Title : Modulators of protein kinase C inhibit hypoxia-induced erythropoietin production.

Pub. Date : 1993 Mar

PMID : 7679999






7 Functional Relationships(s)
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1 The addition of phorbol 12-myristate 13-acetate (PMA) to Hep 3B cells subsequently grown under hypoxic conditions resulted in a dose-dependent inhibition of hypoxia-induced Epo production by as much as 95 +/- 1% with half-maximal inhibition at 8 ng/mL. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens
2 The addition of phorbol 12-myristate 13-acetate (PMA) to Hep 3B cells subsequently grown under hypoxic conditions resulted in a dose-dependent inhibition of hypoxia-induced Epo production by as much as 95 +/- 1% with half-maximal inhibition at 8 ng/mL. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens
3 By Northern blot analysis, Epo mRNA levels were correspondingly decreased after treatment with PMA. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens
4 The PMA-induced inhibition of hypoxia-induced Epo production was shown to occur as early as 3 hours after PMA addition, suggesting that the initial activation, rather than the subsequent decrease in protein kinase C activity, is of primary importance. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens
5 The PMA-induced inhibition of hypoxia-induced Epo production was shown to occur as early as 3 hours after PMA addition, suggesting that the initial activation, rather than the subsequent decrease in protein kinase C activity, is of primary importance. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens
6 The relative specificity of the PMA-induced inhibition of Epo production was demonstrated by 1) the finding that overall protein and RNA synthesis were not similarly decreased as measured by 3H-leucine and 3H-uridine pulse labeling studies and 2) the observation that the biologically inactive phorbol ester, 4 alpha-phorbol didecanoate, failed to have any effect on hypoxia-induced Epo production. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens
7 The relative specificity of the PMA-induced inhibition of Epo production was demonstrated by 1) the finding that overall protein and RNA synthesis were not similarly decreased as measured by 3H-leucine and 3H-uridine pulse labeling studies and 2) the observation that the biologically inactive phorbol ester, 4 alpha-phorbol didecanoate, failed to have any effect on hypoxia-induced Epo production. Tetradecanoylphorbol Acetate erythropoietin Homo sapiens