Evidence map›Paper›PMID 15806162›Full record

ArticleOncogene2005

Mitogen regulated induction of FRA-1 proto-oncogene is controlled by the transcription factors binding to both serum and TPA response elements.

Pavan Adiseshaiah, Suneetha Peddakama, Qin Zhang, Dhanunjaya V Kalvakolanu, Sekhar P Reddy

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  9. Article
  10. FOSL1 Promotes Kras-induced Lung Cancer through Amphiregulin and Cell Survival Gene Regulation.American journal of respiratory cell and molecular biology · 2018
    Article
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  13. Review
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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

5 authors at 3 institutions in 1 country.

Pavan AdiseshaiahDepartment of Environmental Health Sciences, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, MD 21205, USA.
Suneetha Peddakama
Qin Zhang
Dhanunjaya V Kalvakolanu
Sekhar P Reddy
Johns Hopkins University · USSidney Kimmel Comprehensive Cancer Center · USU-M Rogel Cancer Center

Funding

MODULATION OF IFN ACTION VIA NOVEL REGULATORY FACTORSR01CA078282 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI KALVAKOLANU, DHAN V. · 1998 to 2014
$4.4M
Human NRF2 Promoter Functional Polymorphisms and Acute Lung InjuryR01HL066109 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REDDY, SEKHAR P. · 2001 to 2012
$3.5M
The Role and Biology of Fra-1 in Lung Injury and RepairR01ES011863 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REDDY, SEKHAR P. · 2002 to 2013
$3.4M
Cytokine modulated novel growth inhibitory mechanismsR01CA105005 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI KALVAKOLANU, DHAN V. · 2004 to 2013
$2.7M
MOLECULAR BASIS OF AIRWAY SQUAMOUS CELL DIFFERENTIATIONR01HL058122 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI POTHIREDDY, SEKHAR M · 2001 to 2002
$234k
MOLECULAR BASIS OF AIRWAY SQUAMOUS CELL DIFFERENTIATIONR29HL058122 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI POTHIREDDY, SEKHAR M · 1998 to 2000
$112k
NCI NIH HHS CA105005NCI NIH HHS CA78282NHLBI NIH HHS HL58122NHLBI NIH HHS HL66109NIEHS NIH HHS ES011863NIEHS NIH HHS ES30819
6 · The paper itself

Abstract

FRA-1, a member of the FOS family of transcription factors, is overexpressed in a variety of human tumors, and contributes to tumor progression. In addition to mitogens, various toxicants and carcinogens persistently induce FRA-1 expression in vitro and in vivo. Although the mitogen induced expression of c-FOS is relatively well understood, it is poorly defined in the case of FRA-1. Our recent analysis of the FRA-1 promoter has shown a critical role for a TRE located at -318 in mediating the TPA-induced expression. The -379 to -283 bp promoter segment containing a critical TRE (-318), however, is insufficient for the induction of FRA-1 promoter. Here, we show that a 40-bp (-276/-237) segment, comprising a TCF binding site and the CArG box (collectively known as serum response element, SRE), and an ATF site, is also necessary for the FRA-1 induction by TPA and EGF. Interestingly, the -283 to +32 bp FRA-1 promoter fragment containing an SRE and an ATF site alone was also insufficient to confer TPA sensitivity to a reporter gene. However, in association with the -318 TRE, the SRE and ATF sites imparted a strong TPA-inducibility to the reporter. Similarly, EGF also required these motifs for the full induction of this gene. Using ChIP assays we show that, in contrast to c-Jun, SRF, Elk1, ATF1 and CREB proteins bind to SRE and ATF sites of the FRA-1 promoter, constitutively. RNAi-mediated knockdown of endogenous SRF, ELK1 and c-JUN protein expression significantly reduced TPA-stimulated FRA-1 promoter activity. Thus, a bipartite enhancer formed by an upstream TRE and the downstream SRE and ATF sites and the cognate factors is necessary and sufficient for the regulation of FRA-1 in response to mitogens.

Indexed as

Gene Expression Regulation, NeoplasticActivating Transcription FactorsBlood ProteinsBreast NeoplasmsDisease ProgressionFemaleFos-Related Antigen 1HumansLung NeoplasmsMitogensPromoter Regions, GeneticProto-Oncogene MasProto-Oncogene Proteins c-fosSerum Response ElementTetradecanoylphorbol AcetateTranscription Factors12-O-tetradeca-2,4,6,8-tetranoylphorbol-13-acetateActivating Transcription FactorsBlood ProteinsFos-Related Antigen 1MAS1 protein, humanMitogensProto-Oncogene MasProto-Oncogene Proteins c-fosTetradecanoylphorbol AcetateTranscription Factors

Identifiers

PMID15806162
OpenAlexW2070453614

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.