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Supramolecular cyclodextrin nanocarriers for chemo- and gene therapy towards the effective treatment of drug resistant cancers.

Abstract
A tumor active targeting β-cyclodextrin based nanocarrier β-NC-OEI-SS-FA was designed by the modification of star shaped cationic derivatives β-NC-OEI with folic acid through a disulfide bond, to co-deliver chemotherapeutic paclitaxel and the Nur77 gene for overcoming Bcl-2 mediated non-pump resistance by an "enemy to friend" strategy for potential drug resistant cancer therapy.
AuthorsXiaohong Chen, Ying-Kun Qiu, Cally Owh, Xian Jun Loh, Yun-Long Wu
JournalNanoscale (Nanoscale) Vol. 8 Issue 45 Pg. 18876-18881 (Dec 07 2016) ISSN: 2040-3372 [Electronic] England
PMID27819368 (Publication Type: Journal Article)
Chemical References
  • BCL2 protein, human
  • Cyclodextrins
  • Nuclear Receptor Subfamily 4, Group A, Member 1
  • Proto-Oncogene Proteins c-bcl-2
  • Folic Acid
  • Paclitaxel
Topics
  • Animals
  • Cyclodextrins (chemistry)
  • Drug Delivery Systems
  • Drug Resistance, Neoplasm
  • Folic Acid (chemistry)
  • Genetic Therapy
  • HeLa Cells
  • Hep G2 Cells
  • Humans
  • Mice
  • Molecular Structure
  • Nanoparticles
  • Neoplasms (therapy)
  • Nuclear Receptor Subfamily 4, Group A, Member 1 (genetics)
  • Paclitaxel (administration & dosage)
  • Proto-Oncogene Proteins c-bcl-2 (metabolism)
  • Transfection
  • Xenograft Model Antitumor Assays

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