Evidence map›Paper›PMID 2463471›Full record

ArticleMolecular and cellular biology1988

Selective inhibition of growth-related gene expression in murine keratinocytes by transforming growth factor beta.

R J Coffey, C C Bascom, N J Sipes, R Graves-Deal, B E Weissman, H L Moses

Abstract read
In one paragraph

Article in Molecular and cellular biology, 1988. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
–field-weighted citation impact
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

88 citing papers in PubMed.

  1. SMURF2 in Anticancer Therapy: Dual Role in Carcinogenesis and Theranostics.International journal of molecular sciences · 2026
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  9. NGS Analysis Confirms CommonInternational journal of molecular sciences · 2021
    Article
  10. Review
  11. Article
  12. Characterization of Smad3 knockout mouse derived skin cells.In vitro cellular & developmental biology. Animal · 2017
    Article
  13. TGF-β Family Signaling in the Control of Cell Proliferation and Survival.Cold Spring Harbor perspectives in biology · 2017
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Ki-67, TGF-β1, and elastin content are significantly altered in lip carcinogenesis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article

28 more citing papers are in PubMed but not listed here.

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.

R J CoffeyDepartment of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
C C Bascom
N J Sipes
R Graves-Deal
B E Weissman
H L Moses

Funding

CHEMICAL TRANSFORMATION OFMOUSE EPIDERMAL KERATINOCYTESR01CA039602 · NCI · CHILDREN'S HOSPITAL LOS ANGELES · PI WEISSMAN, BERNARD E. · 1986 to 1988
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TRANSFORMING GROWTH FACTORS IN NEOPLASTIC TRANSFORMATIONR35CA042572 · NCI · VANDERBILT UNIVERSITY · PI MOSES, HAROLD L · 1986 to 1999
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NCI NIH HHS CA 39602NCI NIH HHS CA 42572
6 · The paper itself

Abstract

Transforming growth factor beta (TGF beta) is a potent inhibitor of epithelial cell proliferation. A nontumorigenic epidermal growth factor (EGF)-dependent epithelial cell line, BALB/MK, is reversibly growth arrested by TGF beta. TGF beta will also abrogate EGF-stimulated mitogenesis of quiescent BALB/MK cells. Increased levels of calcium (greater than 1.0 mM) will induce differentiation in BALB/MK cells; in contrast, TGF beta-mediated growth inhibition does not result in induction of terminal differentiation. In the present study, the effects of TGF beta and calcium on growth factor-inducible gene expression were examined. TGF beta markedly decreased c-myc and KC gene expression in rapidly growing BALB/MK cells and reduced the EGF induction of c-myc and KC in a quiescent population of cells. TGF beta exerted its control over c-myc expression at a posttranscriptional level, and this inhibitory effect was dependent on protein synthesis. TGF beta had no effect on c-fos gene expression, whereas 1.5 mM calcium attenuated EGF-induced c-fos expression in quiescent cells. Expression of beta-actin, however, was slightly increased in both rapidly growing and EGF-restimulated quiescent BALB/MK cells treated with TGF beta. Thus, in this system, TGF beta selectively reduced expression of certain genes associated with cell proliferation (c-myc and KC), and at least part of the TGF beta effect was at a posttranscriptional level.

Indexed as

Epidermal CellsProto-OncogenesAnimalsCell DivisionCell NucleusCells, CulturedGrowth InhibitorsKeratinsKineticsMiceMice, Inbred BALB CNucleic Acid HybridizationRNARNA Processing, Post-TranscriptionalTranscription, GeneticTransforming Growth FactorsGrowth InhibitorsKeratinsRNATransforming Growth Factors

Identifiers

PMID2463471
PMCPMC363535

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.