Evidence map›Paper›PMID 17911264›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Tumor protein 53-induced nuclear protein 1 expression is repressed by miR-155, and its restoration inhibits pancreatic tumor development.

Meritxell Gironella, Mylène Seux, Min-Jue Xie, Carla Cano, Richard Tomasini, Julien Gommeaux, Stephane Garcia, Jonathan Nowak, Man Lung Yeung, Kuan-Teh Jeang and 12 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 282 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
282citing papers in PubMed, 1 pooled it
15.4field-weighted citation impact, top 1% 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

282 citing papers in PubMed, 1 synthesis or guideline pooled it, 550 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

222 more citing papers are in PubMed but not listed here.

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

22 authors at 9 institutions in 5 countries.

Meritxell GironellaInstitut National de Santé et de Recherche Médicale, U624 Stress Cellulaire, F-13288 Marseille, France.
Mylène Seux
Min-Jue Xie
Carla Cano
Richard Tomasini
Julien Gommeaux
Stephane Garcia
Jonathan Nowak
Man Lung Yeung
Kuan-Teh Jeang
Amandine Chaix
Ladan Fazli
Yoshiharu Motoo
Qing Wang
Palma Rocchi
Antonio Russo
Martin Gleave
Jean-Charles Dagorn
Juan L Iovanna
Alice Carrier
Marie-Josèphe Pébusque
Nelson J Dusetti
University of Toronto · CAInserm · FRUniversity of Palermo · ITAix-Marseille Université · FRInstitut de Neurobiologie de la Méditerranée · FRNational Institute of Allergy and Infectious Diseases · USVancouver General Hospital · CACentre Léon Bérard · FRKanazawa Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is a disease with an extremely poor prognosis. Tumor protein 53-induced nuclear protein 1 (TP53INP1) is a proapoptotic stress-induced p53 target gene. In this article, we show by immunohistochemical analysis that TP53INP1 expression is dramatically reduced in pancreatic ductal adenocarcinoma (PDAC) and this decrease occurs early during pancreatic cancer development. TP53INP1 reexpression in the pancreatic cancer-derived cell line MiaPaCa2 strongly reduced its capacity to form s.c., i.p., and intrapancreatic tumors in nude mice. This anti-tumoral capacity is, at least in part, due to the induction of caspase 3-mediated apoptosis. In addition, TP53INP1(-/-) mouse embryonic fibroblasts (MEFs) transformed with a retrovirus expressing E1A/ras(V12) oncoproteins developed bigger tumors than TP53INP1(+/+) transformed MEFs or TP53INP1(-/-) transformed MEFs with restored TP53INP1 expression. Finally, TP53INP1 expression is repressed by the oncogenic micro RNA miR-155, which is overexpressed in PDAC cells. TP53INP1 is a previously unknown miR-155 target presenting anti-tumoral activity.

Indexed as

AnimalsBase SequenceCarcinoma, Pancreatic DuctalCarrier ProteinsCell Line, TumorCell Transformation, NeoplasticGene ExpressionHeat-Shock ProteinsHumansMiceMice, KnockoutMice, NudeMicroRNAsNeoplasm TransplantationNuclear ProteinsPancreatic NeoplasmsCarrier ProteinsHeat-Shock ProteinsMicroRNAsNuclear ProteinsRNA, NeoplasmTP53INP1 protein, humanTP53 protein, humantumor protein 53-induced nuclear protein 1, mouseTumor Suppressor Protein p53

Identifiers

PMID17911264
PMCPMC2042180
OpenAlexW2047213909

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.