Đorđević, S.

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  • Đorđević, S. (2)
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Marrubium vulgare ethanolic extract induces proliferation block, apoptosis, and cytoprotective autophagy in cancer cells in vitro

Paunović, Verica; Kosic, Milica; Đorđević, S.; Žugić, Ana; Đalinac, Nataša; Gašić, Uroš M.; Trajković, Vladimir S.; Harhaji-Trajkovic, Ljubica

(C M B Assoc, Poitiers, 2016)

TY  - JOUR
AU  - Paunović, Verica
AU  - Kosic, Milica
AU  - Đorđević, S.
AU  - Žugić, Ana
AU  - Đalinac, Nataša
AU  - Gašić, Uroš M.
AU  - Trajković, Vladimir S.
AU  - Harhaji-Trajkovic, Ljubica
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2434
AB  - Marrubium vulgare is a European medicinal plant with numerous beneficial effects on human health. The aim of the study was to isolate the plant ethanolic extract (MVE) and to investigate its anti-melanoma and anti-glioma effects. MVE was prepared by the modified pharmacopoeial percolation method and characterized by UHPLC-LTQ OrbiTrap MS. MVE dose-dependently reduced viability of melanoma (B16) and glioma (U251) cells, but not peripheral blood mononuclear cells. It arrested cell cycle in S+G2/M phase, which was associated with the activation of MAP kinase p38 and up-regulation of antiproliferative genes p53, p21 and p27. MVE induced oxidative stress, while antioxidants abrogated its antitumor effect. Furthermore, MVE induced mitochondrial depolarization, activation of caspase-9 and -3, Parp cleavage, phosphatidylserine exposure and DNA fragmentation. The mitochondrial apoptotic pathway was associated with the up-regulation of proapoptotic genes Pten, Bak1, Apaf1, and Puma and down-regulation of antiapoptotic genes survivin and Xiap. MVE also stimulated the expression of autophagy-related genes Atg5, Atg7, Atg12, Beclin-1, Gabarab and Sqstm1, as well as LC3-I conversion to the autophagosome associated LC3-II, while autophagy inhibitors exacerbated its cytotoxicity. Finally, the most abundant phenolic components of MVE, ferulic, p-hydroxybenzoic, caffeic and chlorogenic acids, did not exert a profound effect on viability of tumor cells, suggesting that other components individually or in concert are the mediators of the extracts' cytotoxicity. By demonstrating the ability of MVE to inhibit proliferation, induce apoptosis and cytoprotective autophagy, our results suggest that MVE, alone or combined with autophagy inhibitors, could be a good candidate for anti-melanoma and anti-glioma therapy.
PB  - C M B  Assoc, Poitiers
T2  - Cellular and Molecular Biology
T1  - Marrubium vulgare ethanolic extract induces proliferation block, apoptosis, and cytoprotective autophagy in cancer cells in vitro
VL  - 62
IS  - 11
SP  - 108
EP  - 114
DO  - 10.14715/cmb/2016.62.11.18
ER  - 
@article{
author = "Paunović, Verica and Kosic, Milica and Đorđević, S. and Žugić, Ana and Đalinac, Nataša and Gašić, Uroš M. and Trajković, Vladimir S. and Harhaji-Trajkovic, Ljubica",
year = "2016",
abstract = "Marrubium vulgare is a European medicinal plant with numerous beneficial effects on human health. The aim of the study was to isolate the plant ethanolic extract (MVE) and to investigate its anti-melanoma and anti-glioma effects. MVE was prepared by the modified pharmacopoeial percolation method and characterized by UHPLC-LTQ OrbiTrap MS. MVE dose-dependently reduced viability of melanoma (B16) and glioma (U251) cells, but not peripheral blood mononuclear cells. It arrested cell cycle in S+G2/M phase, which was associated with the activation of MAP kinase p38 and up-regulation of antiproliferative genes p53, p21 and p27. MVE induced oxidative stress, while antioxidants abrogated its antitumor effect. Furthermore, MVE induced mitochondrial depolarization, activation of caspase-9 and -3, Parp cleavage, phosphatidylserine exposure and DNA fragmentation. The mitochondrial apoptotic pathway was associated with the up-regulation of proapoptotic genes Pten, Bak1, Apaf1, and Puma and down-regulation of antiapoptotic genes survivin and Xiap. MVE also stimulated the expression of autophagy-related genes Atg5, Atg7, Atg12, Beclin-1, Gabarab and Sqstm1, as well as LC3-I conversion to the autophagosome associated LC3-II, while autophagy inhibitors exacerbated its cytotoxicity. Finally, the most abundant phenolic components of MVE, ferulic, p-hydroxybenzoic, caffeic and chlorogenic acids, did not exert a profound effect on viability of tumor cells, suggesting that other components individually or in concert are the mediators of the extracts' cytotoxicity. By demonstrating the ability of MVE to inhibit proliferation, induce apoptosis and cytoprotective autophagy, our results suggest that MVE, alone or combined with autophagy inhibitors, could be a good candidate for anti-melanoma and anti-glioma therapy.",
publisher = "C M B  Assoc, Poitiers",
journal = "Cellular and Molecular Biology",
title = "Marrubium vulgare ethanolic extract induces proliferation block, apoptosis, and cytoprotective autophagy in cancer cells in vitro",
volume = "62",
number = "11",
pages = "108-114",
doi = "10.14715/cmb/2016.62.11.18"
}
Paunović, V., Kosic, M., Đorđević, S., Žugić, A., Đalinac, N., Gašić, U. M., Trajković, V. S.,& Harhaji-Trajkovic, L.. (2016). Marrubium vulgare ethanolic extract induces proliferation block, apoptosis, and cytoprotective autophagy in cancer cells in vitro. in Cellular and Molecular Biology
C M B  Assoc, Poitiers., 62(11), 108-114.
https://doi.org/10.14715/cmb/2016.62.11.18
Paunović V, Kosic M, Đorđević S, Žugić A, Đalinac N, Gašić UM, Trajković VS, Harhaji-Trajkovic L. Marrubium vulgare ethanolic extract induces proliferation block, apoptosis, and cytoprotective autophagy in cancer cells in vitro. in Cellular and Molecular Biology. 2016;62(11):108-114.
doi:10.14715/cmb/2016.62.11.18 .
Paunović, Verica, Kosic, Milica, Đorđević, S., Žugić, Ana, Đalinac, Nataša, Gašić, Uroš M., Trajković, Vladimir S., Harhaji-Trajkovic, Ljubica, "Marrubium vulgare ethanolic extract induces proliferation block, apoptosis, and cytoprotective autophagy in cancer cells in vitro" in Cellular and Molecular Biology, 62, no. 11 (2016):108-114,
https://doi.org/10.14715/cmb/2016.62.11.18 . .
7
14

