O-GlcNAcylation Signal Mediates Proteasome Inhibitor Resistance in Cancer Cells by Stabilizing NRF1

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O-GlcNAcylation Signal Mediates Proteasome Inhibitor Resistance in Cancer Cells by Stabilizing NRF1

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im Juni 2018 veröffentlichter wissenschaftlicher Artikel

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scientific article published on 15 August 2018

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wetenschappelijk artikel

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наукова стаття, опублікована в червні 2018

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O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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P1476

O-GlcNAcylation Signal Mediate ...... ncer Cells by Stabilizing NRF1

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P2093

Akira Kobayashi

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Fumiki Katsuoka

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Hiroki Sekine

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Hiroki Shima

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Kazuhiko Igarashi

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Keito Okazaki

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Koichiro Kato

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M Morshedul Alam

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Masayuki Yamamoto

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Norio Suzuki

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P2860

Model-based analysis of ChIP-Seq (MACS)

Cancer vulnerabilities unveiled by genomic loss

Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1

Oxidative stress sensor Keap1 functions as an adaptor for Cul3-based E3 ligase to regulate proteasomal degradation of Nrf2

O-GlcNAcylation and Metabolic Reprograming in Cancer

Specific SKN-1/Nrf stress responses to perturbations in translation elongation and proteasome activity

Fast gapped-read alignment with Bowtie 2

Loss of nuclear factor E2-related factor 1 in the brain leads to dysregulation of proteasome gene expression and neurodegeneration

Nrf1 is targeted to the endoplasmic reticulum membrane by an N-terminal transmembrane domain. Inhibition of nuclear translocation and transacting function

Proteasome-mediated processing of Nrf1 is essential for coordinate induction of all proteasome subunits and p97

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scholarly article

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10.1128/MCB.00252-18

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English

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http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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Hozumi Motohashi

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2018-08-15T00:00:00Z

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29941490

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molecular biology

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6094050

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