Evidence map›Paper›PMID 32948804›Full record

ArticleCommunications biology2020

An IMiD-induced SALL4 degron system for selective degradation of target proteins.

Satoshi Yamanaka, Yuki Shoya, Saya Matsuoka, Hisayo Nishida-Fukuda, Norio Shibata, Tatsuya Sawasaki

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Targeted Protein Degradation: Clinical Advances in the Field of Oncology.International journal of molecular sciences · 2022
    Review
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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

6 authors at 3 institutions in 1 country.

Satoshi YamanakaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan.ORCID http://orcid.org/0000-0001-8825-7481
Yuki ShoyaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan.
Saya MatsuokaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan.
Hisayo Nishida-FukudaDepartment of Genome Editing, Institute of Biomedical Science, Kansai Medical University, Hirakata, 573-1010, Japan.ORCID http://orcid.org/0000-0002-4661-779X
Norio ShibataDepartment of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Nagoya, 466-8555, Japan.ORCID http://orcid.org/0000-0002-3742-4064
Tatsuya SawasakiDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan. sawasaki@ehime-u.ac.jp.ORCID http://orcid.org/0000-0002-7952-0556
CellFree Sciences (Japan) · JPKansai Medical University · JPNagoya Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulating the amount of proteins in living cells is a powerful approach for understanding the functions of the proteins. Immunomodulatory drugs (IMiDs) induce the degradation of neosubstrates by interacting with celebron (CRBN) in the cullin E3 ubiquitin ligase complex (CRL4

Indexed as

ProteolysisCell MembraneGene Knockdown TechniquesHeLa CellsHumansImmunologic FactorsReceptors, Interleukin-17Substrate SpecificityThalidomideTranscriptional Elongation FactorsTranscription Factor RelATranscription FactorsUbiquitin-Protein Ligases5-hydroxythalidomideElp1 protein, humanIL17RB protein, humanImmunologic FactorsReceptors, Interleukin-17RELA protein, humanSALL4 protein, humanThalidomideTranscriptional Elongation FactorsTranscription Factor RelATranscription FactorsUbiquitin-Protein Ligases

Identifiers

PMID32948804
PMCPMC7501283
OpenAlexW3087018358

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.