Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/178638
Title: Caveolin-1 in sarcomas: friend or foe?
Author: Sáinz Jaspeado, Miguel Guillermo
Martín Liberal, Juan Jesús
Lagares Tena, Laura
Mateo Lozano, Silvia
García del Muro Solans, Xavier
Tirado, Oscar M.
Keywords: Fisiologia
Sarcoma
Diagnòstic
Etiologia
Physiology
Sarcoma
Diagnosis
Etiology
Issue Date: 1-Apr-2011
Publisher: Impact Journals
Abstract: Sarcomas represent a heterogeneous group of tumors with a complex and difficult reproducible classification. Their pathogenesis is poorly understood and there are few effective treatment options for advanced disease. Caveolin-1 is a multifunctional scaffolding protein with multiple binding partners that regulates multiple cancer-associated processes including cellular transformation, tumor growth, cell death and survival, multidrug resistance, angiogenesis, cell migration and metastasis. However, ambiguous roles have been ascribed to caveolin-1 in signal transduction and cancer, including sarcomas. In particular, evidence indicating that caveolin-1 function is cell context dependent has been repeatedly reported. Caveolin-1 appears to act as a tumor suppressor protein at early stages of cancer progression. In contrast, a growing body of evidence indicates that caveolin-1 is up-regulated in several multidrug-resistant and metastatic cancer cell lines and human tumor specimens. This review is focused on the role of caveolin-1 in several soft tissue and bone sarcomas and discusses the use of this protein as a potential diagnostic and prognostic marker and as a therapeutic target.
Note: Reproducció del document publicat a: https://doi.org/10.18632/oncotarget.255
It is part of: Oncotarget, 2011, vol. 2, num. 4, p. 305-312
URI: http://hdl.handle.net/2445/178638
Related resource: https://doi.org/10.18632/oncotarget.255
ISSN: 1949-2553
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Clíniques)

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