Evidence map›Paper›PMID 31857833›Full record

ArticleACS medicinal chemistry letters2019

Evolution of Cereblon-Mediated Protein Degradation as a Therapeutic Modality.

Philip P Chamberlain, Laura A D'Agostino, J Michael Ellis, Joshua D Hansen, Mary E Matyskiela, Joseph J McDonald, Jennifer R Riggs, Lawrence G Hamann

Open access · greenAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. The Role of CELMoD Agents in Multiple Myeloma.OncoTargets and therapy · 2025
    Review
  10. Article
  11. Targeted protein degradation: from mechanisms to clinic.Nature reviews. Molecular cell biology · 2024
    Review
  12. Review
  13. Modulation of CaHandbook of experimental pharmacology · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. PROTAC targeted protein degraders: the past is prologue.Nature reviews. Drug discovery · 2022
    Review
  18. Review
  19. Ligand Enabled Pd(II)-Catalyzed γ-C(spJournal of the American Chemical Society · 2021
    Article
  20. Review
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

8 authors.

Philip P ChamberlainCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
Laura A D'AgostinoCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
J Michael EllisCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
Joshua D HansenCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
Mary E MatyskielaCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
Joseph J McDonaldCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
Jennifer R RiggsCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.
Lawrence G HamannCelgene Corporation, 200 Cambridge Park Drive, Suite 3000, Cambridge, Massachusetts 02140, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many cellular processes and pathways are mediated by the regulation of protein-protein complexes. For example, E3 ubiquitin ligases recruit substrate proteins and transfer a ubiquitin tag to target those proteins for destruction by the proteasome. It has now been shown that this cellular process for protein destruction can be redirected by small molecules in both laboratory and clinical settings. This presents a new paradigm in drug discovery, enabling the rapid removal of target proteins linked to disease. In this Innovations review, we will describe the work done on cereblon as a case study on the different strategies available for targeted protein degradation.

Identifiers

PMID31857833
PMCPMC6912861
OpenAlexW2988308869

What OpenQuestion holds

Textmetadata
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.