Evidence map›Paper›PMID 37279073›Full record

ArticleJCI insight2023

MYC regulates CSF1 expression via microRNA 17/20a to modulate tumor-associated macrophages in osteosarcoma.

Bikesh K Nirala, Tajhal D Patel, Lyazat Kurenbekova, Ryan Shuck, Atreyi Dasgupta, Nino Rainusso, Cristian Coarfa, Jason T Yustein

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 24 citations in OpenAlex.

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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

8 authors at 1 institution in 2 countries.

Bikesh K NiralaTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Tajhal D PatelTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Lyazat KurenbekovaTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Ryan ShuckTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Atreyi DasguptaTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Nino RainussoTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Cristian CoarfaDepartment of Molecular & Human Genetics, and.
Jason T YusteinTexas Children's Cancer and Hematology Centers and The Faris D. Virani Ewing Sarcoma Center.
Baylor College of Medicine · US

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Translational Research Support CoreP30ES030285 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI Casey W Wright · 2019 to 2026
$14.7M
Cutaneous T cell lymphoma: a paradigm for dissecting susceptibility and resistance to checkpoint inhibition therapyR01CA229510 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI QUERFELD, CHRISTIANE · 2019 to 2023
$2.8M
Intratumoral imaging of hypoxia using 1H- and 19F-MRI with redox-responsive Eu-based contrast agentsR01EB026453 · NIBIB · WAYNE STATE UNIVERSITY · PI ALLEN, MATTHEW J, PAUTLER, ROBIA G · 2018 to 2021
$2.7M
Identifying and Targeting Onocgenic MYC Enhancer Control in Pediatric TumorsR01CA215452 · NCI · BAYLOR COLLEGE OF MEDICINE · PI WESTBROOK, THOMAS · 2017 to 2021
$2.0M
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
DISSECTING AND TARGETING THE ROLE OF GALNT14 IN HIGH-RISK OSTEOSARCOMAR21CA267914 · NCI · EMORY UNIVERSITY · PI KOHLER, JENNIFER J, YUSTEIN, JASON · 2022 to 2023
$430k
NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA215452NCI NIH HHS R01 CA229510NCI NIH HHS R21 CA267914NCRR NIH HHS S10 RR024574NIBIB NIH HHS R01 EB026453NIEHS NIH HHS P30 ES030285
6 · The paper itself

Abstract

Osteosarcoma (OS) is the most common primary bone tumor of childhood. Approximately 20%-30% of OSs carry amplification of chromosome 8q24, which harbors the oncogene c-MYC and correlates with a poor prognosis. To understand the mechanisms that underlie the ability of MYC to alter both the tumor and its surrounding tumor microenvironment (TME), we generated and molecularly characterized an osteoblast-specific Cre-Lox-Stop-Lox-c-MycT58A p53fl/+ knockin genetically engineered mouse model (GEMM). Phenotypically, the Myc-knockin GEMM had rapid tumor development with a high incidence of metastasis. MYC-dependent gene signatures in our murine model demonstrated significant homology to the human hyperactivated MYC OS. We established that hyperactivation of MYC led to an immune-depleted TME in OS demonstrated by the reduced number of leukocytes, particularly macrophages. MYC hyperactivation led to the downregulation of macrophage colony-stimulating factor 1, through increased microRNA 17/20a expression, causing a reduction of macrophage population in the TME of OS. Furthermore, we developed cell lines from the GEMM tumors, including a degradation tag-MYC model system, which validated our MYC-dependent findings both in vitro and in vivo. Our studies utilized innovative and clinically relevant models to identify a potentially novel molecular mechanism through which MYC regulates the profile and function of the OS immune landscape.

Indexed as

Bone NeoplasmsMicroRNAsOsteosarcomaAnimalsHumansMacrophage Colony-Stimulating FactorMiceTumor-Associated MacrophagesTumor MicroenvironmentMacrophage Colony-Stimulating FactorMicroRNAsMIRN17 microRNA, humanBone diseaseMouse modelsOncogenesOncology

Identifiers

PMID37279073
PMCPMC10371352
OpenAlexW4379508480

What OpenQuestion holds

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LicenceCC BY
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.