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Geldanamycin, an inhibitor of the chaperone activity of HSP90, induces MAPK-independent cell cycle arrest

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Geldanamycin, an inhibitor of the chaperone activity of HSP90, induces MAPK-independent cell cycle arrest (English)

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Monique Bedin

1

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Anne-Marie Gaben

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2

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Cécile Saucier

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3

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Jan Mester

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4

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language of work or name

English

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publication date

1 May 2004

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published in

International Journal of Cancer

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volume

109

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issue

5

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page(s)

643-52

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cites work

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Regulation of cyclin D-dependent kinase 4 (cdk4) by cdk4-activating kinase

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Ras links growth factor signaling to the cell cycle machinery via regulation of cyclin D1 and the Cdk inhibitor p27KIP1.

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Sustained activation of extracellular-signal-regulated kinase 1 (ERK1) is required for the continued expression of cyclin D1 in G1 phase

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Cyclin D1/Cdk4 regulates retinoblastoma protein-mediated cell cycle arrest by site-specific phosphorylation

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Functional inactivation of the retinoblastoma protein requires sequential modification by at least two distinct cyclin-cdk complexes

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Human cyclin E, a nuclear protein essential for the G1-to-S phase transition

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p50(cdc37) acting in concert with Hsp90 is required for Raf-1 function

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Destabilization of Raf-1 by geldanamycin leads to disruption of the Raf-1-MEK-mitogen-activated protein kinase signalling pathway

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Cell cycle regulation of the murine cyclin E gene depends on an E2F binding site in the promoter.

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Geldanamycin, a new antibiotic

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Identifiers

DOI

10.1002/IJC.20010

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PubMed publication ID

14999769

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ResearchGate publication ID

5364071

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(Q28248254)

Geldanamycin, an inhibitor of the chaperone activity of HSP90, induces MAPK-independent cell cycle arrest

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