Data di Pubblicazione:
2002
Abstract:
Ras genes are evolutionary conserved and codify for a monomeric G protein
binding GTP (active form) or GDP (inactive form). The ras genes are
ubiquitously expressed although mRNA analysis suggests different level
expression in tissue. Mutations in each ras gene frequently were found in
different tumors, suggesting their involvement in the development of
specific neoplasia. These mutations lead to a constitutive active and
potentially oncogenic protein that could cause a deregulation of cell
cycle. Ras protein moderates cellular responses at several mitogens and/or
differentiation factors and at external stimuli. These stimuli activate a
series of signal transduction pathways that either can be independent or
interconnected at different points. Recent observations begin to clarify
the complex relationship between Ras activation, apoptosis, and cellular
proliferation. A greater understanding of these processes would help to
identify the factors directly responsible for cell cycle deregulation in
several tumors, moreover it would help the design of specific therapeutic
strategies, for the control on the proliferation of neoplastic cells. We
summarize here current knowledge of ras genes family: structural and
functional characteristics of Ras proteins and their links with cell cycle
and cancer.
Tipologia CRIS:
01.01 Articolo in rivista
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