Evidence map›Paper›PMID 27425618›Full record

ArticleCell reports2016

Mesenchymal Tumors Can Derive from Ng2/Cspg4-Expressing Pericytes with β-Catenin Modulating the Neoplastic Phenotype.

Shingo Sato, Yuning J Tang, Qingxia Wei, Makoto Hirata, Angela Weng, Ilkyu Han, Atsushi Okawa, Shu Takeda, Heather Whetstone, Puvindran Nadesan and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

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  17. Sarcoma Tumor Microenvironment.Advances in experimental medicine and biology · 2020
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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

13 authors at 5 institutions in 4 countries.

Shingo SatoDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada; Department of Orthopaedic Surgery, Tokyo Medical and Dental, University Graduate School and Faculty of Medicine, Tokyo 113-8510, Japan; Department of Physiology and Cell Biology, Graduate School and Faculty of Medicine, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Yuning J TangDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada; Department of Orthopaedic Surgery, Duke University, Durham, NC 27710, USA.
Qingxia WeiDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada.
Makoto HirataDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada.
Angela WengDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada.
Ilkyu HanDepartment of Orthopaedic Surgery, Seoul National University Hospital, Seoul 151-742, Republic of Korea.
Atsushi OkawaDepartment of Orthopaedic Surgery, Tokyo Medical and Dental, University Graduate School and Faculty of Medicine, Tokyo 113-8510, Japan.
Shu TakedaDepartment of Physiology and Cell Biology, Graduate School and Faculty of Medicine, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Heather WhetstoneDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada.
Puvindran NadesanDepartment of Orthopaedic Surgery, Duke University, Durham, NC 27710, USA.
David G KirschDepartment of Radiation Oncology, Duke University, Durham, NC 27710, USA; Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.
Jay S WunderSamuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, ON M5G 1X5, Canada.
Benjamin A AlmanDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G1X8, Canada; Department of Orthopaedic Surgery, Duke University, Durham, NC 27710, USA. Electronic address: ben.alman@duke.edu.
Hospital for Sick Children · CADuke University · USTokyo Medical and Dental University · JPLunenfeld-Tanenbaum Research Institute · CASeoul National University Hospital · KR

Funding

Targeting Tumor Initiating Cell in Undifferentiated Pleomorphic SarcomaR01CA183811 · NCI · DUKE UNIVERSITY · PI ALMAN, BENJAMIN AARON · 2014 to 2018
$2.2M
CIHR FRN 123493NCI NIH HHS R01 CA183811
6 · The paper itself

Abstract

The cell of origin for most mesenchymal tumors is unclear. One cell type that contributes to this lineages is the pericyte, a cell expressing Ng2/Cspg4. Using lineage tracing, we demonstrated that bone and soft tissue sarcomas driven by the deletion of the Trp53 tumor suppressor, or desmoid tumors driven by a mutation in Apc, can derive from cells expressing Ng2/Cspg4. Deletion of the Trp53 tumor suppressor gene in these cells resulted in the bone and soft tissue sarcomas that closely resemble human sarcomas, while stabilizing β-catenin in this same cell type caused desmoid tumors. Comparing expression between Ng2/Cspg4-expressing pericytes lacking Trp53 and sarcomas that arose from deletion of Trp53 showed inhibition of β-catenin signaling in the sarcomas. Activation of β-catenin inhibited the formation and growth of sarcomas. Thus, pericytes can be a cell of origin for mesenchymal tumors, and β-catenin dysregulation plays an important role in the neoplastic phenotype.

Indexed as

AnimalsAntigensbeta CateninBone NeoplasmsCell LineageCell Line, TumorChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansFemaleGene Expression Regulation, NeoplasticHumansMaleMesodermMiceMice, KnockoutMutationAntigensbeta CateninChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansProteoglycansTumor Suppressor Protein p53

Identifiers

PMID27425618
PMCPMC4963269
OpenAlexW2466486568

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.