Evidence map›Paper›PMID 9671748›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Tumors of DNA mismatch repair-deficient hosts exhibit dramatic increases in genomic instability.

A Baross-Francis, S E Andrew, J E Penney, F R Jirik

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.8field-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

11 citing papers in PubMed, 37 citations in OpenAlex.

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  7. A new mutator phenotype in breast cancer?Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  8. Genetic instability favoring transversions associated with ErbB2-induced mammary tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
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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

4 authors at 1 institution in 1 country.

A Baross-FrancisCenter for Molecular Medicine and Therapeutics, and Department of Medicine, University of British Columbia, Vancouver, BC Canada V5Z 4H4.
S E Andrew
J E Penney
F R Jirik
University of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA mismatch repair (MMR) deficiency is associated with an increased mutational burden and predisposition to certain malignancies. Relatively little is known, however, about gene-specific mutation frequencies within MMR-deficient primary tumors. Thymic lymphomas from Msh2(-/-) mice were thus analyzed by using a lacI-based transgenic shuttle-phage mutation detection system. All tumors exhibited greatly elevated lacI gene mutation frequencies, ranging from 3.2- to 17.4-fold above the approximately 15-fold elevations present within normal Msh2(-/-) thymi. In addition, lacI genes harboring multiple changes, including clusters of mutations, were found in thymic tumor DNA. The results suggest that an additional mutator activity, such as an error-prone DNA polymerase, leads to increased genomic instability in these MMR-deficient tumors.

Indexed as

DNA-Binding ProteinsEscherichia coli ProteinsNucleic Acid HeteroduplexesAnimalsBacterial ProteinsBase SequenceDNADNA RepairLac RepressorsLymphomaMiceMice, TransgenicMutationMutS Homolog 2 ProteinProto-Oncogene ProteinsRepressor ProteinsBacterial ProteinsDNADNA-Binding ProteinsEscherichia coli ProteinsLac RepressorsMsh2 protein, mouseMutS Homolog 2 ProteinNucleic Acid HeteroduplexesProto-Oncogene ProteinsRepressor Proteins

Identifiers

PMID9671748
PMCPMC21146
OpenAlexW2020522324

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.