Metastatic MHC class I-negative mouse cells derived by transformation with human papillomavirus type 16
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
11225590
PubMed Central
PMC2363731
DOI
10.1054/bjoc.2000.1615
PII: S000709200091615X
Knihovny.cz E-zdroje
- MeSH
- buněčné linie MeSH
- experimentální nádory imunologie metabolismus patologie MeSH
- exprese genu MeSH
- histokompatibilita - antigeny třídy I metabolismus MeSH
- histokompatibilita - antigeny třídy II metabolismus MeSH
- imunoblotting MeSH
- imunohistochemie MeSH
- keratiny analýza MeSH
- lidé MeSH
- metastázy nádorů patologie MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- nádorové buňky kultivované cytologie účinky záření MeSH
- onkogenní proteiny virové genetika MeSH
- Papillomaviridae genetika MeSH
- Papillomavirus E7 - proteiny MeSH
- plazmidy aplikace a dávkování genetika imunologie MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- průtoková cytometrie MeSH
- Ras proteiny genetika metabolismus MeSH
- rekombinantní DNA MeSH
- represorové proteiny * MeSH
- RNA genetika metabolismus MeSH
- transfekce MeSH
- transformované buněčné linie MeSH
- transplantace nádorů MeSH
- virová transformace buněk * MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- E6 protein, Human papillomavirus type 16 MeSH Prohlížeč
- histokompatibilita - antigeny třídy I MeSH
- histokompatibilita - antigeny třídy II MeSH
- keratiny MeSH
- oncogene protein E7, Human papillomavirus type 16 MeSH Prohlížeč
- onkogenní proteiny virové MeSH
- Papillomavirus E7 - proteiny MeSH
- Ras proteiny MeSH
- rekombinantní DNA MeSH
- represorové proteiny * MeSH
- RNA MeSH
In the endeavour to develop a model for studying gene therapy of cancers associated with human papillomaviruses (HPVs), mouse cells were transformed with the HPV type 16 (HPV16) and activated H-ras oncogenes. This was done by cotransfection of plasmid p16HHMo, carrying the HPV16 E6/E7 oncogenes, and plasmid pEJ6.6, carrying the gene coding for human H-ras oncoprotein activated by the G12V mutation, into secondary C57BL/6 mouse kidney cells. An oncogenic cell line, designated MK16/1/IIIABC, was derived. The epithelial origin of the cells was confirmed by their expression of cytokeratins. No MHC class I and class II molecules were detected on the surface of MK16/1/IIIABC cells. Spontaneous metastases were observed in lymphatic nodes and lungs after prolonged growth of MK16/1/IIIABC-induced subcutaneous tumours. Lethally irradiated MK16/1/IIIABC cells induced protection against challenge with 10(5) homologous cells, but not against a higher cell dose (5 x 10(5)). Plasmids p16HHMo and pEJ6.6 were also used for preventive immunization of mice. In comparison with a control group injected with pBR322, they exhibited moderate protection, in terms of prolonged survival, against MK16/1/IIIABC challenge (P < 0.03). These data suggest that MK16/1/IIIABC cells may serve as a model for studying immune reactions against HPV16-associated human tumours.
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