Evidence map›Paper›PMID 33161413›Full record

ArticleCell death & disease2020

LINC00174 is a novel prognostic factor in thymic epithelial tumors involved in cell migration and lipid metabolism.

Claudia Tito, Federica Ganci, Andrea Sacconi, Silvia Masciarelli, Giulia Fontemaggi, Claudio Pulito, Enzo Gallo, Valentina Laquintana, Alessia Iaiza, Luciana De Angelis and 16 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  8. Long non‑coding RNAs, lipid metabolism and cancer (Review).Experimental and therapeutic medicine · 2023
    Review
  9. Retinoic acid and proteotoxic stress induce AML cell death overcoming stromal cell protection.Journal of experimental & clinical cancer research : CR · 2023
    Article
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  12. Review
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  16. Thymic Epithelial Neoplasms: Focusing on the Epigenetic Alterations.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Review
  19. Article
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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

26 authors at 8 institutions in 3 countries.

Claudia TitoDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Federica GanciOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Andrea SacconiOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Silvia MasciarelliDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Giulia FontemaggiOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0001-8332-8842
Claudio PulitoMolecular Chemoprevention Unit, "Regina Elena" National Cancer Institute - IFO, Rome, Italy.ORCID 0000-0002-0921-6962
Enzo GalloDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Valentina LaquintanaDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Alessia IaizaDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Luciana De AngelisDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Anna BenedettiDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Jessica CacciottiPathology Unit, ICOT, Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.
Selenia MigliettaDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Human Anatomy, Sapienza University of Rome, Rome, Italy.
Maria BellenghiCenter for Gender-Specific Medicine, Oncology Unit-Istituto Superiore di Sanita', Rome, Italy.
Alessandra CarèCenter for Gender-Specific Medicine, Oncology Unit-Istituto Superiore di Sanita', Rome, Italy.ORCID 0000-0003-4106-3342
Alessandro FaticaDepartment of Biology and Biotechnology 'Charles Darwin', Sapienza University of Rome, Rome, Italy.
Daniele DisoDepartment of Thoracic Surgery, Sapienza University of Rome, Rome, Italy.
Marco AnileDepartment of Thoracic Surgery, Sapienza University of Rome, Rome, Italy.
Vincenzo PetrozzaPathology Unit, ICOT, Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.
Francesco FaccioloThoracic Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Gabriele AlessandriniThoracic Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Edoardo PescarmonaDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Federico VenutaDepartment of Thoracic Surgery, Sapienza University of Rome, Rome, Italy.
Mirella MarinoDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy. mirella.marino@ifo.gov.it.
Giovanni BlandinoOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy. giovanni.blandino@ifo.gov.it.ORCID 0000-0002-6970-2241
Francesco FaziDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy. francesco.fazi@uniroma1.it.
Sapienza University of Rome · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Pasteur · ITIstituto Superiore di Sanità · ITEpigenomics (Germany) · DEIstituti Fisioterapici Ospitalieri · ITNational Cancer Institute · MYUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs are emerging as new molecular players involved in many biological processes, such as proliferation, apoptosis, cell cycle, migration, and differentiation. Their aberrant expression has been reported in variety of diseases. The aim of this study is the identification and functional characterization of clinically relevant lncRNAs responsible for the inhibition of miR-145-5p, a key tumor suppressor in thymic epithelial tumors (TETs). Starting from gene expression analysis by microarray in a cohort of fresh frozen thymic tumors and normal tissues, we identified LINC00174 as upregulated in TET. Interestingly, LINC00174 expression is positively correlated with a 5-genes signature in TETs. Survival analyses, performed on the TCGA dataset, showed that LINC00174 and its associated 5-genes signature are prognostic in TETs. Specifically, we show that LINC00174 favors the expression of SYBU, FEM1B, and SCD5 genes by sponging miR-145-5p, a well-known tumor suppressor microRNA downregulated in a variety of tumors, included TETs. Functionally, LINC00174 impacts on cell migration and lipid metabolism. Specifically, SCD5, one of the LINC00174-associated genes, is implicated in the control of lipid metabolism and promotes thymic cancer cells migration. Our study highlights that LINC00174 and its associated gene signature are relevant prognostic indicators in TETs. Of note, we here show that a key controller of lipid metabolism, SCD5, augments the migration ability of TET cells, creating a link between lipids and motility, and highlighting these pathways as relevant targets for the development of novel therapeutic approaches for TET.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticLipid MetabolismApoptosisBiomarkers, TumorCarrier ProteinsCell Cycle ProteinsCell ProliferationGene Expression ProfilingHumansNeoplasms, Glandular and EpithelialPrognosisRNA, Long NoncodingSurvival RateThymus NeoplasmsTumor Cells, CulturedBiomarkers, TumorCarrier ProteinsCell Cycle ProteinsFEM1B protein, humanRNA, Long Noncoding

Identifiers

PMID33161413
PMCPMC7648846
OpenAlexW3104787810

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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.