Figure 2.Effects of limited glucose availability, resveratrol and DHEA on expression of TXNIP and Sirt1 in cancer cells. Panel A.
SaOS2 cells were incubated in the presence of reduced glucose levels in the
culture medium for 48 hours. Expression of TXNIP and Sirt1 were determined
by Western blot using specific antibodies. Antibody to β-actin was used
as a loading control. Panel B. Respective expression of TXNIP and
Sirt1 in response to limited glucose availability, measured by quantitative
real time PCR (Q-PCR). SaOS2 cells were incubated in the presence of the
indicated amounts of glucose for 48 hours, QPCR was then performed to
detect expression of TXNIP and Sirt1 using specific primers. Panel C
and D, the RGC (panel C) and SaOS2 (panel D) cells
were subjected to treatment with
increasing concentrations of resveratrol (Resv.) for 48 hours followed by
Western blot as described in Panel A. Panel E, SaOS2 cells
were treated with increasing amounts of DHEA and probed for expression of
Sirt1 and TXNIP, β-actin was used as a loading control.
