Evidence map›Paper›PMID 20808935›Full record

ArticlePloS one2010

Mesenchymal stem cells promote mammosphere formation and decrease E-cadherin in normal and malignant breast cells.

Ann H Klopp, Lara Lacerda, Anshul Gupta, Bisrat G Debeb, Travis Solley, Li Li, Erika Spaeth, Wei Xu, Xiaomei Zhang, Michael T Lewis and 9 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

102 citing papers in PubMed, 1 synthesis or guideline pooled it, 171 citations in OpenAlex.

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42 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

19 authors at 4 institutions in 2 countries.

Ann H KloppDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Lara Lacerda
Anshul Gupta
Bisrat G Debeb
Travis Solley
Li Li
Erika Spaeth
Wei Xu
Xiaomei Zhang
Michael T Lewis
James M Reuben
Savitri Krishnamurthy
Mauro Ferrari
Rogério Gaspar
Thomas A Buchholz
Massimo Cristofanilli
Frank Marini
Michael Andreeff
Wendy A Woodward
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · USThe University of Texas Health Science Center at Houston · USUniversity of Lisbon · PT

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UTMDACC SPORE in Breast CancerP50CA116199 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BERRY, DONALD A · 2005 to 2009
$11.9M
CTSA: K12 COMPONENTKL2RR024149 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2011
$6.7M
Human Breast Cancer Stem Cell SurrogatesR01CA138239 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CRISTOFANILLI, MASSIMO, REUBEN, JAMES MARTIN · 2008 to 2012
$2.8M
Regulation of Mammary Stem CellsR01CA127857 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LEWIS, MICHAEL T. · 2008 to 2012
$1.7M
Assembly and disassembly of the stromal architecture in the tumor microenvironmenRC1CA146381 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MARINI, FRANK C. · 2009 to 2010
$1.0M
Gene Delivery Vehicles for Cancer Gene TherapyR01CA109451 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MARINI, FRANK C. · 2005 to 2009
$928k
NCI NIH HHS CA109451NCI NIH HHS CA116199NCI NIH HHS P50 CA116199NCI NIH HHS R01 CA109451NCI NIH HHS R01 CA127857NCI NIH HHS R01 CA138239NCI NIH HHS R01CA138239-01NCI NIH HHS RC1 CA146381NCI NIH HHS RC1CA146381NCRR NIH HHS KL2 RR024149NCRR NIH HHS KL2RR024149
6 · The paper itself

Abstract

introductionNormal and malignant breast tissue contains a rare population of multi-potent cells with the capacity to self-renew, referred to as stem cells, or tumor initiating cells (TIC). These cells can be enriched by growth as "mammospheres" in three-dimensional cultures.

objectiveWe tested the hypothesis that human bone-marrow derived mesenchymal stem cells (MSC), which are known to support tumor growth and metastasis, increase mammosphere formation.

resultsWe found that MSC increased human mammary epithelial cell (HMEC) mammosphere formation in a dose-dependent manner. A similar increase in sphere formation was seen in human inflammatory (SUM149) and non-inflammatory breast cancer cell lines (MCF-7) but not in primary inflammatory breast cancer cells (MDA-IBC-3). We determined that increased mammosphere formation can be mediated by secreted factors as MSC conditioned media from MSC spheroids significantly increased HMEC, MCF-7 and SUM149 mammosphere formation by 6.4 to 21-fold. Mammospheres grown in MSC conditioned media had lower levels of the cell adhesion protein, E-cadherin, and increased expression of N-cadherin in SUM149 and HMEC cells, characteristic of a pro-invasive mesenchymal phenotype. Co-injection with MSC in vivo resulted in a reduced latency time to develop detectable MCF-7 and MDA-IBC-3 tumors and increased the growth of MDA-IBC-3 tumors. Furthermore, E-cadherin expression was decreased in MDA-IBC-3 xenografts with co-injection of MSC.

conclusionsMSC increase the efficiency of primary mammosphere formation in normal and malignant breast cells and decrease E-cadherin expression, a biologic event associated with breast cancer progression and resistance to therapy.

Indexed as

AnimalsBreastBreast NeoplasmsCadherinsCell Culture TechniquesCell Line, TumorCell ProliferationCell Transformation, NeoplasticCulture Media, ConditionedGene Expression RegulationHumansMammary Glands, HumanMesenchymal Stem CellsMiceNeoplasm MetastasisCadherinsCulture Media, Conditioned

Identifiers

PMID20808935
PMCPMC2922340
OpenAlexW2043416876

What OpenQuestion holds

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LicenceCC BY
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.