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pH 敏感的负载酞菁的聚合物纳米颗粒作为乳腺癌的一种新型治疗策略。

pH-sensitive phthalocyanine-loaded polymeric nanoparticles as a novel treatment strategy for breast cancer.

作者信息

Malarz Katarzyna, Borzęcka Wioleta, Ziola Patryk, Domiński Adrian, Rawicka Patrycja, Bialik-Wąs Katarzyna, Kurcok Piotr, Torres Tomas, Mrozek-Wilczkiewicz Anna

机构信息

Department of Systems Biology and Engineering, Silesian University of Technology, Akademicka 2A, 44-100 Gliwice, Poland; A. Chełkowski Institute of Physics, University of Silesia in Katowice, 75 Pułku Piechoty 1a, 41-500 Chorzów, Poland.

Centre of Polymer and Carbon Materials, Polish Academy of Sciences, Marii Skłodowskiej-Curie 34, 41-819 Zabrze, Poland.

出版信息

Bioorg Chem. 2025 Feb;155:108127. doi: 10.1016/j.bioorg.2025.108127. Epub 2025 Jan 3.

DOI:10.1016/j.bioorg.2025.108127
PMID:39798455
Abstract

Novel pH-sensitive polymeric photosensitizer carriers from the phthalocyanine (Pc) group were investigated as potential photodynamic therapy drugs for the treatment of breast cancer. Their high antiproliferative activity was confirmed by photocytotoxicity studies, which indicated their high efficacy and specificity toward the SK-BR-3 cell line. Importantly, the Pcs encapsulated in the polymeric nanoparticle (NP) carrier exhibited a much better penetration into the acidic environment of tumor cells than their free form. The investigated Pc4-NPs and TT1-NPs exhibited a high selectivity to healthy fibroblasts as well as non-toxicity without irradiation. This paper describes the detailed mechanism of action of the evaluated compounds by measuring reactive oxygen species (ROS), including singlet oxygen; imaging cellular localization; and analyzing key signaling pathway proteins. An additional advantage of the evaluated compounds is their ability to inhibit the Akt protein expression, including its phosphorylation, which the Western blot test confirmed. This is particularly important because breast cancers often overexpress the HER-2 receptor-related signaling proteins. Moreover, an analysis of proteins such as GLUT-1, HO-1, phospho-p42/44, and BID revealed the significant involvement of ROS in disrupting cellular homeostasis, thereby leading to the induction of oxidative stress and resulting in apoptotic cell death.

摘要

研究了新型酞菁(Pc)基pH敏感聚合物光敏剂载体作为治疗乳腺癌的潜在光动力治疗药物。光细胞毒性研究证实了它们具有高抗增殖活性,这表明它们对SK-BR-3细胞系具有高效性和特异性。重要的是,封装在聚合物纳米颗粒(NP)载体中的Pc在肿瘤细胞的酸性环境中的穿透性比其游离形式要好得多。所研究的Pc4-NPs和TT1-NPs对健康成纤维细胞具有高选择性且在无辐射时无毒。本文通过测量活性氧(ROS),包括单线态氧;成像细胞定位;以及分析关键信号通路蛋白,描述了所评估化合物的详细作用机制。所评估化合物的另一个优点是它们能够抑制Akt蛋白表达,包括其磷酸化,蛋白质印迹试验证实了这一点。这一点尤为重要,因为乳腺癌通常过度表达HER-2受体相关信号蛋白。此外,对GLUT-1、HO-1、磷酸化p42/44和BID等蛋白质的分析表明,ROS在破坏细胞稳态中起重要作用,从而导致氧化应激的诱导并导致凋亡性细胞死亡。

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引用本文的文献

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RSC Adv. 2025 Aug 21;15(36):29890-29924. doi: 10.1039/d5ra04347f. eCollection 2025 Aug 18.
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Manganese-based nanoparticles plus gambogic acid targeted hypoxic tumor microenvironment by enhancing ROS generation and provided antitumor treatment and improved immunotherapy.基于锰的纳米颗粒联合藤黄酸通过增强活性氧生成靶向缺氧肿瘤微环境,提供抗肿瘤治疗并改善免疫疗法。
RSC Adv. 2025 Apr 11;15(15):11283-11292. doi: 10.1039/d4ra08547g. eCollection 2025 Apr 9.