Evidence map›Paper›PMID 16832349›Full record

ArticleOncogene2007

Role of PSF-TFE3 oncoprotein in the development of papillary renal cell carcinomas.

M Mathur, H H Samuels

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 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
1.3field-weighted citation impact, top 20% 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, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Activators of G protein signaling in the kidney.The Journal of pharmacology and experimental therapeutics · 2015
    Review
  7. Review
  8. Review
  9. Article
  10. Genomic heterogeneity of translocation renal cell carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  11. Article
  12. Oncogenic gene fusions in epithelial carcinomas.Current opinion in genetics & development · 2009
    Review
  13. Fusion of the GenesCancer genomics & proteomics
    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

2 authors at 1 institution in 1 country.

M MathurDepartment of Pharmacology, New York University School of Medicine, New York, NY 10016, USA. mathum01@med.nyu.edu
H H Samuels
New York University · US

Funding

METABOLIC EFFECTS OF THYROID HORMONE IN CELL CULTURER01DK016636 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SAMUELS, HERBERT H · 1986 to 2007
$6.0M
THYROID/RETINOIC ACID RECEPTOR INTERACTING PROTEINSK01AR002083 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MATHUR, MUKUL · 2000 to 2004
$553k
Metabolic Effects of Thyroid HormoneR56DK016636 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SAMUELS, HERBERT H · 2009 to 2009
$211k
METABOLIC EFFECTS OF THYROID HORMONER37DK016636 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SAMUELS, HERBERT H · 1991 to 1998
–
NIAMS NIH HHS AR02083NIDDK NIH HHS DK16636
6 · The paper itself

Abstract

A subset of papillary renal cell carcinomas (RCC) is characterized by the expression of a TFE3 fusion protein, where the fusion partner can be any of the several proteins identified so far such as PSF (PTB associated splicing factor), NonO, PRCC, CLTC and ASPL. These proteins result from chromosomal translocations involving the TFE3 gene located on the X chromosome. Our present study documents the central role of PSF-TFE3 in oncogenic transformation. We show that the inhibition of PSF-TFE3 expression through siRNA or shRNA leads to impaired growth, proliferation, invasion potential and long-term survival of UOK-145 papillary renal carcinoma-derived cells, which endogenously express PSF-TFE3. The oncogenic potential of PSF-TFE3 became evident by stable expression of PSF-TFE3 in NIH-3T3 mouse fibroblast cells, which leads to the acquisition of anchorage-independent growth as revealed by soft agar assay. In addition, the expression of PSF-TFE3 in normal renal proximal tubular epithelial cells from where such tumors originate leads to dedifferentiation and loss of some key functional proteins, which may reflect an initial step in the multistep process of tumor development. This suggests that the expression of PSF-TFE3 in renal epithelial cells plays an important role in the initiation and maintenance of oncogenic phenotype in papillary RCC.

Indexed as

AnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarcinoma, PapillaryCarcinoma, Renal CellCell AdhesionCell ProliferationCells, CulturedCell SurvivalCell Transformation, NeoplasticEpithelial CellsHumansKidney NeoplasmsKidney Tubules, ProximalMiceNeoplasm InvasivenessNeovascularization, PathologicBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsOncogene Proteins, FusionPTB-Associated Splicing FactorRNA-Binding ProteinsRNA, Small InterferingTFE3 protein, human

Identifiers

PMID16832349
OpenAlexW2013121856

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.