Evidence map›Paper›PMID 26993766›Full record

ArticleOncotarget2016

Implication of NPM1 phosphorylation and preclinical evaluation of the nucleoprotein antagonist N6L in prostate cancer.

Damien Destouches, Maha Sader, Stéphane Terry, Charles Marchand, Pascale Maillé, Pascale Soyeux, Gilles Carpentier, Fannie Semprez, Jocelyn Céraline, Yves Allory and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Overexpression of Nucleolin and Associated Genes in Prostate Cancer.International journal of molecular sciences · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
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

13 authors at 4 institutions in 1 country.

Damien DestouchesUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Maha SaderUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Stéphane TerryINSERM, U1186, Gustave Roussy Cancer Campus, Villejuif, F-94805, France.
Charles MarchandUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Pascale MailléUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Pascale SoyeuxUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Gilles CarpentierUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Fannie SemprezUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Jocelyn CéralineINSERM, U1113, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, F-67000, France.
Yves AlloryUniversité Paris-Est, UPEC, Créteil, F-94000, France.
José CourtyUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Alexandre De La TailleUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Francis VacherotUniversité Paris-Est, UPEC, Créteil, F-94000, France.
Université Paris-Est Créteil · FRInserm · FRCentre National de la Recherche Scientifique · FRHôpital Albert-Chenevier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the advent of several new treatment options over the past years, advanced/metastatic prostate carcinoma (PCa) still remains incurable, which justifies the search for novel targets and therapeutic molecules. Nucleophosmin (NPM1) is a shuttling nucleoprotein involved in tumor growth and its targeting could be a potential approach for cancer therapy. We previously demonstrated that the multivalent pseudopeptide N6L binds to NPM1 potently affecting in vitro and in vivo tumor cell growth of various tumor types as well as angiogenesis. Furthermore, NPM1 binds to androgen receptor (AR) and modulate its activity. In this study, we first investigated the implication of the NPM1 and its Thr199 and Thr234/237 phosphorylated forms in PCa. We showed that phosphorylated forms of NPM1 interact with androgen receptor (AR) in nucleoplasm. N6L treatment of prostate tumor cells led to inhibition of NPM1 phosphorylation in conjunction with inhibition of AR activity. We also found that total and phosphorylated NPM1 were overexpressed in castration-resistant PCa. Assessment of the potential therapeutic role of N6L in PCa indicated that N6L inhibited tumor growth both in vitro and in vivo when used either alone or in combination with the standard-of-care first- (hormonotherapy) and second-line (docetaxel) treatments for advanced PCa. Our findings reveal the role of Thr199 and Thr234/237 phosphorylated NPM1 in PCa progression and define N6L as a new drug candidate for PCa therapy.

Indexed as

Xenograft Model Antitumor AssaysAnimalsAntineoplastic AgentsCell Line, TumorDocetaxelHumansMaleMice, NudeNuclear ProteinsNucleophosminNucleoproteinsPeptidesPhosphorylationProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantProtein BindingAntineoplastic AgentsAR protein, humanDocetaxelN6L peptideNPM1 protein, humanNpm1 protein, mouseNuclear ProteinsNucleophosminNucleoproteinsPeptidesReceptors, AndrogenTaxoidsThreonineandrogen receptorN6LNPM1phosphorylated NPM1prostate cancer

Identifiers

PMID26993766
PMCPMC5342486
OpenAlexW2307467276

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.