Evidence map›Paper›PMID 33470442›Full record

ArticleThe EMBO journal2021

Thalidomide and its metabolite 5-hydroxythalidomide induce teratogenicity via the cereblon neosubstrate PLZF.

Satoshi Yamanaka, Hidetaka Murai, Daisuke Saito, Gembu Abe, Etsuko Tokunaga, Takahiro Iwasaki, Hirotaka Takahashi, Hiroyuki Takeda, Takayuki Suzuki, Norio Shibata and 2 more

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 85 citations in OpenAlex.

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  7. Design and Application of Cereblon-Recruiting Prodegraders.Journal of the American Chemical Society · 2025
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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

12 authors at 5 institutions in 1 country.

Satoshi YamanakaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Japan.ORCID 0000-0001-8825-7481
Hidetaka MuraiDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Daisuke SaitoDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Gembu AbeDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Etsuko TokunagaDepartment of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Nagoya, Japan.ORCID 0000-0003-0621-3798
Takahiro IwasakiDivision of Proteo-Drug-Discovery Sciences, Proteo-Science Center, Ehime University, Matsuyama, Japan.
Hirotaka TakahashiDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Japan.
Hiroyuki TakedaDivision of Proteo-Drug-Discovery Sciences, Proteo-Science Center, Ehime University, Matsuyama, Japan.
Takayuki SuzukiAvian Bioscience Research Center, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan.
Norio ShibataDepartment of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Nagoya, Japan.ORCID 0000-0002-3742-4064
Koji TamuraDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Tatsuya SawasakiDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Japan.ORCID 0000-0002-7952-0556
Tohoku University · JPCellFree Sciences (Japan) · JPEhime University · JPNagoya Institute of Technology · JPNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thalidomide causes teratogenic effects by inducing protein degradation via cereblon (CRBN)-containing ubiquitin ligase and modification of its substrate specificity. Human P450 cytochromes convert thalidomide into two monohydroxylated metabolites that are considered to contribute to thalidomide effects, through mechanisms that remain unclear. Here, we report that promyelocytic leukaemia zinc finger (PLZF)/ZBTB16 is a CRBN target protein whose degradation is involved in thalidomide- and 5-hydroxythalidomide-induced teratogenicity. Using a human transcription factor protein array produced in a wheat cell-free protein synthesis system, PLZF was identified as a thalidomide-dependent CRBN substrate. PLZF is degraded by the ubiquitin ligase CRL4

Indexed as

TeratogenesisAdaptor Proteins, Signal TransducingAnimalsChick EmbryoCytochrome P-450 CYP3AHumansMicePromyelocytic Leukemia Zinc Finger ProteinProteolysisSubstrate SpecificityTeratogensThalidomideTranscription FactorsUbiquitin-Protein Ligases5-hydroxythalidomideAdaptor Proteins, Signal TransducingCRBN protein, humanCytochrome P-450 CYP3APromyelocytic Leukemia Zinc Finger ProteinSALL4 protein, humanTeratogensThalidomideTranscription FactorsUbiquitin-Protein LigasesCRBNprotein degradationthalidomide metabolitethalidomide teratogenicityubiquitin

Identifiers

PMID33470442
PMCPMC7883055
OpenAlexW3123177844

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.