Evidence map›Paper›PMID 35348275›Full record

ArticleMolecular oncology2022

TGFβ selects for pro-stemness over pro-invasive phenotypes during cancer cell epithelial-mesenchymal transition.

Yutaro Tsubakihara, Yae Ohata, Yukari Okita, Shady Younis, Jens Eriksson, Mikael E Sellin, Jiang Ren, Peter Ten Dijke, Kohei Miyazono, Atsuhiko Hikita and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

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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

14 authors at 6 institutions in 4 countries.

Yutaro TsubakiharaDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.
Yae OhataDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.ORCID 0000-0002-5518-835X
Yukari OkitaDepartment of Experimental Pathology and Transborder Medical Research Center, Faculty of Medicine, University of Tsukuba, Japan.ORCID 0000-0002-7279-4634
Shady YounisDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.ORCID 0000-0002-4319-1738
Jens ErikssonDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.ORCID 0000-0002-8945-2665
Mikael E SellinDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.ORCID 0000-0002-8355-0803
Jiang RenDepartment of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Peter Ten DijkeDepartment of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-7234-342X
Kohei MiyazonoDepartment of Molecular Pathology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Japan.ORCID 0000-0001-7341-0172
Atsuhiko HikitaDivison of Tissue Engineering, The University of Tokyo Hospital, Bunkyo-ku, Japan.ORCID 0000-0001-9552-2976
Takeshi ImamuraDepartment of Molecular Medicine for Pathogenesis, Graduate School of Medicine, Ehime University, Toon, Japan.ORCID 0000-0001-5101-4304
Mitsuyasu KatoDepartment of Experimental Pathology and Transborder Medical Research Center, Faculty of Medicine, University of Tsukuba, Japan.ORCID 0000-0001-9905-2473
Carl-Henrik HeldinDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.ORCID 0000-0002-9508-896X
Aristidis MoustakasDepartment of Medical Biochemistry and Microbiology, Science for Life Laboratory, Biomedical Center, Uppsala University, Sweden.ORCID 0000-0001-9131-3827
Uppsala University · SELeiden University Medical Center · NLUniversity of Tsukuba · JPBunkyo University · JPEhime University · JPUniversity of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transforming growth factor β (TGFβ) induces epithelial-mesenchymal transition (EMT), which correlates with stemness and invasiveness. Mesenchymal-epithelial transition (MET) is induced by TGFβ withdrawal and correlates with metastatic colonization. Whether TGFβ promotes stemness and invasiveness simultaneously via EMT remains unclear. We established a breast cancer cell model expressing red fluorescent protein (RFP) under the E-cadherin promoter. In 2D cultures, TGFβ induced EMT, generating RFP

Indexed as

Epithelial-Mesenchymal TransitionLung NeoplasmsCell Line, TumorHumansPhenotypeReceptors, Transforming Growth Factor betaTransforming Growth Factor betaReceptors, Transforming Growth Factor betaTransforming Growth Factor betacancer stem cellE-cadherinepithelial-mesenchymal transitioninvasionmetastasistransforming growth factor β

Identifiers

PMID35348275
PMCPMC9208077
OpenAlexW4221110931

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.