Effect of genistein on p90RSK phosphorylation and cell proliferation in T47D breast cancer cells.

Abstract:

BACKGROUND:The molecular mechanisms of genistein's proliferative effects on breast cancer cells are largely unknown. This study aimed to examine estrogen-receptor (ER)-related signaling molecules involved in genistein-associated cell proliferation and survival (ERK1/2, p90RSK, JNK, Akt and NFκB) and to correlate these results to cell proliferation. MATERIALS AND METHODS:The effect of genistein on cell-signaling molecules was determined in T47D breast cancer cells by a Bioplex phosphoprotein detection kit. These results were confirmed by Western blotting and were correlated to cell proliferation by MTT assay. RESULTS:Low and high concentrations of genistein induced an ERK1/2-independent decrease in phosphorylated p90RSK. This effect was accompanied by decreased cell proliferation at high concentrations and an increased response at low concentrations of genistein following a 48-hour exposure. CONCLUSION:Concentration-dependent actions of genistein in T47D cells may be due to differential activation of signaling molecules.

journal_name

Anticancer Res

journal_title

Anticancer research

authors

Gwin J,Drews N,Ali S,Stamschror J,Sorenson M,Rajah TT

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

209-14

issue

1

eissn

0250-7005

issn

1791-7530

pii

31/1/209

journal_volume

31

pub_type

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