DG与ALA-声动力疗法组)中,HepG2细胞呈现出典型的凋亡特征。2-DG还增加了ALA-声动力疗法相关的细胞内活性氧生成以及线粒体膜电位的丧失。此外,声诺维微泡对联合治疗的细胞活力抑制、凋亡、活性氧产生及线粒体膜电位丧失具有促进作用。本研究提示,2-DG、微泡与ALA-声动力疗法联合应用有望成为一种治疗肝癌的有效策略。