Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth

SUMMARY: Following the success of the highly active antiretroviral therapy, the potential of multidrug combination regimen for the management of cancer is intensely researched. The anticancer effects of curcumin on some human cell lines have been documented. Lopinavir is a FDA approved protease inhi...

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Autores principales: Adefolaju-Gbenga,Anthony, Mwakikunga,Anthony
Lenguaje:English
Publicado: Sociedad Chilena de Anatomía 2019
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BAX
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022019000200584
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spelling oai:scielo:S0717-950220190002005842019-09-11Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell GrowthAdefolaju-Gbenga,AnthonyMwakikunga,Anthony Lopinavir Curcumin VEGF165b BAX BCL2 Cervical cancer SUMMARY: Following the success of the highly active antiretroviral therapy, the potential of multidrug combination regimen for the management of cancer is intensely researched. The anticancer effects of curcumin on some human cell lines have been documented. Lopinavir is a FDA approved protease inhibitor with known apoptotic activities. Dysregulated apoptosis is important for the initiation of cancer while angiogenesis is required for cancer growth and development, this study therefore investigated the effects of the combination of lopinavir and curcumin on cell viability, apoptosis and the mRNA expression levels of key apoptotic and angiogenic genes; BAX, BCL2 and VEGF165b in two human cervical cell lines; human squamous cell carcinoma cells - uterine cervix (HCS-2) and transformed normal human cervical cells (NCE16IIA). The two human cervical cell lines were treated with physiologically relevant concentrations of the agents for 120 h following which BAX, BCL2 and VEGF165b mRNA expression were determined by Real Time qPCR. The Acridine Orange staining for the morphological evaluation of apoptotic cells was also performed. The combination of lopinavir and curcumin up-regulated pro-apoptotic BAX and antiangiogenic VEGF165b but down-regulated the mRNA levels of anti-apoptotic BCL2 mRNA in the human squamous cell carcinoma (HCS-2) cells only. The fold changes were statistically significant. Micrographs from Acridine Orange staining showed characteristic evidence of apoptosis in the human squamous cell carcinoma (HCS-2) cells only. The findings reported here suggest that the combination of curcumin and the FDA approved drug-lopinavir modulate the apoptotic and angiogenic pathway towards the inhibition of cervical cancer.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.37 n.2 20192019-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022019000200584en10.4067/S0717-95022019000200584
institution Scielo Chile
collection Scielo Chile
language English
topic Lopinavir
Curcumin
VEGF165b
BAX
BCL2
Cervical cancer
spellingShingle Lopinavir
Curcumin
VEGF165b
BAX
BCL2
Cervical cancer
Adefolaju-Gbenga,Anthony
Mwakikunga,Anthony
Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth
description SUMMARY: Following the success of the highly active antiretroviral therapy, the potential of multidrug combination regimen for the management of cancer is intensely researched. The anticancer effects of curcumin on some human cell lines have been documented. Lopinavir is a FDA approved protease inhibitor with known apoptotic activities. Dysregulated apoptosis is important for the initiation of cancer while angiogenesis is required for cancer growth and development, this study therefore investigated the effects of the combination of lopinavir and curcumin on cell viability, apoptosis and the mRNA expression levels of key apoptotic and angiogenic genes; BAX, BCL2 and VEGF165b in two human cervical cell lines; human squamous cell carcinoma cells - uterine cervix (HCS-2) and transformed normal human cervical cells (NCE16IIA). The two human cervical cell lines were treated with physiologically relevant concentrations of the agents for 120 h following which BAX, BCL2 and VEGF165b mRNA expression were determined by Real Time qPCR. The Acridine Orange staining for the morphological evaluation of apoptotic cells was also performed. The combination of lopinavir and curcumin up-regulated pro-apoptotic BAX and antiangiogenic VEGF165b but down-regulated the mRNA levels of anti-apoptotic BCL2 mRNA in the human squamous cell carcinoma (HCS-2) cells only. The fold changes were statistically significant. Micrographs from Acridine Orange staining showed characteristic evidence of apoptosis in the human squamous cell carcinoma (HCS-2) cells only. The findings reported here suggest that the combination of curcumin and the FDA approved drug-lopinavir modulate the apoptotic and angiogenic pathway towards the inhibition of cervical cancer.
author Adefolaju-Gbenga,Anthony
Mwakikunga,Anthony
author_facet Adefolaju-Gbenga,Anthony
Mwakikunga,Anthony
author_sort Adefolaju-Gbenga,Anthony
title Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth
title_short Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth
title_full Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth
title_fullStr Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth
title_full_unstemmed Lopinavir and Curcumin Directly Alters BAX/BCL2 and VEGF165b mRNA Levels to Suppress Human Squamous Cervical Carcinoma Cell Growth
title_sort lopinavir and curcumin directly alters bax/bcl2 and vegf165b mrna levels to suppress human squamous cervical carcinoma cell growth
publisher Sociedad Chilena de Anatomía
publishDate 2019
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022019000200584
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