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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...

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Autores principales: Bhattacharya, Chandrabali, Yu, Zhiqiang, Rishel, Michael J., Hecht, Sidney M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
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.
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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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