Dobutovic, B.

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  • Dobutovic, B. (2)
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Author's Bibliography

Involvement of the ADAM 12 in Thrombin-Induced Rats VSMCs Proliferation

Smiljanić, Katarina; Dobutovic, B.; Obradović, Milan M.; Nikolić, Dragana; Marche, Pierre; Isenović, Esma R.

(2011)

TY  - JOUR
AU  - Smiljanić, Katarina
AU  - Dobutovic, B.
AU  - Obradović, Milan M.
AU  - Nikolić, Dragana
AU  - Marche, Pierre
AU  - Isenović, Esma R.
PY  - 2011
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4468
AB  - Cardiovascular disease is the largest single cause of mortality and its major underlying pathology is atherosclerosis. The proliferation of vascular smooth muscle cells (VSMCs) is a key event in the pathogenesis of the various vascular diseases, including atherosclerosis and hypertension. Thrombin (Thr) is involved in the abnormal proliferation of VSMCs associated with atherosclerosis and hypertension. ADAMs (A Disintegrin And Metalloproteinase) are transmembrane metalloproteinases, belonging to the adamalysins group, that are distinct from matrix metalloproteinases (MMPs) in a way as they have an extracellular disintegrin domain and cytoplasmic domain that can associate with intracellular proteins. There is limited knowledge about the presence of ADAM metalloproteinase activity in Thr-induced VSMCs proliferation. Therefore, this review examines recent findings in signaling mechanisms employed by Thr in modulating the regulation of proliferation of VSMCs with particular emphasis on involvement of ADAM 12 which has been identified as an important mediator of VSMCs hypertrophy and vascular diseases. These findings are critical for understanding the role of Thr in vascular biology and vascular diseases.
T2  - Current Medicinal Chemistry
T1  - Involvement of the ADAM 12 in Thrombin-Induced Rats VSMCs Proliferation
VL  - 18
IS  - 22
SP  - 3382
EP  - 3386
DO  - 10.2174/092986711796504709
ER  - 
@article{
author = "Smiljanić, Katarina and Dobutovic, B. and Obradović, Milan M. and Nikolić, Dragana and Marche, Pierre and Isenović, Esma R.",
year = "2011",
abstract = "Cardiovascular disease is the largest single cause of mortality and its major underlying pathology is atherosclerosis. The proliferation of vascular smooth muscle cells (VSMCs) is a key event in the pathogenesis of the various vascular diseases, including atherosclerosis and hypertension. Thrombin (Thr) is involved in the abnormal proliferation of VSMCs associated with atherosclerosis and hypertension. ADAMs (A Disintegrin And Metalloproteinase) are transmembrane metalloproteinases, belonging to the adamalysins group, that are distinct from matrix metalloproteinases (MMPs) in a way as they have an extracellular disintegrin domain and cytoplasmic domain that can associate with intracellular proteins. There is limited knowledge about the presence of ADAM metalloproteinase activity in Thr-induced VSMCs proliferation. Therefore, this review examines recent findings in signaling mechanisms employed by Thr in modulating the regulation of proliferation of VSMCs with particular emphasis on involvement of ADAM 12 which has been identified as an important mediator of VSMCs hypertrophy and vascular diseases. These findings are critical for understanding the role of Thr in vascular biology and vascular diseases.",
journal = "Current Medicinal Chemistry",
title = "Involvement of the ADAM 12 in Thrombin-Induced Rats VSMCs Proliferation",
volume = "18",
number = "22",
pages = "3382-3386",
doi = "10.2174/092986711796504709"
}
Smiljanić, K., Dobutovic, B., Obradović, M. M., Nikolić, D., Marche, P.,& Isenović, E. R.. (2011). Involvement of the ADAM 12 in Thrombin-Induced Rats VSMCs Proliferation. in Current Medicinal Chemistry, 18(22), 3382-3386.
https://doi.org/10.2174/092986711796504709
Smiljanić K, Dobutovic B, Obradović MM, Nikolić D, Marche P, Isenović ER. Involvement of the ADAM 12 in Thrombin-Induced Rats VSMCs Proliferation. in Current Medicinal Chemistry. 2011;18(22):3382-3386.
doi:10.2174/092986711796504709 .
Smiljanić, Katarina, Dobutovic, B., Obradović, Milan M., Nikolić, Dragana, Marche, Pierre, Isenović, Esma R., "Involvement of the ADAM 12 in Thrombin-Induced Rats VSMCs Proliferation" in Current Medicinal Chemistry, 18, no. 22 (2011):3382-3386,
https://doi.org/10.2174/092986711796504709 . .
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Insulin Regulation of Proliferation Involves Activation of AKT and ERK 1/2 Signaling Pathways in Vascular Smooth Muscle Cells

Isenović, Esma R.; Fretaud, M.; Korićanac, Goran; Sudar, Emina; Velebit, Jelena; Dobutovic, B.; Marche, Pierre

(2009)

