Evidence map›Paper›PMID 36902215›Full record

ArticleInternational journal of molecular sciences2023

PARP-1 Expression Influences Cancer Stem Cell Phenotype in Colorectal Cancer Depending on p53.

Jose D Puentes-Pardo, Sara Moreno-SanJuan, Jorge Casado, Julia Escudero-Feliu, David López-Pérez, Paula Sánchez-Uceta, Paula González-Novoa, Julio Gálvez, Ángel Carazo, Josefa León

Open access · goldFull text read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 20 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

10 authors at 2 institutions in 1 country.

Jose D Puentes-PardoInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.ORCID 0000-0002-6417-6019
Sara Moreno-SanJuanInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
Jorge CasadoInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
Julia Escudero-FeliuInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
David López-PérezInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
Paula Sánchez-UcetaInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
Paula González-NovoaInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
Julio GálvezInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.ORCID 0000-0001-6876-3782
Ángel CarazoInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.
Josefa LeónInstituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.ORCID 0000-0002-0543-4823
Instituto de Investigación Biosanitaria de Granada · ESUniversidad de Granada · ES

Funding

Instituto de Salud Carlos III PI18/01947
6 · The paper itself

Abstract

Poly(ADP-ribose) polymerase-1 (PARP-1) is a protein involved in multiple physiological processes. Elevated PARP-1 expression has been found in several tumours, being associated with stemness and tumorigenesis. In colorectal cancer (CRC), some controversy among studies has been described. In this study, we analysed the expression of PARP-1 and cancer stem cell (CSC) markers in CRC patients with different p53 status. In addition, we used an in vitro model to evaluate the influence of PARP-1 in CSC phenotype regarding p53. In CRC patients, PARP-1 expression correlated with the differentiation grade, but this association was only maintained for tumours harbouring wild-type p53. Additionally, in those tumours, PARP-1 and CSC markers were positively correlated. In mutated p53 tumours, no associations were found, but PARP-1 was an independent factor for survival. According to our in vitro model, PARP-1 regulates CSC phenotype depending on p53 status. PARP-1 overexpression in a wild type p53 context increases CSC markers and sphere forming ability. By contrast, those features were reduced in mutated p53 cells. These results could implicate that patients with elevated PARP-1 expression and wild type p53 could benefit from PARP-1 inhibition therapies, meanwhile it could have adverse effects for those carrying mutated p53 tumours.

Indexed as

Colorectal NeoplasmsNeoplastic Stem CellsPoly (ADP-Ribose) Polymerase-1Tumor Suppressor Protein p53HumansPhenotypePoly(ADP-ribose) Polymerase InhibitorsPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsTumor Suppressor Protein p53cancer stem cellscolorectal cancerp53PARP-1

Identifiers

PMID36902215
PMCPMC10002521
OpenAlexW4322771003

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read18
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.