Literature DB >> 8822202

Transforming growth factor beta and dexamethasone cooperatively enhance c-jun gene expression and inhibit the growth of human monocytoid leukemia cells.

Y Kanatani1, T Kasukabe, J Okabe-Kado, S Hayashi, Y Yamamoto-Yamaguchi, K Motoyoshi, N Nagata, Y Honma.   

Abstract

Glucocorticoids inhibit the proliferation of lymphoid leukemia cells, whereas most myeloid leukemia cells are resistant to glucocorticoids. However, this study showed that glucocorticoids significantly and preferentially inhibited growth of monocytoid leukemia cells in combination with a low concentration of transforming growth factor beta (TGF beta). Combined 1 alpha,25-dihydroxyvitamin D3 and TGF beta markedly induced monocytic differentiation of U937 cells, whereas dexamethasone (Dex) and TGF beta essentially did not, although both combinations similarly inhibited the growth of U937 cells. The growth inhibition was accompanied by a block in the cell cycle progression from G1 to S phase (G1 arrest). Expression of glucocorticoid receptors was not affected by TGF beta, although they are induced during the monocytic differentiation of myelogenous leukemia cells and have increased sensitivity to glucocorticoids. The expression of TGF beta receptors also was not enhanced by Dex. TGF beta significantly stimulated glucocorticoid responsive element-mediated transcription activity. Combined Dex and TGF beta stimulated the expression of c-jun and c-fos early responsive genes in U937 cells, although Dex or TGF beta alone did not. The combination synergistically induced expression of c-jun gene, reaching a maximum level at 24 h. On the other hand, expression of c-fos gene was induced by TGF beta alone and increased additively in combination with Dex. Treatment with antisense oligonucleotide complementary to the first exon of c-jun mRNA reduced the growth-inhibitory effect of Dex and TGF beta in a dose-dependent manner. However, exposure of U937 cells to the sense oligomer of c-jun mRNA or an antisense oligomer of c-fos mRNA did not affect the growth inhibition. These results suggested that the preferential expression of c-jun and stimulation of glucocorticoid responsive element-mediated transactivation are closely associated with the growth arrest of U937 cells incubated with Dex and TGF beta.

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Year:  1996        PMID: 8822202

Source DB:  PubMed          Journal:  Cell Growth Differ        ISSN: 1044-9523


  4 in total

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Journal:  Horm Cancer       Date:  2018-01-08       Impact factor: 3.869

2.  Vesnarinone and glucocorticoids cooperatively induce G1 arrest and have an anti-tumour effect on human non-small cell lung carcinoma cells grown in nude mice.

Authors:  Y Honma; Y Yamamoto-Yamaguchi; Y Kanatani
Journal:  Br J Cancer       Date:  1999-04       Impact factor: 7.640

3.  Changes of signal transductivity and robustness of gene regulatory network in the carcinogenesis of leukemic subtypes via microarray sample data.

Authors:  Cheng-Wei Li; Tzu-Ying Lai; Bor-Sen Chen
Journal:  Oncotarget       Date:  2018-05-04

4.  African Swine Fever Virus Manipulates the Cell Cycle of G0-Infected Cells to Access Cellular Nucleotides.

Authors:  Hranush R Avagyan; Sona A Hakobyan; Arpine A Poghosyan; Nane V Bayramyan; Hranush H Arzumanyan; Liana O Abroyan; Aida S Avetisyan; Lina A Hakobyan; Elena M Karalova; Zaven A Karalyan
Journal:  Viruses       Date:  2022-07-22       Impact factor: 5.818

  4 in total

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