The functions of the tumor suppressor p53, which is mutated in 50% of cancers, include DNA repair, cell cycle arrest and apoptosis. Recent evidences have suggested that p53 regulates also necrotic cell death, which is implicated in several pathologies, such as cerebral stroke and myocardial infarction. However, the role of p53 in the regulation of necrosis and its in vivo contribution remain unknown. Here, we examined the role of p53 in germ cell death (GCD), a pathway of necrotic cell death that regulates tissue homeostasis during Drosophila spermatogenesis. We found that p53 mutant testes exhibited a reduced GCD, as other mutants of the necrotic pathway. Furthermore inhibition of GCD promoted tumor-like formations in the adult testes. I will present further characterization of p53-dependent necrosis and discuss its importance as a tumor suppressive mechanism during development.

p53-dependent necrosis suppresses tumorigenesis in Drosophila

Napoletano, Francesco;
2014-01-01

Abstract

The functions of the tumor suppressor p53, which is mutated in 50% of cancers, include DNA repair, cell cycle arrest and apoptosis. Recent evidences have suggested that p53 regulates also necrotic cell death, which is implicated in several pathologies, such as cerebral stroke and myocardial infarction. However, the role of p53 in the regulation of necrosis and its in vivo contribution remain unknown. Here, we examined the role of p53 in germ cell death (GCD), a pathway of necrotic cell death that regulates tissue homeostasis during Drosophila spermatogenesis. We found that p53 mutant testes exhibited a reduced GCD, as other mutants of the necrotic pathway. Furthermore inhibition of GCD promoted tumor-like formations in the adult testes. I will present further characterization of p53-dependent necrosis and discuss its importance as a tumor suppressive mechanism during development.
2014
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2940731
 Avviso

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact