Peptide\nNanocarriers for Targeted Delivery of Nucleic\nAcids for Cancer Therapy

Peptides have been extensively studied in nanomedicine\nwith great\nbioactivity and biocompatibility; however, their poor cell-membrane-penetrating\nproperties and nonselectivity greatly limit their clinical applications.\nIn this study, tumor-targeting therapy was achieved by modifying our\npreviously developed efficient peptide vector with the cancer-targeting\npeptide RGD, enabling it to specifically target tumor cells with a\nhigh expression of RGD-binding receptors. B-cell lymphoma-2 antisense\noligonucleotides were selected as the target model to validate the\neffectiveness of the delivery carriers. Results demonstrated that\nthis delivery system can be efficiently and selectively taken up by\nRGD receptor-positive cells (α<sub>v</sub>β<sub>3</sub> integrin receptor), further inducing effective target gene knockdown.\nOverall, this system provided a promising strategy for the targeted\ndelivery of nucleic acid drugs.

Publication Details

Journal
Figshare
Published
2024-12-23
DOI
https://doi.org/10.1021/acs.bioconjchem.4c00324.s001
Primary Topic
RNA Interference and Gene Delivery
Type
article
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article

Peptide\nNanocarriers for Targeted Delivery of Nucleic\nAcids for Cancer Therapy

Figshare
RNA Interference and Gene Delivery
article

Peptide\nNanocarriers for Targeted Delivery of Nucleic\nAcids for Cancer Therapy

article en

Abstract

Peptides have been extensively studied in nanomedicine\nwith great\nbioactivity and biocompatibility; however, their poor cell-membrane-penetrating\nproperties and nonselectivity greatly limit their clinical applications.\nIn this study, tumor-targeting therapy was achieved by modifying our\npreviously developed efficient peptide vector with the cancer-targeting\npeptide RGD, enabling it to specifically target tumor cells with a\nhigh expression of RGD-binding receptors. B-cell lymphoma-2 antisense\noligonucleotides were selected as the target model to validate the\neffectiveness of the delivery carriers. Results demonstrated that\nthis delivery system can be efficiently and selectively taken up by\nRGD receptor-positive cells (α<sub>v</sub>β<sub>3</sub> integrin receptor), further inducing effective target gene knockdown.\nOverall, this system provided a promising strategy for the targeted\ndelivery of nucleic acid drugs.

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RNA Interference and Gene Delivery
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