Copyright
©The Author(s) 2015.
World J Clin Oncol. Dec 10, 2015; 6(6): 299-311
Published online Dec 10, 2015. doi: 10.5306/wjco.v6.i6.299
Published online Dec 10, 2015. doi: 10.5306/wjco.v6.i6.299
Figure 1 Expression levels of proteins along the phosphoinositide 3-kinase/Akt/mammalian target of rapamcyin, mitogen-activated protein kinase/extracellular signal-regulated kinase, and apoptosis pathways vary by cell lines.
Statistically significant and differentially expressed proteins, following (A) 24 h and (B) 48 h treatment of 10 μmol/L FLX, were indicated with stars; (C) Expression of few selected proteins across cell lines after 48 h of 10 μmol/L fluoxetine was confirmed by Western blotting. For detection of p70 S6K and ERK1/2 activation, cell extracts were loaded at 100 μg and 30 μg per lane, respectively. MEK: Mitogen-activated protein kinase; ERK: Extracellular signal-regulated kinase; FLX: Fluoxetine; p70 S6K: p70 S6 Kinase; GSK3: Glycogen synthase kinase 3; eIF4G: Eukaryotic translation initiation factor 4G.
- Citation: Bowie M, Pilie P, Wulfkuhle J, Lem S, Hoffman A, Desai S, Petricoin E, Carter A, Ambrose A, Seewaldt V, Yu D, Ibarra Drendall C. Fluoxetine induces cytotoxic endoplasmic reticulum stress and autophagy in triple negative breast cancer. World J Clin Oncol 2015; 6(6): 299-311
- URL: https://www.wjgnet.com/2218-4333/full/v6/i6/299.htm
- DOI: https://dx.doi.org/10.5306/wjco.v6.i6.299