Evidence map›Paper›PMID 39211557›Full record

ReviewFrontiers in oncology2024

REThinking the role of the RET oncogene in breast cancer.

Giuseppe Di Grazia, Chiara Conti, Sabrina Nucera, Gianmarco Motta, Federica Martorana, Stefania Stella, Michele Massimino, Mario Giuliano, Paolo Vigneri

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. AccurateInternational journal of molecular sciences · 2025
    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

9 authors.

Giuseppe Di GraziaDepartment of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
Chiara ContiDepartment of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
Sabrina NuceraDepartment of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
Gianmarco MottaDepartment of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Federica MartoranaDepartment of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Stefania StellaDepartment of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Michele MassiminoCenter of Experimental Oncology and Hematology, Azienda Ospedaliera Universitaria (A.O.U.) Policlinico "G. Rodolico - S. Marco", Catania, Italy.
Mario GiulianoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Paolo VigneriDepartment of Clinical and Experimental Medicine, University of Catania, Catania, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The REarranged during Transfection (RET) receptor tyrosine kinase plays a crucial role in the development of various anatomical structures during embryogenesis and it is involved in many physiological cellular processes. This protein is also associated with the initiation of various cancer types, such as thyroid cancer, non-small cell lung cancer, and multiple endocrine neoplasms. In breast cancer, and especially in the estrogen receptor-positive (ER+) subtype, the activity of RET is of notable importance. Indeed, RET seems to be involved in tumor progression, resistance to therapies, and cellular proliferation. Nevertheless, the ways RET alterations could impact the prognosis of breast cancer and its response to treatment remain only partially elucidated. Several inhibitors of RET kinase have been developed thus far, with various degrees of selectivity toward RET inhibition. These molecules showed notable efficacy in the treatment of RET-driven tumors, including some breast cancer cases. Despite these encouraging results, further investigation is needed to fully understand the potential role RET inhibition in breast cancer. This review aims to recapitulate the existing evidence about the role of

Indexed as

breast cancerclinical trialsRET oncogenetargeted therapyTKI - tyrosine kinase inhibitor

Identifiers

PMID39211557
PMCPMC11358597

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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.