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<dc:title>Scaffold proteins and cytoskeletal dynamics as modulators of Ras-ERK pathway in cancer</dc:title>
<dc:creator>Fuente Vivas, Dalia de la</dc:creator>
<dc:creator>Casar, Berta</dc:creator>
<dc:creator>Crespo, Pedro</dc:creator>
<dc:description>Póster presentado en: 41 Congreso de la SEBBM, Santander, 10-13 septiembre 2018</dc:description>
<dc:description>An overwhelming body of data unquestionably links the Ras-ERK&#xd;
pathway to the upbringing and progression of human malignancies.&#xd;
About 40% of human cancers harbor activating mutations in proteins&#xd;
involved in this signaling cascade, in particular Ras and Braf. In addition&#xd;
to the main proteins of this signaling pathway, there are several&#xd;
regulatory proteins known as scaffold proteins, that modulate the&#xd;
intensity, amplitude and duration of ERK signals. Interestingly, it can&#xd;
propose the scaffold proteins as antitumoral targets. Considering the&#xd;
hypothesis that scaffold proteins interact and regulate the signal&#xd;
transduction through the Ras-ERK pathway in a coordinated manner&#xd;
we try to find out how these interactions are regulated. Ras proteins&#xd;
are distributed in different types of plasma membrane: microdomains&#xd;
and endomembranes. We have previously demonstrated that&#xd;
compartmentalization dictates Ras utilization of effectors, the intensity&#xd;
of its signals and the biological response of the cells. Cell migration is&#xd;
critical for many physiological processes and is often misregulated in&#xd;
developmental disorders and pathological conditions including cancer.&#xd;
MAPK signaling are known regulators of cytoskeletal dynamics during&#xd;
cellular processes such as cell adhesion and migration. Our hypothesis&#xd;
is that localized ERK signaling mediated through recently identified&#xd;
scaffold proteins and its interactions with the cytoskeleton may&#xd;
regulate specific cellular responses. Here we propose that associations&#xd;
among different scaffold proteins and cytoskeleton will add one further&#xd;
degree of regulation for an already tightly regulated cascade and could&#xd;
provide a novel means for manipulating ERK signals, even with&#xd;
therapeutic purposes.</dc:description>
<dc:date>2026-10-07T10:59:47Z</dc:date>
<dc:date>2026-10-07T10:59:47Z</dc:date>
<dc:date>2018</dc:date>
<dc:type>info:eu-repo/semantics/conferenceObject</dc:type>
<dc:identifier>https://hdl.handle.net/10259/12244</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
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