Literature DB >> 9000007

Fluorescent taxoids.

R Guy1, Z Scott, R Sloboda, K Nicolaou.   

Abstract

BACKGROUND: Taxol is a natural product produced by the Pacific Yew, Taxus brevifolia, that has emerged as a prominent chemotherapeutic agent for the treatment of solid tumors. Taxol's biochemical mode of action has been well studied: it binds to microtubules, stabilizing them and preventing their depolymerization to tubulin subunits. At lower dosage levels, taxol also interferes with the normal dynamics of the tubulin-microtubule equilibrium. This biochemical effect causes taxol's ultimate physiological effect, cell cycle arrest; taxol is thought to block anaphase A of mitosis. Taxol also causes a number of intriguing secondary effects on interphase cells that are poorly understood. We believed that a bio-active fluorescent taxol derivative could be a useful tool in the study of these cellular mechanisms, especially in interphase cells.
RESULTS: We have synthesized and characterized a series of stable, fluorescently labeled derivatives of taxol that bind to microtubules and have cytotoxicities similar to that of taxol. Fluorescence microscopy experiments in interphase human foreskin fibroblast (HFF) cells indicate that one of these, a sulforhodamine taxoid, is particularly well suited for optical microscopy. The use of this taxoid in HFF cells revealed a previously undetected localization of taxoids to the nucleolus during interphase.
CONCLUSIONS: The production of a new fluorescent derivative of taxol provides a useful tool, enabling cellular biologists to study taxol's mechanism of action. It is hoped that this material will prove particularly useful for the study of taxol's effects upon interphase cells. Although in common usage for the last 20 years, Taxol is now a registered trademark of Bristol-Myers Squibb. The copyright of Bristol-Myers Squibb is recognized when Taxol or taxol is used in this article.

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Year:  1996        PMID: 9000007     DOI: 10.1016/s1074-5521(96)90168-4

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  15 in total

Review 1.  Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.

Authors:  K C Nicolaou; Christopher R H Hale; Christian Nilewski; Heraklidia A Ioannidou
Journal:  Chem Soc Rev       Date:  2012-06-28       Impact factor: 54.564

2.  Heat shock protein 90 mediates macrophage activation by Taxol and bacterial lipopolysaccharide.

Authors:  C A Byrd; W Bornmann; H Erdjument-Bromage; P Tempst; N Pavletich; N Rosen; C F Nathan; A Ding
Journal:  Proc Natl Acad Sci U S A       Date:  1999-05-11       Impact factor: 11.205

3.  FRET measurements of kinesin neck orientation reveal a structural basis for processivity and asymmetry.

Authors:  Douglas S Martin; Reza Fathi; Timothy J Mitchison; Jeff Gelles
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-08       Impact factor: 11.205

4.  Rapid, photoactivatable turn-on fluorescent probes based on an intramolecular photoclick reaction.

Authors:  Zhipeng Yu; Lok Yin Ho; Qing Lin
Journal:  J Am Chem Soc       Date:  2011-07-15       Impact factor: 15.419

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

Authors:  Molly M Lee; Zhe Gao; Blake R Peterson
Journal:  Angew Chem Int Ed Engl       Date:  2017-05-09       Impact factor: 15.336

6.  Perspectives from nearly five decades of total synthesis of natural products and their analogues for biology and medicine.

Authors:  K C Nicolaou; Stephan Rigol
Journal:  Nat Prod Rep       Date:  2020-04-22       Impact factor: 13.423

7.  Biomedical applications of tetrazine cycloadditions.

Authors:  Neal K Devaraj; Ralph Weissleder
Journal:  Acc Chem Res       Date:  2011-05-31       Impact factor: 22.384

8.  Bioorthogonal turn-on probes for imaging small molecules inside living cells.

Authors:  Neal K Devaraj; Scott Hilderbrand; Rabi Upadhyay; Ralph Mazitschek; Ralph Weissleder
Journal:  Angew Chem Int Ed Engl       Date:  2010-03-19       Impact factor: 15.336

9.  Synthesis and Biological Evaluation of a Biotinylated Paclitaxel With an Extra-Long Chain Spacer Arm.

Authors:  Lev G Lis; Mary A Smart; Anna Luchniak; Mohan L Gupta; Vadim J Gurvich
Journal:  ACS Med Chem Lett       Date:  2012-07-30       Impact factor: 4.345

10.  Paclitaxel induces nucleolar enlargement in dorsal root ganglion neurons in vivo reducing oxaliplatin toxicity.

Authors:  S M F Jamieson; J Liu; T Hsu; B C Baguley; M J McKeage
Journal:  Br J Cancer       Date:  2003-06-16       Impact factor: 7.640

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