Pregled bibliografske jedinice broj: 970756
De novo expression of transfected Sirt3 enhances susceptibility of human MCF-7 breast cancer cells to hyperoxia treatment
De novo expression of transfected Sirt3 enhances susceptibility of human MCF-7 breast cancer cells to hyperoxia treatment // Free Radical Biology and Medicine, Volume 120, Supplement 1
Lisabon, Portugal, 2018. str. S56-S56 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 970756 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
De novo expression of transfected Sirt3 enhances susceptibility of human MCF-7 breast cancer cells to hyperoxia treatment
Autori
Podgorski, Iva I ; Pinterić, Marija ; Sobočanec, Sandra ; Popović Hadžija, Marijana ; Paradžik, Mladen ; Dekanić, Ana ; Marinović, Maja ; Halasz, Mirna ; Belužić, Robert ; Davidović, Grazia ; Ambriović Ristov, Andreja ; Balog, Tihomir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Free Radical Biology and Medicine, Volume 120, Supplement 1
/ - , 2018, S56-S56
Skup
19th biennial meeting for the Society for Free Radical Research International (SFRRI)
Mjesto i datum
Lisabon, Portugal, 04.06.2018. - 07.06.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Hyperoxia ; MCF-7 ; ROS ; mitochondrial function ; sirtuin 3
Sažetak
Sirtuin 3 (Sirt3) has a promising role in cancer tumorigenesis and treatment, but there have been controversies about its role as tumor suppressor or promoter in different types of cancer. Hyperoxic treatment (i.e. generator of reactive oxygen species (ROS)) was shown to suppress growth of certain mammary carcinoma cells. Due to strikingly reduced Sirt3 level in many breast cancer cells and changes in its expression associated with the production of ROS, we studied the effect of de novo Sirt3 expression in the human MCF-7 breast cancer cells upon 44 hours long hyperoxic treatment. Effects of Sirt3 were enhanced upon hyperoxic treatment: decreased metabolic activity and cellular growth, reduced expression of pro-angiogenic genes, induced metabolic switch from glycolysis to OXPHOS, decreased cellular senescence, induced DNA damage and upregulated p53, increased ROS levels followed by mitochondrial and antioxidant dysfunction. The mitigation of tumorigenic properties and enhancement of the susceptibility of the MCF-7 breast cancer cells to the hyperoxic treatment upon de novo Sirt3 expression, gives rationale for further in vitro and particularly in vivo studies which would combine these two factors as an adjuvant tumor therapy in breast cancer malignancies.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
HRZZ-IP-2014-09-4533 - Sirtuin3 kao posrednik mitohondrijske funkcije u estrogen-ovisnoj otpornosti na oksidativni stres i prehranu s visokim udjelom masti (SuMERA) (Balog, Tihomir, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Ana Tadijan
(autor)
Tihomir Balog
(autor)
Mirna Halasz
(autor)
Iva Škrinjar
(autor)
Marija Pinterić
(autor)
Mladen Paradžik
(autor)
Robert Belužić
(autor)
Andreja Ambriović Ristov
(autor)
Marijana Popović-Hadžija
(autor)
Maja Marinović
(autor)
Sandra Sobočanec
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Conference Proceedings Citation Index - Science (CPCI-S)
- Scopus
- MEDLINE