| Literature DB >> 31075256 |
Daniel W Cole1, Peter F Svider1, Kerolos G Shenouda1, Paul B Lee2, Nicholas G Yoo1, Thomas M McLeod1, Sean A Mutchnick1, George H Yoo3, Randal J Kaufman4, Michael U Callaghan5, Andrew M Fribley6.
Abstract
Many FDA-approved anti-cancer therapies, targeted toward a wide array of molecular targets and signaling networks, have been demonstrated to activate the unfolded protein response (UPR). Despite a critical role for UPR signaling in the apoptotic execution of cancer cells by many of these compounds, the authors are currently unaware of any instance whereby a cancer drug was developed with the UPR as the intended target. With the essential role of the UPR as a driving force in the genesis and maintenance of the malignant phenotype, a great number of pre-clinical studies have surged into the medical literature describing the ability of dozens of compounds to induce UPR signaling in a myriad of cancer models. The focus of the current work is to review the literature and explore the role of the UPR as a mediator of chemotherapy-induced cell death in squamous cell carcinomas of the head and neck (HNSCC) and oral cavity (OCSCC), with an emphasis on preclinical studies.Entities:
Keywords: ER stress; HNSCC; Head and neck squamous cell carcinoma; Natural products; Oral cavity squamous cell carcinoma; Unfolded protein response
Mesh:
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Year: 2019 PMID: 31075256 PMCID: PMC6867800 DOI: 10.1016/j.yexcr.2019.04.007
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905