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Optimized HSP90 mediated fluorescent probes for cancer-specific bioimaging

  • Shulei Zhu
  • , Yalei Li
  • , Yushu Huang
  • , Minmin Zhang
  • , Xiaofan Gu
  • , Yang He
  • , Hongchun Liu
  • , Mingliang Ma*
  • , Wei Lu
  • *此作品的通讯作者
  • CAS - Shanghai Institute of Materia Medica
  • East China Normal University

科研成果: 期刊稿件文章同行评审

摘要

Cancer-specific bioimaging has been correlated with fluorescence-guided tumor therapy, garnering extensive interest from researchers. Herein, a highly efficient tumor-targeting fluorescent probe (NP-001), which is integrated with 4-hydroxy-1,8-naphthalimide and NVP-AUY922, for tumor imaging has been established. 4-Hydroxy-1,8-naphthalimide is a fluorescent molecule with remarkable imaging compatibility. NVP-AUY922 is a heat shock protein 90 (HSP90) inhibitor with preferential tumor selectivity that is conjugated to 4-hydroxy-1,8-naphthalimide as a tumor-targeting ligand. NP-002, a resorcinol-blocked probe which prevented binding with an amino acid residue of the HSP90 ATP binding pocket, was also synthesized as a control. In vitro and ex vivo assays showed that NP-001 could arrest cell proliferation, induce apoptosis and accumulate to inhibit HSP90. Confocal laser scanning microscopy (CLSM) also confirmed that NP-001 could be selectively internalized by tumor cells for cancer-specific bioimaging. Moreover, pharmacokinetic studies and histological analysis also indicated that NP-001 had a relatively longer retention time and showed no major organ-related toxicities. Overall, these encouraging data suggest that NP-001 is a promising new candidate for the early diagnosis of metastatic disease as well as targeted tumor imaging.

源语言英语
页(从-至)1878-1896
页数19
期刊Journal of Materials Chemistry B
8
9
DOI
出版状态已出版 - 7 3月 2020

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