Cancer Microenvironment and Endoplasmic Reticulum Stress Response (Q26778533)

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scientific article

Language	Label	Description	Also known as
English	Cancer Microenvironment and Endoplasmic Reticulum Stress Response	scientific article

Statements

instance of

scholarly article

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title

Cancer Microenvironment and Endoplasmic Reticulum Stress Response (English)

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main subject

cell biology

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author name string

Claudia Giampietri

series ordinal

1

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Simonetta Petrungaro

series ordinal

2

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Silvia Conti

series ordinal

3

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Antonio Facchiano

series ordinal

4

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Antonio Filippini

series ordinal

5

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Elio Ziparo

series ordinal

6

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original language of film or TV show

English

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publication date

2015

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published in

Mediators of Inflammation

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volume

2015

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page(s)

417281

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cites work

The unfolded protein response induces the angiogenic switch in human tumor cells through the PERK/ATF4 pathway

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PubMed Central

Blockade of XBP1 splicing by inhibition of IRE1α is a promising therapeutic option in multiple myeloma

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PubMed Central

Identification of an Ire1alpha endonuclease specific inhibitor with cytotoxic activity against human multiple myeloma

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PubMed Central

One step at a time: endoplasmic reticulum-associated degradation

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PubMed Central

Endoplasmic reticulum stress activates cleavage of CREBH to induce a systemic inflammatory response

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PubMed Central

Endoplasmic reticulum chaperone protein GRP78 protects cells from apoptosis induced by topoisomerase inhibitors: role of ATP binding site in suppression of caspase-7 activation

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stated in

PubMed Central

Regulation of protein synthesis by hypoxia via activation of the endoplasmic reticulum kinase PERK and phosphorylation of the translation initiation factor eIF2alpha

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stated in

PubMed Central

ASK1 is essential for endoplasmic reticulum stress-induced neuronal cell death triggered by expanded polyglutamine repeats

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PubMed Central

Coupling endoplasmic reticulum stress to the cell death program: role of the ER chaperone GRP78

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PubMed Central

XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor

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PubMed Central

Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress

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PubMed Central

Oxidative stress and cytokines in the pathogenesis of pancreatic cancer

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PubMed Central

Discovery of 7-methyl-5-(1-{[3-(trifluoromethyl)phenyl]acetyl}-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (GSK2606414), a potent and selective first-in-class inhibitor of protein kinase R (PKR)-like endoplasmic reticulum kinase (P

1 reference

stated in

PubMed Central

Signal integration in the endoplasmic reticulum unfolded protein response

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PubMed Central

A regulatory link between ER-associated protein degradation and the unfolded-protein response

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PubMed Central

Der1, a novel protein specifically required for endoplasmic reticulum degradation in yeast

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PubMed Central

Transcriptional induction of genes encoding endoplasmic reticulum resident proteins requires a transmembrane protein kinase

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PubMed Central

IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA

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PubMed Central

Perk is essential for translational regulation and cell survival during the unfolded protein response

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PubMed Central

Secretion of ERP57 is important for extracellular matrix accumulation and progression of renal fibrosis, and is an early sign of disease onset

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PubMed Central

Endoplasmic reticulum stress controls M2 macrophage differentiation and foam cell formation

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PubMed Central

The regulation of Bax by c-Jun N-terminal protein kinase (JNK) is a prerequisite to the mitochondrial-induced apoptotic pathway

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stated in

PubMed Central

Identifiers

DOI

10.1155/2015/417281

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PMC publication ID

4600498

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PubMed publication ID

26491226

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