Pubblicazioni

Pancreatic cancer stem cells characterization and secretome analysis  (2014)

Autori:
Dando, Ilaria; Biondani, Giulia; DALLA POZZA, Elisa; Brandi, Jessica; Costanzo, Chiara; Cecconi, Daniela; Palmieri, Marta
Titolo:
Pancreatic cancer stem cells characterization and secretome analysis
Anno:
2014
Tipologia prodotto:
Abstract in Atti di convegno
Tipologia ANVUR:
Abstract in Atti di convegno
Lingua:
Inglese
Titolo del Convegno:
FEBS EMBO 2014 Conference
Luogo:
Paris, FRANCE
Periodo:
AUG 30-SEP 04, 2014
Intervallo pagine:
780-780
Parole chiave:
pancreatic cancer; secretome; stem cells
Breve descrizione dei contenuti:
Pancreatic ductal adenocarcinoma (PDAC) is generally asymptomatic until the late stage of the disease and it often metastasizes. Cellular dissemination leading to metastasis occurs prior to the formation of an identifiable primary tumour and this event strictly correlates with the presence of cancer stem cells (CSC). These observations render imperative the identification of the specific biological features of CSC, in order to improve PDAC diagnosis and prognosis. We obtained in vitro CSC from different pancreatic ductal adenocarcinoma (PDAC) cell lines, named parental cell lines (P), using a selective medium. After the formation of spheres, which represent the first evidence of the staminal traits, cells have been characterized for the expression profile of different markers, e.g. CD44v6, Ep-CAM, E-caderin via FACS or Western Blot (WB) analyses. Furthermore, since CSC have been shown to represent the most threatening and resistant portion of the tumour, we tested their aggressiveness in mice subcutaneously injected with Panc1 P or CSC, at different cell concentrations. At the higher cell concentration (1*106 cells/mouse), mice injected with CSC displayed a significant higher tumour volume, as well as the tumour cellular morphology appeared to be very different, by histochemical analysis, compared to the mice injected with P cells. We are now performing other analyses, in particular immunohistochemistry on the tumour tissues, WB and real-time PCR on the tumour cells, to evaluate differences in morphology and marker expression between the two cell types. Moreover, to test the capacity of CSC to metastasize, we injected Panc1 P or CSC in the spleen, which was then excised after 5 minutes, with the advantage to follow metastasis formation, without the presence of a primary tumour. The invasive capacity of CSC is still under evaluation, through the monitoring of metastasis formation by MRI. Since it is known that cells secrete proteins for cell-cell communication and that the specificity of the secreted proteins can direct cells to distinct environments, we analysed the difference in protein secretion between Panc1 P and CSC by iTRAQ, an innovative protein quantification technique. The results showed that 71 proteins were secreted by CSC with an average fold change higher than 1.5 (p<0.001) relative to P cells, and 9 proteins were secreted only by CSC. We are validating these results with other techniques, mainly by WB on the secreted proteins in the culture medium, and by ELISA, using patient serum. The study of CSC and the analyses of secreted molecules is an approach with the strong potential to improve PDAC biology knowledge and to identify new potential early diagnostic markers.
Id prodotto:
94318
Handle IRIS:
11562/952673
ultima modifica:
18 settembre 2022
Citazione bibliografica:
Dando, Ilaria; Biondani, Giulia; DALLA POZZA, Elisa; Brandi, Jessica; Costanzo, Chiara; Cecconi, Daniela; Palmieri, Marta, Pancreatic cancer stem cells characterization and secretome analysis  in FEBS JOURNALAtti di "FEBS EMBO 2014 Conference" , Paris, FRANCE , AUG 30-SEP 04, 2014 , 2014pp. 780-780

Consulta la scheda completa presente nel repository istituzionale della Ricerca di Ateneo IRIS

Progetti Collegati
Titolo Dipartimento Responsabili
Ricerca di marcatori molecolari proteici nel tumore pancreatico tramite analisi proteomiche di cellule staminali tumorali Dipartimento Biotecnologie Daniela Cecconi, Marta Palmieri
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