| Literature DB >> 28433699 |
Nicole M Jackson1, Brian P Ceresa2.
Abstract
The Epidermal Growth Factor Receptor (EGFR) is a cell surface receptor with primary implications in cell growth in both normal and malignant tissue. Paradoxically, cell lines that hyperexpress the EGFR have been documented to undergo receptor-mediated apoptosis. The underlying mechanism by which EGF-induced apoptosis occurs however remains inexplicit. In an attempt to identify this mechanism, we assessed downstream effectors of EGFR in MDA-MB-468 cells during conditions of EGF-induced apoptosis. The effector assessment revealed STAT3 as a potential mediator of EGF-induced apoptosis. Alternative strategies for activating STAT3, independent of EGFR stimulation, resulted in the induction of the apoptotic pathways. A reduction in STAT3 expression via RNAi resulted in a significant attenuation of EGF-induced PARP cleavage. Our findings support STAT3 as a positive mediator of EGF-induced apoptosis in MDA-MB-468 cells.Entities:
Keywords: A431 Cells; Apoptosis; Epidermal Growth Factor Receptor; MDA-MB-468 Cells; Oncostatin M; S3I-201; STAT3; Stattic
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Year: 2017 PMID: 28433699 PMCID: PMC5514375 DOI: 10.1016/j.yexcr.2017.04.016
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905