Evidence map›Paper›PMID 32940810›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2021

Autophagy induced by Helicobacter pylori infection is necessary for gastric cancer stem cell emergence.

Sarah Courtois, Maria Haykal, Clément Bodineau, Elodie Sifré, Lamia Azzi-Martin, Armelle Ménard, Francis Mégraud, Philippe Lehours, Raúl V Durán, Christine Varon and 1 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.2field-weighted citation impact, top 5% of its field
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

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Beyond the Stomach: Exploring the Role ofExpert reviews in molecular medicine · 2026
    Review
  2. Article
  3. Increasing autophagy activity suppressesAmerican journal of cancer research · 2026
    Article
  4. Article
  5. Iranian journal of microbiology · 2025
    Article
  6. Review
  7. Review
  8. RSC advances · 2025
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Programmed cell death inFrontiers in cellular and infection microbiology · 2024
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Gastric Cancer Due to ChronicDiseases (Basel, Switzerland) · 2022
    Review
  20. 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

11 authors at 4 institutions in 2 countries.

Sarah CourtoisUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Maria HaykalUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Clément BodineauCentro Andaluz de Biología Molecular Y Medicina Regenerativa-CABIMER, Consejo Superior de Investigaciones Científicas, Universidad de Sevilla, Universidad Pablo de Olavide, Américo Vespucio 24, 41092, Sevilla, Spain.
Elodie SifréUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Lamia Azzi-MartinUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Armelle MénardUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Francis MégraudUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Philippe LehoursUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Raúl V DuránCentro Andaluz de Biología Molecular Y Medicina Regenerativa-CABIMER, Consejo Superior de Investigaciones Científicas, Universidad de Sevilla, Universidad Pablo de Olavide, Américo Vespucio 24, 41092, Sevilla, Spain.
Christine VaronUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France.
Emilie BessèdeUniv. Bordeaux, INSERM, BaRITOn, U1053, F-33000, Bordeaux, France. emilie.bessede@u-bordeaux.fr.
Bordeaux Population Health · FRInserm · FRUniversité de Bordeaux · FRCentro Andaluz de Biología Molecular y Medicina Regenerativa · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe main cause of gastric cancer is the infection by the bacterium Helicobacter pylori which induces a chronic inflammation and an epithelial-to-mesenchymal transition (EMT) leading to the emergence of cells with cancer stem cell (CSC) properties. However, the underlying mechanisms have not been fully characterized. Moreover, H. pylori modulates the host cell autophagic process, but a few studies have investigated the role of this process in tumoral transformation. The aim of this study was to determine whether H. pylori-induced autophagy has a role in CSC emergence.

methodsAutophagic flux in response to H. pylori infection was characterized in AGS cell line expressing the tandem-tagged mCherry-GFP-LC3 protein and using a ratiometric flow cytometry analysis. Then, AGS and MKN45 cell lines were treated with bafilomycin or chloroquine, two pharmaceutical well-known inhibitors of autophagy, and different EMT and CSC characteristics were analyzed.

resultsFirst, a co-expression of the gastric CSC marker CD44 and the autophagic marker LC3 in mice and human stomach tissues infected with H. pylori was observed. Then, we demonstrated in vitro that H. pylori was able to activate the autophagy process with a reduced autophagic flux. Finally, infected cells were treated with autophagy inhibitors, which reduced (i) appearance of mesenchymal phenotypes and migration ability related to EMT and (ii) CD44 expression as well as tumorsphere formation capacities reflecting CSC properties.

conclusionIn conclusion, all these data show that H. pylori-induced autophagy is implicated in gastric CSC emergence and could represent an interesting therapeutic target.

Indexed as

AnimalsAutophagyCell Line, TumorEpithelial-Mesenchymal TransitionHelicobacter InfectionsHelicobacter pyloriHumansHyaluronan ReceptorsMiceMicrotubule-Associated ProteinsNeoplastic Stem CellsStomachStomach NeoplasmsHyaluronan ReceptorsMAP1LC3A protein, humanMap1lc3b protein, mouseMicrotubule-Associated ProteinsAutophagic fluxCD44Epithelial-to-mesenchymal transitionmTORC1Tumorspheres

Identifiers

PMID32940810
OpenAlexW3087270406

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.