Growth arrest-specific 5 lncRNA as a valuable biomarker of chemoresistance in osteosarcoma.


Journal

Anti-cancer drugs
ISSN: 1473-5741
Titre abrégé: Anticancer Drugs
Pays: England
ID NLM: 9100823

Informations de publication

Date de publication:
01 03 2022
Historique:
pubmed: 20 1 2022
medline: 3 5 2022
entrez: 19 1 2022
Statut: ppublish

Résumé

Osteosarcoma is the most common primary malignant bone tumour in children and teenagers, and it is characterised by drug resistance and high metastatic potential. Increasing studies have highlighted the critical roles of long noncoding RNAs (lncRNAs) as oncogenes or tumour suppressors as well as new biomarkers and therapeutic targets in osteosarcoma. The growth arrest-specific 5 (GAS5) lncRNA can function as a tumour suppressor in several cancers. The present study aimed to validate GAS5 and other chemoresistance-associated lncRNAs as biomarkers in a cohort of primary osteosarcoma samples, to obtain predictive information on resistance or sensitivity to treatment. The GAS5 and a panel of lncRNAs related to chemoresistance [SNGH1, FOXD2-AS1, deleted in lymphocytic leukemia (DLEU2) and LINC00963] were evaluated in a cohort of osteosarcoma patients enrolled at the Careggi University Hospital. Total RNA was extracted from formalin-fixed paraffin-embedded (FFPE) tissue sections and the expression levels of the lncRNAs were quantified by qPCR. A bioinformatic analysis on deposited RNA-seq data was performed to validate the qPCR results. Clustering analysis shows that GAS5 could be linked to the expression of isoforms 02 and 04 of the lncRNA DLEU2, whereas the DLEU2 isoform 08 is linked to the lncRNA LINC00963. We found that GAS5 is significantly increased in patients with a good prognosis and is expressed differently between chemosensitive and chemoresistant osteosarcoma patients. However, the results obtained are not concordant with the in-silico analysis performed on the TARGET osteosarcoma dataset. In the future, we would enlarge the case series, including different disease settings.

Identifiants

pubmed: 35045526
doi: 10.1097/CAD.0000000000001263
pii: 00001813-202203000-00006
doi:

Substances chimiques

Biomarkers 0
RNA, Long Noncoding 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

278-285

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Références

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Auteurs

Simone Polvani (S)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence.

Filippo Martignano (F)

Core Research Laboratory, ISPRO, Firenze.

Guido Scoccianti (G)

Orthopaedic Oncology Unit.

Adriano Pasqui (A)

Medical Oncology Unit, Florence.

Anna Rita Palomba (AR)

Histopathology and Molecular Diagnostic Unit, Careggi University Hospital.

Silvo Conticello (S)

Core Research Laboratory, ISPRO, Firenze.

Andrea Galli (A)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence.

Ilaria Palchetti (I)

Department of Chemistry Ugo Schiff, Univerisity of Florence, Sesto Fiorentino.

Chiara Caporalini (C)

Pathology Unit, Anna Meyer Children's University Hospital.

Lorenzo Antonuzzo (L)

Medical Oncology Unit, Florence.
Department of Experimental and Clinical Medicine, University of Florence.

Domenico Andrea Campanacci (DA)

Orthopaedic Oncology Unit.
Department of Health Sciences, Orthopaedic Oncology Unit, Careggi University Hospital, University of Florence, Florence Italy.

Serena Pillozzi (S)

Medical Oncology Unit, Florence.

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