Evidence map›Paper›PMID 15467753›Full record

ArticleOncogene2004

NHERF (Na+/H+ exchanger regulatory factor) gene mutations in human breast cancer.

Jia Le Dai, Lei Wang, Aysegul A Sahin, Lyle D Broemeling, Mieke Schutte, Yong Pan

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 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.5field-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

45 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. New roles of the NaAmerican journal of physiology. Renal physiology · 2020
    Review
  6. Article
  7. Loss of the NaThe American journal of pathology · 2019
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells.International journal of molecular sciences · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Novel bioactivity of NHERF1 in corneal neovascularization.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2012
    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

6 authors at 2 institutions in 2 countries.

Jia Le DaiDepartment of Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. jldai@mdanderson.org
Lei Wang
Aysegul A Sahin
Lyle D Broemeling
Mieke Schutte
Yong Pan
The University of Texas MD Anderson Cancer Center · USMeertens Institute · NL

Funding

SYK SIGNALING AND BREAST CANCER INVASIONR01CA100278 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DAI, JIALE · 2003 to 2007
$1.3M
NCI NIH HHS R01 CA100278
6 · The paper itself

Abstract

Yeast two-hybrid screening was used to explore novel proteins that interact with a breast tumor or metastasis suppressor, SYK (spleen tyrosine kinase). The screening yielded NHERF (Na+/H+ exchanger regulatory factor, also known as NHERF1 or EBP-50) that binds to the interdomain B of SYK. NHERF is an estrogen-responsive gene that encodes an inhibitory factor for epithelial Na+/H+ exchanger isoform 3 (NHE3). We found intragenic mutation of the NHERF gene accompanied by loss of heterzygosity (LOH) in approximately 3% (3/85) of breast cancer cell lines and primary breast tumors. Mutations occurred at the conserved PDZ domains at NHERF NH2-terminus that bound to SYK, or at its COOH-terminus motif that binds to MERLIN, the product of Neurofibromatosis 2 (NF2) tumor suppressor gene. NHERF tumorigenic mutations decreased or abolished its interaction with SYK or MERLIN, suggesting a pathway link among these three molecules that may play a critical role in mammary neoplastic progression. Primary breast tumors with LOH at the NHERF locus had clinical presentations of higher aggressiveness, indicating that deregulated NHERF signaling may be associated with disease progression. Moreover, the LOH was inversely correlated with SYK promoter methylation, suggesting that NHERF and SYK may transduce a common suppressive signal. Taken together, the results indicated NHERF to be a candidate tumor suppressor gene in human breast carcinoma that may be interconnected to the SYK and MERLIN suppressors.

Indexed as

Base SequenceBreast NeoplasmsConserved SequenceDisease ProgressionEnzyme PrecursorsHumansIntracellular Signaling Peptides and ProteinsLoss of HeterozygosityMutationNeurofibromin 2PhosphoproteinsProtein BindingProtein Structure, TertiaryProtein-Tyrosine KinasesSodium-Hydrogen ExchangersSyk KinaseEnzyme PrecursorsIntracellular Signaling Peptides and ProteinsNeurofibromin 2PhosphoproteinsProtein-Tyrosine Kinasessodium-hydrogen exchanger regulatory factorSodium-Hydrogen ExchangersSyk KinaseSYK protein, human

Identifiers

PMID15467753
OpenAlexW2152086857

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.