Copyright
©The Author(s) 2020.
World J Stem Cells. Nov 26, 2020; 12(11): 1410-1428
Published online Nov 26, 2020. doi: 10.4252/wjsc.v12.i11.1410
Published online Nov 26, 2020. doi: 10.4252/wjsc.v12.i11.1410
Figure 5 Inhibition of glutathione synthesis and recycling decreases self-renewal and CD133 expression.
Cells from the indicated patient-derived xenografts (PDXs) were treated with 100 µmol/L buthionine-sulfoximine or 1 µmol/L 6-Aminonicotinamide as indicated. A: Expression of stemness gene expression following 72 h of treatment; B: Sphere formation ability after 7 d of treatment, replenished every other day. Data are shown as fold change vs untreated conditions (Cont) for each PDX model, mean ± SE; C: Representative flow cytometry plots for CD133 expression after 48 h of treatment. aP < 0.05; bP < 0.01; cP < 0.001. BSO: Buthionine-sulfoximine; PDX: Patient-derived xenograft; 6-AN: 6-Aminonicotinamide.
- Citation: Jagust P, Alcalá S, Sainz Jr B, Heeschen C, Sancho P. Glutathione metabolism is essential for self-renewal and chemoresistance of pancreatic cancer stem cells. World J Stem Cells 2020; 12(11): 1410-1428
- URL: https://www.wjgnet.com/1948-0210/full/v12/i11/1410.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v12.i11.1410