Evidence map›Paper›PMID 42043872›Full record

ArticleCancer medicine2026

TYRO3, AXL, MERTK and Their Ligands in Brain Metastases From Colorectal Cancers.

Anaïs Noblanc, Fatima Dkhissi, Pierre-Olivier Guichet, Lucie Lebeau, Serge Milin, Sheik Emambux, Pauline Roussille, Camille Evrard, Lucie Karayan-Tapon, David Tougeron and 2 more

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Anaïs NoblancPRODICET, UR24144, Université de Poitiers, Poitiers, France.
Fatima DkhissiPRODICET, UR24144, Université de Poitiers, Poitiers, France.
Pierre-Olivier GuichetPRODICET, UR24144, Université de Poitiers, Poitiers, France.
Lucie LebeauDepartment of Pathology, CHU de Poitiers, Poitiers, France.
Serge MilinDepartment of Pathology, CHU de Poitiers, Poitiers, France.
Sheik EmambuxPRODICET, UR24144, Université de Poitiers, Poitiers, France.
Pauline RoussilleDepartment of Radiotherapy, CHU de Poitiers, Poitiers, France.
Camille EvrardPRODICET, UR24144, Université de Poitiers, Poitiers, France.ORCID https://orcid.org/0000-0003-3147-1350
Lucie Karayan-TaponPRODICET, UR24144, Université de Poitiers, Poitiers, France.
David TougeronPRODICET, UR24144, Université de Poitiers, Poitiers, France.
Omar BenzakourPRODICET, UR24144, Université de Poitiers, Poitiers, France.
Violaine RandrianPRODICET, UR24144, Université de Poitiers, Poitiers, France.ORCID https://orcid.org/0000-0002-0155-1766

Funding

Sport et Collection 2020
6 · The paper itself

Abstract

introductionTYRO3, AXL, and MERTK (TAM receptor tyrosine kinases) represent potential therapeutic targets in metastatic colorectal cancer. Pre-clinical and clinical data are needed to explore further how TAM receptors interact with the central nervous system, which could impact brain metastases from colorectal cancer (BM-CRC).

methodsWe analyzed TAM receptor expression in established brain metastasis stem cell lines from patients with CRC (BM-SC-CRC) (RNA and protein), a local cohort of BM-CRC patients (protein), and a cohort of metastatic CRC from The Cancer Genome Atlas (TCGA) (RNA).

resultsWhen orthotopically injected into mice, BM-SC-CRC derived from two patients expressed TYRO3 and Protein S (PROS1) but poorly AXL and GAS6. When we analyzed both patients' primary tumors and metastatic sites, TYRO3 and AXL proteins were expressed in all tumor sites, but hardly MERTK. AXL was located primarily in endothelial cells, and TYRO3 in tumor cells. We examined the protein expression of TAM receptors in a cohort of BM-CRC patients, considering tissue from the primary tumor (N = 85), the matched brain metastases (N = 40), and another metastatic site (N = 29). AXL was expressed through primary tumors to brain metastases, as 72.7% of samples in BM (versus 44% with TYRO3 and 53% with MERTK) had a stable (45.5%) or increased (27.2%) protein expression compared to their paired primary tumor. None of the TAM receptors or PROS1 were found prognostic in a TCGA metastatic CRC cohort (n = 80), but GAS6 was, in univariate (HR = 2.141 [95% CI 1.018-4.506], p = 0.045) and multivariate analysis (HR = 2.382 [95% CI 1.124-5.048], p = 0.024). In exploratory analysis, patients with Low AXL/High GAS6 had a poorer prognosis (p = 0.046). DISCUSSION AND

conclusionThe TAM receptors' ligand GAS6 and the AXL/GAS6 ratio could help to monitor patients' prognosis in metastatic CRC settings including BM-CRC. Further research is needed to validate the TAM receptors' impact on prognosis in BM-CRC.

Indexed as

Brain Neoplasmsc-Mer Tyrosine KinaseColorectal NeoplasmsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAgedAnimalsAxl Receptor Tyrosine KinaseCell Line, TumorFemaleGrowth Arrest-Specific Protein 6HumansIntercellular Signaling Peptides and ProteinsLigandsMaleMiceAXL protein, humanAxl Receptor Tyrosine Kinasec-Mer Tyrosine KinaseGrowth Arrest-Specific Protein 6Intercellular Signaling Peptides and ProteinsLigandsMERTK protein, humanPROS1 protein, humanProtein SProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesTYRO3 protein, humanAXLbrain metastasiscolorectal cancerGAS6

Identifiers

PMID42043872
PMCPMC13117217

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.