Evidence map›Paper›PMID 31979076›Full record

ReviewInternational journal of molecular sciences2020

High Mobility Group A (HMGA): Chromatin Nodes Controlled by a Knotty miRNA Network.

Riccardo Sgarra, Silvia Pegoraro, Daniela D'Angelo, Gloria Ros, Rossella Zanin, Michela Sgubin, Sara Petrosino, Sabrina Battista, Guidalberto Manfioletti

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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 2 institutions in 1 country.

Riccardo SgarraDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
Silvia PegoraroDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
Daniela D'AngeloIstituto per l'Endocrinologia e l'Oncologia Sperimentale (IEOS) "G. Salvatore", Consiglio Nazionale delle Ricerche (CNR) c/o Dipartimento di Medicina Molecolare e Biotecnologie Mediche (DMMBM), Università degli Studi di Napoli "Federico II", Via Pansini 5, 80131 Napoli, Italy.
Gloria RosDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
Rossella ZaninDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
Michela SgubinDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
Sara PetrosinoDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
Sabrina BattistaIstituto per l'Endocrinologia e l'Oncologia Sperimentale (IEOS) "G. Salvatore", Consiglio Nazionale delle Ricerche (CNR) c/o Dipartimento di Medicina Molecolare e Biotecnologie Mediche (DMMBM), Università degli Studi di Napoli "Federico II", Via Pansini 5, 80131 Napoli, Italy.
Guidalberto ManfiolettiDipartimento di Scienze della Vita, Università degli Studi di Trieste, 34127 Trieste, Italy.
University of Trieste · ITInstitute for Experimental Endocrinology and Oncology · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG18385Regione Autonoma Friuli Venezia Giulia RiFTRegione Autonoma Friuli Venezia Giulia TNBCneo
6 · The paper itself

Abstract

High mobility group A (HMGA) proteins are oncofoetal chromatin architectural factors that are widely involved in regulating gene expression. These proteins are unique, because they are highly expressed in embryonic and cancer cells, where they play a relevant role in cell proliferation, stemness, and the acquisition of aggressive tumour traits, i.e., motility, invasiveness, and metastatic properties. The HMGA protein expression levels and activities are controlled by a connected set of events at the transcriptional, post-transcriptional, and post-translational levels. In fact, microRNA (miRNA)-mediated RNA stability is the most-studied mechanism of HMGA protein expression modulation. In this review, we contribute to a comprehensive overview of HMGA-targeting miRNAs; we provide detailed information regarding HMGA gene structural organization and a comprehensive evaluation and description of HMGA-targeting miRNAs, while focusing on those that are widely involved in HMGA regulation; and, we aim to offer insights into HMGA-miRNA mutual cross-talk from a functional and cancer-related perspective, highlighting possible clinical implications.

Indexed as

AnimalsChromatinGene Expression Regulation, NeoplasticHMGA ProteinsHumansMicroRNAsNeoplasmsChromatinHMGA ProteinsMicroRNAscancerHigh mobility group AmiRNApost-transcriptional regulation

Identifiers

PMID31979076
PMCPMC7038092
OpenAlexW3001730383

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.