Pregled bibliografske jedinice broj: 626863
Defective signaling in a spontaneous transformation model of rat prostate epithelial cells
Defective signaling in a spontaneous transformation model of rat prostate epithelial cells // The FASEB Journal, 2012, Volume 26 (Meeting Abstract)
San Diego (CA), Sjedinjene Američke Države, 2012. str. lb474-lb474 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 626863 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Defective signaling in a spontaneous transformation model of rat prostate epithelial cells
Autori
Srajer Gajdosik, Martina ; Yang, DongQin ; Catterjee, Devasis ; Cross-Knorr, Sam ; Brilliant, Kate E. ; Gorman, Megan ; Hixson, Douglas C. ; Mills, David R.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
The FASEB Journal, 2012, Volume 26 (Meeting Abstract)
/ - , 2012, Lb474-lb474
Skup
Experimental Biology 2012
Mjesto i datum
San Diego (CA), Sjedinjene Američke Države, 21.04.2012. - 25.04.2012
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
cell signaling ; spontaneous transformation ; soft agar invasion ; prostate cancer
Sažetak
We describe an in vitro model of spontaneous transformation using normal rat prostate epithelial cells (PEC) that culminates at high passage (p>85) in anchorage independent growth when plated on soft agar. High passage PEC also formed large tumors in immunodeficient mice. We identified a small subpopulation of cells derived from the high passage anchorage independent cells that migrate through soft agar and expand on the underlying plastic substratum. In addition, several antibodies generated against rat liver epithelial cells of ductal origin that react strongly with rat prostate cells were examined. OC.2 was expressed by a low percentage of low and high passage PEC but was expressed by 100% of freshly isolated soft agar invasive (SAI) cells. Conversely, OC.4 and OC.5 were expressed by a high percentage of low and high passage PEC but were absent in SAI cells. Tumorigenicity experiments demonstrated that the SAI subpopulation was considerably more tumorigenic than high passage cells, evidenced by decreased latency period and increased tumor size. Immunoblot analysis identified alterations in signaling proteins belonging to EGFR and JAK/STAT pathways between low pass, high pass and SAI cells. We are investigating the role of these pathways on the phenotype of the 3 PEC models by examining anchorage independent growth, invasion, and tumorigenicity.
Izvorni jezik
Engleski
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE