Layered Double Hydroxide Nanoparticles Loaded with Resveratrol Inhibit Glycolysis and Show Efficacy in the Treatment of Breast Cancer.

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-03-17 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S492145
Chenchen Geng, Liuyang Yan, Yunhao Li, Houcong Li, Yuxin Ji, Yuhan Xiao, Zhifa Wang, Xiaoqi Chen, Changjie Chen, Qingling Yang, Baoding Tang, Wenrui Wang
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引用次数: 0

Abstract

Background: Breast cancer is one of the most common cancers among women. Tumor cell proliferation is highly dependent on aerobic glycolysis, so regulating aerobic glycolysis in breast cancer cells is a promising therapeutic strategy. Resveratrol (Res), as a potential new anti-breast cancer drug, has been shown to regulate the glycolysis of cancer cells and inhibit the metastasis and recurrence of breast cancer. The nano drug delivery system can regulate the aerobic glycolysis metabolism by targeting the signaling factors and reaction products of the tumor aerobic glycolysis process to enhance the anti-tumor effect.

Methods: A new albumin-modified layered double hydroxide resveratrol dosage form (BSA@LDHs-Res) was synthesized by hydrothermal co-precipitation. Characterization was carried out to determine the successful synthesis of the nanocarrier system. The bioactivity, glycolytic activity and biocompatibility were examined by in vitro cellular assays; in vivo experiments were performed to further evaluate the anti-tumor effects of the BSA@LDHs-Res dosage form for breast cancer.

Results: In this study, we obtained for the first time a bovine serum albumin-modified BSA@LDHs-Res loaded dosage form, which was able to enter breast cancer cells SKBR3 and MDA-MB-231 via endocytosis and successfully escaped from lysosomal capture. BSA@LDHs-Res inhibited the proliferation, migration, and invasion of two types of breast cancer cells, induced apoptosis, and promoted the reduction of mitochondrial membrane potential and ROS. BSA@LDHs-Res inhibited the expression and viability of the key enzymes of glycolysis, hexokinase 2 (HK2), pyruvate kinase (PK), and lactate dehydrogenase, resulting in decreased glucose consumption, decreased lactate accumulation, and decreased intracellular ATP levels. BSA@LDHs-Res was examined in the mouse model with good anti-tumor effects.

Conclusion: BSA@LDHs-Res is an efficient nanoreagent for the treatment of breast cancer. The albumin-modified resveratrol layered double hydroxide delivery system developed in this study will provide some theoretical references for further research and clinical application of tumor aerobic glycolysis.

负载白藜芦醇的层状双氢氧化物纳米颗粒抑制糖酵解并显示治疗乳腺癌的疗效。
背景:乳腺癌是女性中最常见的癌症之一。肿瘤细胞的增殖高度依赖于有氧糖酵解,因此调节乳腺癌细胞的有氧糖酵解是一种很有前景的治疗策略。白藜芦醇(Resveratrol, Res)作为一种潜在的抗乳腺癌新药,具有调节癌细胞糖酵解,抑制乳腺癌转移和复发的作用。纳米给药系统通过靶向肿瘤好氧糖酵解过程的信号因子和反应产物调节好氧糖酵解代谢,增强抗肿瘤作用。方法:采用水热共沉淀法合成一种新的白蛋白修饰层状双氢氧化物白藜芦醇剂型(BSA@LDHs-Res)。进行表征以确定纳米载体体系的成功合成。体外细胞法检测其生物活性、糖酵解活性和生物相容性;通过体内实验进一步评价BSA@LDHs-Res剂型对乳腺癌的抗肿瘤作用。结果:在本研究中,我们首次获得了牛血清白蛋白修饰的BSA@LDHs-Res负载剂型,该剂型能够通过内吞作用进入乳腺癌细胞SKBR3和MDA-MB-231,并成功逃脱溶酶体捕获。BSA@LDHs-Res抑制两类乳腺癌细胞的增殖、迁移和侵袭,诱导凋亡,促进线粒体膜电位和ROS的降低。BSA@LDHs-Res抑制糖酵解、己糖激酶2 (HK2)、丙酮酸激酶(PK)和乳酸脱氢酶等关键酶的表达和活力,导致葡萄糖消耗减少,乳酸积累减少,细胞内ATP水平降低。BSA@LDHs-Res经小鼠模型检验,具有良好的抗肿瘤作用。结论:BSA@LDHs-Res是一种有效的治疗乳腺癌的纳米药物。本研究建立的白蛋白修饰白藜芦醇层状双氢氧化物递送体系将为肿瘤有氧糖酵解的进一步研究和临床应用提供一定的理论参考。
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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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