Evidence map›Paper›PMID 22878936›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2012

Characterization of mammary cancer stem cells in the MMTV-PyMT mouse model.

Jun Ma, Denise Grant Lanza, Ian Guest, Chang Uk-Lim, Anna Glinskii, Gennadi Glinsky, Stewart Sell

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 52 citations in OpenAlex.

  1. Targeted Degradation of sGRP78 Alleviates the Immunosuppressive Tumor Microenvironment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  12. Regulatory T Cells Control the Switch FromFrontiers in immunology · 2019
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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

7 authors at 3 institutions in 1 country.

Jun MaTranslational and Functional Genomics Laboratory, Ordway Research Institute, Albany, NY 12208, USA.
Denise Grant Lanza
Ian Guest
Chang Uk-Lim
Anna Glinskii
Gennadi Glinsky
Stewart Sell
Albany Medical Center Hospital · USAlbany State University · USWadsworth Center · US

Funding

STEM CELLS AND HEPATOCARCINOGENESISR01CA112481 · NCI · ORDWAY RESEARCH INSTITUTE, INC. · PI SELL, STEWART · 2005 to 2009
$1.3M
NCI NIH HHS NIH R01 CA 112481
6 · The paper itself

Abstract

Breast cancer stem cells, the root of tumor growth, present challenges to investigate: Primary human breast cancer cells are difficult to establish in culture and inconsistently yield tumors after transplantation into immune-deficient recipient mice. Furthermore, there is limited characterization of mammary cancer stem cells in mice, the ideal model for the study of breast cancer. We herein describe a pre-clinical breast cancer stem cell model, based on the properties of cancer stem cells, derived from transgenic MMTV-PyMT mice. Using a defined set of cell surface markers to identify cancer stem cells by flow cytometry, at least four cell populations were recovered from primary mammary cancers. Only two of the four populations, one epithelial and one mesenchymal, were able to survive and proliferate in vitro. The epithelial population exhibited tumor initiation potential with as few as 10 cells injected into syngeneic immune-competent recipients. Tumors initiated from injected cell lines recapitulated the morphological and physiological components of the primary tumor. To highlight the stemness potential of the putative cancer stem cells, B lymphoma Mo-MLV insertion region 1 homolog (Bmi-1) expression was knocked down via shRNA targeting Bmi-1. Without Bmi-1 expression, putative cancer stem cells could no longer initiate tumors, but tumor initiation was rescued with the introduction of a Bmi-1 overexpression vector in the Bmi-1 knockdown cells. In conclusion, our data show that primary mammary cancers from MMTV-PyMT mice contain putative cancer stem cells that survive in culture and can be used to create a model for study of mammary cancer stem cells.

Indexed as

Disease Models, AnimalAnimalsCell Line, TumorCell Transformation, NeoplasticFemaleFlow CytometryHumansImmunoenzyme TechniquesMaleMammary Neoplasms, ExperimentalMammary Tumor Virus, MouseMiceMice, TransgenicNeoplastic Stem CellsPolycomb Repressive Complex 1Proto-Oncogene ProteinsBmi1 protein, mousePolycomb Repressive Complex 1Proto-Oncogene ProteinsRNA, Messenger

Identifiers

PMID22878936
OpenAlexW2002818028

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.