Geldanamycin Induces Cell Cycle Arrest in K562 Erythroleukemic Cells

IUBMB Life - Tập 48 Số 4 - Trang 425-428 - 1999
Hong Ro Kim1, Chang Hoon Lee1, Yung Hyun Choi2, Ho Sung Kang1, Han Do Kim1
1Department of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan, 609-735, Korea
2Vincent T. Lombardi Cancer Center, Georgetown University Medical Center, Washington, DC 20007, U.S.A.

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Abstract

Geldanamycin (GA), a benzoquinone ansamycin, is one of the specific inhibitors of 90‐kDa heat shock protein and induces growth inhibition and apoptosis in certain cancer cell lines. We have investigated the mechanism of GA‐induced growth inhibition in K562 erythroleukemic cells. DNA flow‐cytometric analysis indicated that GA‐induced growth arrest was associated with G2/M phase arrest of the cell cycle. GA treatment down‐regulated the expression of cyclin B1 and inhibited phosphorylation of Cdc2 protein, both key regulatory proteins at the G2/M boundary. GA also markedly inhibited the Cdc2 kinase activity, which may be in part a result of up‐regulation of p27KIP1 by GA. The present results suggest a novel mechanism that p27KIP1 could be involved in the regulation of G2 to M phase transition.

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