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Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017)
In article 1600202, CD44v6 peptide functionalized nanoparticles are fabricated in a facile and controllable way to selectively bind to tumor cells with highly efficient anticancer and antimetastatic properties by Veronique Orian‐Rousseau, Pavel A. Levkin, and co‐workers. The modular synthesis and fa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238733/ http://dx.doi.org/10.1002/advs.201770001 |
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author | Li, Linxian Schmitt, Mark Matzke‐Ogi, Alexandra Wadhwani, Parvesh Orian‐Rousseau, Veronique Levkin, Pavel A. |
author_facet | Li, Linxian Schmitt, Mark Matzke‐Ogi, Alexandra Wadhwani, Parvesh Orian‐Rousseau, Veronique Levkin, Pavel A. |
author_sort | Li, Linxian |
collection | PubMed |
description | In article 1600202, CD44v6 peptide functionalized nanoparticles are fabricated in a facile and controllable way to selectively bind to tumor cells with highly efficient anticancer and antimetastatic properties by Veronique Orian‐Rousseau, Pavel A. Levkin, and co‐workers. The modular synthesis and facile preparation makes this system highly potent for developing novel multifunctional nanocarriers for therapeutic and/or diagnostic anticancer applications. [Image: see text] |
format | Online Article Text |
id | pubmed-5238733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52387332017-01-19 Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) Li, Linxian Schmitt, Mark Matzke‐Ogi, Alexandra Wadhwani, Parvesh Orian‐Rousseau, Veronique Levkin, Pavel A. Adv Sci (Weinh) Cover Picture In article 1600202, CD44v6 peptide functionalized nanoparticles are fabricated in a facile and controllable way to selectively bind to tumor cells with highly efficient anticancer and antimetastatic properties by Veronique Orian‐Rousseau, Pavel A. Levkin, and co‐workers. The modular synthesis and facile preparation makes this system highly potent for developing novel multifunctional nanocarriers for therapeutic and/or diagnostic anticancer applications. [Image: see text] John Wiley and Sons Inc. 2017-01-16 /pmc/articles/PMC5238733/ http://dx.doi.org/10.1002/advs.201770001 Text en © 2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Cover Picture Li, Linxian Schmitt, Mark Matzke‐Ogi, Alexandra Wadhwani, Parvesh Orian‐Rousseau, Veronique Levkin, Pavel A. Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) |
title | Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) |
title_full | Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) |
title_fullStr | Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) |
title_full_unstemmed | Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) |
title_short | Cancer Therapy: CD44v6‐Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells (Adv. Sci. 1/2017) |
title_sort | cancer therapy: cd44v6‐peptide functionalized nanoparticles selectively bind to metastatic cancer cells (adv. sci. 1/2017) |
topic | Cover Picture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238733/ http://dx.doi.org/10.1002/advs.201770001 |
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