Enhanced ZNF521 expression induces an aggressive phenotype in human ovarian carcinoma cell lines.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 28 06 2022
accepted: 05 09 2022
entrez: 3 10 2022
pubmed: 4 10 2022
medline: 6 10 2022
Statut: epublish

Résumé

Epithelial ovarian carcinoma (EOC) is the most lethal gynecological tumor, that almost inevitably relapses and develops chemo-resistance. A better understanding of molecular events underlying the biological behavior of this tumor, as well as identification of new biomarkers and therapeutic targets are the prerequisite to improve its clinical management. ZNF521 gene amplifications are present in >6% of OCs and its overexpression is associated with poor prognosis, suggesting that it may play an important role in OC. Increased ZNF521 expression resulted in an enhancement of OC HeyA8 and ES-2 cell growth and motility. Analysis of RNA isolated from transduced cells by RNA-Seq and qRT-PCR revealed that several genes involved in growth, proliferation, migration and tumor invasiveness are differentially expressed following increased ZNF521 expression. The data illustrate a novel biological role of ZNF521 in OC that, thanks to the early and easy detection by RNA-Seq, can be used as biomarker for identification and treatment of OC patients.

Identifiants

pubmed: 36191006
doi: 10.1371/journal.pone.0274785
pii: PONE-D-22-18337
pmc: PMC9529122
doi:

Substances chimiques

DNA-Binding Proteins 0
Transcription Factors 0
zinc finger protein 521, human 0
RNA 63231-63-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0274785

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Stefania Scicchitano (S)

Laboratory of Molecular Haematopoiesis and Stem Cell Biology, Department of Experimental and Clinical Medicine, University Magna Græcia, Catanzaro, Italy.

Ylenia Montalcini (Y)

Laboratory of Molecular Haematopoiesis and Stem Cell Biology, Department of Experimental and Clinical Medicine, University Magna Græcia, Catanzaro, Italy.

Valeria Lucchino (V)

Laboratory of Stem Cell Biology Department of Experimental and Clinical Medicine University Magna Graecia, Catanzaro, Italy.

Valentina Melocchi (V)

Unit of Cancer Biomarkers, Fondazione IRCCS-Casa Sollievo Della Sofferenza, San Giovanni Rotondo (FG), Italy.

Valerio Gigantino (V)

Laboratory of Molecular Medicine and Genomics, Department of Medicine, Surgery and Dentistry, University of Salerno, Baronissi (SA), Italy.

Emanuela Chiarella (E)

Laboratory of Molecular Haematopoiesis and Stem Cell Biology, Department of Experimental and Clinical Medicine, University Magna Græcia, Catanzaro, Italy.

Fabrizio Bianchi (F)

Unit of Cancer Biomarkers, Fondazione IRCCS-Casa Sollievo Della Sofferenza, San Giovanni Rotondo (FG), Italy.

Alessandro Weisz (A)

Laboratory of Molecular Medicine and Genomics, Department of Medicine, Surgery and Dentistry, University of Salerno, Baronissi (SA), Italy.
Genome Research Center for Health, University of Salerno Campus, Baronissi (SA), Italy.

Maria Mesuraca (M)

Laboratory of Molecular Haematopoiesis and Stem Cell Biology, Department of Experimental and Clinical Medicine, University Magna Græcia, Catanzaro, Italy.

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Classifications MeSH