Pregled bibliografske jedinice broj: 1138381
PDZ-domain Containing Protein NHERF-2 is a Novel Target of Human Papillomavirus type 16 (HPV-16) and HPV- 18
PDZ-domain Containing Protein NHERF-2 is a Novel Target of Human Papillomavirus type 16 (HPV-16) and HPV- 18 // ICGEB DNA Tumour Virus Meeting
Udine: Lithostampa SrL, 2019. str. 119-119 (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1138381 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
PDZ-domain Containing Protein NHERF-2 is a
Novel Target of
Human Papillomavirus type 16 (HPV-16) and HPV-
18
Autori
Saidu, Nathaniel Edward Bennett ; Filić Mileta, Vedrana ; Thomas, Miranda ; Miljković, Frane ; Banks, Lawrence ; Tomaić, Vjekoslav
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
ICGEB DNA Tumour Virus Meeting
/ - Udine : Lithostampa SrL, 2019, 119-119
Skup
ICGEB DNA Tumour Virus Meeting
Mjesto i datum
Trst, Italija, 09.07.2019. - 14.07.2019
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
HPV ; E6 oncoprotein ; cervical cancer ; NHERF-2 ; p27 ; cyclin D1 ; cell proliferation
Sažetak
Cancer causing HPV E6 oncoproteins have a Class I PDZ- binding motif (PBM) on their C-termini, which play critical roles that are related to HPV life cycle and HPV-induced malignancies. E6 oncoproteins use these PBMs to interact and target for a proteasome mediated degradation a plethora of cellular substrates that contain PDZ domains and are involved in the regulation of various cellular pathways. In this study, we show that both HPV-16 and HPV-18 E6 can interact with Na+/H+ exchange regulatory factor 2 (NHERF-2), a PDZ domain containing protein, which among other cellular functions also behaves as a tumor suppressor that regulates endothelial proliferation. The interaction between the E6 oncoproteins and NHERF-2 is PBM dependent and this consequently results in a proteasome-mediated degradation of NHERF-2. We further confirmed this effect in cells derived from HPV-16 and HPV- 18 positive cervical tumors, where we show that NHERF-2 protein turnover is increased in the presence of E6. Finally, our data indicate that E6-mediated NHERF-2 degradation results in p27 downregulation and cyclin D1 upregulation, which leads to an accelerated cellular proliferation. To our knowledge, this is the first report which demonstrates that E6 oncoproteins can stimulate cell proliferation by indirectly regulating p27 via targeting a PDZ-domain containing protein.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Projekti:
HRZZ-IP-2016-06-2246 - Rasvjetljivanje onkogenih funkcija E6/E7 HPV-a na različitim anatomskim mjestima (HPVHNC) (Tomaić, Vjekoslav, HRZZ - 2016-06) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb