NONO is a member of the Drosophila behavior/human splicing (DBHS) family of proteins. NONO is a multifunctional protein that acts as a "molecular scaffold" to carry out versatile biological activities in many aspects of gene regulation, cell proliferation, apoptosis, migration, DNA damage repair, and maintaining cellular circadian rhythm coupled to the cell cycle. Besides these physiological activities, emerging evidence strongly indicates that NONO-altered expression levels promote tumorigenesis. In addition, NONO can undergo various post-transcriptional or post-translational modifications, including alternative splicing, phosphorylation, methylation, and acetylation, whose impact on cancer remains largely to be elucidated. Overall, altered NONO expression and/or activities are a common feature in cancer. This review provides an integrated scenario of the current understanding of the molecular mechanisms and the biological processes affected by NONO in different tumor contexts, suggesting that a better elucidation of the pleiotropic functions of NONO in physiology and tumorigenesis will make it a potential therapeutic target in cancer. In this respect, due to the complex landscape of NONO activities and interactions, we highlight caveats that must be considered during experimental planning and data interpretation of NONO studies.

The pleiotropic nature of NONO, a master regulator of essential biological pathways in cancers / D. Ronchetti, V. Traini, I. Silvestris, G. Fabbiano, F. Passamonti, N. Bolli, E. Taiana. - In: CANCER GENE THERAPY. - ISSN 0929-1903. - (2024), pp. 1-11. [Epub ahead of print] [10.1038/s41417-024-00763-x]

The pleiotropic nature of NONO, a master regulator of essential biological pathways in cancers

D. Ronchetti
Primo
;
V. Traini
Secondo
;
I. Silvestris;F. Passamonti;N. Bolli
Penultimo
;
E. Taiana
Ultimo
2024

Abstract

NONO is a member of the Drosophila behavior/human splicing (DBHS) family of proteins. NONO is a multifunctional protein that acts as a "molecular scaffold" to carry out versatile biological activities in many aspects of gene regulation, cell proliferation, apoptosis, migration, DNA damage repair, and maintaining cellular circadian rhythm coupled to the cell cycle. Besides these physiological activities, emerging evidence strongly indicates that NONO-altered expression levels promote tumorigenesis. In addition, NONO can undergo various post-transcriptional or post-translational modifications, including alternative splicing, phosphorylation, methylation, and acetylation, whose impact on cancer remains largely to be elucidated. Overall, altered NONO expression and/or activities are a common feature in cancer. This review provides an integrated scenario of the current understanding of the molecular mechanisms and the biological processes affected by NONO in different tumor contexts, suggesting that a better elucidation of the pleiotropic functions of NONO in physiology and tumorigenesis will make it a potential therapeutic target in cancer. In this respect, due to the complex landscape of NONO activities and interactions, we highlight caveats that must be considered during experimental planning and data interpretation of NONO studies.
No
English
Settore MED/06 - Oncologia Medica
Review essay
Esperti anonimi
Pubblicazione scientifica
Goal 3: Good health and well-being
   spontaneous Evolution and Clonal heterOgeneity in MoNoclonal Gammopathies: from mechanisms of progression to clinical management (bECOMiNG)
   bECOMiNG
   EUROPEAN COMMISSION
   H2020
   817997
2024
16-mar-2024
Springer Nature
1
11
11
Epub ahead of print
Periodico con rilevanza internazionale
pubmed
Aderisco
info:eu-repo/semantics/article
The pleiotropic nature of NONO, a master regulator of essential biological pathways in cancers / D. Ronchetti, V. Traini, I. Silvestris, G. Fabbiano, F. Passamonti, N. Bolli, E. Taiana. - In: CANCER GENE THERAPY. - ISSN 0929-1903. - (2024), pp. 1-11. [Epub ahead of print] [10.1038/s41417-024-00763-x]
open
Prodotti della ricerca::01 - Articolo su periodico
7
262
Article (author)
Periodico con Impact Factor
D. Ronchetti, V. Traini, I. Silvestris, G. Fabbiano, F. Passamonti, N. Bolli, E. Taiana
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1050620
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