Evidence map›Paper›PMID 17325033›Full record

ArticleMolecular and cellular biology2007

Phosphorylation of the cyclic AMP response element binding protein mediates transforming growth factor beta-induced downregulation of cyclin A in vascular smooth muscle cells.

Kentaro Kamiya, Kenji Sakakibara, Evan J Ryer, Raymond P Hom, Edward B Leof, K Craig Kent, Bo Liu

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  5. TGF-β and Smad3 modulate PI3K/Akt signaling pathway in vascular smooth muscle cells.American journal of physiology. Heart and circulatory physiology · 2012
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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

7 authors at 2 institutions in 1 country.

Kentaro KamiyaDepartment of Surgery, Weill Cornell Medical College of Cornell University, New York, NY 1002, USA.
Kenji Sakakibara
Evan J Ryer
Raymond P Hom
Edward B Leof
K Craig Kent
Bo Liu
Cornell University · USMayo Clinic · US

Funding

PKC-Delta in Intimal Hyperplasia after Vascular BypassR01HL081424 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LIU, BO · 2005 to 2008
$1.6M
SURGICAL ONCOLOGY RESEARCH TRAINING PROGRAMT32CA068971 · NCI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI KENT, K CRAIG · 1996 to 2005
$1.3M
NCI NIH HHS T32 CA068971NCI NIH HHS T32CA68917-07NHLBI NIH HHS HL-081424NHLBI NIH HHS R01 HL081424
6 · The paper itself

Abstract

Transforming growth factor beta (TGFbeta), a multifunctional cytokine associated with vascular injury, is a potent inhibitor of cell proliferation. The current results demonstrate that the TGFbeta-induced growth arrest of vascular smooth muscle cells (VSMCs) is associated with cyclin A downregulation. TGFbeta represses the cyclin A gene through a cyclic AMP (cAMP) response element, which complexes with the cAMP response element binding protein (CREB). The CREB-cyclin A promoter interaction is hindered by TGFbeta, preceded by a TGFbeta receptor-dependent CREB phosphorylation. Induction of CREB phosphorylation with forskolin or 6bnz-cAMP mimics TGFbeta's inhibitory effect on cyclin A expression. Conversely, inhibition of CREB phosphorylation with a CREB mutant in which the phosphorylation site at serine 133 was changed to alanine (CREB-S133A) upregulated cyclin A gene expression. Furthermore, the CREB-S133A mutant abolished TGFbeta-induced CREB phosphorylation, cyclin A downregulation, and growth inhibition. Since we have previously shown that the novel PKC isoform protein kinase C delta (PKCdelta) is activated by TGFbeta in VSMCs, we tested the role of this kinase in CREB phosphorylation and cyclin A downregulation. Inhibition of PKCdelta by a dominant-negative mutant or by targeted gene deletion blocked TGFbeta-induced CREB phosphorylation and cyclin A downregulation. Taken together, our data indicate that phosphorylation of CREB stimulated by TGFbeta is a critical step leading to the inhibition of cyclin A expression and, thus, VSMC proliferation.

Indexed as

AnimalsCell LineCyclic AMP Response Element-Binding ProteinCyclin ADown-RegulationMiceMice, KnockoutMuscle, Smooth, VascularPhosphorylationPromoter Regions, GeneticProtein Kinase C-deltaRatsResponse ElementsTransforming Growth Factor betaCyclic AMP Response Element-Binding ProteinCyclin AProtein Kinase C-deltaTransforming Growth Factor beta

Identifiers

PMID17325033
PMCPMC1899963
OpenAlexW2171796334

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.