Evidence map›Paper›PMID 37052491›Full record

ReviewMolecular cancer research : MCR2023

Small Non-Coding RNAs in Soft-Tissue Sarcomas: State of the Art and Future Directions.

Alessandro La Ferlita, Nipin Sp, Marina Goryunova, Giovanni Nigita, Raphael E Pollock, Carlo M Croce, Joal D Beane

Open access · greenAbstract readReview
In one paragraph

Review in Molecular cancer research : MCR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. miR-497 Target Gene Regulatory Network in Angiosarcoma.Molecular cancer research : MCR · 2024
    Article
  2. Target gene regulatory network of miR-497 in angiosarcoma.bioRxiv : the preprint server for biology · 2023
    Article
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.

Alessandro La FerlitaDepartment of Cancer Biology and Genetics, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0002-3680-3177
Nipin SpDivision of Surgical Oncology, Department of Surgery, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0003-1826-3135
Marina GoryunovaDivision of Surgical Oncology, Department of Surgery, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-8251-1469
Giovanni NigitaDepartment of Cancer Biology and Genetics, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-8880-4334
Raphael E PollockDivision of Surgical Oncology, Department of Surgery, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0002-0443-1583
Carlo M CroceDepartment of Cancer Biology and Genetics, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0003-3788-1457
Joal D BeaneDivision of Surgical Oncology, Department of Surgery, The James Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.ORCID 0000-0002-4160-4340
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
Tissue and Pathology ResourcesU54CA168512 · NCI · SARC · PI CROWLEY, JOHN J · 2012 to 2016
$11.0M
Ex vivo generation of tumor-reactive T cells for adoptive cell transfer using an immune enhanced, patient derived tumor organoid-on-a-chip (iTOC)R21CA263137 · NCI · OHIO STATE UNIVERSITY · PI BEANE, JOAL D, SKARDAL, ALEKSANDER · 2022 to 2023
$396k
NCI NIH HHS P30 CA016058NCI NIH HHS R21 CA263137NCI NIH HHS U54 CA168512
6 · The paper itself

Abstract

Soft-tissue sarcomas (STS) are a rare and heterogeneous group of tumors that arise from connective tissue and can occur anywhere in the body. Among the plethora of over 50 different STS types, liposarcoma (LPS) is one of the most common. The subtypes of STS are characterized by distinct differences in tumor biology that drive responses to pharmacologic therapy and disparate oncologic outcomes. Small non-coding RNAs (sncRNA) are a heterogeneous class of regulatory RNAs involved in the regulation of gene expression by targeting mRNAs. Among the several types of sncRNAs, miRNAs and tRNA-derived ncRNAs are the most studied in the context of tumor biology, and we are learning more about the role of these molecules as important regulators of STS tumorigenesis and differentiation. However, challenges remain in translating these findings and no biomarkers or therapeutic approaches targeting sncRNAs have been developed for clinical use. In this review, we summarize the current landscape of sncRNAs in the context of STS with an emphasis on LPS, including the role of sncRNAs in the tumorigenesis and differentiation of these rare malignancies and their potential as novel biomarkers and therapeutic targets. Finally, we provide an appraisal of published studies and outline future directions to study sncRNAs in STS, including tRNA-derived ncRNAs.

Indexed as

RNA, Small UntranslatedSarcomaBiomarkersCarcinogenesisHumansLipopolysaccharidesRNA, TransferBiomarkersLipopolysaccharidesRNA, Small UntranslatedRNA, Transfer

Identifiers

PMID37052491
PMCPMC10238653
OpenAlexW4365442669

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.