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靶向细胞焦亡诱导增强胶质母细胞瘤治疗。

Boosting Glioblastoma Therapy with Targeted Pyroptosis Induction.

机构信息

Clinical College of Traditional Chinese Medicine, Taihe Hospital, Hubei University of Chinese Medicine, Wuhan, Hubei, 430065, P. R. China.

Department of Neurosurgery, Hubei Key Laboratory of Embryonic Stem Cell Research, Hubei Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, 442000, P. R. China.

出版信息

Small. 2023 Jul;19(30):e2207604. doi: 10.1002/smll.202207604. Epub 2023 Apr 17.

Abstract

Glioblastoma (GBM) is a highly aggressive cancer that currently lacks effective treatments. Pyroptosis has emerged as a promising therapeutic approach for cancer, but there is still a need for new pyroptosis boosters to target cancer cells. In this study, it is reported that Aloe-emodin (AE), a natural compound derived from plants, can inhibit GBM cells by inducing pyroptosis, making it a potential booster for pyroptosis-mediated GBM therapy. However, administering AE is challenging due to the blood-brain barrier (BBB) and its non-selectivity. To overcome this obstacle, AE@ZIF-8 NPs are developed, a biomineralized nanocarrier that releases AE in response to the tumor's acidic microenvironment (TAM). Further modification of the nanocarrier with transferrin (Tf) and polyethylene glycol-poly (lactic-co-glycolic acid) (PEG-PLGA) improves its penetration through the BBB and tumor targeting, respectively. The results show that AE-NPs (Tf-PEG-PLGA modified AE@ZIF-8 NPs) significantly increase the intracranial distribution and tumor tissue accumulation, enhancing GBM pyroptosis. Additionally, AE-NPs activate antitumor immunity and reduce AE-related toxicity. Overall, this study provides a new approach for GBM therapy and offers a nanocarrier that is capable of penetrating the BBB, targeting tumors, and attenuating toxicity.

摘要

胶质母细胞瘤(GBM)是一种高度侵袭性的癌症,目前缺乏有效的治疗方法。细胞焦亡已成为癌症治疗的一种有前途的方法,但仍需要新的细胞焦亡增强剂来靶向癌细胞。在这项研究中,据报道,大黄素(AE),一种来源于植物的天然化合物,可以通过诱导细胞焦亡来抑制 GBM 细胞,使其成为一种潜在的细胞焦亡介导的 GBM 治疗增强剂。然而,由于血脑屏障(BBB)及其非选择性,给予 AE 具有挑战性。为了克服这一障碍,开发了 AE@ZIF-8 NPs,这是一种生物矿化纳米载体,可响应肿瘤酸性微环境(TAM)释放 AE。进一步用转铁蛋白(Tf)和聚乙二醇-聚(乳酸-共-羟基乙酸)(PEG-PLGA)对纳米载体进行修饰,分别提高了其穿透 BBB 和肿瘤靶向的能力。结果表明,AE-NPs(Tf-PEG-PLGA 修饰的 AE@ZIF-8 NPs)显著增加了颅内分布和肿瘤组织积累,增强了 GBM 细胞焦亡。此外,AE-NPs 激活了抗肿瘤免疫并降低了 AE 相关毒性。总的来说,这项研究为 GBM 治疗提供了一种新方法,并提供了一种能够穿透 BBB、靶向肿瘤和减轻毒性的纳米载体。

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