Electroacupuncture in Combination with Bevacizumab Hydrogel Provides a Therapeutic Strategy for Bladder Cancer

贝伐单抗 膀胱癌 电针 医学 免疫系统 阿霉素 药理学 癌症研究 肿瘤微环境 联合疗法 癌症 药品 药物输送 细胞因子 免疫疗法 血管生成 化疗 透明质酸 马拉特1 癌细胞 髓样 肿瘤坏死因子α 系统药理学 中医药 治疗效果 肿瘤科 功效
作者
Lisha Liu,Ting Liang,Guixiao Huang,Dashi Deng,Chengnan Li,Yu Wang,Xuyuan Liu,Guangzhi Li
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:18 (4): 6668-6686
标识
DOI:10.1021/acsami.6c00404
摘要

Acupuncture, a promising treatment for various diseases and a crucial component of traditional Chinese medicine (TCM), shows potential in enhancing immune function and prognosis in patients with cancer. However, its mechanisms of action in solid tumors remain unclear. This study evaluated the antitumor efficacy of electroacupuncture (EA) in bladder cancer (BC), using doxorubicin (DOX) as a reference treatment. Both DOX and EA significantly inhibited tumor growth and prolonged survival in a BC mouse model. To further investigate the underlying mechanisms, RNA sequencing (RNA-seq) and network pharmacology analyses were conducted to explore the organ-protective and neuromodulatory effects of EA. Single-cell RNA sequencing (scRNA-seq) was performed to assess the impact of DOX and EA on the heterogeneity of the tumor immune microenvironment (TIME). EA treatment led to an increased proportion of immune cells, particularly T cells and myeloid cells. Additionally, EA activated CD8+ T cells, suppressed fibroblast-mediated tumor angiogenesis, and reduced pro-inflammatory cytokine expression, contributing to organ protection and highlighting its potential for combination therapy with antiangiogenic agents. Based on these findings, bevacizumab (BEV), an antiangiogenic drug, was selected and a hyaluronic acid (HA)@sodium alginate (SA)-BEV hydrogel was developed as a drug delivery system for combination therapy with EA. HA@SA-BEV exhibited stable release in the acidic tumor microenvironment, prolonging local drug retention at the tumor site. EA combined with HA@SA-BEV effectively suppressed BC progression, enhancing antitumor efficacy. These findings provide insights into the integration of EA with anticancer agents and support its potential clinical value in cancer treatment.
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