Evidence map›Paper›PMID 19276366›Full record

ArticleCancer research2009

Immune-induced epithelial to mesenchymal transition in vivo generates breast cancer stem cells.

Marta Santisteban, Jennifer M Reiman, Michael K Asiedu, Marshall D Behrens, Aziza Nassar, Kimberly R Kalli, Paul Haluska, James N Ingle, Lynn C Hartmann, Masoud H Manjili and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 232 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
232citing papers in PubMed, 1 pooled it
17.1field-weighted citation impact, top 1% 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

232 citing papers in PubMed, 1 synthesis or guideline pooled it, 378 citations in OpenAlex.

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  14. NOP16 promotes hepatocellular carcinoma progression and triggers EMT through the Keap1-Nrf2 signaling pathway.Technology and health care : official journal of the European Society for Engineering and Medicine · 2024
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172 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

13 authors at 6 institutions in 3 countries.

Marta SantistebanDepartment of Oncology, Mayo Clinic, Rochester, Minnesota 55905, USA.
Jennifer M Reiman
Michael K Asiedu
Marshall D Behrens
Aziza Nassar
Kimberly R Kalli
Paul Haluska
James N Ingle
Lynn C Hartmann
Masoud H Manjili
Derek C Radisky
Soldano Ferrone
Keith L Knutson
Institute of Neuroimmunology of the Slovak Academy of Sciences · SKClinica Universidad de Navarra · ESMayo Clinic · USMayo Clinic in Florida · USUPMC Hillman Cancer Center · USVCU Massey Comprehensive Cancer Center

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Combinatorial targeting of melanoma initiating cellsR01CA138188 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRONE, SOLDANO · 2008 to 2012
$1.5M
HLA classl complex expression in breast cancer immunityR01CA113861 · NCI · MAYO CLINIC ROCHESTER · PI KNUTSON, KEITH L. · 2005 to 2009
$1.1M
Ex vivo expansion of HER-2/neu specific T helper cellsK01CA100764 · NCI · UNIVERSITY OF WASHINGTON · PI KNUTSON, KEITH L. · 2004 to 2008
$742k
NCI NIH HHS K01 CA100764NCI NIH HHS K01-CA100764NCI NIH HHS P50 CA116201NCI NIH HHS P50-CA116201NCI NIH HHS R01 CA113861NCI NIH HHS R01-CA113861NCI NIH HHS R01 CA138188
6 · The paper itself

Abstract

The breast cancer stem cell (BCSC) hypotheses suggest that breast cancer is derived from a single tumor-initiating cell with stem-like properties, but the source of these cells is unclear. We previously observed that induction of an immune response against an epithelial breast cancer led in vivo to the T-cell-dependent outgrowth of a tumor, the cells of which had undergone epithelial to mesenchymal transition (EMT). The resulting mesenchymal tumor cells had a CD24(-/lo)CD44(+) phenotype, consistent with BCSCs. In the present study, we found that EMT was induced by CD8 T cells and the resulting tumors had characteristics of BCSCs, including potent tumorigenicity, ability to reestablish an epithelial tumor, and enhanced resistance to drugs and radiation. In contrast to the hierarchal cancer stem cell hypothesis, which suggests that breast cancer arises from the transformation of a resident tissue stem cell, our results show that EMT can produce the BCSC phenotype. These findings have several important implications related to disease progression and relapse.

Indexed as

AnimalsCD24 AntigenCD8-Positive T-LymphocytesDNA Repair EnzymesEpithelial CellsFemaleGene ExpressionGenes, erbB-2Hyaluronan ReceptorsMammary Neoplasms, ExperimentalMesodermMiceMice, TransgenicMitoxantroneNeoplastic Stem CellsCD24 AntigenDNA Repair EnzymesHyaluronan ReceptorsMitoxantrone

Identifiers

PMID19276366
PMCPMC2664865
OpenAlexW2058763255

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.