Evidence map›Paper›PMID 35856839›Full record

ReviewBiochemistry2023

Molecular Glues: The Adhesive Connecting Targeted Protein Degradation to the Clinic.

Janet M Sasso, Rumiana Tenchov, DaSheng Wang, Linda S Johnson, Xinmei Wang, Qiongqiong Angela Zhou

Abstract readReview
In one paragraph

Review in Biochemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
–field-weighted citation impact
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

116 citing papers in PubMed.

  1. Article
  2. Article
  3. E3 Ubiquitin Ligases in MASH-Associated Liver Fibrosis: Mechanisms and Therapeutic Opportunities.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  4. Review
  5. Article
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  7. Article
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  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
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  16. Article
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  18. Review
  19. Bellerophon: An Automated Tool for PROTAC Decomposition.ACS medicinal chemistry letters · 2026
    Article
  20. Article

56 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

6 authors.

Janet M SassoCAS, a division of the American Chemical Society, 2540 Olentangy River Road, Columbus, Ohio 43202, United States.ORCID 0000-0002-1156-5184
Rumiana TenchovCAS, a division of the American Chemical Society, 2540 Olentangy River Road, Columbus, Ohio 43202, United States.ORCID 0000-0003-4698-6832
DaSheng WangCAS, a division of the American Chemical Society, 2540 Olentangy River Road, Columbus, Ohio 43202, United States.
Linda S JohnsonCAS, a division of the American Chemical Society, 2540 Olentangy River Road, Columbus, Ohio 43202, United States.ORCID 0000-0002-5926-6124
Xinmei WangCAS, a division of the American Chemical Society, 2540 Olentangy River Road, Columbus, Ohio 43202, United States.
Qiongqiong Angela ZhouCAS, a division of the American Chemical Society, 2540 Olentangy River Road, Columbus, Ohio 43202, United States.ORCID 0000-0001-6711-369X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted protein degradation is a rapidly exploding drug discovery strategy that uses small molecules to recruit disease-causing proteins for rapid destruction mainly via the ubiquitin-proteasome pathway. It shows great potential for treating diseases such as cancer and infectious, inflammatory, and neurodegenerative diseases, especially for those with "undruggable" pathogenic protein targets. With the recent rise of the "molecular glue" type of protein degraders, which tighten and simplify the connection of an E3 ligase with a disease-causing protein for ubiquitination and subsequent degradation, new therapies for unmet medical needs are being designed and developed. Here we use data from the CAS Content Collection and the publication landscape of recent research on targeted protein degraders to provide insights into these molecules, with a special focus on molecular glues. We also outline the advantages of the molecular glues and summarize the advances in drug discovery practices for molecular glue degraders. We further provide a thorough review of drug candidates in targeted protein degradation through E3 ligase recruitment. Finally, we highlight the progression of molecular glues in drug discovery pipelines and their targeted diseases. Overall, our paper provides a comprehensive reference to support the future development of molecular glues in medicine.

Indexed as

ProteinsUbiquitin-Protein LigasesDrug DiscoveryProteasome Endopeptidase ComplexProteolysisUbiquitinationProteasome Endopeptidase ComplexProteinsUbiquitin-Protein Ligases

Identifiers

PMID35856839
PMCPMC9910052

What OpenQuestion holds

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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.