Evidence map›Paper›PMID 39201551›Full record

ArticleInternational journal of molecular sciences2024

ICAM1 (CD54) Contributes to the Metastatic Capacity of Gastric Cancer Stem Cells.

José Manuel Tinajero-Rodríguez, Lizbeth Ramírez-Vidal, Jared Becerril-Rico, Eduardo Alvarado-Ortiz, Dámaris P Romero-Rodríguez, Fernando López-Casillas, Daniel Hernández-Sotelo, Fernando Fernández-Ramírez, Adriana Contreras-Paredes, Elizabeth Ortiz-Sánchez

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. World journal of gastroenterology · 2026
    Article
  3. Article
  4. 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

10 authors.

José Manuel Tinajero-RodríguezSubdirección de Investigación Básica, Instituto Nacional de Cancerología, Av. San Fernando 22, Colonia Sección XVI, Mexico City 14080, Mexico.ORCID 0000-0002-4460-2906
Lizbeth Ramírez-VidalPosgrado de Ciencias Biomédicas, Facultad de Medicina, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, Mexico City 04510, Mexico.
Jared Becerril-RicoPosgrado en Ciencias Biológicas, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico.
Eduardo Alvarado-OrtizPosgrado en Ciencias Biológicas, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico.ORCID 0000-0003-2201-2793
Dámaris P Romero-RodríguezLaboratorio Nacional Conahcyt de Investigación y Diagnóstico por Inmunocitofluorometría (LANCIDI), INER, Mexico City 14080, Mexico.
Fernando López-CasillasInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, Mexico City 04510, Mexico.ORCID 0000-0002-3689-1824
Daniel Hernández-SoteloFacultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.
Fernando Fernández-RamírezUnidad de Genética, Hospital General de México, Mexico City 06720, Mexico.ORCID 0000-0002-7016-1948
Adriana Contreras-ParedesSubdirección de Investigación Básica, Instituto Nacional de Cancerología, Av. San Fernando 22, Colonia Sección XVI, Mexico City 14080, Mexico.ORCID 0000-0001-9965-4108
Elizabeth Ortiz-SánchezSubdirección de Investigación Básica, Instituto Nacional de Cancerología, Av. San Fernando 22, Colonia Sección XVI, Mexico City 14080, Mexico.ORCID 0000-0001-9855-9491

Funding

CONAHCYT A1-S-40601CONAHCYT CF-2019-263979
6 · The paper itself

Abstract

Gastric cancer is the fourth leading cause of cancer deaths worldwide. The presence of chemoresistant cells has been used to explain this high mortality rate. These higher tumorigenic and chemoresistant cells involve cancer stem cells (CSCs), which have the potential for self-renewal, a cell differentiation capacity, and a greater tumorigenic capacity. Our research group identified gastric cancer stem cells (GCSCs) with the CD24+CD44+CD326+ICAM1+ immunophenotype isolated from gastric cancer patients. Interestingly, this GCSC immunophenotype was absent in cells isolated from healthy people, who presented a cell population with a CD24+CD44+CD326+ immunophenotype, lacking ICAM1. We aimed to explore the role of ICAM1 in these GCSCs; for this purpose, we isolated GCSCs from the AGS cell line and generated a GCSC line knockout for ICAM1 using CRISPR/iCas9, which we named GCSC-ICAM1

Indexed as

Cell MovementDrug Resistance, NeoplasmIntercellular Adhesion Molecule-1Neoplastic Stem CellsStomach NeoplasmsZebrafishAnimalsCell Line, TumorCisplatinHumansNeoplasm MetastasisSTAT3 Transcription FactorCisplatinICAM1 protein, humanIntercellular Adhesion Molecule-1STAT3 Transcription Factorcancer stem cellgastric cancermetastasizetumorigenic

Identifiers

PMID39201551
PMCPMC11354656

What OpenQuestion holds

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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.