Evidence map›Paper›PMID 2040702›Full record

ArticleThe Journal of clinical investigation1991

Regulation of transforming growth factor expression in rat intestinal epithelial cell lines.

S Suemori, C Ciacci, D K Podolsky

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
  2. Article
  3. Smad7 inhibits autocrine expression of TGF-β2 in intestinal epithelial cells in baboon necrotizing enterocolitis.American journal of physiology. Gastrointestinal and liver physiology · 2013
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  15. Functional interleukin-2 receptors on intestinal epithelial cells.The Journal of clinical investigation · 1993
    Article
  16. 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

3 authors at 2 institutions in 1 country.

S SuemoriDepartment of Medicine, Massachusetts General Hospital, Boston 02114.
C Ciacci
D K Podolsky
Massachusetts General Hospital · USHarvard University Press · US

Funding

PEPTIDE GROWTH FACTORS IN INTESTINAL EPITHELIAL REPAIRR37DK041557 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI PODOLSKY, DANIEL K · 1997 to 2006
$2.9M
PEPTIDE GROWTH FACTORS IN INTESTINAL EPITHELIAL REPAIRR01DK041557 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI PODOLSKY, DANIEL K · 1988 to 1997
–
NIDDK NIH HHS DK41557
6 · The paper itself

Abstract

Autocrine and paracrine modulation of transforming growth factor expression was assessed in rat intestinal epithelial cell lines designated IEC-6 and IEC-7. Addition of the transforming growth factor alpha (TGF alpha) homologue epidermal growth factor (EGF) to media of subconfluent IEC-6 cells led to autocrine stimulation of TGF alpha expression as well as increased expression of the transforming growth factor beta 1 (TGF beta 1). Increased expression of TGF alpha was maximal between 3 and 6 h after addition of EGF and subsequently declined coincident with increasing level of expression of TGF beta 1, which achieved maximal levels 6 h after addition of EGF and was sustained for more than 12 h. Addition of TGF beta 1 also led to autocrine induction of its own expression coincident with suppression of TGF alpha expression. Addition of TGF beta 1 was associated with increased expression of beta-actin when standardized to a constitutive transcript (GAPDH). Similar responses to addition of EGF and TGF beta 1, were observed in another intestinal epithelial cell line, designated IEC-17. Modulation of expression of TGFs was attenuated when cells were grown on the complex extracellular matrix produced by the Engelbreth-Holm-Swarm tumor (Matrigel), reflecting the baseline induction of TGF beta 1 expression when compared to IEC-6 and IEC-17 cells maintained on plastic. These observations suggest that expression of TGFs is controlled by autocrine mechanisms in intestinal epithelial cell lines and proliferation stimulated by TGF alpha may be initially self-reinforcing but ultimately downregulated by induction of TGF beta 1.

Indexed as

Gene Expression RegulationActinsAnimalsBlotting, NorthernCell LineEpidermal Growth FactorEpitheliumExtracellular MatrixIntestinesIn Vitro TechniquesRatsRNA, MessengerTransforming Growth FactorsActinsEpidermal Growth FactorRNA, MessengerTransforming Growth Factors

Identifiers

PMID2040702
PMCPMC296982
OpenAlexW2115601920

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.