Effects of fentanyl and its analogs on electric field-stimulated contractions of rat ileum

Jankovic, S.M.; Beleslin, D.; Ivanović, Milovan; Kouvelas, D.; Argyriou, A.; Đorđević, S.; Mirtsou-Fidani, V.

(1997)

TY  - JOUR
AU  - Jankovic, S.M.
AU  - Beleslin, D.
AU  - Ivanović, Milovan
AU  - Kouvelas, D.
AU  - Argyriou, A.
AU  - Đorđević, S.
AU  - Mirtsou-Fidani, V.
PY  - 1997
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/45
AB  - Opiates inhibit electrically-stimulated contractions of isolated rat ileum acting on δ-receptors. We have examined effects of fentanyl and its three analogues on contractions of isolated rat ileum stimulated by electric field (20 V, 22 ms, 1 Hz). Fentanyl (from 10-9 M to 10-7 M) and trans-3-(carbomethoxy) fentanyl (from 10-7 M to 10-5 M) produced concentration-dependent decrease in amplitude of stimulated contractions, only fentanyl was about 40 times more potent. Cis-3-(methyl) fentanyl and Cis-3-(carbomethoxy) fentanyl did not affect stimulated contractions. Our study suggested that introduction of methyl and carbomethoxy moieties on position 3 of piperidine ring produced loss of fentanyl activity on δ-opioid receptors, cis-orientation being specially uafavourable.
T2  - Archives of Gastroenterohepatology
T1  - Effects of fentanyl and its analogs on electric field-stimulated contractions of rat ileum
VL  - 16
IS  - 2
SP  - 29
EP  - 32
UR  - https://hdl.handle.net/21.15107/rcub_cherry_45
ER  - 
@article{
author = "Jankovic, S.M. and Beleslin, D. and Ivanović, Milovan and Kouvelas, D. and Argyriou, A. and Đorđević, S. and Mirtsou-Fidani, V.",
year = "1997",
abstract = "Opiates inhibit electrically-stimulated contractions of isolated rat ileum acting on δ-receptors. We have examined effects of fentanyl and its three analogues on contractions of isolated rat ileum stimulated by electric field (20 V, 22 ms, 1 Hz). Fentanyl (from 10-9 M to 10-7 M) and trans-3-(carbomethoxy) fentanyl (from 10-7 M to 10-5 M) produced concentration-dependent decrease in amplitude of stimulated contractions, only fentanyl was about 40 times more potent. Cis-3-(methyl) fentanyl and Cis-3-(carbomethoxy) fentanyl did not affect stimulated contractions. Our study suggested that introduction of methyl and carbomethoxy moieties on position 3 of piperidine ring produced loss of fentanyl activity on δ-opioid receptors, cis-orientation being specially uafavourable.",
journal = "Archives of Gastroenterohepatology",
title = "Effects of fentanyl and its analogs on electric field-stimulated contractions of rat ileum",
volume = "16",
number = "2",
pages = "29-32",
url = "https://hdl.handle.net/21.15107/rcub_cherry_45"
}
Jankovic, S.M., Beleslin, D., Ivanović, M., Kouvelas, D., Argyriou, A., Đorđević, S.,& Mirtsou-Fidani, V.. (1997). Effects of fentanyl and its analogs on electric field-stimulated contractions of rat ileum. in Archives of Gastroenterohepatology, 16(2), 29-32.
https://hdl.handle.net/21.15107/rcub_cherry_45
Jankovic S, Beleslin D, Ivanović M, Kouvelas D, Argyriou A, Đorđević S, Mirtsou-Fidani V. Effects of fentanyl and its analogs on electric field-stimulated contractions of rat ileum. in Archives of Gastroenterohepatology. 1997;16(2):29-32.
https://hdl.handle.net/21.15107/rcub_cherry_45 .
Jankovic, S.M., Beleslin, D., Ivanović, Milovan, Kouvelas, D., Argyriou, A., Đorđević, S., Mirtsou-Fidani, V., "Effects of fentanyl and its analogs on electric field-stimulated contractions of rat ileum" in Archives of Gastroenterohepatology, 16, no. 2 (1997):29-32,
https://hdl.handle.net/21.15107/rcub_cherry_45 .