Evidence map›Paper›PMID 37958963›Full record

ReviewInternational journal of molecular sciences2023

Analysis of CD74 Occurrence in Oncogenic Fusion Proteins.

Jasmine Vargas, Georgios Pantouris

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Molecular Characterization of a ComplexJCO precision oncology · 2026
    Article
  5. Generation of MIF Peptides via Solid Phase Peptide Synthesis.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Insight into NSCLC through novel analysis of gene interactions and characteristics.American journal of clinical and experimental immunology · 2024
    Article
  11. Article
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

2 authors.

Jasmine VargasDepartment of Chemistry, University of the Pacific, Stockton, CA 95211, USA.ORCID 0009-0005-8080-0992
Georgios PantourisDepartment of Chemistry, University of the Pacific, Stockton, CA 95211, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD74 is a type II cell surface receptor found to be highly expressed in several hematological and solid cancers, due to its ability to activate pathways associated with tumor cell survival and proliferation. Over the past 16 years, CD74 has emerged as a commonly detected fusion partner in multiple oncogenic fusion proteins. Studies have found CD74 fusion proteins in a range of cancers, including lung adenocarcinoma, inflammatory breast cancer, and pediatric acute lymphoblastic leukemia. To date, there are five known CD74 fusion proteins, CD74-ROS1, CD74-NTRK1, CD74-NRG1, CD74-NRG2α, and CD74-PDGFRB, with a total of 16 different variants, each with unique genetic signatures. Importantly, the occurrence of CD74 in the formation of fusion proteins has not been well explored despite the fact that ROS1 and NRG1 families utilize CD74 as the primary partner for the formation of oncogenic fusions. Fusion proteins known to be oncogenic drivers, including those of CD74, are typically detected and targeted after standard chemotherapeutic plans fail and the disease relapses. The analysis reported herein provides insights into the early intervention of CD74 fusions and highlights the need for improved routine assessment methods so that targeted therapies can be applied while they are most effective.

Indexed as

Adenocarcinoma of LungLung NeoplasmsChildHumansOncogene Proteins, FusionProtein-Tyrosine KinasesProto-Oncogene ProteinsOncogene Proteins, FusionProtein-Tyrosine KinasesProto-Oncogene ProteinscancerCD74-NRG1CD74-NRG2αCD74-NTRK1CD74-PDGFRBCD74-ROS1cluster of differentiation 74 (CD74)fusion geneoncogenic fusion protein

Identifiers

PMID37958963
PMCPMC10650716

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Registered trials

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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.