Evidence map›Paper›PMID 30643193›Full record

ArticleOncogene2019

Increased type III TGF-β receptor shedding decreases tumorigenesis through induction of epithelial-to-mesenchymal transition.

Jennifer J Huang, Armando L Corona, Brian P Dunn, Elise M Cai, Jesse N Prakken, Gerard C Blobe

Abstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Matrix proteoglycans in tumor inflammation and immunity.American journal of physiology. Cell physiology · 2022
    Review
  10. Article
  11. Article
  12. A tumor-promoting role for soluble TβRIII in glioblastoma.Molecular and cellular biochemistry · 2021
    Article
  13. Article
  14. Observational
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

6 authors at 2 institutions in 1 country.

Jennifer J HuangDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
Armando L CoronaDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
Brian P DunnDivision of Medical Oncology, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Elise M CaiDivision of Medical Oncology, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Jesse N PrakkenDivision of Medical Oncology, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Gerard C BlobeDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA. gerard.blobe@duke.edu.
Duke Medical Center · USDuke University Hospital · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Role of TbRIII in Regulating Motility and InvasionR01CA135006 · NCI · DUKE UNIVERSITY · PI BLOBE, GERARD C · 2009 to 2013
$2.2M
Role of Type III TGF-beta Receptor Shedding in Lung Cancer Initiation and ProgressionF30CA196162 · NCI · DUKE UNIVERSITY · PI HUANG, JENNIFER J · 2015 to 2016
$90k
NCI NIH HHS F30 CA196162NCI NIH HHS P30 CA014236NCI NIH HHS R01 CA135006NIGMS NIH HHS T32 GM007171U.S. Department of Health & Human Services | National Institutes of Health (NIH) F30CA196162U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01CA135006
6 · The paper itself

Abstract

The type III TGF-β receptor (TβRIII) is a TGF-β co-receptor that presents ligand to the type II TGF-β receptor to initiate signaling. TβRIII also undergoes ectodomain shedding to release a soluble form (sTβRIII) that can bind ligand, sequestering it away from cell surface receptors. We have previously identified a TβRIII extracellular mutant that has enhanced ectodomain shedding ("super shedding (SS)"-TβRIII-SS). Here, we utilize TβRIII-SS to study the balance of cell surface and soluble TβRIII in the context of lung cancer. We demonstrate that expressing TβRIII-SS in lung cancer cell models induces epithelial-to-mesenchymal transition (EMT) and that these TβRIII-SS (EMT) cells are less migratory, invasive and adhesive and more resistant to gemcitabine. Moreover, TβRIII-SS (EMT) cells exhibit decreased tumorigenicity but increased growth rate in vitro and in vivo. These studies suggest that the balance of cell surface and soluble TβRIII may regulate a dichotomous role for TβRIII during cancer progression.

Indexed as

A549 CellsAnimalsCarcinogenesisCell LineCell Line, TumorCell MovementDisease ProgressionDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHEK293 CellsHumansLung NeoplasmsMiceMice, NudebetaglycanProteoglycansReceptors, Transforming Growth Factor beta

Identifiers

PMID30643193
PMCPMC6586422
OpenAlexW2910223575

What OpenQuestion holds

Textmetadata
LicenceTDM
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.