Evidence map›Paper›PMID 27413734›Full record

ReviewBioMed research international2016

Manipulation of DNA Repair Proficiency in Mouse Models of Colorectal Cancer.

Michael A Mcilhatton, Gregory P Boivin, Joanna Groden

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Investigating Tumor Heterogeneity in Mouse Models.Annual review of cancer biology · 2020
    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

3 authors at 2 institutions in 1 country.

Michael A McilhattonDepartment of Cancer Biology and Genetics, The Ohio State University, 460 West 12th Avenue, Columbus, OH 43210, USA.ORCID 0000-0002-7304-4528
Gregory P BoivinDepartment of Pathology, Boonshoft School of Medicine, Wright State University, Health Sciences Building 053, 3640 Colonel Glenn Highway, Dayton, OH 45435, USA.
Joanna GrodenDepartment of Cancer Biology and Genetics, The Ohio State University, 460 West 12th Avenue, Columbus, OH 43210, USA.ORCID 0000-0001-8507-6423
The Ohio State University · USWright State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
CHARACTERIZATION OF TUMOR SUPPRESSION BY THE APC GENER01CA063507 · NCI · UNIVERSITY OF CINCINNATI · PI GRODEN, JOANNA LOUISE · 2000 to 2010
$2.7M
Functions of the BLM Helicase in Telomere MaintenanceR01CA117898 · NCI · OHIO STATE UNIVERSITY · PI GRODEN, JOANNA LOUISE · 2008 to 2012
$1.5M
TUMOR SUPPRESSION BY THE APC GENER29CA063507 · NCI · UNIVERSITY OF CINCINNATI · PI GRODEN, JOANNA LOUISE · 1995 to 1999
–
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA063507NCI NIH HHS R01 CA117898NCI NIH HHS R29 CA063507
6 · The paper itself

Abstract

Technical and biological innovations have enabled the development of more sophisticated and focused murine models that increasingly recapitulate the complex pathologies of human diseases, in particular cancer. Mouse models provide excellent in vivo systems for deciphering the intricacies of cancer biology within the context of precise experimental settings. They present biologically relevant, adaptable platforms that are amenable to continual improvement and refinement. We discuss how recent advances in our understanding of tumorigenesis and the underlying deficiencies of DNA repair mechanisms that drive it have been informed by using genetically engineered mice to create defined, well-characterized models of human colorectal cancer. In particular, we focus on how mechanisms of DNA repair can be manipulated precisely to create in vivo models whereby the underlying processes of tumorigenesis are accelerated or attenuated, dependent on the composite alleles carried by the mouse model. Such models have evolved to the stage where they now reflect the initiation and progression of sporadic cancers. The review is focused on mouse models of colorectal cancer and how insights from these models have been instrumental in shaping our understanding of the processes and potential therapies for this disease.

Indexed as

AnimalsCarcinogenesisColorectal NeoplasmsDisease Models, AnimalDNA RepairHumansMice

Identifiers

PMID27413734
PMCPMC4931062
OpenAlexW2443550871

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.