Evidence map›Paper›PMID 19901968›Full record

ArticleOncogene2010

A 'DNA replication' signature of progression and negative outcome in colorectal cancer.

M-J Pillaire, J Selves, K Gordien, P-A Gourraud, P-A Gouraud, C Gentil, M Danjoux, C Do, V Negre, A Bieth and 6 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
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  11. The mJournal of cancer research and clinical oncology · 2024
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  19. RIP140 regulatesCancer drug resistance (Alhambra, Calif.) · 2022
    Article
  20. Article

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

4 · The record

Corrections and comments

  • Erratum issued
    Gouraud, P-A [corrected to Gourraud, P-A]
5 · Who and what money

Authors and funding

16 authors at 7 institutions in 1 country.

M-J PillaireGenetic Instability and Cancer Group, Department Biology of Cancer, Institute of Pharmacology and Structural Biology, UMR5089 CNRS, University of Toulouse, University Paul Sabatier, Toulouse, France.
J Selves
K Gordien
P-A Gourraud
P-A Gouraud
C Gentil
M Danjoux
C Do
V Negre
A Bieth
R Guimbaud
D Trouche
P Pasero
M Méchali
J-S Hoffmann
C Cazaux
Inserm · FRInstitut de Pharmacologie et de Biologie Structurale · FRUniversité Toulouse III - Paul Sabatier · FRInstitut de Génétique Humaine · FRCentre National de la Recherche Scientifique · FRLaboratoire de Biologie Cellulaire et Moléculaire du Contrôle de la Prolifération · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is one of the most frequent cancers worldwide. As the tumor-node-metastasis (TNM) staging classification does not allow to predict the survival of patients in many cases, additional prognostic factors are needed to better forecast their outcome. Genes involved in DNA replication may represent an underexplored source of such prognostic markers. Indeed, accidents during DNA replication can trigger 'replicative stress', one of the main features of cancer from earlier stages onward. In this study, we assessed the expression of 47 'DNA replication' genes in primary tumors and adjacent normal tissues from a homogeneous series of 74 patients. We found that genes coding for translesional (TLS) DNA polymerases, initiation of DNA replication, S-phase signaling and protection of replication forks were significantly deregulated in tumors. We also observed that the overexpression of either the MCM7 helicase or the TLS DNA polymerase POLQ (if also associated with a concomitant overexpression of firing genes) was significantly related to poor patient survival. Our data suggest the existence of a 'DNA replication signature' that might represent a source of new prognostic markers. Such a signature could help in understanding the molecular mechanisms underlying tumor progression in colorectal cancer patients.

Indexed as

Disease ProgressionDNA ReplicationCell Cycle ProteinsColorectal NeoplasmsDNA-Binding ProteinsDNA-Directed DNA PolymeraseDNA Polymerase thetaGene Expression Regulation, NeoplasticHumansMinichromosome Maintenance Complex Component 7Multigene FamilyNuclear ProteinsPrognosisCell Cycle ProteinsDNA-Binding ProteinsDNA-Directed DNA PolymeraseDNA Polymerase thetaMCM7 protein, humanMinichromosome Maintenance Complex Component 7Nuclear Proteins

Identifiers

PMID19901968
OpenAlexW2044671527

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.