Evidence map›Paper›PMID 15064745›Full record

ArticleOncogene2004

Deregulated expression of LRBA facilitates cancer cell growth.

Jia-Wang Wang, Joshua J Gamsby, Steven L Highfill, Linda B Mora, Gregory C Bloom, Tim J Yeatman, Tien-chi Pan, Anna L Ramne, Lewis A Chodosh, W Douglas Cress and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

42 citing papers in PubMed, 79 citations in OpenAlex.

  1. LRBA organizes distinct vesicular trafficking systems in distal nephron segments for water and sodium conservation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Transcriptomic Changes ofFrontiers in microbiology · 2022
    Article
  9. Review
  10. Review
  11. Observational
  12. Discovery and validation of surfaceJournal for immunotherapy of cancer · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. LRBA in the endomembrane system.Colombia medica (Cali, Colombia) · 2018
    Review
  18. Article
  19. Article
  20. Immunological phenotype of the murine Lrba knockout.Immunology and cell biology · 2017
    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

12 authors at 6 institutions in 1 country.

Jia-Wang WangImmunology Programs and Department of Interdisciplinary Oncology, H Lee Moffitt Comprehensive Cancer Center and Research Institute, University of South Florida College of Medicine, Tampa, FL 33612, USA.
Joshua J Gamsby
Steven L Highfill
Linda B Mora
Gregory C Bloom
Tim J Yeatman
Tien-chi Pan
Anna L Ramne
Lewis A Chodosh
W Douglas Cress
Jiandong Chen
William G Kerr
Florida College · USMoffitt Cancer Center · USUniversity of South Florida · USUniversity of Tampa · USUPMC Hillman Cancer Center · USUniversity of Pennsylvania · US

Funding

SCID HU MODEL FOR HIV INFECTION OF THE CNSP01NS027405 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI GONZALEZ-SCARANO, FRANCISCO · 1989 to 2007
$8.2M
Role of SHIP in NK Cell BiologyR01HL072523 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI KERR, WILLIAM GARROW · 2002 to 2014
$4.3M
C-MPL AND EARLY HUMAN HEMATOPOIESISR01DK054767 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI KERR, WILLIAM GARROW · 1999 to 2003
$1.3M
NHLBI NIH HHS R01 HL72523NIDDK NIH HHS R01 DK54767NINDS NIH HHS P01 NS27405
6 · The paper itself

Abstract

LRBA expression is induced by mitogens in lymphoid and myeloid cells. The Drosophila LRBA orthologue rugose/DAKAP550 is involved in Notch, Ras and EGFR pathways. These findings suggest that LRBA could play a role in cell types that have increased proliferative and survival capacity. Here, we show by microarray and real-time PCR analyses that LRBA is overexpressed in several different cancers relative to their normal tissue controls. We also show that LRBA promoter activity and endogenous LRBA mRNA levels are reduced by p53 and increased by E2F1, indicating that mutations in the tumor suppressors p53 and Rb could contribute to the deregulation of LRBA. Furthermore, inhibition of LRBA expression by RNA interference, or inhibition of its function by a dominant-negative mutant, leads to significant growth inhibition of cancer cells, demonstrating that deregulated expression of LRBA contributes to the altered growth properties of a cancer cell. Finally, we show that the phosphorylation of EGFR is affected by the dominant-negative mutant, suggesting LRBA plays a role in the mammalian EGFR pathway. These findings demonstrate that LRBA facilitates cancer cell growth and thus LRBA may represent a novel molecular target for cancer therapy.

Indexed as

Cell Cycle ProteinsAdaptor Proteins, Signal TransducingBase SequenceBreast NeoplasmsCarrier ProteinsCyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsE2F1 Transcription FactorE2F Transcription FactorsFemaleHeLa CellsHumansMolecular Sequence DataNeoplasmsPromoter Regions, GeneticReceptors, EstrogenAdaptor Proteins, Signal TransducingCarrier ProteinsCell Cycle ProteinsCyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsE2F1 protein, humanE2F1 Transcription FactorE2F Transcription FactorsLRBA protein, humanprotein p23Receptors, EstrogenTranscription Factors

Identifiers

PMID15064745
OpenAlexW2048531148

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.