Evidence map›Paper›PMID 28433655›Full record

ArticleStem cell research2017

Targeting sarcoma tumor-initiating cells through differentiation therapy.

Dan Han, Veronica Rodriguez-Bravo, Elizabeth Charytonowicz, Elizabeth Demicco, Josep Domingo-Domenech, Robert G Maki, Carlos Cordon-Cardo

Open access · goldAbstract read
In one paragraph

Article in Stem cell research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Dan HanDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Veronica Rodriguez-BravoDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Elizabeth CharytonowiczDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Elizabeth DemiccoDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Josep Domingo-DomenechDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Robert G MakiDepartment of Hematology-Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Carlos Cordon-CardoDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: carlos.cordon-cardo@mssm.edu.
Icahn School of Medicine at Mount Sinai · US

Funding

Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL · 2000 to 2021
$35.4M
A New Disease Platform Leveraging Complex Drosophila and Mammalian ModelsU54OD020353 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAGAN, ROSS LEIGH · 2015 to 2019
$10.3M
Role of GATA2 signaling network in Lethal Prostate CancerR01CA207311 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DOMINGO-DOMENECH, JOSEP MARIA · 2016 to 2020
$2.2M
Genome Stability Regulation by the Nuclear Pore-Chromosome Axis and Defects in Tumor CellsK22CA207458 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RODRIGUEZ-BRAVO, VERONICA · 2016 to 2018
$551k
NCI NIH HHS K22 CA207458NCI NIH HHS P01 CA087497NCI NIH HHS R01 CA207311NIH HHS U54 OD020353
6 · The paper itself

Abstract

Human leukocyte antigen class I (HLA-I) down-regulation has been reported in many human cancers to be associated with poor clinical outcome. However, its connection to tumor-initiating cells (TICs) remains unknown. In this study, we report that HLA-I is down-regulated in a subpopulation of cells that have high tumor initiating capacity in different types of human sarcomas. Detailed characterization revealed their distinct molecular profiles regarding proliferation, apoptosis and stemness programs. Notably, these TICs can be induced to differentiate along distinct mesenchymal lineages, including the osteogenic pathway. The retinoic acid receptor signaling pathway is overexpressed in HLA-1 negative TICs. All-trans retinoic acid treatment successfully induced osteogenic differentiation of this subpopulation, in vitro and in vivo, resulting in significantly decreased tumor formation. Thus, our findings indicate down-regulated HLA-I is a shared feature of TICs in a variety of human sarcomas, and differentiation therapy strategies may specifically target undifferentiated TICs and inhibit tumor formation.

Indexed as

Cell DifferentiationCarcinogenesisCell Line, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHLA AntigensHumansNeoplastic Stem CellsOsteogenesisPhenotypeSarcomaTretinoinHLA AntigensTretinoinHuman leukocyte antigen class ISarcomasTumor-initiating cells

Identifiers

PMID28433655
PMCPMC5988213
OpenAlexW2606342071

What OpenQuestion holds

Textmetadata
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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.