Evidence map›Paper›PMID 17653086›Full record

ArticleOncogene2008

Activation of estrogen signaling pathways collaborates with loss of Brca1 to promote development of ERalpha-negative and ERalpha-positive mammary preneoplasia and cancer.

L P Jones, M T Tilli, S Assefnia, K Torre, E D Halama, A Parrish, E M Rosen, P A Furth

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

43 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Article
  3. Bilateral Salpingo-oophorectomy and Breast Cancer Risk forCancer prevention research (Philadelphia, Pa.) · 2021
    Review
  4. Article
  5. Review
  6. Environmental Exposures during Puberty: Window of Breast Cancer Risk and Epigenetic Damage.International journal of environmental research and public health · 2020
    Review
  7. Review
  8. Review
  9. Article
  10. Responsiveness ofCancer prevention research (Philadelphia, Pa.) · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Small-molecule "BRCA1-mimetics" are antagonists of estrogen receptor-α.Molecular endocrinology (Baltimore, Md.) · 2014
    Article
  17. Review
  18. Article
  19. Review
  20. BRCA1 and estrogen/estrogen receptor in breast cancer: where they interact?International journal of biological sciences · 2014
    Review
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

8 authors at 4 institutions in 1 country.

L P JonesDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA.
M T Tilli
S Assefnia
K Torre
E D Halama
A Parrish
E M Rosen
P A Furth
Georgetown University Medical Center · USGeorgetown University · USSalk Institute for Biological Studies · USVirginia Commonwealth University · US

Funding

TRAINING GRANT IN TUMOR BIOLOGYT32CA009686 · NCI · GEORGETOWN UNIVERSITY · PI ANNA Tate RIEGEL, DAVID J ROBBINS · 1996 to 2026
$10.8M
Progression and regression of mammary preneoplasiaR01CA112176 · NCI · GEORGETOWN UNIVERSITY · PI FURTH, PRISCILLA A. · 2005 to 2018
$3.1M
SCREENING OF VARIOUS CHEMOPREVENTIVE AGENTS IN THE MNU-IN01CN005024 · CN · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PEZZUTO, JOHN M · 2000 to 2000
$180k
NCI NIH HHS 2T32CA09686-08NCI NIH HHS N01-CN-05024NCI NIH HHS R01CA08000NCI NIH HHS R01 CA112176NCI NIH HHS T32 CA009686
6 · The paper itself

Abstract

BRCA1 can regulate estrogen receptor-alpha (ERalpha) activity. This study tested the hypotheses that Brca1 loss in mammary epithelium alters the estrogenic growth response and that exposure to increased estrogen or ERalpha collaborates with Brca1 deficiency to accelerate preneoplasia and cancer development. Longer ductal extension was found in mammary glands of Brca1(f/f;MMTV-Cre) mice during puberty as compared to wild-type mice. Terminal end bud differentiation was impaired in Brca1 mutant mice with preservation of prolactin-induced alveolar differentiation. Exogenous estrogen stimulated an abnormal sustained increase in mammary epithelial cell proliferation and the appearance of ERalpha-negative preneoplasia in postpubertal Brca1 mutant mice. Carcinogenesis was investigated using Brca1(f/f;MMTV-Cre) mice hemizygous for p53. Exogenous estrogen increased the percentage of mice with multiple hyperplastic alveolar nodules. Targeted conditional ERalpha overexpression in mammary epithelial cells of mice that were Brca1 mutant and hemizygous for p53 increased the percentage of mice exhibiting multiple hyperplastic nodules, invasive mammary cancers and cancer multiplicity. Significantly more than half of the preneoplasia and cancers were ERalpha negative even as their initiation was promoted by ERalpha overexpression.

Indexed as

AnimalsBRCA1 ProteinCell ProliferationEstrogen Receptor alphaEstrogensFemaleMammary Neoplasms, ExperimentalMiceMice, Mutant StrainsNeoplasm InvasivenessPrecancerous ConditionsBRCA1 ProteinEstrogen Receptor alphaEstrogens

Identifiers

PMID17653086
PMCPMC3045705
OpenAlexW2030954815

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.