Evidence map›Paper›PMID 19258514›Full record

ArticleCancer research2009

Heterogeneous nuclear ribonucleoprotein K is a novel regulator of androgen receptor translation.

Nishit K Mukhopadhyay, Jayoung Kim, Bekir Cinar, Aruna Ramachandran, Martin H Hager, Dolores Di Vizio, Rosalyn M Adam, Mark A Rubin, Pradip Raychaudhuri, Arrigo De Benedetti and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. The Nuclear Translocation of Heme Oxygenase-1 in Human Diseases.Frontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Covid-19 pathogenesis in prostatic cancer and TMPRSS2-ERG regulatory genetic pathway.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 4 institutions in 1 country.

Nishit K MukhopadhyayUrological Diseases Research Center, Department of Urology, Children's Hospital Boston, Boston, MA 02115, USA.
Jayoung Kim
Bekir Cinar
Aruna Ramachandran
Martin H Hager
Dolores Di Vizio
Rosalyn M Adam
Mark A Rubin
Pradip Raychaudhuri
Arrigo De Benedetti
Michael R Freeman
Harvard University · USCornell University · USLouisiana State University Health Sciences Center Shreveport · USUniversity of Illinois Chicago · US

Funding

HEPARIN-BINDING EGF-LIKE FACTORS IN PROSTATE GROWTHR37DK047556 · NIDDK · CHILDREN'S HOSPITAL BOSTON · PI FREEMAN, MICHAEL R · 2000 to 2009
$3.0M
Membrane Microdomains in Prostate CancerR01CA112303 · NCI · CHILDREN'S HOSPITAL BOSTON · PI FREEMAN, MICHAEL R · 2005 to 2009
$1.4M
Fatty Acid Synthase, Caveolin-1 and Membrane Microdomains in Prostate CancerK99CA131472 · NCI · BOSTON CHILDREN'S HOSPITAL · PI DI VIZIO, DOLORES · 2008 to 2009
$273k
NCI NIH HHS K99 CA131472NCI NIH HHS R01 CA112303NIDDK NIH HHS R37 DK047556NIDDK NIH HHS R37 DK47556
6 · The paper itself

Abstract

The regulation of androgen receptor (AR) expression in prostate cancer is still poorly understood. The activation of the epidermal growth factor receptor (EGFR) in prostate cancer cells was previously shown to lower AR expression by a rapamycin-sensitive, posttranscriptional mechanism involving the AR mRNA 5'-untranslated region (5'-UTR). In a search for an intermediate within the EGFR/phosphoinositide 3-kinase/Akt/mammalian target of rapamycin pathway that regulates AR at this site, we identified the nucleic acid-binding protein, heterogeneous nuclear ribonucleoprotein K (hnRNP-K), by mass spectrometric analysis of Akt immune complexes from lipid raft-enriched subcellular fractions. We show here that hnRNP-K is a novel inhibitor of AR mRNA translation that regulates androgen-responsive gene expression and prostate cancer cell proliferation. A functional hnRNP-K binding site involved in down-regulating AR protein levels was identified in the AR mRNA 5'-UTR. Further analysis revealed that hnRNP-K is also able to inhibit AR translation in the absence of the 5'-UTR, consistent with the presence of additional predicted hnRNP-K binding sites within the AR open reading frame and in the 3'-UTR. Immunohistochemical analysis of a human prostate cancer tissue microarray revealed an inverse correlation between hnRNP-K expression and AR protein levels in organ-confined prostate tumors and a substantial decline in cytoplasmic hnRNP-K in metastases, despite an overall increase in hnRNP-K levels in metastatic tumors. These data suggest that translational inhibition of AR by hnRNP-K may occur in organ-confined tumors but possibly at a reduced level in metastases. HnRNP-K is the first protein identified that directly interacts with and regulates the AR translational apparatus.

Indexed as

Androgen Receptor AntagonistsAnimalsBinding SitesCell Line, TumorChlorocebus aethiopsCOS CellsDown-RegulationHeLa CellsHeterogeneous-Nuclear Ribonucleoprotein KHumansMalePromoter Regions, GeneticProstate-Specific AntigenProstatic NeoplasmsProtein BiosynthesisReceptors, AndrogenAndrogen Receptor AntagonistsHeterogeneous-Nuclear Ribonucleoprotein KProstate-Specific AntigenReceptors, AndrogenRNA, Messenger

Identifiers

PMID19258514
PMCPMC2659763
OpenAlexW2102576322

What OpenQuestion holds

Textmetadata
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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.