Evidence map›Paper›PMID 28588009›Full record

ArticleCancer research2017

Exosome-Derived miR-25-3p and miR-92a-3p Stimulate Liposarcoma Progression.

Lucia Casadei, Federica Calore, Chad J Creighton, Michele Guescini, Kara Batte, O Hans Iwenofu, Abeba Zewdu, Danielle A Braggio, Kate Lynn Bill, Paolo Fadda and 9 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

127 citing papers in PubMed, 196 citations in OpenAlex.

  1. Article
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  11. 5'-tRNABiophysical journal · 2025
    Article
  12. Article
  13. Review
  14. Potential biological roles of exosomal non-coding RNAs in breast cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
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  16. Article
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  19. Article
  20. Downregulation ofJournal of clinical medicine research · 2024
    Article

67 more citing papers are in PubMed but not listed here.

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

19 authors at 5 institutions in 3 countries.

Lucia CasadeiThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Federica CaloreDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Chad J CreightonDepartment of Medicine and Dan L. Duncan Comprehensive Cancer Center Division of Biostatistics, Houston, Texas.
Michele GuesciniDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Kara BatteThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
O Hans IwenofuDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Abeba ZewduThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Danielle A BraggioThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Kate Lynn BillThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Paolo FaddaDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Francesca LovatDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Gonzalo LopezThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Pierluigi GaspariniDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
James L ChenThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Raleigh D KladneyDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Gustavo LeoneDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Dina LevDepartment of Surgery 'B', Sheba Medical Center and The Tel Aviv University, Tel Aviv, Israel.
Carlo M CroceDepartment of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio. carlo.croce@osumc.edu Raphael.pollock@osumc.edu.
Raphael E PollockThe James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio. carlo.croce@osumc.edu Raphael.pollock@osumc.edu.
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USSheba Medical Center · ILThe Ohio State University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Urbino · IT

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Tissue and Pathology ResourcesU54CA168512 · NCI · SARC · PI REINKE, DENISE · 2012 to 2016
$11.0M
Cancer Gene Discovery to Identify Targetable TargetsR35CA197706 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2015 to 2021
$6.4M
NCI NIH HHS P30 CA016058NCI NIH HHS R35 CA197706NCI NIH HHS U54 CA168512
6 · The paper itself

Abstract

Despite the development of combined modality treatments against liposarcoma in recent years, a significant proportion of patients respond only modestly to such approaches, possibly contributing to local or distant recurrence. Early detection of recurrent or metastatic disease could improve patient prognosis by triggering earlier clinical intervention. However, useful biomarkers for such purposes are lacking. Using both patient plasma samples and cell lines, we demonstrate here that miR-25-3p and miR-92a-3p are secreted by liposarcoma cells through extracellular vesicles and may be useful as potential biomarkers of disease. Both miR-25-3p and miR-92a-3p stimulated secretion of proinflammatory cytokine IL6 from tumor-associated macrophages in a TLR7/8-dependent manner, which in turn promoted liposarcoma cell proliferation, invasion, and metastasis via this interaction with the surrounding microenvironment. Our findings provide novel and previously unreported insight into liposarcoma progression, identifying communication between liposarcoma cells and their microenvironment as a process critically involved in liposarcoma progression. This study establishes the possibility that the pattern of circulating miRNAs may identify recurrence prior to radiological detectability while providing insight into disease outcome and as a possible approach to monitor treatment efficacy.

Indexed as

AnimalsCase-Control StudiesCell Line, TumorCell ProliferationDisease ProgressionExosomesHEK293 CellsHumansLiposarcomaMiceMice, Inbred C57BLMicroRNAsTransfectionMicroRNAsMIRN25 microRNA, humanMIRN25 microRNA, mouseMIRN92 microRNA, humanMirn92 microRNA, mouse

Identifiers

PMID28588009
PMCPMC6033276
OpenAlexW2622355554

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.