Evidence map›Paper›PMID 10630642›Full record

ArticleOncogene1999

BRCA1 deficient embryonic stem cells display a decreased homologous recombination frequency and an increased frequency of non-homologous recombination that is corrected by expression of a brca1 transgene.

J N Snouwaert, L C Gowen, A M Latour, A R Mohn, A Xiao, L DiBiase, B H Koller

Abstract read
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In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

82 citing papers in PubMed, 195 citations in OpenAlex.

  1. Article
  2. Repetitive Sequence Stability in Embryonic Stem Cells.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
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  19. Article
  20. Unsolved mystery: the role of BRCA1 in DNA end-joining.Journal of radiation research · 2016
    Review

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

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

7 authors at 1 institution in 1 country.

J N SnouwaertDepartment of Medicine, University of North Carolina at Chapel Hill, 27599-7248, USA.
L C Gowen
A M Latour
A R Mohn
A Xiao
L DiBiase
B H Koller
University of North Carolina at Chapel Hill · US

Funding

ROLE OF BRCA1 IN NORMAL CELL GROWTH AND TUMORGENESISR01CA082423 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI KOLLER, BEVERLY H · 1999 to 2003
$826k
NCI NIH HHS CA82423
6 · The paper itself

Abstract

BRCA1 is a nuclear phosphoprotein that has been classified as a tumor suppressor based on the fact that women carrying a mutated copy of the BRCA1 gene are at increased risk of developing breast and ovarian cancer. The association of BRCA1 with RAD51 has led to the hypothesis that BRCA1 is involved in DNA repair. We describe here the generation and analysis of murine embryonic stem (ES) cell lines in which both copies of the murine homologue of the human BRCA1 gene have been disrupted by gene targeting. We show that exogenous DNA introduced into these BRCA1 deficient cells by electroporation is randomly integrated into the genome at a significantly higher rate than in wild type ES cells. In contrast, integration of exogenous DNA by homologous recombination occurs in BRCA1 deficient cells at a significantly lower rate than in wild type controls. When BRCA1 expression is re-established at 5-10% of normal levels by introduction of a Brca1 transgene into BRCA1 deficient ES cells, the frequency of random integration is reduced to wild type levels, although the frequency of homologous recombination is not significantly improved. These results suggest that BRCA1 plays a role in determining the response of cells to double stranded DNA breaks.

Indexed as

Genes, BRCA1Recombination, GeneticAnimalsBreast NeoplasmsCells, CulturedEmbryo, MammalianFemaleGene DeletionHumansMiceMice, KnockoutMice, TransgenicOvarian NeoplasmsRestriction MappingReverse Transcriptase Polymerase Chain ReactionRisk Factors

Identifiers

PMID10630642
OpenAlexW2039435798

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.