Evidence map›Paper›PMID 23247610›Full record

ArticleBreast cancer research and treatment2013

Estrogen switches pure mucinous breast cancer to invasive lobular carcinoma with mucinous features.

Purevsuren Jambal, Melanie M Badtke, J Chuck Harrell, Virginia F Borges, Miriam D Post, Grace E Sollender, Monique A Spillman, Kathryn B Horwitz, Britta M Jacobsen

Open access · greenAbstract readCase Reports
In one paragraph

Article in Breast cancer research and treatment, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

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  13. Mucin 2 (MUC2) modulates the aggressiveness of breast cancer.Breast cancer research and treatment · 2019
    Article
  14. Article
  15. Loss of E-cadherin Enhances IGF1-IGF1R Pathway Activation and Sensitizes Breast Cancers to Anti-IGF1R/InsR Inhibitors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    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

9 authors at 2 institutions in 1 country.

Purevsuren JambalDivision of Endocrinology, Department of Medicine, University of Colorado, Anschutz Medical Campus, Mail Stop 8106, Aurora, CO 80045, USA.
Melanie M Badtke
J Chuck Harrell
Virginia F Borges
Miriam D Post
Grace E Sollender
Monique A Spillman
Kathryn B Horwitz
Britta M Jacobsen
University of Colorado Anschutz Medical Campus · USUniversity of North Carolina at Chapel Hill · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
PROGESTERONE RECEPTORS IN BREAST CANCERR01CA026869 · NCI · UNIVERSITY OF COLORADO DENVER · PI HORWITZ, KATHRYN B · 1985 to 2014
$5.6M
PROGESTERONE RECEPTORS IN BREAST CANCERR37CA026869 · NCI · UNIVERSITY OF COLORADO DENVER · PI HORWITZ, KATHRYN B · 1993 to 1999
–
NCI NIH HHS CA026869NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA026869NCI NIH HHS R37 CA026869
6 · The paper itself

Abstract

Mucinous breast cancer (MBC) is mainly a disease of postmenopausal women. Pure MBC is rare and augurs a good prognosis. In contrast, MBC mixed with other histological subtypes of invasive disease loses the more favorable prognosis. Because of the relative rarity of pure MBC, little is known about its cell and tumor biology and relationship to invasive disease of other subtypes. We have now developed a human breast cancer cell line called BCK4, in which we can control the behavior of MBC. BCK4 cells were derived from a patient whose poorly differentiated primary tumor was treated with chemotherapy, radiation and tamoxifen. Malignant cells from a recurrent pleural effusion were xenografted in mammary glands of a nude mouse. Cells from the solid tumor xenograft were propagated in culture to generate the BCK4 cell line. Multiple marker and chromosome analyses demonstrate that BCK4 cells are human, near diploid and luminal, expressing functional estrogen, androgen, and progesterone receptors. When xenografted back into immunocompromised cycling mice, BCK4 cells grow into small pure MBC. However, if mice are supplemented with continuous estradiol, tumors switch to invasive lobular carcinoma (ILC) with mucinous features (mixed MBC), and growth is markedly accelerated. Tamoxifen prevents the expansion of this more invasive component. The unexpected ability of estrogens to convert pure MBC into mixed MBC with ILC may explain the rarity of the pure disease in premenopausal women. These studies show that MBC can be derived from lobular precursors and that BCK4 cells are new, unique models to study the phenotypic plasticity, hormonal regulation, optimal therapeutic interventions, and metastatic patterns of MBC.

Indexed as

AgedAnimalsBreast NeoplasmsCarcinoma, LobularCell Line, TumorCell ProliferationEstradiolEstrogensFemaleHumansKaryotypingMiceMice, NudeNeoplasms, Cystic, Mucinous, and SerousTamoxifenXenograft Model Antitumor AssaysEstradiolEstrogensTamoxifen

Identifiers

PMID23247610
PMCPMC3543987
OpenAlexW1979032468

What OpenQuestion holds

Textmetadata
LicenceTDM
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.