U87MG cells were seeded at 1 × 104 cells/well in 12-well flat-bottomed plates. U87MG was exposed to GiNK at a GiNK:GBM cell ratio of 1:1 in the presence/absence of 50 μM TMZ for 96 h. Adherent cells were stained with SA-β-gal, and the stained cells were counted under an inverted microscope. (a) Representative photographs of SA-β-gal-stained U87MG cells under each treatment condition. (b) The graphs show the percentages of SA-β-gal-positive cells of U87MG (n = 4) cells. Data indicated as mean ± SE. P values were determined using one-way ANOVA followed by Tukey’s test. Statistically significant differences: **P < 0.01.</p
<p>Western blot analysis of senescence markers in <b>A</b>) LβT2 cells transiently transfected with ...
<p>(A and B) U87 MG cells were treated with 400 µM TMZ for the indicated time periods and then analy...
<p>A) The TGFβ data-set from GSE15871 was compared to probe-set changes between P3 and P5 wild type ...
<p>HCT116 cells were treated with different concentrations of TMZ for 48 h and then processed for SA...
<p>The HCT116 cells were pretreated with different concentrations of NSC666715 for 2 h followed by t...
<p>T98G, U118MG, U251MG and U87MG cells were treated with TMZ [100μM] for 3 h, and then cultured in ...
<p>Senescence induction 24–144 h after TMZ treatment (100 µM) determined by C<sub>12</sub>FDG positi...
<p>U251MG and U87MG cells were treated with TMZ [100μM] for 3 h, and then cultured in medium contain...
<p>HCT116 cells with or without p53 and p21 expression were treated with 500 μM TMZ for 48 h, and th...
U87MG and T98G were exposed to GiNK at a GiNK:GBM cell ratio of 1:1, and LN-18 was exposed to GiNK a...
<p>Cells were grown in 24-well plate and repeatedly treated with PROG and TMZ at different concentra...
<p>Representative images of (A) U87-MG and U–SC, and (B) L0627 morphology after 48 h treatment with ...
<p>Normal (MCF12A) ± siMGMT undergo ≥ 75% senescence at equitoxic concentrations of MNNG (2 µM + siM...
<p>(<b>A</b>) SA-β-gal staining at 48 h after transfection of expression plasmids for E12, p21 and F...
<p>(A) HepG2 cells were cultured in RPMI medium with 0.1% DMSO or 10 µM etoposide for 0, 12, 24, 36 ...
<p>Western blot analysis of senescence markers in <b>A</b>) LβT2 cells transiently transfected with ...
<p>(A and B) U87 MG cells were treated with 400 µM TMZ for the indicated time periods and then analy...
<p>A) The TGFβ data-set from GSE15871 was compared to probe-set changes between P3 and P5 wild type ...
<p>HCT116 cells were treated with different concentrations of TMZ for 48 h and then processed for SA...
<p>The HCT116 cells were pretreated with different concentrations of NSC666715 for 2 h followed by t...
<p>T98G, U118MG, U251MG and U87MG cells were treated with TMZ [100μM] for 3 h, and then cultured in ...
<p>Senescence induction 24–144 h after TMZ treatment (100 µM) determined by C<sub>12</sub>FDG positi...
<p>U251MG and U87MG cells were treated with TMZ [100μM] for 3 h, and then cultured in medium contain...
<p>HCT116 cells with or without p53 and p21 expression were treated with 500 μM TMZ for 48 h, and th...
U87MG and T98G were exposed to GiNK at a GiNK:GBM cell ratio of 1:1, and LN-18 was exposed to GiNK a...
<p>Cells were grown in 24-well plate and repeatedly treated with PROG and TMZ at different concentra...
<p>Representative images of (A) U87-MG and U–SC, and (B) L0627 morphology after 48 h treatment with ...
<p>Normal (MCF12A) ± siMGMT undergo ≥ 75% senescence at equitoxic concentrations of MNNG (2 µM + siM...
<p>(<b>A</b>) SA-β-gal staining at 48 h after transfection of expression plasmids for E12, p21 and F...
<p>(A) HepG2 cells were cultured in RPMI medium with 0.1% DMSO or 10 µM etoposide for 0, 12, 24, 36 ...
<p>Western blot analysis of senescence markers in <b>A</b>) LβT2 cells transiently transfected with ...
<p>(A and B) U87 MG cells were treated with 400 µM TMZ for the indicated time periods and then analy...
<p>A) The TGFβ data-set from GSE15871 was compared to probe-set changes between P3 and P5 wild type ...