Literature DB >> 28485901

Synthesis of a Fluorescent Analogue of Paclitaxel That Selectively Binds Microtubules and Sensitively Detects Efflux by P-Glycoprotein.

Molly M Lee1, Zhe Gao1, Blake R Peterson1.   

Abstract

The anticancer drug paclitaxel (Taxol) exhibits paradoxical and poorly understood effects against slow-growing tumors. To investigate its biological activity, fluorophores such as Oregon Green have been linked to this drug. However, this modification increases its polarity by approximately 1000-fold and reduces the toxicity of Taxol towards cancer cell lines by over 200-fold. To construct more drug-like fluorescent probes suitable for imaging by confocal microscopy and analysis by flow cytometry, we synthesized derivatives of Taxol linked to the drug-like fluorophore Pacific Blue (PB). We found that PB-Gly-Taxol bound the target protein β-tubulin with both high affinity in vitro and high specificity in living cells, exhibited substantial cytotoxicity towards HeLa cells, and was a highly sensitive substrate of the multidrug resistance transporter P-glycoprotein (P-gp).
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  antitumor agents; confocal microscopy; drug design; fluorescent probes; paclitaxel

Mesh:

Substances:

Year:  2017        PMID: 28485901      PMCID: PMC5679005          DOI: 10.1002/anie.201703298

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  31 in total

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Journal:  Bioorg Med Chem Lett       Date:  2001-09-03       Impact factor: 2.823

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7.  Interaction of a fluorescent paclitaxel analogue with tubulin.

Authors:  S Sengupta; T C Boge; G I Georg; R H Himes
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10.  The expression of P-glycoprotein does influence the distribution of novel fluorescent compounds in solid tumour models.

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