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Hereditary prostate cancer – Primetime for genetic testing?

Articolo
Data di Pubblicazione:
2019
Abstract:
Prostate cancer (PCa) remains the most common cancer in men. The proportion of all PCa attributable to high-risk hereditary factors has been estimated to 5–15%. Recent landmark discoveries in PCa genetics led to the identification of germline mutations/alterations (eg. BRCA1, BRCA2, ATM or HOXB13), single nucleotide polymorphisms or copy number variations associated with PCa incidence and progression. However, offering germline testing to men with an assumed hereditary component is currently controversial. In the present review article, we provide an overview about the epidemiology and the genetic basis of PCa predisposition and critically discuss the significance and consequence in the clinical routine. In addition, we give an overview about genetic tests and report latest findings from ongoing clinical studies. Lastly, we discuss the impact of genetic testing in personalized therapy in advanced stages of the disease.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Genetic testing; Hereditary; Precision oncology; Prostate cancer; BRCA1 Protein; BRCA2 Protein; Checkpoint Kinase 2; Clinical Trials as Topic; DNA Copy Number Variations; Genetic Predisposition to Disease; Homeodomain Proteins; Humans; Male; Mutation; Polymorphism, Single Nucleotide; Precision Medicine; Prostatic Neoplasms; Genetic Testing
Elenco autori:
Heidegger, I.; Tsaur, I.; Borgmann, H.; Surcel, C.; Kretschmer, A.; Mathieu, R.; Visschere, P. D.; Valerio, M.; van den Bergh, R. C. N.; Ost, P.; Tilki, D.; Gandaglia, G.; Ploussard, G.
Autori di Ateneo:
GANDAGLIA GIORGIO
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/118415
Pubblicato in:
CANCER TREATMENT REVIEWS
Journal
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