Evidence map›Paper›PMID 36433954›Full record

ArticleNature communications2022

circCsnk1g3- and circAnkib1-regulated interferon responses in sarcoma promote tumorigenesis by shaping the immune microenvironment.

Roberta Piras, Emily Y Ko, Connor Barrett, Marco De Simone, Xianzhi Lin, Marina T Broz, Fernando H G Tessaro, Mireia Castillo-Martin, Carlos Cordon-Cardo, Helen S Goodridge and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 18 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

16 authors at 4 institutions in 2 countries.

Roberta Piras *Department of Radiation Oncology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID 0000-0002-0254-5122
Emily Y Ko *Department of Radiation Oncology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Connor BarrettDepartment of Medical and Molecular Sciences, University of Delaware, Newark, DE, USA.
Marco De SimoneDepartment of Radiation Oncology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Xianzhi LinWomen's Cancer Research Program at Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID 0000-0001-9802-9896
Marina T BrozDepartment of Radiation Oncology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Fernando H G TessaroDepartment of Radiation Oncology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Mireia Castillo-MartinDepartment of Pathology, Mount Sinai School of Medicine, The Mount Sinai Medical Center, New York, NY, 10029, USA.
Carlos Cordon-CardoDepartment of Pathology, Mount Sinai School of Medicine, The Mount Sinai Medical Center, New York, NY, 10029, USA.ORCID 0000-0003-0858-5624
Helen S GoodridgeBoard of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Dolores Di VizioDepartment of Surgery and Department of Pathology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Mona BatishDepartment of Medical and Molecular Sciences, University of Delaware, Newark, DE, USA.
Kate LawrensonWomen's Cancer Research Program at Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID 0000-0002-6469-2515
Y Grace ChenDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-3574-5734
Keith Syson ChanDepartment of Pathology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Jlenia GuarnerioDepartment of Radiation Oncology, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA. jlenia.guarnerio@cshs.org.ORCID 0000-0001-7576-7095
Cedars-Sinai Medical Center · USMount Sinai Medical Center · USUniversity of Delaware · USYale University · US

Funding

Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI CORDON-CARDO, CARLOS · 2000 to 2021
$35.4M
Distinct Tumor and Metastatic Collagen Microenvironments: Divergent Targeting ApproachesR01CA175397 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHAN, KEITH SYSON · 2013 to 2025
$4.8M
Comparative modeling of sarcoma microenvironments for the discovery of biomarkers and tumor vulnerabilitiesR01CA258265 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GUARNERIO, JLENIA · 2021 to 2025
$2.3M
Targeting tumor repopulation and the immune microenvironment to overcome chemoresistanceR01CA255609 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHAN, KEITH SYSON · 2021 to 2025
$2.2M
The Regulation of Circular RNA FunctionsR35GM142687 · NIGMS · YALE UNIVERSITY · PI CHEN, YE GRACE · 2021 to 2025
$2.2M
DETECTION OF CHROMOSOMAL TRANSLOCATIONS BY SINGLE MOLECULE RNA IMAGINGDP5OD012160 · OD · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI BATISH, MONA · 2012 to 2016
$2.1M
Investigation and functional characterization of new drivers of mesenchymal tumorigenesis.R00CA212200 · NCI · CEDARS-SINAI MEDICAL CENTER · PI GUARNERIO, JLENIA · 2018 to 2020
$710k
Investigation and functional characterization of new drivers of mesenchymal tumorigenesis.K99CA212200 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GUARNERIO, JLENIA · 2016 to 2017
$204k
NCI NIH HHS K99 CA212200NCI NIH HHS P01 CA087497NCI NIH HHS R00 CA212200NCI NIH HHS R01 CA175397NCI NIH HHS R01 CA255609NCI NIH HHS R01 CA258265NIGMS NIH HHS R35 GM142687NIH HHS DP5 OD012160
6 · The paper itself

Abstract

Exonic circular RNAs (circRNAs) produce predominantly non-coding RNA species that have been recently profiled in many tumors. However, their functional contribution to cancer progression is still poorly understood. Here, we identify the circRNAs expressed in soft tissue sarcoma cells and explore how the circRNAs regulate sarcoma growth in vivo. We show that circCsnk1g3 and circAnkib1 promote tumor growth by shaping a pro-tumorigenic microenvironment, possibly due to their capabilities to regulate tumor-promoting elements extrinsic to the tumor cells. Accordingly, circCsnk1g3 and circAnkib1 can control the expression of interferon-related genes and pro-inflammatory factors in the sarcoma cells, thus directing immune cell recruitment into the tumor mass, and hence their activation. Mechanistically, circRNAs may repress pro-inflammatory elements by buffering activation of the pathways mediated by RIG-I, the cytosolic viral RNA sensor. The current findings suggest that the targeting of specific circRNAs could augment the efficacy of tumor and immune response to mainstay therapies.

Indexed as

CarcinogenesisInterferonsRNA, CircularSarcomaSoft Tissue NeoplasmsTumor MicroenvironmentCasein Kinase IDEAD Box Protein 58HumansProteinsReceptors, ImmunologicANKIB1 protein, humanCasein Kinase IDEAD Box Protein 58InterferonsProteinsReceptors, ImmunologicRIGI protein, humanRNA, Circular

Identifiers

PMID36433954
PMCPMC9700836
OpenAlexW4309961593

What OpenQuestion holds

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Registered trials

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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.