Evidence map›Paper›PMID 37596276›Full record

ArticleNature communications2023

Lenalidomide derivatives and proteolysis-targeting chimeras for controlling neosubstrate degradation.

Satoshi Yamanaka, Hirotake Furihata, Yuta Yanagihara, Akihito Taya, Takato Nagasaka, Mai Usui, Koya Nagaoka, Yuki Shoya, Kohei Nishino, Shuhei Yoshida and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Evolving CRBN ligands enhance the drug-like properties of protein degraders.Journal of enzyme inhibition and medicinal chemistry · 2026
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  12. Characterization of a dual degrader of MDM2 and GSPT1.European journal of medicinal chemistry · 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

16 authors at 6 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
Hirotake FurihataDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan.
Yuta YanagiharaDivision of Integrative Pathophysiology, Proteo-Science Center, Ehime University, Toon, 791-0295, Japan.
Akihito TayaDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, 466-8555, Japan.
Takato NagasakaDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, 466-8555, Japan.
Mai UsuiDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, 466-8555, Japan.
Koya NagaokaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan.
Yuki ShoyaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, 790-8577, Japan.
Kohei NishinoDivision of Cell Signaling, Fujii Memorial Institute of Medical Sciences, Tokushima University, Tokushima, 770-8503, Japan.
Shuhei YoshidaDivision of Integrative Pathophysiology, Proteo-Science Center, Ehime University, Toon, 791-0295, Japan.
Hidetaka KosakoDivision of Cell Signaling, Fujii Memorial Institute of Medical Sciences, Tokushima University, Tokushima, 770-8503, Japan.ORCID http://orcid.org/0000-0003-3228-6368
Masaru TanokuraDepartment of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, 113-8657, Japan.ORCID http://orcid.org/0000-0001-5072-2480
Takuya MiyakawaDepartment of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, 113-8657, Japan.ORCID http://orcid.org/0000-0001-5957-3549
Yuuki ImaiDivision of Integrative Pathophysiology, Proteo-Science Center, Ehime University, Toon, 791-0295, Japan.ORCID http://orcid.org/0000-0002-6119-0034
Norio ShibataDepartment of Life Science and Applied Chemistry, 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) · JPNagoya Institute of Technology · JPEhime University · JPTokushima University · JPKyoto University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lenalidomide, an immunomodulatory drug (IMiD), is commonly used as a first-line therapy in many haematological cancers, such as multiple myeloma (MM) and 5q myelodysplastic syndromes (5q MDS), and it functions as a molecular glue for the protein degradation of neosubstrates by CRL4

Indexed as

Hematologic NeoplasmsMultiple MyelomaMyelodysplastic SyndromesChromosome AberrationsFemaleHumansImmunomodulating AgentsLenalidomidePregnancyProteolysisProteolysis Targeting ChimeraImmunomodulating AgentsLenalidomideProteolysis Targeting Chimera

Identifiers

PMID37596276
PMCPMC10439208
OpenAlexW4385980910

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.