<p>(A) Flow cytometric analysis of cell surface gp96 levels in breast cancer cells. (B) Cells were treated with 50 μg/ml of p37 for 48 h. Cellular apoptosis were analyzed by FACS, and the percentage of apoptotic cells (Annexin V single positive and Annexin V/PI double positive) was determined. (C) CCK-8 assay of cell proliferation upon treatment with various concentrations of p37 peptide for 48 h. Results are presented as means ± SD from three independent experiments. (D) SK-BR-3 cells were transfected with gp96 or control siRNA for 48 h. Cells were treated with 20 μg/ml of p37 or control peptide for additional 48 h. Cellular apoptosis were analyzed by FACS. Results are presented as means ± SD from three independent experiments. (E) Represe...
<p>(A) Cell cycle distribution was analyzed by flow cytometry 72 h after transfection. Bars are show...
<p>(A) TUNEL assay shows the apoptotic tumor cells in PGPIPN-treated samples extracted from xenograf...
Longfei Yang,* Ying Cui,* Jianjun Shen, Fang Lin, Xi Wang, Min Long, Junxia Wei, Huizhong Zhang Dep...
<p>(A) SK-BR-3 cells were treated with 20 μg/ml of p37 or control peptide, and 20 μg/ml of trastuzum...
<p>(A) Flow cytometric analysis of HER2 levels in SK-BR-3 cells treated with the indicated concentra...
<p><b>A</b>) Daudi, Jurkat, and HeLa cell lines were cultured in the presence of DPT-C9h, DPT-Sh1, C...
<p>Cells were pretreated with or without inhibitor (SB202190 or SP600125, 20 uM/ml) for 30 min. Afte...
<div><p>(A) TA3/St cells were recovered from an A/J mouse treated with RI-TATp53C′ peptide and grown...
The tumor suppressor p53 is a potent inducer of tumor cell death, and strategies exist to exploit p...
The tumor suppressor p53 is a potent inducer of tumor cell death, and strategies exist to exploit p5...
<p>(A) Cells treated with vehicle and CDRI-85/287 were analyzed by flow cytometry of annexin-V/PI st...
<p>Cells were treated with the indicated concentrations of PD for 48 h, stained with Muse Annexin V ...
Objective: To test cell penetrating and interfering peptide Mut3DPT-PP2A/SET in interaction between ...
<p>(A) MCF-7, MDA-MB-231 cells were stained with Annexin V/PI and subjected to flow cytometric analy...
<p>(A) Total cell lysate from MCF10A normal breast cell line or MDA-MB 468 and MDA-MB 231 TNBC cell ...
<p>(A) Cell cycle distribution was analyzed by flow cytometry 72 h after transfection. Bars are show...
<p>(A) TUNEL assay shows the apoptotic tumor cells in PGPIPN-treated samples extracted from xenograf...
Longfei Yang,* Ying Cui,* Jianjun Shen, Fang Lin, Xi Wang, Min Long, Junxia Wei, Huizhong Zhang Dep...
<p>(A) SK-BR-3 cells were treated with 20 μg/ml of p37 or control peptide, and 20 μg/ml of trastuzum...
<p>(A) Flow cytometric analysis of HER2 levels in SK-BR-3 cells treated with the indicated concentra...
<p><b>A</b>) Daudi, Jurkat, and HeLa cell lines were cultured in the presence of DPT-C9h, DPT-Sh1, C...
<p>Cells were pretreated with or without inhibitor (SB202190 or SP600125, 20 uM/ml) for 30 min. Afte...
<div><p>(A) TA3/St cells were recovered from an A/J mouse treated with RI-TATp53C′ peptide and grown...
The tumor suppressor p53 is a potent inducer of tumor cell death, and strategies exist to exploit p...
The tumor suppressor p53 is a potent inducer of tumor cell death, and strategies exist to exploit p5...
<p>(A) Cells treated with vehicle and CDRI-85/287 were analyzed by flow cytometry of annexin-V/PI st...
<p>Cells were treated with the indicated concentrations of PD for 48 h, stained with Muse Annexin V ...
Objective: To test cell penetrating and interfering peptide Mut3DPT-PP2A/SET in interaction between ...
<p>(A) MCF-7, MDA-MB-231 cells were stained with Annexin V/PI and subjected to flow cytometric analy...
<p>(A) Total cell lysate from MCF10A normal breast cell line or MDA-MB 468 and MDA-MB 231 TNBC cell ...
<p>(A) Cell cycle distribution was analyzed by flow cytometry 72 h after transfection. Bars are show...
<p>(A) TUNEL assay shows the apoptotic tumor cells in PGPIPN-treated samples extracted from xenograf...
Longfei Yang,* Ying Cui,* Jianjun Shen, Fang Lin, Xi Wang, Min Long, Junxia Wei, Huizhong Zhang Dep...