Evidence map›Paper›PMID 41916916›Full record

ReviewZhongguo fei ai za zhi = Chinese journal of lung cancer2026

[Role of Receptor Tyrosine Kinase AXL in Cancer Targeted Therapy Drug Resistance].

Sutong Zhan, Peilin Chen, Tangfeng Lv, Yong Song

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 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

4 authors.

Sutong ZhanNanjing Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210000, China.
Peilin ChenNanjing Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210000, China.
Tangfeng LvNanjing Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210000, China.
Yong SongNanjing Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although targeted therapy has made significant advances in cancer treatment throughout these years, drug resistance still remains a major obstacle. Plenty of evidence has proved that abnormal expression of receptor tyrosine kinase AXL is associated with targeted therapy resistance and poor clinical outcomes. AXL drives drug resistance through diverse mechanisms, including altering tumor cell phenotypes, orchestrating DNA damage response process, promoting the activation of bypass signals, or interacting with other receptor tyrosine kinases. Preclinical and clinical studies have demonstrated that combined inhibition of AXL and the other target can enhance the efficacy of various targeted therapies and improve outcomes for patients with drug resistance. This review summarizes recent advances in the specific roles of AXL in targeted therapy resistance and AXL-targeted treatment strategies. It further explores the potential clinical value of combinatorial approaches involving AXL inhibition and discusses future directions for its application in developing novel targeted therapies and advancing precision oncology treatment. 
.

Indexed as

Drug Resistance, NeoplasmMolecular Targeted TherapyNeoplasmsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAnimalsAntineoplastic AgentsAxl Receptor Tyrosine KinaseHumansProtein Kinase InhibitorsAntineoplastic AgentsAXL protein, humanAxl Receptor Tyrosine KinaseProtein Kinase InhibitorsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAXLCancerDrug resistanceTargeted therapy

Identifiers

PMID41916916
PMCPMC13046439

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.