Evidence map›Paper›PMID 35170763›Full record

ReviewThe EMBO journal2022

Order through destruction: how ER-associated protein degradation contributes to organelle homeostasis.

John C Christianson, Pedro Carvalho

Open access · hybridAbstract readReview
In one paragraph

Review in The EMBO journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
14.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 133 citations in OpenAlex.

  1. More than the 'master regulator of cytosolic proteostasis': new roles for HSF1 in promoting tissue health.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
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  11. TMEM33 deletion potentiates anti-tumor CD8bioRxiv : the preprint server for biology · 2026
    Article
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  14. Competition between Der1 and ERAD-M substrates controls Hrd1 complex function.Proceedings of the National Academy of Sciences of the United States of America · 2025
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15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

John C ChristiansonNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.ORCID 0000-0002-0474-1207
Pedro CarvalhoSir William Dunn School of Pathology, University of Oxford, Oxford, UK.ORCID 0000-0002-9691-5277
Nuffield Orthopaedic Centre · GBUniversity of Oxford · GB

Funding

Cancer Research UK 29217Cancer Research UK C68569/A29217Wellcome TrustWellcome Trust 202642/Z/16/Z
6 · The paper itself

Abstract

The endoplasmic reticulum (ER) is a large, dynamic, and multifunctional organelle. ER protein homeostasis is essential for the coordination of its diverse functions and depends on ER-associated protein degradation (ERAD). The latter process selects target proteins in the lumen and membrane of the ER, promotes their ubiquitination, and facilitates their delivery into the cytosol for degradation by the proteasome. Originally characterized for a role in the degradation of misfolded proteins and rate-limiting enzymes of sterol biosynthesis, the many branches of ERAD now appear to control the levels of a wider range of substrates and influence more broadly the organization and functions of the ER, as well as its interactions with adjacent organelles. Here, we discuss recent mechanistic advances in our understanding of ERAD and of its consequences for the regulation of ER functions.

Indexed as

Endoplasmic Reticulum-Associated DegradationSaccharomyces cerevisiae ProteinsEndoplasmic ReticulumHomeostasisProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae Proteinsendoplasmic reticulumERADprotein degradationprotein quality controlubiquitin ligase

Identifiers

PMID35170763
PMCPMC8922271
OpenAlexW4213287704

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.