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. 1986 Apr;5(4):701-5.
doi: 10.1002/j.1460-2075.1986.tb04270.x.

Activation of the pp60c-src kinase during differentiation of monomyelocytic cells in vitro

Activation of the pp60c-src kinase during differentiation of monomyelocytic cells in vitro

A Barnekow et al. EMBO J. 1986 Apr.

Abstract

The proto-oncogene c-src, the cellular homolog of the Rous sarcoma virus (RSV) transforming gene v-src, is expressed in a tissue-specific and age-dependent manner. Its physiological function, although still unknown, appears to be more closely related to differentiation processes than to proliferation processes. To obtain more information about the physiological role of the c-src gene in cells, we have studied differentiation-dependent alterations using the human HL-60 leukaemia cell line as a model system. Induction of monocytic and granulocytic differentiation of HL-60 cells by 12-O-tetradecanoylphorbol-13-acetate (TPA) and dimethylsulfoxide (DMSO) is associated with an activation of the pp60c-src tyrosine kinase, but not with increased c-src gene expression. Control experiments exclude an interaction of TPA and DMSO themselves with the pp60c-src kinase.

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References

    1. Cancer Res. 1985 Feb;45(2):847-50 - PubMed
    1. Cancer Res. 1985 Feb;45(2):822-5 - PubMed
    1. Biochem Biophys Res Commun. 1985 Feb 15;126(3):999-1005 - PubMed
    1. Nature. 1985 Apr 11-17;314(6011):546-8 - PubMed
    1. Nature. 1985 Jul 4-10;316(6023):64-6 - PubMed

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