Evidence map›Paper›PMID 17322389›Full record

ArticleThe American journal of pathology2007

Human breast fibroblasts inhibit growth of the MCF10AT xenograft model of proliferative breast disease.

Andrea Sadlonova, Shibani Mukherjee, Damon B Bowe, Sandra R Gault, Nicole A Dumas, Brian A Van Tine, Natalya Frolova, Grier P Page, Danny R Welch, Lea Novak and 1 more

Abstract read
In one paragraph

Article in The American journal of pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Exosomes: recruits for tumour surveillance?Journal of thoracic disease · 2017
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Differential gene expression of Wnt signaling pathway in benign, premalignant, and malignant human breast epithelial cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2012
    Article
  13. Active roles of tumor stroma in breast cancer metastasis.International journal of breast cancer · 2012
    Article
  14. Article
  15. Article
  16. Identification of molecular distinctions between normal breast-associated fibroblasts and breast cancer-associated fibroblasts.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2009
    Article
  17. Article
  18. 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

11 authors.

Andrea SadlonovaDepartment of Pathology, The University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Shibani Mukherjee
Damon B Bowe
Sandra R Gault
Nicole A Dumas
Brian A Van Tine
Natalya Frolova
Grier P Page
Danny R Welch
Lea Novak
Andra R Frost

Funding

Prevention of Breast Cancer by Targeting MyofibroblastsR03CA105950 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FROST, ANDRA R · 2003 to 2004
$145k
Role of Fibroblasts and IGF-II in Breast CarcinogenesisR03CA097472 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FROST, ANDRA R · 2002 to 2003
$145k
NCI NIH HHS CA097472NCI NIH HHS CA105950NCI NIH HHS R03 CA105950
6 · The paper itself

Abstract

Stromal fibroblasts are important for normal breast homeostasis and regulation of epithelial growth; however, this regulatory function is altered during carcinogenesis. To study the role of fibroblasts in the development of breast cancer, fibroblasts derived from normal breast (NAFs) were incorporated into the MCF10AT xenograft model of progressive proliferative breast disease. The persistence of human NAFs in xenografts was established by intracellular labeling and tyramide-coupled fluorescent in situ hybridization. Overall, the number of MCF10AT epithelial structures was decreased, and the rate of epithelial cell apoptosis was increased in xenografts containing NAFs. However, these changes were primarily in low-grade epithelial structures, corresponding to normal or mildly hyperplastic ductal epithelium. The level and rate of apoptosis of high-grade epithelial structures, corresponding to in situ and invasive carcinoma, were not consistently altered by NAFs. In addition, there was variability in the growth-inhibitory capacity of NAFs derived from different individuals. NAFs induced changes in the morphology of high-grade MCF10AT structures and in xenograft stroma, including the composition of extracellular matrix, and increased angiogenesis and lymphocytic infiltration. These findings imply that NAFs can inhibit the growth of normal and hyperplastic epi-thelium but are less able to regulate the more transformed epithelial cells that arise during carcino-genesis.

Indexed as

AnimalsApoptosisBreast NeoplasmsCells, CulturedDisease Models, AnimalEpithelial CellsFemaleFibroblastsHumansImmunohistochemistryIn Situ Hybridization, FluorescenceMicePrecancerous ConditionsTransplantation, Heterologous

Identifiers

PMID17322389
PMCPMC1864888

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.