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  5. Mapping prostate cancer pathobiology: A review of genetically engineered mouse models (GEMMs)

Mapping prostate cancer pathobiology: A review of genetically engineered mouse models (GEMMs)

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File(s)
41905611.pdf (2.38 MB)
No Access Until
2027-03-27
Permanent Link(s)
https://hdl.handle.net/1813/126890
Collections
Department of Pathology and Laboratory Medicine
Author
Pederzoli, Filippo
Pakula, Hubert
Rodrigues, Silvia
Garner, Richard
Nuzzo, Pier Vitale
Bleve, Sara
Rickman, David S.
Fanelli, Giuseppe Nicolò.
Loda, Massimo
Abstract

Prostate cancer (PCa) is the second most common malignancy in men and represents about 7% of newly diagnosed tumors worldwide (and up to 15% in developed countries). At the genomic level, PCa is generally characterized by copy number alterations and/or gene structural rearrangements that encompass multiple genes, including oncogenes such as ERG and MYC and tumor suppressor genes such as TP53 and PTEN. To advance our understanding of the role of specific genomic alterations in PCa, genetically engineered mouse models (GEMMs) have been pivotal in complementing large-scale human sequencing initiatives. In this Review, we focus on the main altered genes in PCa and how they have been modeled in different GEMMs to study the molecular mechanisms underlying PCa tumorigenesis and progression.

Journal / Series
Gene
Volume & Issue
996
Date Issued
2026-03-27
Publisher
Elsevier
Keywords
WCM Library Coordinated Deposit
•
Animals
•
Prostatic Neoplasms/genetics/pathology
•
Male
•
Mice
•
Humans
•
Disease Models, Animal
•
Mice, Transgenic
•
Genetic Engineering
•
GEMMs
•
Genetically engineered mouse models
•
Genomic alterations
•
Prostate cancer
•
Transgenic mice
Related DOI
https://doi.org/10.1016/j.gene.2026.150131
Previously Published as
Pederzoli F, Pakula H, Rodrigues S, Garner R, Nuzzo PV, Bleve S, Rickman DS, Fanelli GNò, Loda M. Mapping prostate cancer pathobiology: A review of genetically engineered mouse models (GEMMs). Gene. 2026;996:150131. doi: 10.1016/j.gene.2026.150131. PMID: 41905611.
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International
Rights URI
https://creativecommons.org/licenses/by-nc-nd/4.0/
Type
article

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