Evidence mapPaperPMID 40076599Full record

ReviewInternational journal of molecular sciences2025

Untangling the Role of MYC in Sarcomas and Its Potential as a Promising Therapeutic Target.

Fabio Sias, Stefano Zoroddu, Rossana Migheli, Luigi Bagella

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Frontiers in pharmacology · 2026
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. 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

4 authors.

Fabio SiasDepartment of Biomedical Sciences, University of Sassari, Viale San Pietro 43/b, 07100 Sassari, Italy.ORCID 0009-0006-4833-444X
Stefano ZorodduDepartment of Biomedical Sciences, University of Sassari, Viale San Pietro 43/b, 07100 Sassari, Italy.ORCID 0000-0003-4423-9745
Rossana MigheliDepartment of Medical, Surgical and Experimental Sciences, University of Sassari, 07100 Sassari, Italy.
Luigi BagellaDepartment of Biomedical Sciences, University of Sassari, Viale San Pietro 43/b, 07100 Sassari, Italy.ORCID 0000-0003-2815-037X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MYC plays a pivotal role in the biology of various sarcoma subtypes, acting as a key regulator of tumor growth, proliferation, and metabolic reprogramming. This oncogene is frequently dysregulated across different sarcomas, where its expression is closely intertwined with the molecular features unique to each subtype. MYC interacts with critical pathways such as cell cycle regulation, apoptosis, and angiogenesis, amplifying tumor aggressiveness and resistance to standard therapies. Furthermore, MYC influences the tumor microenvironment by modulating cell-extracellular matrix interactions and immune evasion mechanisms, further complicating therapeutic management. Despite its well-established centrality in sarcoma pathogenesis, targeting MYC directly remains challenging due to its "undruggable" protein structure. However, emerging therapeutic strategies, including indirect MYC inhibition via epigenetic modulators, transcriptional machinery disruptors, and metabolic pathway inhibitors, offer new hope for sarcoma treatment. This review underscores the importance of understanding the intricate roles of MYC across sarcoma subtypes to guide the development of effective targeted therapies. Given MYC's central role in tumorigenesis and progression, innovative approaches aiming at MYC inhibition could transform the therapeutic landscape for sarcoma patients, providing a much-needed avenue to overcome therapeutic resistance and improve clinical outcomes.

Indexed as

Antineoplastic AgentsProto-Oncogene Proteins c-mycSarcomaAnimalsApoptosisCell CycleCell ProliferationDrug Resistance, NeoplasmEpigenesis, GeneticGene Expression Regulation, NeoplasticHumansMetabolic ReprogrammingMolecular Targeted TherapyTumor MicroenvironmentAntineoplastic AgentsProto-Oncogene Proteins c-mycEwing’s sarcomaleiomyosarcomamalignant rhabdoid tumorMYCosteosarcomarhabdomyosarcomasarcomasynovial sarcoma

Identifiers

PMID40076599
PMCPMC11900228

What Socratic 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 Socratic graph.