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Imaging Cellular Distribution of Bcl Inhibitors Using Small Molecule Drug Conjugates
[Image: see text] Overexpression of anti-apoptotic proteins such as Bcl-2 is a cellular mechanism to evade apoptosis; consequently, Bcl-2 inhibitors are being developed as anticancer agents. In this work, we have synthesized a fluorescent version of ABT-199 in an effort to visualize a drug surrogate...
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/PMC4240345/ https://www.ncbi.nlm.nih.gov/pubmed/25333750 http://dx.doi.org/10.1021/bc500433k |
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author | Giedt, Randy J. Sprachman, Melissa M. Yang, Katherine S. Weissleder, Ralph |
author_facet | Giedt, Randy J. Sprachman, Melissa M. Yang, Katherine S. Weissleder, Ralph |
author_sort | Giedt, Randy J. |
collection | PubMed |
description | [Image: see text] Overexpression of anti-apoptotic proteins such as Bcl-2 is a cellular mechanism to evade apoptosis; consequently, Bcl-2 inhibitors are being developed as anticancer agents. In this work, we have synthesized a fluorescent version of ABT-199 in an effort to visualize a drug surrogate by high resolution imaging. We show that this fluorescent conjugate has comparable Bcl-2 binding efficacy and cell line potency to the parent compound and can be used as an imaging agent in several cancer cell types. We anticipate that this agent will be a valuable tool for studying the single-cell distribution and pharmacokinetics of ABT-199 as well the broader group of BH3-mimetics. |
format | Online Article Text |
id | pubmed-4240345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42403452015-10-21 Imaging Cellular Distribution of Bcl Inhibitors Using Small Molecule Drug Conjugates Giedt, Randy J. Sprachman, Melissa M. Yang, Katherine S. Weissleder, Ralph Bioconjug Chem [Image: see text] Overexpression of anti-apoptotic proteins such as Bcl-2 is a cellular mechanism to evade apoptosis; consequently, Bcl-2 inhibitors are being developed as anticancer agents. In this work, we have synthesized a fluorescent version of ABT-199 in an effort to visualize a drug surrogate by high resolution imaging. We show that this fluorescent conjugate has comparable Bcl-2 binding efficacy and cell line potency to the parent compound and can be used as an imaging agent in several cancer cell types. We anticipate that this agent will be a valuable tool for studying the single-cell distribution and pharmacokinetics of ABT-199 as well the broader group of BH3-mimetics. American Chemical Society 2014-10-21 2014-11-19 /pmc/articles/PMC4240345/ /pubmed/25333750 http://dx.doi.org/10.1021/bc500433k Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Giedt, Randy J. Sprachman, Melissa M. Yang, Katherine S. Weissleder, Ralph Imaging Cellular Distribution of Bcl Inhibitors Using Small Molecule Drug Conjugates |
title | Imaging Cellular Distribution of Bcl Inhibitors Using
Small Molecule Drug Conjugates |
title_full | Imaging Cellular Distribution of Bcl Inhibitors Using
Small Molecule Drug Conjugates |
title_fullStr | Imaging Cellular Distribution of Bcl Inhibitors Using
Small Molecule Drug Conjugates |
title_full_unstemmed | Imaging Cellular Distribution of Bcl Inhibitors Using
Small Molecule Drug Conjugates |
title_short | Imaging Cellular Distribution of Bcl Inhibitors Using
Small Molecule Drug Conjugates |
title_sort | imaging cellular distribution of bcl inhibitors using
small molecule drug conjugates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240345/ https://www.ncbi.nlm.nih.gov/pubmed/25333750 http://dx.doi.org/10.1021/bc500433k |
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