TY  - JOUR
AU  - Isenović, Esma R.
AU  - Fretaud, M.
AU  - Korićanac, Goran
AU  - Sudar, Emina
AU  - Velebit, Jelena
AU  - Dobutovic, B.
AU  - Marche, Pierre
PY  - 2009
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3718
AB  - This investigation used primary cultured rat vascular smooth muscle cells (VSMCs) to examine the effect of insulin (INS) on proliferation of VSMCs. In this study, we investigated the role of protein kinase B (Akt) and p42/44 mitogen-activated protein kinase (ERK 1/2) signaling pathways in mediating the mitogenic action of INS in VSMCs. Incubation of rat VSMCs with INS (100 nM) for 10 min resulted man increase of Akt phosphorylation by 6-fold (p LT 0.001) and ERK 1/2 phosphorylation by 3-fold (p LT 0.001). Pretreatment for 15 min with 10 mu M of PI3K/Akt inhibitor LY294002 or with 20 mu M PD98059, inhibitor of ERK 1/2, significantly reduced INS-stimulated Akt and ERK 1/2 phosphorylation by 76 and 75%, respectively. Prolonged treatment of VSMCs with INS for 24 h did not have an effect on either Akt or ERK 1/2 phosphorylation. Incubation of rat VSMCs with INS resulted in an increase of VSMCs proliferation by 87% (p LT 0.001.) The effect of INS on VSMCs proliferation was significantly reduced by 68% by pretreatment with LY294002 (p GT 0.01) and by 71% (p GT 0.01) by pretreatment with PD98059. These results indicate that INS acts through Akt and ERK 1/2 signaling pathways to Up-regulate proliferation of VSMCs.
T2  - Experimental and Clinical Endocrinology and Diabetes
T1  - Insulin Regulation of Proliferation Involves Activation of AKT and ERK 1/2 Signaling Pathways in Vascular Smooth Muscle Cells
VL  - 117
IS  - 5
SP  - 214
EP  - 219
DO  - 10.1055/s-0028-1085470
ER  - 
@article{
author = "Isenović, Esma R. and Fretaud, M. and Korićanac, Goran and Sudar, Emina and Velebit, Jelena and Dobutovic, B. and Marche, Pierre",
year = "2009",
abstract = "This investigation used primary cultured rat vascular smooth muscle cells (VSMCs) to examine the effect of insulin (INS) on proliferation of VSMCs. In this study, we investigated the role of protein kinase B (Akt) and p42/44 mitogen-activated protein kinase (ERK 1/2) signaling pathways in mediating the mitogenic action of INS in VSMCs. Incubation of rat VSMCs with INS (100 nM) for 10 min resulted man increase of Akt phosphorylation by 6-fold (p LT 0.001) and ERK 1/2 phosphorylation by 3-fold (p LT 0.001). Pretreatment for 15 min with 10 mu M of PI3K/Akt inhibitor LY294002 or with 20 mu M PD98059, inhibitor of ERK 1/2, significantly reduced INS-stimulated Akt and ERK 1/2 phosphorylation by 76 and 75%, respectively. Prolonged treatment of VSMCs with INS for 24 h did not have an effect on either Akt or ERK 1/2 phosphorylation. Incubation of rat VSMCs with INS resulted in an increase of VSMCs proliferation by 87% (p LT 0.001.) The effect of INS on VSMCs proliferation was significantly reduced by 68% by pretreatment with LY294002 (p GT 0.01) and by 71% (p GT 0.01) by pretreatment with PD98059. These results indicate that INS acts through Akt and ERK 1/2 signaling pathways to Up-regulate proliferation of VSMCs.",
journal = "Experimental and Clinical Endocrinology and Diabetes",
title = "Insulin Regulation of Proliferation Involves Activation of AKT and ERK 1/2 Signaling Pathways in Vascular Smooth Muscle Cells",
volume = "117",
number = "5",
pages = "214-219",
doi = "10.1055/s-0028-1085470"
}
Isenović, E. R., Fretaud, M., Korićanac, G., Sudar, E., Velebit, J., Dobutovic, B.,& Marche, P.. (2009). Insulin Regulation of Proliferation Involves Activation of AKT and ERK 1/2 Signaling Pathways in Vascular Smooth Muscle Cells. in Experimental and Clinical Endocrinology and Diabetes, 117(5), 214-219.
https://doi.org/10.1055/s-0028-1085470
Isenović ER, Fretaud M, Korićanac G, Sudar E, Velebit J, Dobutovic B, Marche P. Insulin Regulation of Proliferation Involves Activation of AKT and ERK 1/2 Signaling Pathways in Vascular Smooth Muscle Cells. in Experimental and Clinical Endocrinology and Diabetes. 2009;117(5):214-219.
doi:10.1055/s-0028-1085470 .
Isenović, Esma R., Fretaud, M., Korićanac, Goran, Sudar, Emina, Velebit, Jelena, Dobutovic, B., Marche, Pierre, "Insulin Regulation of Proliferation Involves Activation of AKT and ERK 1/2 Signaling Pathways in Vascular Smooth Muscle Cells" in Experimental and Clinical Endocrinology and Diabetes, 117, no. 5 (2009):214-219,
https://doi.org/10.1055/s-0028-1085470 . .
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