Cyclin D1 interacts and collaborates with Ral GTPases enhancing cell detachment and motility
Fecha de publicación
2011Cita recomendada
Fernández, Rosa M. H.;
Ruiz Miró, Maria;
Dolcet Roca, Xavier;
Aldea, Martí;
Garí Marsol, Eloi;
.
(2011)
.
Cyclin D1 interacts and collaborates with Ral GTPases enhancing cell detachment and motility.
Oncogene, 2011, vol. 30, p. 1936-1946.
https://doi.org/10.1038/onc.2010.577.
Metadatos
Mostrar el registro completo del ítemResumen
Alterations in the levels of adhesion and motility of cells
are critical events in the development of metastasis. Cyclin
D1 (CycD1) is one of the most frequently amplified
oncogenes in many types of cancers and it is also
associated with the development of metastasis. Despite
this, we still do not know which are all the relevant
pathways by which CycD1 induces oncogenic processes.
CycD1 functions can be either dependent or independent
of the cyclin-dependent kinase Cdk4, and they affect
several cellular aspects such as proliferation, cell attachment
and migration. In this work, we reveal a novel
function of CycD1 that fosters our understanding of the
oncogenic potential of CycD1. We show that CycD1 binds
to the small GTPases Ral A and B, which are involved,
through exocyst regulation, in the progression of metastatic
cancers, inducing anchorage-independent growth
and cell survival of transformed cells. We show that
CycD1 binds active Ral complexes and the exocyst
protein Sec6, and co-localizes with Ral GTPases in
trans-Golgi and exocyst-rich regions. We have also
observed that CycD1–Cdk4 phosphorylates the Ral GEF
Rgl2 ‘in vitro’ and that CycD1–Cdk4 activity stimulates
accumulation of the Ral GTP active forms. In accordance
with this, our data suggest that CycD1–Cdk4 enhances
cell detachment and motility in collaboration with Ral
GTPases. This new function may help explain the
contribution of CycD1 to tumor spreading.