(Q84263450)

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Nanosecond pulsed electric fields act as a novel cellular stress that induces translational suppression accompanied by eIF2α phosphorylation and 4E-BP1 dephosphorylation

scientific article published on 28 May 2012

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2 February 2020

Nanosecond pulsed electric fields act as a novel cellular stress that induces translational suppression accompanied by eIF2α phosphorylation and 4E-BP1 dephosphorylation (English)

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2 February 2020

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Keiko Morotomi-Yano

1

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2 February 2020

Seiichi Oyadomari

2

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2 February 2020

Hidenori Akiyama

3

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2 February 2020

Ken-ichi Yano

4

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2 February 2020

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28 May 2012

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2 February 2020

Experimental Cell Research

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2 February 2020

318

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2 February 2020

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2 February 2020

1733-1744

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2 February 2020

Mechanisms of cell membrane electropermeabilization: a minireview of our present (lack of ?) knowledge.

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Membrane permeabilization and cell damage by ultrashort electric field shocks

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Nanosecond pulsed electric fields perturb membrane phospholipids in T lymphoblasts

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Intracellular effect of ultrashort electrical pulses

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Activation of the JNK pathway by nanosecond pulsed electric fields.

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Nanosecond pulsed electric fields activate MAPK pathways in human cells.

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Calcium bursts induced by nanosecond electric pulses

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Stimulation of capacitative calcium entry in HL-60 cells by nanosecond pulsed electric fields

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Nanosecond, high-intensity pulsed electric fields induce apoptosis in human cells

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In vitro and in vivo evaluation and a case report of intense nanosecond pulsed electric field as a local therapy for human malignancies

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Nanosecond pulsed electric fields stimulate apoptosis without release of pro-apoptotic factors from mitochondria in B16f10 melanoma

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A new pulsed electric field therapy for melanoma disrupts the tumor's blood supply and causes complete remission without recurrence.

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Apoptosis initiation and angiogenesis inhibition: melanoma targets for nanosecond pulsed electric fields.

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Optimized nanosecond pulsed electric field therapy can cause murine malignant melanomas to self-destruct with a single treatment

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Translational control in stress and apoptosis

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Signalling to translation: how signal transduction pathways control the protein synthetic machinery

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Translational control in cancer.

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Coping with stress: eIF2 kinases and translational control

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Regulation of mRNA translation by protein folding in the endoplasmic reticulum

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Identification and characterization of pancreatic eukaryotic initiation factor 2 alpha-subunit kinase, PEK, involved in translational control

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Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase

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7 January 2021

Signal integration in the endoplasmic reticulum unfolded protein response

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7 January 2021

Activation of GCN2 in UV-irradiated cells inhibits translation

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GCN2 phosphorylation of eIF2alpha activates NF-kappaB in response to UV irradiation

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Regulated translation initiation controls stress-induced gene expression in mammalian cells

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The GCN2 eIF2alpha kinase is required for adaptation to amino acid deprivation in mice

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The dsRNA protein kinase PKR: virus and cell control

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Regulation of protein synthesis by the heme-regulated eIF2alpha kinase: relevance to anemias

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Endoplasmic reticulum stress links obesity, insulin action, and type 2 diabetes

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Phosphorylation of the translational repressor PHAS-I by the mammalian target of rapamycin

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

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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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Both Transcriptional Regulation and Translational Control of ATF4 Are Central to the Integrated Stress Response

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A family of stress-inducible GADD45-like proteins mediate activation of the stress-responsive MTK1/MEKK4 MAPKKK

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10.1016/J.YEXCR.2012.04.016

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22652449%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22652449%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

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