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LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells
Functionalized multi‐walled carbon nanotubes have been extensively gained popularity in pancreatic cancer gene therapy. LyP‐1, a peptide, has been proved to specifically bind pancreatic cancer cells. The potential therapeutic effect of LyP‐1–conjugated functionalized multi‐walled carbon nanotubes in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077559/ https://www.ncbi.nlm.nih.gov/pubmed/31968405 http://dx.doi.org/10.1111/jcmm.14864 |
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author | Lin, Quan‐Jun Xie, Zhi‐Bo Gao, Ya Zhang, Yi‐Fan Yao, Lie Fu, De‐Liang |
author_facet | Lin, Quan‐Jun Xie, Zhi‐Bo Gao, Ya Zhang, Yi‐Fan Yao, Lie Fu, De‐Liang |
author_sort | Lin, Quan‐Jun |
collection | PubMed |
description | Functionalized multi‐walled carbon nanotubes have been extensively gained popularity in pancreatic cancer gene therapy. LyP‐1, a peptide, has been proved to specifically bind pancreatic cancer cells. The potential therapeutic effect of LyP‐1–conjugated functionalized multi‐walled carbon nanotubes in treating pancreatic cancer is still unknown. In this study, LyP‐1–conjugated functionalized multi‐walled carbon nanotubes were successfully synthesized, characterized and showed satisfactory size distribution and zeta potential. Compared with functionalized multi‐walled carbon nanotubes, cellular uptake of LyP‐1–functionalized multi‐walled carbon nanotubes was shown to be increased. Compound of LyP‐1–functionalized multi‐walled carbon nanotubes and MBD1siRNA showed superior gene transfection efficiency. Moreover, LyP‐1‐fMWNTs/MBD1siRNA complex could significantly decrease the viability and proliferation and promoted apoptosis of pancreatic cancer cells in vitro. Further xenograft assays revealed that the tumour burden in the nude mice injected with LyP‐1–functionalized multi‐walled carbon nanotubes/MBD1siRNA was significantly relieved. The study demonstrated that LyP‐1–functionalized multi‐walled carbon nanotubes/MBD1siRNA could be a promising candidate for tumour active targeting therapy in pancreatic cancer. |
format | Online Article Text |
id | pubmed-7077559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70775592020-03-19 LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells Lin, Quan‐Jun Xie, Zhi‐Bo Gao, Ya Zhang, Yi‐Fan Yao, Lie Fu, De‐Liang J Cell Mol Med Original Articles Functionalized multi‐walled carbon nanotubes have been extensively gained popularity in pancreatic cancer gene therapy. LyP‐1, a peptide, has been proved to specifically bind pancreatic cancer cells. The potential therapeutic effect of LyP‐1–conjugated functionalized multi‐walled carbon nanotubes in treating pancreatic cancer is still unknown. In this study, LyP‐1–conjugated functionalized multi‐walled carbon nanotubes were successfully synthesized, characterized and showed satisfactory size distribution and zeta potential. Compared with functionalized multi‐walled carbon nanotubes, cellular uptake of LyP‐1–functionalized multi‐walled carbon nanotubes was shown to be increased. Compound of LyP‐1–functionalized multi‐walled carbon nanotubes and MBD1siRNA showed superior gene transfection efficiency. Moreover, LyP‐1‐fMWNTs/MBD1siRNA complex could significantly decrease the viability and proliferation and promoted apoptosis of pancreatic cancer cells in vitro. Further xenograft assays revealed that the tumour burden in the nude mice injected with LyP‐1–functionalized multi‐walled carbon nanotubes/MBD1siRNA was significantly relieved. The study demonstrated that LyP‐1–functionalized multi‐walled carbon nanotubes/MBD1siRNA could be a promising candidate for tumour active targeting therapy in pancreatic cancer. John Wiley and Sons Inc. 2020-01-22 2020-03 /pmc/articles/PMC7077559/ /pubmed/31968405 http://dx.doi.org/10.1111/jcmm.14864 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Lin, Quan‐Jun Xie, Zhi‐Bo Gao, Ya Zhang, Yi‐Fan Yao, Lie Fu, De‐Liang LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells |
title | LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells |
title_full | LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells |
title_fullStr | LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells |
title_full_unstemmed | LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells |
title_short | LyP‐1‐fMWNTs enhanced targeted delivery of MBD1siRNA to pancreatic cancer cells |
title_sort | lyp‐1‐fmwnts enhanced targeted delivery of mbd1sirna to pancreatic cancer cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077559/ https://www.ncbi.nlm.nih.gov/pubmed/31968405 http://dx.doi.org/10.1111/jcmm.14864 |
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