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      The Unfolded Protein Response in Breast Cancer

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          Abstract

          In 2018, in the US alone, it is estimated that 268,670 people will be diagnosed with breast cancer, and that 41,400 will die from it. Since breast cancers often become resistant to therapies, and certain breast cancers lack therapeutic targets, new approaches are urgently required. A cell-stress response pathway, the unfolded protein response (UPR), has emerged as a promising target for the development of novel breast cancer treatments. This pathway is activated in response to a disturbance in endoplasmic reticulum (ER) homeostasis but has diverse physiological and disease-specific functions. In breast cancer, UPR signalling promotes a malignant phenotype and can confer tumours with resistance to widely used therapies. Here, we review several roles for UPR signalling in breast cancer, highlighting UPR-mediated therapy resistance and the potential for targeting the UPR alone or in combination with existing therapies.

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          Most cited references99

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          Patterns of somatic mutation in human cancer genomes.

          Cancers arise owing to mutations in a subset of genes that confer growth advantage. The availability of the human genome sequence led us to propose that systematic resequencing of cancer genomes for mutations would lead to the discovery of many additional cancer genes. Here we report more than 1,000 somatic mutations found in 274 megabases (Mb) of DNA corresponding to the coding exons of 518 protein kinase genes in 210 diverse human cancers. There was substantial variation in the number and pattern of mutations in individual cancers reflecting different exposures, DNA repair defects and cellular origins. Most somatic mutations are likely to be 'passengers' that do not contribute to oncogenesis. However, there was evidence for 'driver' mutations contributing to the development of the cancers studied in approximately 120 genes. Systematic sequencing of cancer genomes therefore reveals the evolutionary diversity of cancers and implicates a larger repertoire of cancer genes than previously anticipated.
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            The integrated stress response.

            In response to diverse stress stimuli, eukaryotic cells activate a common adaptive pathway, termed the integrated stress response (ISR), to restore cellular homeostasis. The core event in this pathway is the phosphorylation of eukaryotic translation initiation factor 2 alpha (eIF2α) by one of four members of the eIF2α kinase family, which leads to a decrease in global protein synthesis and the induction of selected genes, including the transcription factor ATF4, that together promote cellular recovery. The gene expression program activated by the ISR optimizes the cellular response to stress and is dependent on the cellular context, as well as on the nature and intensity of the stress stimuli. Although the ISR is primarily a pro-survival, homeostatic program, exposure to severe stress can drive signaling toward cell death. Here, we review current understanding of the ISR signaling and how it regulates cell fate under diverse types of stress.
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              Gene-expression signatures in breast cancer.

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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                21 September 2018
                October 2018
                : 10
                : 10
                : 344
                Affiliations
                [1 ]Apoptosis Research Centre, National University of Ireland (NUI), Galway, University Road, Galway, H91 TK33 Galway, Ireland; E.MCGRATH14@ 123456nuigalway.ie (E.P.M.); susan.logue@ 123456nuigalway.ie (S.E.L.); katarzyna.mnich@ 123456nuigalway.ie (K.M.); shane.deegan@ 123456nuigalway.ie (S.D.); adrienne.gorman@ 123456nuigalway.ie (A.M.G.)
                [2 ]School of Natural Sciences, NUI Galway, University Road, H91 TK33 Galway, Ireland
                [3 ]Department of Natural Sciences, Bonn-Rhein-Sieg University of Applied Sciences, 53359 Rheinbach, Germany; Richard.Jaeger@ 123456h-brs.de
                Author notes
                [* ]Correspondence: afshin.samali@ 123456nuigalway.ie ; Tel.: +353-91-492440
                Author information
                https://orcid.org/0000-0001-7686-8584
                https://orcid.org/0000-0001-7938-3558
                https://orcid.org/0000-0003-2137-9163
                https://orcid.org/0000-0002-1623-1917
                https://orcid.org/0000-0002-6068-0058
                https://orcid.org/0000-0002-8610-8375
                Article
                cancers-10-00344
                10.3390/cancers10100344
                6211039
                30248920
                31d3476a-9276-4360-b39c-f5a4176f671a
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 03 August 2018
                : 18 September 2018
                Categories
                Review

                breast cancer,endoplasmic reticulum (er) stress,unfolded protein response (upr),therapy,cell death,autophagy

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