首页> 外文期刊>Chemical engineering journal >Bicompatible porous Co3O4 nanoplates with intrinsic tumor metastasis inhibition for multimodal imaging and DNA damage-mediated tumor synergetic photothermal/photodynamic therapy
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Bicompatible porous Co3O4 nanoplates with intrinsic tumor metastasis inhibition for multimodal imaging and DNA damage-mediated tumor synergetic photothermal/photodynamic therapy

机译:具有内在肿瘤转移抑制的双脉络多孔CO3O4纳米多数制成像和DNA损伤介导的肿瘤协同摄热光热/光动力治疗的抑制作用

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摘要

It will be interesting and yet challenging to develop a near-infrared (NIR) laser trigger phototheranostics agent for multimodal imaging guided synergistic phototherapy. In addition, the mechanisms of phototheranostics agent or in combination with NIR for tumor therapy remain unclear. Herein, we fabricate porous Co3O4 nanoplates (pCo(3)O(4) NPs) using a hydrothermal process followed by a calcination treatment. We demonstrate that pCo(3)O(4) NPs are a promising phototheranostics agent for multimodal imaging (photoacoustic/magnetic resonance imaging) and a NIR laser triggered photothermal therapy (PTT) and photodynamic therapy (PDT) of tumors without apparent side effects. Moreover, RNA sequencing (RNA-seq) analysis highlights that pCo(3)O(4) NPs can suppress tumor metastasis via inhibiting epithelial-mesenchymal transition (EMT) pathway. In addition, pCo(3)O(4) NPs could kill tumor cells via inducing DNA damage after NIR irradiation. In summary, the data reveal that pCo(3)O(4) NPs + NIR could effectively suppress tumorigenesis, and further highlight their potential as a nanomaterial-based multimodal imaging contrast agent and precise DNA damage-mediated tumor synergetic phototherapy, providing new insights to fully understand and use phototheranostics agent in the future.
机译:开发近红外(NIR)激光触发光热试剂对多模式成像引导协同光疗法进行有趣且挑战性挑战。另外,光热性药剂或与NIR用于肿瘤疗法的机制仍不清楚。在此,我们使用水热过程制造多孔CO 3 O 4纳米板(PCO(3)O(4)NPS),然后进行煅烧处理。我们证明PCO(3)O(4)NPS是用于多模式成像(光声/磁共振成像)的有前途的光炎剂,并且鼻炎激光触发的光热疗(PTT)和光动力治疗(PDT)的肿瘤而没有明显的副作用。此外,RNA测序(RNA-SEQ)分析突出显示PCO(3)O(4)NPS可以通过抑制上皮 - 间充质转换(EMT)途径来抑制肿瘤转移。此外,PCO(3)O(4)NPS可以通过在NIR辐射后诱导DNA损伤杀死肿瘤细胞。总之,数据显示,PCO(3)O(4)NPS + NIR可以有效地抑制肿瘤发生,并进一步突出其作为基于纳米材料的多模式成像造影剂和精确的DNA损伤介导的肿瘤协同光疗法,提供新的见解在将来完全理解和使用光热仪剂。

著录项

  • 来源
    《Chemical engineering journal》 |2020年第1期|共12页
  • 作者单位

    Sun Yat Sen Univ Affiliated Hosp 8 Shenzhen 518033 Guangdong Peoples R China;

    Southern Med Univ Canc Res Inst Sch Basic Med Sci Guangzhou 510515 Peoples R China;

    Southern Med Univ Canc Res Inst Sch Basic Med Sci Guangzhou 510515 Peoples R China;

    Southern Med Univ Canc Res Inst Sch Basic Med Sci Guangzhou 510515 Peoples R China;

    Southern Med Univ Canc Res Inst Sch Basic Med Sci Guangzhou 510515 Peoples R China;

    Sun Yat Sen Univ Affiliated Hosp 8 Shenzhen 518033 Guangdong Peoples R China;

    Sun Yat Sen Univ Affiliated Hosp 8 Shenzhen 518033 Guangdong Peoples R China;

    Southern Med Univ Canc Res Inst Sch Basic Med Sci Guangzhou 510515 Peoples R China;

    Southern Med Univ Nanfang Hosp Dept Med Imaging Ctr Guangzhou 510515 Peoples R China;

    Sun Yat Sen Univ Affiliated Hosp 8 Shenzhen 518033 Guangdong Peoples R China;

    Sun Yat Sen Univ Affiliated Hosp 8 Shenzhen 518033 Guangdong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    pCo(3)O(4) NPs; Phototheranostics; Tumor metastasis; Epithelial-mesenchymal transition pathway; DNA damage;

    机译:PCO(3)O(4)NPS;光热器;肿瘤转移;上皮 - 间充质转换途径;DNA损伤;

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