Kim Eun Ho, Kim Mi-Sook, Takahashi Akihisa, Suzuki Masao, Vares Guillaume, Uzawa Akiko, Fujimori Akira, Ohno Tatsuya, Sai Sei
Department of Biochemistry, School of Medicine, Daegu Catholic University, Nam-gu, Daegu 42472, Korea.
Department of Radiation Oncology, Korea Institute of Radiological and Medical Sciences, Seoul 139-706, Korea.
Cancers (Basel). 2020 Mar 16;12(3):698. doi: 10.3390/cancers12030698.
Osteosarcoma (OSA) is the most common malignant bone tumor in children and adolescents. The overall five-year survival rate for all bone cancers is below 70%; however, when the cancer has spread beyond the bone, it is about 15-30%. Herein, we evaluated the effects of carbon-ion beam irradiation alone or in combination with zoledronic acid (ZOL) on OSA cells. Carbon-ion beam irradiation in combination with ZOL significantly inhibited OSA cell proliferation by arresting cell cycle progression and initiating KHOS and U2OS cell apoptosis, compared to treatments with carbon-ion beam irradiation, X-ray irradiation, and ZOL alone. Moreover, we observed that this combination greatly inhibited OSA cell motility and invasion, accompanied by the suppression of the Pi3K/Akt and MAPK signaling pathways, which are related to cell proliferation and survival, compared to individual treatments with carbon-ion beam or X-ray irradiation, or ZOL. Furthermore, ZOL treatment upregulated microRNA (miR)-29b expression; the combination with a miR-29b mimic further decreased OSA cell viability via activation of the caspase 3 pathway. Thus, ZOL-mediated enhancement of carbon-ion beam radiosensitivity may occur via miR-29b upregulation; co-treatment with the miR-29b mimic further decreased OSA cell survival. These findings suggest that the carbon-ion beam irradiation in combination with ZOL has high potential to increase OSA cell death.
骨肉瘤(OSA)是儿童和青少年中最常见的恶性骨肿瘤。所有骨癌的总体五年生存率低于70%;然而,当癌症扩散到骨骼以外时,生存率约为15%-30%。在此,我们评估了碳离子束照射单独或与唑来膦酸(ZOL)联合对OSA细胞的影响。与单独使用碳离子束照射、X射线照射和ZOL治疗相比,碳离子束照射联合ZOL通过阻止细胞周期进程并引发KHOS和U2OS细胞凋亡,显著抑制了OSA细胞增殖。此外,我们观察到,与单独使用碳离子束或X射线照射或ZOL治疗相比,这种联合治疗极大地抑制了OSA细胞的运动性和侵袭性,同时抑制了与细胞增殖和存活相关的Pi3K/Akt和MAPK信号通路。此外,ZOL治疗上调了微小RNA(miR)-29b的表达;与miR-29b模拟物联合使用通过激活半胱天冬酶3途径进一步降低了OSA细胞活力。因此,ZOL介导的碳离子束放射敏感性增强可能通过miR-29b上调发生;与miR-29b模拟物联合治疗进一步降低了OSA细胞存活率。这些发现表明,碳离子束照射联合ZOL具有很高的潜力来增加OSA细胞死亡。