Phosphatidylinositol 3-kinases (PI3Ks) are a group of lipid kinases that regulate signaling pathways involved in cell proliferation, adhesion, survival and motility. The PI3K pathway is considered to play an important role in tumorigenesis. Activating mutations of the p110a subunit of PI3K (PIK3CA) have been identified in a broad spectrum of tumors. Analyses of PIK3CA mutations reveals that they increase the PI3K signal, stimulate downstream Akt signaling, promote growth factor-independent growth and increase cell invasion and metastasis. In this review, we analyze the contribution of the PIK3CA mutations in cancer, and their possible implications for diagnosis and therapy.

PIK3CA mutations in human solid tumors: role in sensitivity to various therapeutic approaches

BASILE, Francesco;NICOLETTI, FERDINANDO;LIBRA, Massimo
2009-01-01

Abstract

Phosphatidylinositol 3-kinases (PI3Ks) are a group of lipid kinases that regulate signaling pathways involved in cell proliferation, adhesion, survival and motility. The PI3K pathway is considered to play an important role in tumorigenesis. Activating mutations of the p110a subunit of PI3K (PIK3CA) have been identified in a broad spectrum of tumors. Analyses of PIK3CA mutations reveals that they increase the PI3K signal, stimulate downstream Akt signaling, promote growth factor-independent growth and increase cell invasion and metastasis. In this review, we analyze the contribution of the PIK3CA mutations in cancer, and their possible implications for diagnosis and therapy.
2009
AKT; Cancer; Gene mutations; PI3K pathway; PIK3CA
File in questo prodotto:
File Dimensione Formato  
PIK3CA mutations in human solid tumors Role in sensitivity to various therapeutic approaches.pdf

accesso aperto

Tipologia: Versione Editoriale (PDF)
Dimensione 169.96 kB
Formato Unknown
169.96 kB Unknown Visualizza/Apri

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/20.500.11769/24907
Citazioni
  • ???jsp.display-item.citation.pmc??? 84
  • Scopus 164
  • ???jsp.display-item.citation.isi??? 155
social impact