Evidence map›Paper›PMID 37013641›Full record

ArticleJournal of hematology & oncology2023

PARP1 negatively regulates MAPK signaling by impairing BRAF-X1 translation.

Andrea Marranci, Antonella Prantera, Simona Masotti, Raffaella De Paolo, Caterina Baldanzi, Maurizio S Podda, Serena Mero, Marianna Vitiello, Cinzia Franchin, Mariavittoria Laezza and 5 more

Open access · goldAbstract readLetter
In one paragraph

Article in Journal of hematology & oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.5field-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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. MAP2K6 reprograms NADCell death & disease · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. 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

15 authors at 7 institutions in 2 countries.

Andrea MarranciInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy. andrea.marranci@gmail.com.ORCID 0000-0002-8334-8795
Antonella PranteraInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Simona MasottiInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Raffaella De PaoloInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Caterina BaldanziInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Maurizio S PoddaInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Serena MeroInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Marianna VitielloInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Cinzia FranchinDepartment of Biomedical Sciences, University of Padova, Padua, Italy.
Mariavittoria LaezzaInstitute of Genetics and Biophysics "Adriano Buzzati Traverso", CNR, Naples, Italy.
Laura ComelliInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Giorgio ArrigoniDepartment of Biomedical Sciences, University of Padova, Padua, Italy.
Tiziana CervelliInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy.
Giovanna Del PozzoInstitute of Genetics and Biophysics "Adriano Buzzati Traverso", CNR, Naples, Italy.
Laura PolisenoInstitute of Clinical Physiology (IFC), CNR, Via Moruzzi 1, 56124, Pisa, Italy. laura.poliseno@cnr.it.ORCID 0000-0001-6557-955X
Istituto di Fisiologia Clinica · ITUniversity of Siena · ITInstitute of Genetics and Biophysics · ITUniversity of Padua · ITFondazione Pisa · ITIstituto di Scienza e Tecnologie dell'Informazione "Alessandro Faedo" · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In human cells BRAF oncogene is invariably expressed as a mix of two coding transcripts: BRAF-ref and BRAF-X1. These two mRNA isoforms, remarkably different in the sequence and length of their 3'UTRs, are potentially involved in distinct post-transcriptional regulatory circuits. Herein, we identify PARP1 among the mRNA Binding Proteins that specifically target the X1 3'UTR in melanoma cells. Mechanistically, PARP1 Zinc Finger domain down-regulates BRAF expression at the translational level. As a consequence, it exerts a negative impact on MAPK pathway, and sensitizes melanoma cells to BRAF and MEK inhibitors, both in vitro and in vivo. In summary, our study unveils PARP1 as a negative regulator of the highly oncogenic MAPK pathway in melanoma, through the modulation of BRAF-X1 expression.

Indexed as

MelanomaProto-Oncogene Proteins B-rafCell Line, TumorHumansIndolesMAP Kinase Signaling SystemPoly (ADP-Ribose) Polymerase-1Protein Kinase InhibitorsSulfonamidesVemurafenibBRAF protein, humanIndolesPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Protein Kinase InhibitorsProto-Oncogene Proteins B-rafSulfonamidesVemurafenibBRAF-X1MAPK pathwayMelanomamRBPPARP1Vemurafenib

Identifiers

PMID37013641
PMCPMC10071733
OpenAlexW4362521332

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.