Literature DB >> 3654591

Inhibition of microtubule polymerization by synthetic estrogens: formation of a ribbon structure.

Y Sato1, T Murai, T Oda, H Saitô, M Kodama, A Hirata.   

Abstract

Dienestrol, meso-hexestrol, and dl-hexestrol, synthetic nonsteroidal estrogens, were shown to be inhibitors of microtubule assembly in vitro using microtubule proteins isolated from porcine brains. The order of activity of the synthetic estrogens as inhibitors of microtubule assembly is: dienestrol greater than diethylstilbestrol greater than meso-hexestrol greater than dl-hexestrol greater than isodienestrol. The activity of dienestrol as an inhibitor was of the same order as that of (+)-griseofulvin, as determined by turbidity measurement. Electron microscopic observation revealed that twisted ribbon structures are formed from microtubule proteins in the presence of some synthetic estrogens (dienestrol, meso-hexestrol, and dl-hexestrol).

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Year:  1987        PMID: 3654591     DOI: 10.1093/oxfordjournals.jbchem.a121988

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  2 in total

1.  Interaction of the tumor inhibitor IKP-104, a 4(1H)-pyridinone derivative, with microtubule proteins.

Authors:  F Mizuhashi; K Murata; T Kitagaki; I Tomita
Journal:  Jpn J Cancer Res       Date:  1992-02

Review 2.  Estrogens-Origin of Centrosome Defects in Human Cancer?

Authors:  Miriam Bühler; Ailine Stolz
Journal:  Cells       Date:  2022-01-27       Impact factor: 6.600

  2 in total

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