4.7 Article

Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells

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SCIENTIFIC REPORTS
卷 9, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-019-44388-9

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资金

  1. FCT - Foundation for Science and Technology [SFRH/BD/122953/2016]
  2. project Acoes Integradas Luso-Francesas [TC-15/17]
  3. FCT - Fundo Social Europeu [IF/00959/2015]
  4. Programa Operacional Potencial Humano, FCT [UID/Multi/04349/2019]
  5. project Fundacao Luso-Americana (FLAD) Healthcare 2020 [45/2018]
  6. MIT Portugal FCT project BIODEVICE [MIT-EXPL/BIO/0008/2017]
  7. UTAustin Portugal Program Exploratory project DREAM [UTAP-EXPL/NTec/0015/2017]
  8. POCI - COMPETE 2020 -Operational Programme Competitiveness and Internationalisation in Axis I Strengthening research, technological development and innovation [POCI-01-0145-FEDER-007491]
  9. Symbit project - ERDF [CZ.02.1.01/0.0/0.0/15_003/0000477]
  10. Fundação para a Ciência e a Tecnologia [MIT-EXPL/BIO/0008/2017] Funding Source: FCT

向作者/读者索取更多资源

AS1411 is a G-rich DNA oligonucleotide that functions as an aptamer of the protein nucleolin, found at high levels on the surface of cancer cells but not on the surface of normal cells. Herein, we have studied AS1411 as a supramolecular carrier for the delivery of an acridine-based G-quadruplex ligand, C-8, to HeLa cancer cells. Two AS1411 derivatives, LNA-AS1411 and U-AS1411, were also tested, in an attempt to compare AS1411 pharmacological properties. The results showed that AS1411-C-8 complexation was made with great binding strength and that it lowered the ligand's cytotoxicity towards non-malignant cells. This effect was suggested to be due to a decreased internalization of the complexed versus free C-8 as shown by flow cytometry. The AS1411 derivatives, despite forming a stable complex with C-8, lacked the necessary tumour-selective behaviour. The binding of C-8 to AS1411 G-quadruplex structure did not negatively affect the recognition of nucleolin by the aptamer. The AS1411-C-8 repressed c-MYC expression at the transcriptional level, possibly due to C-8 ability to stabilize the c-MYC promoter G-quadruplexes. Overall, this study demonstrates the usefulness of AS1411 as a supramolecular carrier of the G-quadruplex binder C-8 and the potential of using its tumour-selective properties for the delivery of ligands for cancer therapy.

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