Evidence map›Paper›PMID 22139073›Full record

ArticleOncogene2012

Downregulation of HMGA-targeting microRNAs has a critical role in human pituitary tumorigenesis.

D Palmieri, D D'Angelo, T Valentino, I De Martino, A Ferraro, A Wierinckx, M Fedele, J Trouillas, A Fusco

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 90 citations in OpenAlex.

  1. High mobility group A protein-2 as a tumor cancer diagnostic and prognostic marker: a systematic review and meta-analysis.European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) · 2020
    Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Architects of Pituitary Tumour Growth.Frontiers in endocrinology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. IncreasedDiagnostics (Basel, Switzerland) · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. MicroRNA in Acupuncture Studies: Does Small RNA Shed Light on the Biological Mechanism of Acupuncture?Evidence-based complementary and alternative medicine : eCAM · 2019
    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

9 authors at 4 institutions in 2 countries.

D PalmieriIstituto di Endocrinologia ed Oncologia Sperimentale del CNR Dipartimento di Biologia e Patologia Cellulare e Molecolare Facoltà di Medicina e Chirurgia di Napoli, Università degli Studi di Napoli Federico II, Naples, Italy.
D D'Angelo
T Valentino
I De Martino
A Ferraro
A Wierinckx
M Fedele
J Trouillas
A Fusco
Institute for Experimental Endocrinology and Oncology · ITUniversity of Naples Federico II · ITCentre de Recherche en Neurosciences de Lyon · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have demonstrated that high mobility group A proteins have a critical role on the onset of human pituitary adenomas. Indeed, both high mobility group A (HMGA) genes are overexpressed in pituitary adenomas, and consistently transgenic mice overexpressing either the Hmga1 or the Hmga2 gene develop mixed growth hormone/prolactin (GH-PRL)-secreting pituitary adenomas. Trisomy of chromosome 12, where HMGA2 is located, and/or amplification of the HMGA2 gene locus account for the HMGA2 overexpression in most human prolactinomas. Conversely, HMGA1 overexpression is not associated to any rearrangement or amplification of the HMGA1 locus. We have first identified micro RNAs (miRNAs) able to target both HMGA1 and HMGA2 messenger RNAs. Then, all of these miRNAs have been found downregulated in pituitary adenomas of different histotypes, compared with normal pituitary. Interestingly, their downregulation was also observed in nonfunctioning pituitary adenomas where HMGA2 overexpression is not associated to any alteration of the HMGA2 locus. Functional studies show that all these HMGA-targeting miRNAs inhibit the proliferation of the rat pituitary adenoma cell line GH3. Therefore, these results indicate that the downregulation of the miRNAs able to target the HMGA genes could contribute to increase HMGA protein levels in human pituitary adenomas, and then to pituitary tumorigenesis.

Indexed as

3' Untranslated RegionsAnimalsBase SequenceBinding SitesBlotting, WesternCell LineCell Line, TumorCell Transformation, NeoplasticHMGA1a ProteinHMGA2 ProteinHMGA ProteinsHumansMicroRNAsPituitary NeoplasmsReverse Transcriptase Polymerase Chain ReactionSequence Homology, Nucleic Acid3' Untranslated RegionsHMGA1a ProteinHMGA2 ProteinHMGA ProteinsMicroRNAsMIRN15 microRNA, humanMIRN16 microRNA, humanMIRN196 microRNA, humanMIRN26 microRNA, humanmirnlet7 microRNA, human

Identifiers

PMID22139073
OpenAlexW2037170170

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.