Pregled bibliografske jedinice broj: 1054718
Oleanolic acid attenuates cisplatin-induced nephrotoxicity in mice and chemosensitizes human cervical cancer cells to cisplatin cytotoxicity
Oleanolic acid attenuates cisplatin-induced nephrotoxicity in mice and chemosensitizes human cervical cancer cells to cisplatin cytotoxicity // HDBMB2019 Crossroads in Life Sciences Book of Abstracts / Katalinić, Maja ; Dulić, Morana ; Stuparević Igor (ur.).
Zagreb, 2019. str. 107-107 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1054718 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Oleanolic acid attenuates cisplatin-induced
nephrotoxicity in mice and chemosensitizes
human cervical cancer cells to cisplatin
cytotoxicity
Autori
Potočnjak, Iva ; Šimić, Lidija ; Vukelić, Iva ; Domitrović, Robert
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
HDBMB2019 Crossroads in Life Sciences Book of Abstracts
/ Katalinić, Maja ; Dulić, Morana ; Stuparević Igor - Zagreb, 2019, 107-107
ISBN
978-953-95551-7-5
Skup
Congress of the Croatian Society of Biochemistry and Molecular Biology "Crossroads in Life Sciences" (HDBMB2019)
Mjesto i datum
Lovran, Hrvatska, 25.09.2019. - 28.09.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
oleanolic acid ; cisplatin ; kidney ; cervical cancer cells ; apoptosis ; autophagy
Sažetak
Oleanolic acid (OA) is a natural triterpenoid that possesses numerous beneficial health effects such as antioxidant, anti-inflammatory and anti- apoptotic activities. In this study, we investigated the therapeutic effect of OA (10 and 40 mg/kg) on cisplatin (CP)-induced (13 mg/kg) nephrotoxicity. Treatment with OA 40 mg/kg once daily for 2 days, 48 h after CP- intoxication, ameliorated the increased serum markers and histological features of kidney injury. CP administration increased renal expression of antioxidant and anti-inflammatory markers, which was reduced by OA. The increase in proapoptotic caspase-3 and -9 activations, with concomitant increase in poly (ADP-ribose) polymerase (PARP) cleavage, were dose- dependently inhibited by OA. Treatment with OA also ameliorated microtubule- associated protein 1A/1B-light chain 3B (LC3B)-II and autophagy- related protein (Atg) 5 expression induced by CP. The suppression of CP-induced oxidative stress, apoptosis, autophagy and inflammatory response by OA coincided with the inhibition of extracellular-regulated kinase (ERK) 1/2, signal transducer and activator of transcription (STAT) 3 and nuclear factor-kappa B (NF-κB). Interestingly, OA increased CP cytotoxicity in HeLa cervical cancer cells by inducing cytotoxic autophagy. The chemosensitization of HeLa cells to CP suggests a potential beneficial effect of OA in cervical cancer patients due to reduced CP dosage requirements, which requires further investigation.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Farmacija