1. Biological impact of advanced glycation endproducts on estrogen receptor-positive MCF-7 breast cancer cells.
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Matou-Nasri, Sabine, Sharaf, Hana, Wang, Qiuyu, Almobadel, Nasser, Rabhan, Zaki, Al-Eidi, Hamad, Yahya, Wesam Bin, Trivilegio, Thadeo, Ali, Rizwan, Al-Shanti, Nasser, and Ahmed, Nessar
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DIABETES risk factors , *BREAST cancer , *ADVANCED glycation end-products , *ESTROGEN receptors , *POLYMERASE chain reaction , *MATRIX metalloproteinases - Abstract
Diabetes mellitus potentiates the risk of breast cancer. We have previously described the pro-tumorigenic effects of advanced glycation endproducts (AGEs) on estrogen receptor (ER)-negative MDA-MB-231 breast cancer cell line mediated through the receptor for AGEs (RAGE). However, a predominant association between women with ER-positive breast cancer and type 2 diabetes mellitus has been reported. Therefore, we have investigated the biological impact of AGEs on ER-positive human breast cancer cell line MCF-7 using in vitro cell-based assays including cell count, migration, and invasion assays. Western blot, FACS analyses and quantitative real time-PCR were also performed. We found that AGEs at 50–100 μg/mL increased MCF-7 cell proliferation and cell migration associated with an enhancement of pro-matrix metalloproteinase (MMP)-9 activity, without affecting their poor invasiveness. However, 200 μg/mL AGEs inhibited MCF-7 cell proliferation through induction of apoptosis indicated by caspase-3 cleavage detected using Western blotting. A phospho-protein array analysis revealed that AGEs mainly induce the phosphorylation of extracellular-signal regulated kinase (ERK)1/2 and cAMP response element binding protein-1 (CREB1), both signaling molecules considered as key regulators of AGEs pro-tumorigenic effects. We also showed that AGEs up-regulate RAGE and ER expression at the protein and transcript levels in MCF-7 cells, in a RAGE-dependent manner after blockade of AGEs/RAGE interaction using neutralizing anti-RAGE antibody. Throughout the study, BSA had no effect on cellular processes. These findings pave the way for future studies investigating whether the exposure of AGEs-treated ER-positive breast cancer cells to estrogen could lead to a potentiation of breast cancer development and progression. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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