Tao Liangsong, Gu Rongrong, Yang Junfa, Wang Jiewei, Wu Tiling, Rao Xianyue, Wang Hao, Qian Cheng, Liu Jian, Ye Sheng, Xu Tao
Inflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmaceutical Sciences, Anhui Medical University, Hefei, 230032, China.
Agricultural Photocatalysis Laboratory, School of Materials and Chemistry, Anhui Agricultural University, Hefei, 230036, China.
Mater Today Bio. 2025 Jun 19;33:102001. doi: 10.1016/j.mtbio.2025.102001. eCollection 2025 Aug.
Hepatocellular carcinoma (HCC), a leading cause of tumor-related mortality globally, demands innovative therapeutic strategies to overcome limitations of conventional treatments. Photodynamic therapy (PDT), reliant on reactive oxygen species (ROS) generation, has emerged as a promising therapeutic strategy for neoplastic diseases. But it is constrained by inefficient charge separation in traditional photosensitizers. Here, we engineered a pea-like Au@BiS nanoreactors by anchoring gold nanoparticles onto BiS surfaces to establish a Schottky junction with interfacial Au-S covalent bonds, which suppresses electron-hole recombination and amplifies ROS production. Under light irradiation, Au@BiS exhibited remarkable inhibitory efficacy against HepG-2 cells, producing twice the ROS yield of BiS. Transcriptomic analysis via RNA sequencing identified activation of the Hippo/Yap signaling pathway, which orchestrated endoplasmic reticulum stress and autophagic flux in malignant cells, ultimately driving apoptotic elimination of HepG-2 populations. These findings delineate a mechanistic paradigm wherein Schottky junction engineering potentiates ROS-mediated cytotoxicity, thereby advancing precise photodynamic interventions for HCC management.
肝细胞癌(HCC)是全球肿瘤相关死亡的主要原因之一,需要创新的治疗策略来克服传统治疗的局限性。光动力疗法(PDT)依赖于活性氧(ROS)的产生,已成为一种有前途的肿瘤疾病治疗策略。但它受到传统光敏剂中电荷分离效率低下的限制。在这里,我们通过将金纳米颗粒锚定在BiS表面上,构建了一种豌豆状的Au@BiS纳米反应器,以形成具有界面Au-S共价键的肖特基结,从而抑制电子-空穴复合并增强ROS的产生。在光照下,Au@BiS对HepG-2细胞表现出显著的抑制效果,其产生的ROS产量是BiS的两倍。通过RNA测序进行的转录组分析确定了Hippo/Yap信号通路的激活,该通路协调了恶性细胞中的内质网应激和自噬通量,最终促使HepG-2细胞群体发生凋亡清除。这些发现描绘了一种机制范式,即肖特基结工程增强了ROS介导的细胞毒性,从而推动了针对HCC治疗的精确光动力干预。