Yue Jing, Liang Lijia, Shen Yanting, Guan Xin, Zhang Jing, Li Zhiyuan, Deng Rong, Xu Shuping, Liang Chongyang, Shi Wei, Xu Weiqing
State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, Jilin University, Changchun, China.
Institute of Frontier Medical Science, Jilin University, Changchun, China.
Front Chem. 2019 Jan 28;6:665. doi: 10.3389/fchem.2018.00665. eCollection 2018.
Photodynamic therapy (PDT) involves the uptake of photosensitizers by cancer cells and the irradiation of a light with a specific wavelength to trigger a series of photochemical reactions based on the generation of reactive oxygen, leading to cancer cell death. PDT has been widely used in various fields of biomedicine. However, the molecular events of the cancer cell nucleus during the PDT process are still unclear. In this work, a nuclear-targeted gold nanorod Raman nanoprobe combined with surface-enhanced Raman scattering spectroscopy (SERS) was exploited to investigate the dynamic intranuclear molecular changes of B16 cells (a murine melanoma cell line) treated with a photosensitizer (Chlorin e6) and the specific light (650 nm). The SERS spectra of the cell nucleus during the PDT treatment were recorded and the spectroscopic analysis of the dynamics of the nucleus uncovered two main events in the therapeutic process: the protein degradation and the DNA fragmentation. We expect that these findings are of vital significance in having a better understanding of the PDT mechanism acting on the cancer cell nucleus and can further help us to design and develop more effective therapeutic platforms and methods.
光动力疗法(PDT)包括癌细胞摄取光敏剂以及用特定波长的光照射,以基于活性氧的产生引发一系列光化学反应,从而导致癌细胞死亡。光动力疗法已在生物医学的各个领域广泛应用。然而,光动力疗法过程中癌细胞核的分子事件仍不清楚。在这项工作中,利用一种核靶向金纳米棒拉曼纳米探针结合表面增强拉曼散射光谱(SERS),来研究用光敏剂(叶绿素e6)和特定光(650nm)处理的B16细胞(一种小鼠黑色素瘤细胞系)的核内分子动态变化。记录了光动力疗法治疗过程中细胞核的SERS光谱,并且对细胞核动态的光谱分析揭示了治疗过程中的两个主要事件:蛋白质降解和DNA片段化。我们期望这些发现对于更好地理解作用于癌细胞核的光动力疗法机制具有至关重要的意义,并且能够进一步帮助我们设计和开发更有效的治疗平台和方法。