Evidence map›Paper›PMID 11500377›Full record

ArticleThe EMBO journal2001

Negative regulation of the Wnt-beta-catenin pathway by the transcriptional repressor HBP1.

E M Sampson, Z K Haque, M C Ku, S G Tevosian, C Albanese, R G Pestell, K E Paulson, A S Yee

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

75 citing papers in PubMed, 152 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Cooperative defenses during enteropathogenic infection.Current opinion in microbiology · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. miR-335-5P contributes to human osteoarthritis by targeting HBP1.Experimental and therapeutic medicine · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

15 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

8 authors at 1 institution in 1 country.

E M SampsonDepartment of Biochemistry, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA.
Z K Haque
M C Ku
S G Tevosian
C Albanese
R G Pestell
K E Paulson
A S Yee
Tufts University · US

Funding

PILOT AND FEASIBILITY STUDIESP30DK034928 · NIDDK · TUFTS MEDICAL CENTER · PI PLAUT, ANDREW GEORGE · 1986 to 2007
$8.5M
TRANSCRIPTIONAL REPRESSION AND CELL CYCLE MECHANISMSR01GM044634 · NIGMS · TUFTS UNIVERSITY BOSTON · PI YEE, AMY S. · 1991 to 2000
$363k
NIDDK NIH HHS P30 DK034928NIDDK NIH HHS P30 DK34928NIGMS NIH HHS GM44634
6 · The paper itself

Abstract

In certain cancers, constitutive Wnt signaling results from mutation in one or more pathway components. The result is the accumulation and nuclear localization of beta-catenin, which interacts with the lymphoid enhancer factor-1 (LEF)/T-cell factor (TCF) family of HMG-box transcription factors, which activate important growth regulatory genes, including cyclin D1 and c-myc. As exemplified by APC and axin, the negative regulation of beta-catenin is important for tumor suppression. Another potential mode of negative regulation is transcriptional repression of cyclin D1 and other Wnt target genes. In mammals, the transcriptional repressors in the Wnt pathway are not well defined. We have previously identified HBP1 as an HMG-box repressor and a cell cycle inhibitor. Here, we show that HBP1 is a repressor of the cyclin D1 gene and inhibits the Wnt signaling pathway. The inhibition of Wnt signaling and growth requires a common domain of HBP1. The apparent mechanism is an inhibition of TCF/LEF DNA binding through a physical interaction with HBP1. These data suggest that the suppression of Wnt signaling by HBP1 may be a mechanism to prevent inappropriate proliferation.

Indexed as

Gene Expression Regulation, NeoplasticSignal TransductionTrans-ActivatorsZebrafish Proteinsbeta CateninCaco-2 CellsCell Line, TransformedCyclin D1Cytoskeletal ProteinsDNADNA-Binding ProteinsGrowth InhibitorsHigh Mobility Group ProteinsHumansLymphoid Enhancer-Binding Factor 1Proto-Oncogene Proteinsbeta CateninCTNNB1 protein, humanCyclin D1Cytoskeletal ProteinsDNADNA-Binding ProteinsGrowth InhibitorsHBP1 protein, humanHigh Mobility Group ProteinsLymphoid Enhancer-Binding Factor 1Proto-Oncogene ProteinsRepressor ProteinsTCF7L2 protein, humanTCF Transcription FactorsTrans-ActivatorsTranscription Factor 7-Like 2 ProteinTranscription FactorsWnt ProteinsZebrafish Proteins

Identifiers

PMID11500377
PMCPMC125566
OpenAlexW2000813640

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.