Evidence map›Paper›PMID 35879421›Full record

ArticleCommunications biology2022

PI3Kδ activity controls plasticity and discriminates between EMT and stemness based on distinct TGFβ signaling.

Jean Agnetti, Vanessa Bou Malham, Christophe Desterke, Nassima Benzoubir, Juan Peng, Sophie Jacques, Souad Rahmouni, Emanuel Di Valentin, Tuan Zea Tan, Didier Samuel and 2 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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

12 authors at 4 institutions in 4 countries.

Jean Agnetti *INSERM, Unité 1193, Villejuif, F-94800, France.
Vanessa Bou Malham *INSERM, Unité 1193, Villejuif, F-94800, France.
Christophe Desterke *Université Paris-Saclay, UFR Médecine- INSERM UA9, Villejuif, France.
Nassima BenzoubirINSERM, Unité 1193, Villejuif, F-94800, France.
Juan PengINSERM, Unité 1193, Villejuif, F-94800, France.
Sophie JacquesLaboratory of animal Genomics, GIGA-Medical Genomics, GIGA-institute, Université de Liège, Liège, Belgium.
Souad RahmouniLaboratory of animal Genomics, GIGA-Medical Genomics, GIGA-institute, Université de Liège, Liège, Belgium.
Emanuel Di ValentinPlateforme des vecteurs viraux, GIGA B34, GIGA-institute, Université de Liège, Liège, Belgium.
Tuan Zea TanCancer Science Institute of Singapore National University of Singapore, Center for Translational Medicine, 14 Medical Drive, #12-01, 117599, Singapore, Singapore.ORCID http://orcid.org/0000-0001-6624-1593
Didier SamuelINSERM, Unité 1193, Villejuif, F-94800, France.
Jean Paul ThieryGuangzhou Laboratory, International biological Island Guangzhou, 510005, Guangzhou, China.ORCID http://orcid.org/0000-0003-0478-5020
Ama Gassama-DiagneINSERM, Unité 1193, Villejuif, F-94800, France. ama.gassama@inserm.fr.ORCID http://orcid.org/0000-0002-9878-7811
Inserm · FRUniversity of Liège · BEGuangzhou Experimental Station · CNNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The stem cells involved in formation of the complex human body are epithelial cells that undergo apicobasal polarization and form a hollow lumen. Epithelial plasticity manifests as epithelial to mesenchymal transition (EMT), a process by which epithelial cells switch their polarity and epithelial features to adopt a mesenchymal phenotype. The connection between the EMT program and acquisition of stemness is now supported by a substantial number of reports, although what discriminates these two processes remains largely elusive. In this study, based on 3D organoid culture of hepatocellular carcinoma (HCC)-derived cell lines and AAV8-based protein overexpression in the mouse liver, we show that activity modulation of isoform δ of phosphoinositide 3-kinase (PI3Kδ) controls differentiation and discriminates between stemness and EMT by regulating the transforming growth factor β (TGFβ) signaling. This study provides an important tool to control epithelial cell fate and represents a step forward in understanding the development of aggressive carcinoma.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsClass I Phosphatidylinositol 3-KinasesEpithelial-Mesenchymal TransitionHumansMicePhosphatidylinositol 3-KinasesTransforming Growth Factor betaClass I Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-KinasesPIK3CD protein, humanPik3cd protein, mouseTransforming Growth Factor beta

Identifiers

PMID35879421
PMCPMC9314410
OpenAlexW4287147672

What OpenQuestion 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 OpenQuestion graph.