Zhao Kaili, Shen Guizhi, Liu Yamei, Chen Kaiwei, Chang Rui, Liu Yazhou, Chen Wanting, Liu Huazhen, Yang Meng, Xing Ruirui, Yan Xuehai
State Key Laboratory of Biochemical Engineering, Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
ACS Appl Mater Interfaces. 2024 Dec 11;16(49):67532-67544. doi: 10.1021/acsami.4c18320. Epub 2024 Nov 22.
Triple-negative breast cancer (TNBC) is known for its poor prognosis and aggressive behavior, being highly prone to recurrence and metastasis, and currently has limited effective treatment options. Photothermal therapy (PTT) is an emerging, minimally invasive, low-drug-resistance, and precisely controllable therapeutic method for cancer treatment, offering hope to break through the bottleneck in TNBC therapy. The antitumor efficiency of PTT is predominantly contingent upon the performance of the photothermal drugs. Therefore, there is an urgent need to develop photothermal drugs that not only have excellent photothermal conversion efficiency but also possess strong tumor-targeting capabilities and good biosafety. Here, we have developed a tumor-targeted photothermal agent with near-infrared (NIR) absorption capability based on the strategy of biomolecular assembly, utilizing biliverdin manganese complexes (MnBV) and amphiphilic phospholipid-polymer conjugates (DSPE-PEG and DSPE-PEG-cKNGRE). This photothermal assembled drug exhibits a uniform size, good stability, and ideal photothermal conversion efficiency. In the 4T1 tumor-bearing mouse model of TNBC, it shows good tumor dual-targeting capabilities and a significant drug enrichment performance. While ablating the primary tumor, PTT further stimulates the maturation of dendritic cells (DCs), enhancing the infiltration of T lymphocytes into the spleen and tumor, thus reshaping the immune microenvironment of TNBC and thereby effectively inhibiting tumor metastasis and recurrence. The developed photothermal assembled drug provides an innovative candidate treatment paradigm for TNBC, offering the potential to advance precise, targeted, and safe therapy for highly invasive and aggressive malignancies.
三阴性乳腺癌(TNBC)以其预后差和侵袭性强而闻名,极易复发和转移,目前有效的治疗选择有限。光热疗法(PTT)是一种新兴的、微创的、低耐药性且可精确控制的癌症治疗方法,为突破TNBC治疗的瓶颈带来了希望。PTT的抗肿瘤效率主要取决于光热药物的性能。因此,迫切需要开发不仅具有优异光热转换效率,而且具有强大肿瘤靶向能力和良好生物安全性的光热药物。在此,我们基于生物分子组装策略,利用胆绿素锰配合物(MnBV)和两亲性磷脂-聚合物偶联物(DSPE-PEG和DSPE-PEG-cKNGRE),开发了一种具有近红外(NIR)吸收能力的肿瘤靶向光热剂。这种光热组装药物具有均匀的尺寸、良好的稳定性和理想的光热转换效率。在TNBC的4T1荷瘤小鼠模型中,它表现出良好的肿瘤双靶向能力和显著的药物富集性能。在消融原发性肿瘤的同时,PTT进一步刺激树突状细胞(DCs)成熟,增强T淋巴细胞向脾脏和肿瘤的浸润,从而重塑TNBC的免疫微环境,进而有效抑制肿瘤转移和复发。所开发的光热组装药物为TNBC提供了一种创新的候选治疗模式,为推进对高度侵袭性恶性肿瘤的精准、靶向和安全治疗提供了潜力。