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基于钙介导细胞黏附增强的共轭聚合物-钙复合纳米粒子的抗肿瘤转移及协同治疗。

Calcium-Mediated Cell Adhesion Enhancement-Based Antimetastasis and Synergistic Antitumor Therapy by Conjugated Polymer-Calcium Composite Nanoparticles.

机构信息

Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, Shaanxi 710119, P. R. China.

出版信息

ACS Nano. 2024 Sep 10;18(36):24953-24967. doi: 10.1021/acsnano.4c05771. Epub 2024 Aug 28.

DOI:10.1021/acsnano.4c05771
PMID:39197151
Abstract

Strengthening tumor cellular adhesion through regulating the concentration of extracellular Ca is highly challenging and promising for antimetastasis. Herein, a pH-responsive conjugated polymer-calcium composite nanoparticle (PFV/CaCO/PDA@PEG) is developed for calcium-mediated cell adhesion enhancement-based antimetastasis and reactive oxygen species (ROS)-triggered calcium overload and photodynamic therapy (PDT) synergistic tumor treatment. PFV/CaCO/PDA@PEG is mainly equipped with conjugated poly(fluorene--vinylene) (PFV-COOH)-composited CaCO nanoparticles, which can be rapidly decomposed under the tumor acidic microenvironment, effectively releasing Ca and the photosensitizer PFV-COOH. The high extracellular Ca concentration facilitates the generation of dimers between two adjacent cadherin ectodomains, which greatly enhances cell-cell adhesion and suppresses tumor metastasis. The inhibition rates are 97 and 87% for highly metastatic tumor cells 4T1 and MCF-7, respectively. Such a well-designed nanoparticle also contributes to realizing PDT, mitochondrial dysfunction, and ROS-triggered Ca overload synergistic therapy. Furthermore, PFV/CaCO/PDA@PEG displayed superior inhibition of 4T1 tumor growth and demonstrated a marked antimetastatic effect by both intravenous and intratumoral injection modes. Thus, this study provides a powerful strategy for calcium-mediated metastasis inhibition for tumor therapy.

摘要

通过调节细胞外 Ca 浓度来增强肿瘤细胞黏附对于抗肿瘤转移是极具挑战性和前景的。在此,开发了一种 pH 响应性的聚合物-钙复合纳米粒子(PFV/CaCO/PDA@PEG),用于基于钙介导的细胞黏附增强的抗肿瘤转移和活性氧(ROS)触发的钙超载和光动力治疗(PDT)协同肿瘤治疗。PFV/CaCO/PDA@PEG 主要配备了由共轭聚(芴-乙烯)(PFV-COOH)复合的 CaCO 纳米粒子,这些纳米粒子在肿瘤酸性微环境下可以迅速分解,有效地释放 Ca 和光敏剂 PFV-COOH。高细胞外 Ca 浓度有助于两个相邻钙黏蛋白胞外结构域之间二聚体的生成,从而大大增强了细胞-细胞黏附并抑制了肿瘤转移。对于高度转移性肿瘤细胞 4T1 和 MCF-7,抑制率分别为 97%和 87%。这种精心设计的纳米粒子还有助于实现 PDT、线粒体功能障碍和 ROS 触发的 Ca 超载协同治疗。此外,PFV/CaCO/PDA@PEG 对 4T1 肿瘤生长的抑制作用明显,通过静脉内和瘤内注射两种方式均表现出显著的抗肿瘤转移作用。因此,该研究为肿瘤治疗中基于钙介导的转移抑制提供了一种强大的策略。

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