Evidence map›Paper›PMID 38092952›Full record

ReviewNature reviews. Drug discovery2024

Therapeutic targeting of the functionally elusive TAM receptor family.

Yu Rebecca Miao, Erinn B Rankin, Amato J Giaccia

Abstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
  2. Radiation-induced AXL upregulation in CCR2Clinical and translational medicine · 2026
    Article
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  4. Review
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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

3 authors.

Yu Rebecca MiaoDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, USA.
Erinn B RankinDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, USA.
Amato J GiacciaDepartment of Oncology, University of Oxford, Oxford, UK. amato.giaccia@oncology.ox.ac.uk.

Funding

Translational Biology CoreP01CA257907 · NCI · STANFORD UNIVERSITY · PI Maximilian Diehn, Quynh-Thu Xuan Le · 2022 to 2026
$12.0M
The role of the RNA demethylase FTO in metabolic reprogramming of renal cell carcinomaR01CA272432 · NCI · STANFORD UNIVERSITY · PI Erinn B Rankin · 2023 to 2026
$1.8M
NCI NIH HHS P01 CA257907NCI NIH HHS R01 CA272432NCI NIH HHS R01CA272432-01
6 · The paper itself

Abstract

The TAM receptor family of TYRO3, AXL and MERTK regulates tissue and immune homeostasis. Aberrant TAM receptor signalling has been linked to a range of diseases, including cancer, fibrosis and viral infections. Specifically, the dysregulation of TAM receptors can enhance tumour growth and metastasis due to their involvement in multiple oncogenic pathways. For example, TAM receptors have been implicated in the epithelial-mesenchymal transition, maintaining the stem cell phenotype, immune modulation, proliferation, angiogenesis and resistance to conventional and targeted therapies. Therapeutically, multiple TAM receptor inhibitors are in preclinical and clinical development for cancers and other indications, with those targeting AXL being the most clinically advanced. Although there has been notable clinical advancement in recent years, challenges persist. This Review aims to provide both biological and clinical insights into the current therapeutic landscape of TAM receptor inhibitors, and evaluates their potential for the treatment of cancer and non-malignant diseases.

Indexed as

NeoplasmsReceptor Protein-Tyrosine KinasesAxl Receptor Tyrosine Kinasec-Mer Tyrosine KinaseHumansProto-Oncogene ProteinsAxl Receptor Tyrosine Kinasec-Mer Tyrosine KinaseProto-Oncogene ProteinsReceptor Protein-Tyrosine Kinases

Identifiers

PMID38092952
PMCPMC11335090

What OpenQuestion holds

Textmetadata
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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.