Ge Yu-Xiang, Zhuang Hong-Jun, Zhang Tai-Wei, Liang Hai-Feng, Ding Wang, Zhou Lei, Dong Zhi-Rui, Hu Zhi-Chao, Chen Qing, Dong Jian, Jiang Li-Bo, Yin Xiao-Fan
Department of Orthopedics Surgery, Minhang Hospital, Fudan University, Shanghai 201100, China.
Department of Orthopaedic Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Mater Today Bio. 2023 Jan 26;19:100547. doi: 10.1016/j.mtbio.2023.100547. eCollection 2023 Apr.
Circadian rhythm (CR) disruption contributes to tumor initiation and progression, however the pharmacological targeting of circadian regulators reversely inhibits tumor growth. Precisely controlling CR in tumor cells is urgently required to investigate the exact role of CR interruption in tumor therapy. Herein, based on KL001, a small molecule that specifically interacts with the clock gene cryptochrome (CRY) functioning at disruption of CR, we fabricated a hollow MnO nanocapsule carrying KL001 and photosensitizer BODIPY with the modification of alendronate (ALD) on the surface (H-MnSiO/K&B-ALD) for osteosarcoma (OS) targeting. The H-MnSiO/K&B-ALD nanoparticles reduced the CR amplitude in OS cells without affecting cell proliferation. Furthermore, nanoparticles-controlled oxygen consumption by inhibiting mitochondrial respiration via CR disruption, thus partially overcoming the hypoxia limitation for photodynamic therapy (PDT) and significantly promoting PDT efficacy. An orthotopic OS model demonstrated that KL001 significantly enhanced the inhibitory effect of H-MnSiO/K&B-ALD nanoparticles on tumor growth after laser irradiation. CR disruption and oxygen level enhancement induced by H-MnSiO/K&B-ALD nanoparticles under laser irradiation were also confirmed in vivo. This discovery first demonstrated the potential of CR controlling for tumor PDT ablation and provided a promising strategy for overcoming tumor hypoxia.
昼夜节律(CR)紊乱促进肿瘤的发生和发展,然而,对昼夜节律调节因子进行药物靶向反而会抑制肿瘤生长。迫切需要精确控制肿瘤细胞中的CR,以研究CR中断在肿瘤治疗中的确切作用。在此,基于KL001(一种与在CR破坏时起作用的生物钟基因隐花色素(CRY)特异性相互作用的小分子),我们制备了一种携带KL001和光敏剂BODIPY的中空MnO纳米胶囊,并在其表面修饰了阿仑膦酸盐(ALD),用于靶向骨肉瘤(OS)。H-MnSiO/K&B-ALD纳米颗粒降低了OS细胞中的CR振幅,而不影响细胞增殖。此外,纳米颗粒通过CR破坏抑制线粒体呼吸来控制氧气消耗,从而部分克服了光动力疗法(PDT)的缺氧限制,并显著提高了PDT疗效。原位OS模型表明,KL001显著增强了H-MnSiO/K&B-ALD纳米颗粒在激光照射后对肿瘤生长的抑制作用。激光照射下H-MnSiO/K&B-ALD纳米颗粒诱导的CR破坏和氧水平升高在体内也得到了证实。这一发现首次证明了控制CR用于肿瘤PDT消融的潜力,并为克服肿瘤缺氧提供了一种有前景的策略。