Pregled bibliografske jedinice broj: 1062813
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 // FEBS3+ Conference: From Molecules to Living Systems : Final Programme & Book of Abstracts / Szuts, David ; Buday, Laszlo (ur.).
Veszprém, 2018. str. 236-236 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1062813 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
Pinterić, Marija ; Podgorski, Iva I. ; 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
FEBS3+ Conference: From Molecules to Living Systems : Final Programme & Book of Abstracts
/ Szuts, David ; Buday, Laszlo - Veszprém, 2018, 236-236
ISBN
978-615-527047-5
Skup
FEBS3+ conference "From molecules to living systems"
Mjesto i datum
Siófok, Mađarska, 02.09.2018. - 05.09.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
hyperoxia ; sirtuin 3 ; breast cancer ; mitochondria ; oxidative stress
Sažetak
Sirtuin 3 (Sirt3) has a promising role in cancer treatment, but there are controversies about its role in different types of cancer. Since its expression is reduced in many breast cancer cells and is associated with the production of reactive oxygen species (ROS), and hyperoxia supresses growth of certain mammary carcinoma cells, we studied the effect of de novo Sirt3 expression in human MCF-7 breast cancer cells upon 44 h long hyperoxic treatment. Sirt3 effects were enhanced upon hyperoxia: decreased metabolic activity, cellular growth and senescence, reduced expression of pro-angiogenic genes, induced metabolic switch from glycolysis towards OXPHOS, induced DNA damage, mitochondrial and antioxidant dysfunction, upregulated p53 and ROS levels. The mitigation of tumorigenic properties of MCF-7 cells and enhancement of their susceptibility to the hyperoxic treatment upon de novo Sirt3 expression indicates the promising therapeutic effect of these factors in breast cancer malignancies.
Izvorni jezik
Hrvatski
Znanstvena područja
Biologija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Ana Tadijan
(autor)
Tihomir Balog
(autor)
Iva Škrinjar
(autor)
Mirna Halasz
(autor)
Marija Pinterić
(autor)
Mladen Paradžik
(autor)
Robert Belužić
(autor)
Andreja Ambriović Ristov
(autor)
Marijana Popović-Hadžija
(autor)
Maja Marinović
(autor)
Sandra Sobočanec
(autor)