Inhibition of Mitosis and Microtubule Function through Direct Tubulin Binding by a Novel Antiproliferative Naphthopyran LY290181

Abstract

The mechanism of action of a novel antiproliferative compound LY290181 [2-amino-4-(3-pyridyl)-4H-naphtho(1,2-b)pyran-3-carbonitrile] was characterized. LY290181 is a potent inhibitor of cell proliferation, producing 50% inhibition of vascular smooth muscle, endothelial, Chinese hamster ovary, HeLa, and human erythroleukemia cells at concentrations of 8–40 nm. Cell cycle analysis showed that LY290181 caused accumulation of smooth muscle cells at the G2/M phase and induced mitotic arrest in Chinese hamster ovary cells and HeLa cells. At low concentrations (3–30 nm), LY290181 blocked transition of cells from metaphase to anaphase and disrupted mitotic spindle organization. At high concentrations (≥100 nm), LY290181 produced a concentration-dependent loss of cytoplasmic and spindle microtubules. LY290181 inhibited the polymerization of purified bovine brain microtubule protein into microtubules, and it depolymerized preformed microtubules. Using tubulin-1-anilino-8-naphthalene sulfonate complex fluorescence, we have shown that LY290181 directly interacted with tubulin in a unique manner. These studies show that LY290181 induces cell growth arrest in prometaphase/metaphase, and tubulin appears to be its molecular target.

Footnotes

  • Send reprint requests to: Dr. Jai Pal Singh, Lilly Research Laboratories, DC 0520, Indianapolis, IN 46285.

  • This work was supported in part by National Institute of Neurological Disorders and Stroke Grant NS13560.

  • Abbreviations:
    DMEM
    Dulbecco’s modified Eagle’s medium
    FBS
    fetal bovine serum
    FACS
    fluorescence-activated cell sorting
    FITC
    fluorescein isothiocyanate, BSA, bovine serum albumin
    MAP
    microtubule-associated protein
    PBS
    phosphate-buffered saline
    ANS
    1-anilino-8-naphthalene sulfonate
    CHO
    Chinese hamster ovary
    PEG
    polyethylene glycol
    PIPES
    1,4-piperazinediethanesulfonic acid
    EGTA
    ethylene glycol bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
    • Received February 10, 1996.
    • Accepted May 15, 1997.
« Previous | Next Article »Table of Contents