超声响应的乳腺癌纳米气泡:通过cGAS-STING途径的协同声动力学、化疗和免疫激活

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Huan Pu, Jia Huang, Bin Gui, Yueying Chen, Yuxin Guo, Yingtao Lian, Juhong Pan, Yugang Hu, Nan Jiang, Qing Deng* and Qing Zhou*, 
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引用次数: 0

摘要

乳腺癌仍然是全世界妇女癌症相关死亡的主要原因,因此需要更有效的治疗策略。化疗联合免疫治疗是乳腺癌的一线治疗方法,但由于其递送效率差、肿瘤细胞耐药、肿瘤微环境免疫抑制等原因,其治疗效果有限,副作用严重。本研究探讨超声响应纳米泡(Ce6/PTX Nbs)在乳腺癌靶向成像和超声免疫治疗中的发展。通过整合声动力疗法(SDT)、化疗和免疫疗法,纳米气泡旨在解决传统疗法中药物递送不良、全身毒性和免疫抑制等挑战。该纳米泡由声敏剂氯e6 (Ce6)修饰的磷脂组成,并装载化疗药物紫杉醇(PTX),以增强载药能力,通过环rgd肽精确靶向肿瘤部位。超声激活后,Ce6诱导活性氧(ROS),促进免疫原性细胞死亡(ICD),而PTX破坏肿瘤细胞有丝分裂,增强免疫应答。纳米气泡的超声响应性有助于实时成像和控制药物释放,最大限度地提高治疗效果,同时最大限度地减少副作用。关键研究结果表明,Ce6/PTX Nbs在4T1乳腺癌模型中显著降低肿瘤生长,通过cGAS-STING途径增强免疫激活,并增加原发性和远处肿瘤中CD8+ T细胞的浸润。与抗pd - l1检查点抑制剂联合使用,该疗法可显著抑制肿瘤转移。这种创新的方法提供了一种高度靶向、有效和毒性最小的乳腺癌治疗方法,由于其双重成像和治疗能力,具有临床转化的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasound-Responsive Nanobubbles for Breast Cancer: Synergistic Sonodynamic, Chemotherapy, and Immune Activation through the cGAS-STING Pathway

Ultrasound-Responsive Nanobubbles for Breast Cancer: Synergistic Sonodynamic, Chemotherapy, and Immune Activation through the cGAS-STING Pathway

Breast cancer remains the leading cause of cancer-related deaths among women worldwide, necessitating more effective treatment strategies. Chemotherapy combined with immunotherapy is the first-line treatment for breast cancer, but it still suffers from limited therapeutic efficiency and serious side effects, which are usually due to the poor delivery efficiency, drug resistance of tumor cells, and immunosuppressive tumor microenvironment. This study explores the development of ultrasound-responsive nanobubbles (Ce6/PTX Nbs) for targeted imaging and sonoimmunotherapy in breast cancer treatment. By integrating sonodynamic therapy (SDT), chemotherapy, and immunotherapy, the nanobubbles aim to address challenges such as poor drug delivery, systemic toxicity, and immune suppression in conventional therapies. The nanobubbles, composed of sonosensitizer chlorin e6 (Ce6)-modified phospholipid and loaded with the chemotherapeutic agent paclitaxel (PTX) enhancing drug-loading capacity, are designed to precisely target tumor sites via cyclic-RGD peptides. Upon ultrasound activation, Ce6 induces reactive oxygen species (ROS), promoting immunogenic cell death (ICD), while PTX disrupts tumor cell mitosis, enhancing the immune response. The nanobubbles’ ultrasound responsiveness facilitates real-time imaging and controlled drug release, maximizing therapeutic efficacy while minimizing side effects. Key findings demonstrate that Ce6/PTX Nbs significantly reduced tumor growth in a 4T1 breast cancer model, enhanced immune activation via the cGAS-STING pathway, and increased the infiltration of CD8+ T cells in both primary and distant tumors. In combination with anti-PD-L1 checkpoint inhibitors, the treatment achieved a substantial suppression of tumor metastasis. This innovative approach offers a highly targeted, effective, and minimally toxic breast cancer treatment with potential for clinical translation due to its dual imaging and therapeutic capabilities.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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