Evidence map›Paper›PMID 27203217›Full record

ArticleOncotarget2016

Quantitation of TGF-β proteins in mouse tissues shows reciprocal changes in TGF-β1 and TGF-β3 in normal vs neoplastic mammary epithelium.

Kathleen C Flanders, Yu-An Yang, Michelle Herrmann, JinQiu Chen, Nerissa Mendoza, Amer M Mirza, Lalage M Wakefield

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.3field-weighted citation impact, top 32% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Review
  6. Article
  7. Commensal skin bacteria exacerbate inflammation and delay skin healing.bioRxiv : the preprint server for biology · 2023
    Article
  8. TGF-β broadly modifies rather than specifically suppresses reactivated memory CD8 T cells in a dose-dependent manner.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Targeting TGFβ signal transduction for cancer therapy.Signal transduction and targeted therapy · 2021
    Review
  18. TGFβ biology in cancer progression and immunotherapy.Nature reviews. Clinical oncology · 2021
    Review
  19. Article
  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

7 authors at 2 institutions in 1 country.

Kathleen C FlandersLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
Yu-An YangLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
Michelle HerrmannLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
JinQiu ChenLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
Nerissa MendozaXOMA Corporation, Berkeley, California, United States of America.
Amer M MirzaXOMA Corporation, Berkeley, California, United States of America.
Lalage M WakefieldLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America.
National Cancer Institute · USXOMA (United States) · US

Funding

Spatial Imaging Technology ResourceZICBC011434 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MALIK, MARIAM · 2012 to 2025
$12.8M
Development of TGF-beta antagonists for cancer therapyZIABC010881 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WAKEFIELD, LALAGE · 2009 to 2025
$12.5M
Intramural NIH HHS ZIA BC010881
6 · The paper itself

Abstract

Transforming growth factor-βs (TGF-βs) regulate tissue homeostasis, and their expression is perturbed in many diseases. The three isoforms (TGF-β1, -β2, and -β3) have similar bioactivities in vitro but show distinct activities in vivo. Little quantitative information exists for expression of TGF-β isoform proteins in physiology or disease. We developed an optimized method to quantitate protein levels of the three isoforms, using a Luminex® xMAP®-based multianalyte assay following acid-ethanol extraction of tissues. Analysis of multiple tissues and plasma from four strains of adult mice showed that TGF-β1 is the predominant isoform with TGF-β2 being ~10-fold lower. There were no sex-specific differences in isoform expression, but some tissues showed inter-strain variation, particularly for TGF-β2. The only adult tissue expressing appreciable TGF-β3 was the mammary gland, where its levels were comparable to TGF-β1. In situ hybridization showed the luminal epithelium as the major source of all TGF-β isoforms in the normal mammary gland. TGF-β1 protein was 3-8-fold higher in three murine mammary tumor models than in normal mammary gland, while TGF-β3 protein was 2-3-fold lower in tumors than normal tissue, suggesting reciprocal regulation of these isoforms in mammary tumorigenesis.

Indexed as

AnimalsFemaleHumansMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CProtein IsoformsTransforming Growth Factor betaTransforming Growth Factor beta1Transforming Growth Factor beta3Protein IsoformsTransforming Growth Factor betaTransforming Growth Factor beta1Transforming Growth Factor beta3mammary glandmouse tissuesproteinquantitationTGF-β isoforms

Identifiers

PMID27203217
PMCPMC5122380
OpenAlexW2404501987

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.