Evidence map›Paper›PMID 41582591›Full record

ReviewCurrent medicinal chemistry2026

RTK AXL and its Isoforms: Regulation and Implications in Cancer.

Ilona Malikova, Aizhan Syzdykova, Nazia Islam, Marina Kriajevskaia, Eugene Tulchinsky

Abstract readReview
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In one paragraph

Review in Current medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Ilona MalikovaSchool of Medicine, Nazarbayev University, Astana, Kazakhstan.ORCID 0009-0005-9417-2325
Aizhan SyzdykovaSchool of Medicine, Nazarbayev University, Astana, Kazakhstan.
Nazia IslamSchool of Medicine, Nazarbayev University, Astana, Kazakhstan.ORCID 0000-0002-5826-4960
Marina KriajevskaiaSchool of Medicine, Nazarbayev University, Astana, Kazakhstan.
Eugene TulchinskySchool of Medicine, Nazarbayev University, Astana, Kazakhstan.ORCID 0000-0001-8684-0315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a member of the TAM family of receptor kinases, the AXL protein plays an essential role in biological processes that maintain tissue homeostasis. Deregulated AXL signalling in tumour cells is linked to cancer progression, poor prognosis, metastasis, and reduced sensitivity to anti-cancer therapies. The underlying mechanisms are the activation of downstream signalling routes that promote cell survival, invasion and epithelial-mesenchymal transition. Two major AXL isoforms are expressed in human and rodent cells due to alternative splicing. Despite extensive research on AXL in cancer, little is known regarding the functional differences between these isoforms and whether they contribute to cancer differently. This review paper first outlines the structural and functional aspects of TAM biology with a particular focus on AXL. Next, we discuss the different levels of AXL regulation in tumour cells, including proteolytic cleavage, which leads to the formation of both extracellular and nuclear forms of AXL. Finally, we review articles investigating the variations in the function of AXL isoforms and report their associations with cancer. Notably, the formation of isoform 1 is likely to determine the presence of soluble AXL, elevated levels of which have been correlated with cancer progression in several tumour types. The review identifies areas deserving further investigation, such as how changes in isoform expression impact levels of soluble AXL in cancer. Additionally, isoform-specific downstream signalling effects and their impact on metastasis and drug resistance warrant more in-depth investigation.

Indexed as

NeoplasmsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAlternative SplicingAnimalsAxl Receptor Tyrosine KinaseHumansProtein IsoformsSignal TransductionAXL protein, humanAxl Receptor Tyrosine KinaseProtein IsoformsProto-Oncogene ProteinsReceptor Protein-Tyrosine Kinasesalternative splicingAXLAXL isoformscancercell signalingproteolytic cleavageTAM receptors

Identifiers

What Socratic holds

Textmetadata
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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.