Evidence map›Paper›PMID 39563861›Full record

ArticleFrontiers in cell and developmental biology2024

Representing ECM composition and EMT pathways in gastric cancer using a new metastatic gene signature.

Francesco Albano, Sabino Russi, Simona Laurino, Pellegrino Mazzone, Giuseppina Di Paola, Pietro Zoppoli, Elena Amendola, Chiara Balzamo, Ottavia Bartolo, Mario Ciuffi and 6 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Do Metastatic Cells Arise from PD-L1International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Article
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

16 authors.

Francesco AlbanoLaboratory of Preclinical and Translational Research, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.
Sabino RussiLaboratory of Preclinical and Translational Research, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.
Simona LaurinoLaboratory of Preclinical and Translational Research, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.
Pellegrino MazzoneLaboratory of Stemness and Tissue Regeneration, Biogem S.c.a.r.l., Ariano Irpino, Italy.
Giuseppina Di PaolaLaboratory of Stemness and Tissue Regeneration, Biogem S.c.a.r.l., Ariano Irpino, Italy.
Pietro ZoppoliDepartment of Molecular Medicine and Medical Biotechnologies, University Federico II, Napoli, Italy.
Elena AmendolaLaboratory of Stem Cell Biology, Department of Biology, University Federico II of Napoli, Napoli, Italy.
Chiara BalzamoLaboratory of Stem Cell Biology, Department of Biology, University Federico II of Napoli, Napoli, Italy.
Ottavia BartoloEndoscopy Unit, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.
Mario CiuffiEndoscopy Unit, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.
Orazio IgnomirelliEndoscopy Unit, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.
Alessandro SgambatoDepartment of Translational Medicine and Surgery, Catholic University of Sacro Cuore, Roma, Italy.
Rocco GalassoScientific Direction, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB) Via Padre Pio 1, Rionero inVulture, Italy.
Mario De FeliceDepartment of Molecular Medicine and Medical Biotechnologies, University Federico II, Napoli, Italy.
Geppino Falco *Laboratory of Stem Cell Biology, Department of Biology, University Federico II of Napoli, Napoli, Italy.
Giovanni Calice *Laboratory of Preclinical and Translational Research, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Rionero inVulture, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gastric cancer (GC) is an aggressive and heterogeneous malignancy marked by cellular and molecular diversity. In GC, cancer cells invade locally in the stomach at stage I and can progress to metastasis in distant organs by stage IV, where it often becomes fatal. Methods: We analyzed gene expression profiles from 719 stage I and stage IV GC patients across seven public datasets, conducting functional enrichment analysis to identify a gene signature linked to disease progression. Additionally, we developed an Results: Our analysis identified a progression-associated gene signature ( Discussion: This gene signature may help identify stage I GC patients at higher risk, offering potential utility in early-stage patient management. Furthermore, our experimental ECM model may serve as a platform for investigating molecular mechanisms underlying metastatic spread in gastric cancer.

Indexed as

cell invasionepithelial-to-mesenchymal transitionextracellular matrixgastric cancermetastasistranscriptomics and enrichment analysis

Identifiers

PMID39563861
PMCPMC11573575

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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.