张申武, 单新竹, 孙新新, 孔志强, 罗聪, 何仲贵*. 基于纳米递送技术诱导肿瘤铁死亡的研究进展J. 药学学报, 2022,57(1): 36-45. doi: 10.16438/j.0513-4870.2021-1152
引用本文: 张申武, 单新竹, 孙新新, 孔志强, 罗聪, 何仲贵*. 基于纳米递送技术诱导肿瘤铁死亡的研究进展J. 药学学报, 2022,57(1): 36-45. doi: 10.16438/j.0513-4870.2021-1152
ZHANG Shen-wu, SHAN Xin-zhu, SUN Xin-xin, KONG Zhi-qiang, LUO Cong, HE Zhong-gui*. Advance on inducing ferroptosis of tumor cells based on nanodelivery technologyJ. Acta Pharmaceutica Sinica, 2022,57(1): 36-45. doi: 10.16438/j.0513-4870.2021-1152
Citation: ZHANG Shen-wu, SHAN Xin-zhu, SUN Xin-xin, KONG Zhi-qiang, LUO Cong, HE Zhong-gui*. Advance on inducing ferroptosis of tumor cells based on nanodelivery technologyJ. Acta Pharmaceutica Sinica, 2022,57(1): 36-45. doi: 10.16438/j.0513-4870.2021-1152

基于纳米递送技术诱导肿瘤铁死亡的研究进展

Advance on inducing ferroptosis of tumor cells based on nanodelivery technology

  • 摘要: 目前癌症仍是对人类健康最具威胁的重大疾病之一。尽管多种疗法已经被应用于临床,但多数癌症的临床治疗效果仍不佳。近年来,调节性细胞死亡过程的发现为癌症治疗提供了新思路。其中,铁死亡(ferroptosis)是一种铁离子催化细胞膜不饱和脂肪酸发生脂质过氧化引发的调节性细胞死亡方式。随着生物纳米技术的蓬勃发展,铁死亡作为一种新兴的癌症治疗靶点,已引起了人们的广泛关注。鉴于生物纳米技术诱导铁死亡研究的快速发展,本文对铁死亡和生物纳米技术交叉这一领域的最新进展进行概括。首先,对铁死亡与纳米制剂的研究背景以及基于铁死亡的纳米递药系统用于癌症治疗的可行性进行介绍和分析;其次,对基于纳米递药技术诱导铁死亡的策略进行总结,主要包括:促进芬顿(Fenton)反应、抑制谷胱甘肽过氧化物酶4(glutathione peroxidase 4,GPX-4)和抑制半胱氨酸-谷氨酸交换转运体(system Xc-)等;此外,还对基于生物纳米技术诱导铁死亡的联合治疗策略进行了探讨;最后,着重讨论了基于铁死亡的纳米制剂在癌症临床治疗中的应用前景和挑战。

     

    Abstract: At present, cancer is still one of the most serious threats to human health. Despite the wide application of multiple cancer therapies in clinical practice, the therapeutic effects of most cancers are still far from satisfactory. In recent years, the discovery of regulated cell death may be a good first step on the road to treat cancer. Ferroptosis is triggered by lipid peroxidation of unsaturated fatty acids in cell membrane catalyzed by iron ion. It has been widely concerned as an emerging target for cancer therapy. With the booming of biomedical nanotechnology, ferroptosis as an emerging therapeutic target has attracted extensive attention. Here, we review the advance on the intersection of ferroptosis and biomedical nanotechnology. First, the research background of ferroptosis and nano-preparation as well as the feasibility of ferroptosis-based nano-drug delivery systems (nano-DDS) for cancer treatment are presented and analyzed. Then, the strategies for inducing ferroptosis based on nano-DDS are summarized, mainly including:the promotion of Fenton reaction, the inhibition of glutathione peroxidase 4 (GPX-4) and the restriction of the cysteine-glutamate exchange transporter (system Xc-). Furthermore, the combination therapy strategies based on biomedical nanotechnology induced ferroptosis are also discussed. Finally, we shine the spotlight on the prospects and challenges of ferroptosis-based nanotherapeutics in clinical application.

     

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