CDC20 in and out of mitosis: a prognostic factor and therapeutic target in hematological malignancies.


Journal

Journal of experimental & clinical cancer research : CR
ISSN: 1756-9966
Titre abrégé: J Exp Clin Cancer Res
Pays: England
ID NLM: 8308647

Informations de publication

Date de publication:
30 Apr 2022
Historique:
received: 14 01 2022
accepted: 11 04 2022
entrez: 30 4 2022
pubmed: 1 5 2022
medline: 4 5 2022
Statut: epublish

Résumé

Cell division cycle 20 homologue (CDC20) is a well-known regulator of cell cycle, as it controls the correct segregation of chromosomes during mitosis. Many studies have focused on the biological role of CDC20 in cancer development, as alterations of its functionality have been linked to genomic instability and evidence demonstrated that high CDC20 expression levels are associated with poor overall survival in solid cancers. More recently, novel CDC20 functions have been demonstrated or suggested, including the regulation of apoptosis and stemness properties and a correlation with immune cell infiltration. Here, we here summarize and discuss the role of CDC20 inside and outside mitosis, starting from its network of interacting proteins. In the last years, CDC20 has also attracted more interest in the blood cancer field, being overexpressed and showing an association with prognosis both in myeloid and lymphoid malignancies. Preclinical findings showed that selective CDC20 and APC/C

Identifiants

pubmed: 35490245
doi: 10.1186/s13046-022-02363-9
pii: 10.1186/s13046-022-02363-9
pmc: PMC9055704
doi:

Substances chimiques

Cdc20 Proteins 0
Cell Cycle Proteins 0
CDC20 protein, human 156288-95-8

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

159

Subventions

Organisme : ERA-Per-Med
ID : ERAPERMED2018-275

Informations de copyright

© 2022. The Author(s).

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Auteurs

Samantha Bruno (S)

Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna and Institute of Hematology "L. e A. Seràgnoli", Bologna, Italy.

Andrea Ghelli Luserna di Rorà (A)

Biosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", via Piero Maroncelli 40, 47014, Meldola, FC, Italy. andrea.ghellilusernadirora@irst.emr.it.

Roberta Napolitano (R)

Biosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", via Piero Maroncelli 40, 47014, Meldola, FC, Italy.

Simona Soverini (S)

Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna and Institute of Hematology "L. e A. Seràgnoli", Bologna, Italy.

Giovanni Martinelli (G)

Scientific Directorate, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", via Piero Maroncelli 40, 47014, Meldola, FC, Italy.

Giorgia Simonetti (G)

Biosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", via Piero Maroncelli 40, 47014, Meldola, FC, Italy.

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