http://www.cnr.it/ontology/cnr/individuo/prodotto/ID175006
Proteomic Profiling of Human Melanoma Metastatic Cell Line Secretomes (Articolo in rivista)
- Type
- Label
- Proteomic Profiling of Human Melanoma Metastatic Cell Line Secretomes (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/pr200511f (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Micaela Rocco; Livia Malorni;Rosaria Cozzolino; Giuseppe Palmieri;Carla Rozzo; Antonella Manca;
Augusto Parente; Angela Chambery (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Life Sciences, Via Vivaldi 43, Second University of Naples, I-81100 Caserta, Italy
Proteomic and Biomolecular Mass Spectrometry Center, Institute of Food Science and Technology, National Research Council
(CNR), Via Roma 64, I-83100 Avellino, Italy
Unit of Cancer Genetics, Institute of Biomolecular Chemistry, National Research Council (CNR), Traversa La Crucca 3,
Baldinca Li Punti, I-07100 Sassari, Italy (literal)
- Titolo
- Proteomic Profiling of Human Melanoma Metastatic Cell Line Secretomes (literal)
- Abstract
- During the last few years, the incidence and mortality of
human melanoma have rapidly increased. Metastatic spread of malignant
melanoma is often associated with cancer progression with poor prognosis
and survival. These processes are controlled by dynamic interactions
between tumor melanocytes and neighboring stromal cells, whose deregulation
leads to the acquisition of cell proliferation capabilities and invasiveness.
It is increasingly clear that a key role in carcinogenesis is played by
secreted molecules either by tumor and surrounding stromal cells. To
address the issue of the proteins secreted during cancer progression, the
proteomic profiling of secretomes of cancer cell lines from different
melanoma metastases of the same patient (PE-MEL-41, PE-MEL-47, and
PE-MEL-43) was performed by applying a shotgun LC?MS/MS-based
approach. The results provide a list of candidate proteins associated with the
metastatic potential of PE-MEL melanoma cell lines. Among them, several matricellular proteins previously reported as involved in
melanoma aggressiveness were identified (i.e., SPARC, osteopontin). In addition, the extracellular matrix protein 1 that stimulates
proliferation and angiogenesis of endothelial cells as well as the fibronectin, involved in cell adhesion and motility, were identified.
The present work provides the basis to clarify the complex extracellular protein networks implicated in human melanoma cell
invasion, migration, and motility. (literal)
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