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The Carbamoylmannose Moiety of Bleomycin Mediates Selective Tumor Cell Targeting
[Image: see text] Recently, we reported that both bleomycin (BLM) and its disaccharide, conjugated to the cyanine dye Cy5**, bound selectively to cancer cells. Thus, the disaccharide moiety alone recapitulates the tumor cell targeting properties of BLM. Here, we demonstrate that the conjugate of the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038340/ https://www.ncbi.nlm.nih.gov/pubmed/24811347 http://dx.doi.org/10.1021/bi500482q |
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author | Bhattacharya, Chandrabali Yu, Zhiqiang Rishel, Michael J. Hecht, Sidney M. |
author_facet | Bhattacharya, Chandrabali Yu, Zhiqiang Rishel, Michael J. Hecht, Sidney M. |
author_sort | Bhattacharya, Chandrabali |
collection | PubMed |
description | [Image: see text] Recently, we reported that both bleomycin (BLM) and its disaccharide, conjugated to the cyanine dye Cy5**, bound selectively to cancer cells. Thus, the disaccharide moiety alone recapitulates the tumor cell targeting properties of BLM. Here, we demonstrate that the conjugate of the BLM carbamoylmannose moiety with Cy5** showed tumor cell selective binding and also enhanced cellular uptake in most cancer cell lines. The carbamoyl functionality was required for tumor cell targeting. A dye conjugate prepared from a trivalent cluster of carbamoylmannose exhibited levels of tumor cell binding and internalization significantly greater than those of the simple carbamoylmannose–dye conjugate, consistent with a possible multivalent receptor. |
format | Online Article Text |
id | pubmed-4038340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40383402015-05-08 The Carbamoylmannose Moiety of Bleomycin Mediates Selective Tumor Cell Targeting Bhattacharya, Chandrabali Yu, Zhiqiang Rishel, Michael J. Hecht, Sidney M. Biochemistry [Image: see text] Recently, we reported that both bleomycin (BLM) and its disaccharide, conjugated to the cyanine dye Cy5**, bound selectively to cancer cells. Thus, the disaccharide moiety alone recapitulates the tumor cell targeting properties of BLM. Here, we demonstrate that the conjugate of the BLM carbamoylmannose moiety with Cy5** showed tumor cell selective binding and also enhanced cellular uptake in most cancer cell lines. The carbamoyl functionality was required for tumor cell targeting. A dye conjugate prepared from a trivalent cluster of carbamoylmannose exhibited levels of tumor cell binding and internalization significantly greater than those of the simple carbamoylmannose–dye conjugate, consistent with a possible multivalent receptor. American Chemical Society 2014-05-08 2014-05-27 /pmc/articles/PMC4038340/ /pubmed/24811347 http://dx.doi.org/10.1021/bi500482q Text en Copyright © 2014 American Chemical Society |
spellingShingle | Bhattacharya, Chandrabali Yu, Zhiqiang Rishel, Michael J. Hecht, Sidney M. The Carbamoylmannose Moiety of Bleomycin Mediates Selective Tumor Cell Targeting |
title | The Carbamoylmannose Moiety of Bleomycin Mediates
Selective Tumor Cell Targeting |
title_full | The Carbamoylmannose Moiety of Bleomycin Mediates
Selective Tumor Cell Targeting |
title_fullStr | The Carbamoylmannose Moiety of Bleomycin Mediates
Selective Tumor Cell Targeting |
title_full_unstemmed | The Carbamoylmannose Moiety of Bleomycin Mediates
Selective Tumor Cell Targeting |
title_short | The Carbamoylmannose Moiety of Bleomycin Mediates
Selective Tumor Cell Targeting |
title_sort | carbamoylmannose moiety of bleomycin mediates
selective tumor cell targeting |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038340/ https://www.ncbi.nlm.nih.gov/pubmed/24811347 http://dx.doi.org/10.1021/bi500482q |
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