Evidence map›Paper›PMID 25614485›Full record

ArticleCancer discovery2015

A genetic platform to model sarcomagenesis from primary adult mesenchymal stem cells.

Jlenia Guarnerio, Luisa Riccardi, Riccardo Taulli, Takahiro Maeda, Guocan Wang, Robin M Hobbs, Min Sup Song, Paolo Sportoletti, Rosa Bernardi, Roderick T Bronson and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  9. MicroRNA-22 Is a Key Regulator of Lipid and Metabolic Homeostasis.International journal of molecular sciences · 2023
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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

14 authors at 5 institutions in 2 countries.

Jlenia GuarnerioCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Luisa RiccardiCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Riccardo TaulliCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Takahiro MaedaDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Guocan WangCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Robin M HobbsCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Min Sup SongCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Paolo SportolettiCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Rosa BernardiDivision of Molecular Oncology, Leukemia Unit, San Raffaele Scientific Institute, Milan, Italy.
Roderick T BronsonDepartment of Microbiology and Immunology, Rodent Histopathology Care, Harvard Medical School, Boston, Massachusetts.
Mireia Castillo-MartinDepartment of Pathology, Mount Sinai School of Medicine, The Mount Sinai Medical Center, New York, New York.
Carlos Cordon-CardoDepartment of Pathology, Mount Sinai School of Medicine, The Mount Sinai Medical Center, New York, New York.
Andrea LunardiCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA. ppandolf@bidmc.harvard.edu andrea.lunardi@unitn.it.
Pier Paolo PandolfiCancer Research Institute, Beth Israel Deaconess Cancer Center, Departments of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA. ppandolf@bidmc.harvard.edu andrea.lunardi@unitn.it.
Beth Israel Deaconess Medical Center · USMount Sinai Medical Center · USBrigham and Women's Hospital · USHarvard University · USSan Raffaele University of Rome · IT

Funding

Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL · 2000 to 2021
$35.4M
Role of POZ-zinc in hemopoietic malignaciesR01CA102142 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PANDOLFI, PIER PAOLO · 2004 to 2014
$3.3M
NCI NIH HHS P01 CA087497NCI NIH HHS R01 CA102142NCI NIH HHS R01 CA102142-7
6 · The paper itself

Abstract

unlabelledThe regulatory factors governing adult mesenchymal stem cell (MSC) physiology and their tumorigenic potential are still largely unknown, which substantially delays the identification of effective therapeutic approaches for the treatment of aggressive and lethal forms of MSC-derived mesenchymal tumors, such as undifferentiated sarcomas. Here, we have developed a novel platform to screen and quickly identify genes and pathways responsible for adult MSC transformation, modeled undifferentiated sarcoma in vivo, and, ultimately, tested the efficacy of targeting the identified oncopathways. Importantly, by taking advantage of this new platform, we demonstrate the key role of an aberrant LRF-DLK1-SOX9 pathway in the pathogenesis of undifferentiated sarcoma, with important therapeutic implications. SIGNIFICANCE: The paucity of therapeutic options for the treatment of sarcoma calls for a rapid and effective preclinical assessment of new therapeutic modalities. We have here developed a new platform to deconstruct the molecular genetics underlying the pathogenesis of sarcoma and to evaluate in vivo the efficacy of novel targeted therapies.

Indexed as

Models, BiologicalAdultAnimalsCalcium-Binding ProteinsCell Culture TechniquesCell DifferentiationCell LineCell ProliferationCell Transformation, NeoplasticDNA-Binding ProteinsGene Expression Regulation, NeoplasticHumansImmunophenotypingIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsMiceCalcium-Binding ProteinsDlk1 protein, mouseDNA-Binding ProteinsIntercellular Signaling Peptides and ProteinsTranscription FactorsTumor Suppressor ProteinsZbtb7a protein, mouse

Identifiers

PMID25614485
PMCPMC4418175
OpenAlexW2161615897

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.