Evidence map›Paper›PMID 41563267›Full record

ArticleArquivos brasileiros de cirurgia digestiva : ABCD = Brazilian archives of digestive surgery2026

Prognostic and predictive value of AXL and C-MET in patients with rectal cancer.

Carmen Austrália Paredes Marcondes Ribas, Efstathia N Doelken, Sudipta Tripathi, Bülent Polat, Reinhard Lissner, Thomas Böeldicke, Jurandir Marcondes Ribas-Filho, Osvaldo Malafaia, Martin Gasser, Ana Maria Waaga-Gasser

Abstract read
In one paragraph

Article in Arquivos brasileiros de cirurgia digestiva : ABCD = Brazilian archives of digestive surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

10 authors.

Carmen Austrália Paredes Marcondes RibasFaculdade Evangélica Mackenzie do Paraná - Curitiba (PR), Brazil.ORCID http://orcid.org/0000-0002-6195-046X
Efstathia N DoelkenUniversity of Wuerzburg, Molecular Oncology and Immunology, Department of Surgery I - Wuerzburg (BY), Germany.ORCID http://orcid.org/0009-0001-1683-6780
Sudipta TripathiUniversity of Massachusetts Chan Medical School, Department of Medicine, Division of Renal Medicine - Worcester (MA), USA.ORCID http://orcid.org/0000-0001-7729-9002
Bülent PolatUniversity of Wurzburg, University Hospital, Department of Radiation Oncology - Wurzburg (BY), Germany.ORCID http://orcid.org/0000-0003-4677-424X
Reinhard LissnerUniversity of Wuerzburg, Molecular Oncology and Immunology, Department of Surgery I - Wuerzburg (BY), Germany.ORCID http://orcid.org/0009-0000-6091-2640
Thomas BöeldickeHelmholtz Centre for Infection Research - Braunschweig, Germany.ORCID http://orcid.org/0000-0003-2869-1133
Jurandir Marcondes Ribas-FilhoFaculdade Evangélica Mackenzie do Paraná - Curitiba (PR), Brazil.ORCID http://orcid.org/0000-0002-5251-7672
Osvaldo MalafaiaFaculdade Evangélica Mackenzie do Paraná - Curitiba (PR), Brazil.ORCID http://orcid.org/0000-0002-1829-7071
Martin GasserUniversity of Wuerzburg, Molecular Oncology and Immunology, Department of Surgery I - Wuerzburg (BY), Germany.ORCID http://orcid.org/0000-0002-0797-169X
Ana Maria Waaga-GasserUniversity of Wuerzburg, Molecular Oncology and Immunology, Department of Surgery I - Wuerzburg (BY), Germany.ORCID http://orcid.org/0000-0001-5437-716X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRectal cancer remains a significant clinical challenge with demand for conclusive biomarkers, essential in prognostication and therapy monitoring of neoadjuvant and adjuvant treatment strategies.

aimsThe aim of the study was to evaluate AXL and cellular mesenchymal-epithelial transition factor (C-MET) biomarkers for cancer stem cells and to correlate them with clinicopathological characteristics and patient outcome data with respect to neoadjuvant chemoradiotherapy.

methodsSerum levels of soluble surface markers AXL and C-MET were retrospectively analyzed in 164 rectal cancer patients with additional immunofluorescent analyses of their primary tumor tissues.

resultsKaplan-Meier analysis confirmed the prognostic significance of Union for International Cancer Control stages, but with no significant correlation between investigated markers with patient age, gender, or tumor stage. In contrast, tumor tissues demonstrated stage-dependently increased marker expression. While AXL was detected at low levels, C-MET exhibited a bimodal distribution, with elevated levels seen in most patients, particularly post-neoadjuvant therapy and non-significantly in the subgroup with poorer response to neoadjuvant therapy (p=0.074).

conclusionsAXL serum levels in the rectal cancer cohort were significantly different from healthy subjects but did not correlate with tumor stage or survival during and after neoadjuvant/adjuvant therapy. Soluble C-MET levels in the blood, influenced by neoadjuvant chemoradiotherapy, may serve as a predictive marker for treatment response.

Indexed as

Biomarkers, TumorProto-Oncogene ProteinsProto-Oncogene Proteins c-metReceptor Protein-Tyrosine KinasesRectal NeoplasmsAdultAgedAxl Receptor Tyrosine KinaseFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesAXL protein, humanAxl Receptor Tyrosine KinaseBiomarkers, TumorProto-Oncogene ProteinsProto-Oncogene Proteins c-metReceptor Protein-Tyrosine Kinases

Identifiers

PMID41563267
PMCPMC12815463

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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.