An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines
Aim: We sought to assess the effect of sunitinib and lapatinib applied either alone or in combination, on U87 and M059K glioma cells. Methods: Both cell lines were cultured as recommended by the manufacturer. Sunitinib and lapatinib were applied, either separately or in combination, in the culture...
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nemertes-10889-64582022-09-05T13:58:48Z An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines Giannopoulou, Efstathia Dimitropoulos, Konstantinos Argyriou, Andreas Koutras, Angelos Dimitrakopoulos, Fotinos Kalofonos, Haralabos Γιαννοπούλου, Ευσταθία Δημητρόπουλος, Κωνσταντίνος Αργυρίου, Ανδρέας Κούτρας, Άγγελος Δημητρακόπουλος, Φωτεινός Καλόφωνος, Χαράλαμπος Lapatinib Sunitinib Malignant glioma Proliferation Apoptosis Migration MMPs Κακοήθες γλοίωμα Πολλαπλασιασμός Απόπτωση Μετανάστευση Aim: We sought to assess the effect of sunitinib and lapatinib applied either alone or in combination, on U87 and M059K glioma cells. Methods: Both cell lines were cultured as recommended by the manufacturer. Sunitinib and lapatinib were applied, either separately or in combination, in the cultured cells after cell attachment at doses of 10nM, 100nM, 1μM and 10 μM. To determine whether the agents affect the proliferation of glioma cells, the 3-[4,5-dimethylthiazol-2-yl]-2,5 dimethyltetrazolium bromide assay was used. Apoptosis was detected using annexin V/propidium iodide detection assay, migration assay was performed in 24-well microchemotaxis chambers. The release of MMPs into the culture medium of U87 and M059K cells was measured by zymography. Results: Both agents, administered either alone or in combination, decreased cell proliferation in a dose-dependent manner 48 h after their application in both cell lines. The inhibition of their combination was statistically different than the inhibition of each agent alone. Apoptosis was increased and migration of U87 and M059K cells was inhibited either by each agent alone or their combination. MMPs levels remained unaffected by the application of both agents in U87 cells. However, MMP-9 and MMP-2 levels were decreased 48h after treatment of M059K cells with sunitinib either alone or in combination with lapatinib. Conclusion: Sunitinib and/or lapatinib appear to exhibit significant effects on proliferation, apoptosis and migration of glioma cells. When applied alone, sunitinib appears to be a more potent inhibitor than lapatinib. 2013-12-03T10:43:48Z 2013-12-03T10:43:48Z 2010-10 2013-12-03 Journal (paper) Giannopoulou E, Dimitropoulos K, Argyriou AA, Koutras AK, Dimitrakopoulos F, Kalofonos HP. An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines. Invest New Drugs, 2010; 28:554-60 http://hdl.handle.net/10889/6458 en application/pdf Investigational New Drugs |
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Nemertes |
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English |
topic |
Lapatinib Sunitinib Malignant glioma Proliferation Apoptosis Migration MMPs Κακοήθες γλοίωμα Πολλαπλασιασμός Απόπτωση Μετανάστευση |
spellingShingle |
Lapatinib Sunitinib Malignant glioma Proliferation Apoptosis Migration MMPs Κακοήθες γλοίωμα Πολλαπλασιασμός Απόπτωση Μετανάστευση Giannopoulou, Efstathia Dimitropoulos, Konstantinos Argyriou, Andreas Koutras, Angelos Dimitrakopoulos, Fotinos Kalofonos, Haralabos An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
description |
Aim: We sought to assess the effect of sunitinib and lapatinib applied either alone or in combination, on U87 and M059K glioma cells.
Methods: Both cell lines were cultured as recommended by the manufacturer. Sunitinib and lapatinib were applied, either separately or in combination, in the cultured cells after cell attachment at doses of 10nM, 100nM, 1μM and 10 μM. To determine whether the agents affect the proliferation of glioma cells, the 3-[4,5-dimethylthiazol-2-yl]-2,5 dimethyltetrazolium bromide assay was used. Apoptosis was detected using annexin V/propidium iodide detection assay, migration assay was performed in 24-well microchemotaxis chambers. The release of MMPs into the culture medium of U87 and M059K cells was measured by zymography.
Results: Both agents, administered either alone or in combination, decreased cell proliferation in a dose-dependent manner 48 h after their application in both cell lines. The inhibition of their combination was statistically different than the inhibition of each agent alone. Apoptosis was increased and migration of U87 and M059K cells was inhibited either by each agent alone or their combination. MMPs levels remained unaffected by the application of both agents in U87 cells. However, MMP-9 and MMP-2 levels were decreased 48h after treatment of M059K cells with sunitinib either alone or in combination with lapatinib.
Conclusion: Sunitinib and/or lapatinib appear to exhibit significant effects on proliferation, apoptosis and migration of glioma cells. When applied alone, sunitinib appears to be a more potent inhibitor than lapatinib. |
author2 |
Γιαννοπούλου, Ευσταθία |
author_facet |
Γιαννοπούλου, Ευσταθία Giannopoulou, Efstathia Dimitropoulos, Konstantinos Argyriou, Andreas Koutras, Angelos Dimitrakopoulos, Fotinos Kalofonos, Haralabos |
format |
Journal (paper) |
author |
Giannopoulou, Efstathia Dimitropoulos, Konstantinos Argyriou, Andreas Koutras, Angelos Dimitrakopoulos, Fotinos Kalofonos, Haralabos |
author_sort |
Giannopoulou, Efstathia |
title |
An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
title_short |
An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
title_full |
An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
title_fullStr |
An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
title_full_unstemmed |
An in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
title_sort |
in vitro study, evaluating the effect of sunitinib and/or lapatinib on two glioma cell lines |
publishDate |
2013 |
url |
http://hdl.handle.net/10889/6458 |
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