Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line

Background: Every year, many people around the world die from cancers. Among all types of cancers, brain cancer has been recognized as one of the most deadly cancers due to the late detection and limitations of current therapies, and thus it remains an unresolved problem. Glioblastoma occurs in diff...

Full description

Bibliographic Details
Main Authors: Zeinolabedin Sharifian Dastjerdi, Elyas Kargar Abargouei, Salman Jafari, Ebrahim Eftekhar, Majid Pourentezari, Fahimeh Zamani Rarani, Reza Afzalipour, Javad Mohajer Ansari, Mohammad Zamani Rarani
Format: Article
Language:English
Published: Hormozgan University of Medical Sciences 2020-09-01
Series:Disease and Diagnosis
Subjects:
Online Access:https://ddj.hums.ac.ir/PDF/iejm-175.pdf
_version_ 1818437637846859776
author Zeinolabedin Sharifian Dastjerdi
Elyas Kargar Abargouei
Salman Jafari
Ebrahim Eftekhar
Majid Pourentezari
Fahimeh Zamani Rarani
Reza Afzalipour
Javad Mohajer Ansari
Mohammad Zamani Rarani
author_facet Zeinolabedin Sharifian Dastjerdi
Elyas Kargar Abargouei
Salman Jafari
Ebrahim Eftekhar
Majid Pourentezari
Fahimeh Zamani Rarani
Reza Afzalipour
Javad Mohajer Ansari
Mohammad Zamani Rarani
author_sort Zeinolabedin Sharifian Dastjerdi
collection DOAJ
description Background: Every year, many people around the world die from cancers. Among all types of cancers, brain cancer has been recognized as one of the most deadly cancers due to the late detection and limitations of current therapies, and thus it remains an unresolved problem. Glioblastoma occurs in different parts of the central nervous system and is one of the most important causes of cancer death in people. In addition, there are many problems for the treatment of cancer cells. One of the limiting factors is the resistance of cancer cells to chemotherapy drugs. In this regard, the use of nanoparticles (NPs) is an effective method for overcoming this problem. Materials and Methods: In this study, iron oxide-NPs were synthesized and loaded on the folic and lomustine. Further, the size and morphology of NPs were assessed by transmission electron microscopy, X-ray photoelectron spectroscopy, and dynamic light scattering. Then, the U87-MG cell line was cultured in the Dulbecco’s Modified Eagle Medium and treated with nano, nano-folic, nano-lomustine (LUM), LUM, and complex, followed by evaluating 50% inhibitory concentration, tetrazolium assay, and caspase-6 activity. Results: Our results showed that cell viability decreased in LUM container groups by increasing the incubation time. Based on the caspase-6 activity analysis, the mortality rate increased in LUM container groups after 3 days. These findings indicated that LUM, complex, and nano-LUM increase cell death in U87MG. Conclusion: Finally, the results suggested that LUM in NPs could be applied as a safer form of drug delivery for targeting cancer.
first_indexed 2024-12-14T17:27:51Z
format Article
id doaj.art-280ecb4ffea94d36884af2dae8c61c6b
institution Directory Open Access Journal
issn 2717-3232
language English
last_indexed 2024-12-14T17:27:51Z
publishDate 2020-09-01
publisher Hormozgan University of Medical Sciences
record_format Article
series Disease and Diagnosis
spelling doaj.art-280ecb4ffea94d36884af2dae8c61c6b2022-12-21T22:53:11ZengHormozgan University of Medical SciencesDisease and Diagnosis2717-32322020-09-019312412910.34172/iejm.2020.23iejm-175Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell LineZeinolabedin Sharifian Dastjerdi0Elyas Kargar Abargouei1Salman Jafari2Ebrahim Eftekhar3Majid Pourentezari4Fahimeh Zamani Rarani5Reza Afzalipour6Javad Mohajer Ansari7Mohammad Zamani Rarani8Department of Anatomical Sciences, Medical School, Hormozgan University of Medical Sciences, Hormozgan, Iran.Department of Anatomical Sciences, Medical School, Hormozgan University of Medical Sciences, Hormozgan, Iran.Department of Radiology Technology, School of Paramedicine, Hamadan University of Medical Sciences, Hamadan, Iran.Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.Department of Biology and Anatomical Sciences, Medical School, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.Department of Anatomical Sciences, Medical School, Hormozgan University of Medical Sciences, Hormozgan, Iran.Department of Anatomical Sciences, Medical School, Hormozgan University of Medical Sciences, Hormozgan, Iran.Background: Every year, many people around the world die from cancers. Among all types of cancers, brain cancer has been recognized as one of the most deadly cancers due to the late detection and limitations of current therapies, and thus it remains an unresolved problem. Glioblastoma occurs in different parts of the central nervous system and is one of the most important causes of cancer death in people. In addition, there are many problems for the treatment of cancer cells. One of the limiting factors is the resistance of cancer cells to chemotherapy drugs. In this regard, the use of nanoparticles (NPs) is an effective method for overcoming this problem. Materials and Methods: In this study, iron oxide-NPs were synthesized and loaded on the folic and lomustine. Further, the size and morphology of NPs were assessed by transmission electron microscopy, X-ray photoelectron spectroscopy, and dynamic light scattering. Then, the U87-MG cell line was cultured in the Dulbecco’s Modified Eagle Medium and treated with nano, nano-folic, nano-lomustine (LUM), LUM, and complex, followed by evaluating 50% inhibitory concentration, tetrazolium assay, and caspase-6 activity. Results: Our results showed that cell viability decreased in LUM container groups by increasing the incubation time. Based on the caspase-6 activity analysis, the mortality rate increased in LUM container groups after 3 days. These findings indicated that LUM, complex, and nano-LUM increase cell death in U87MG. Conclusion: Finally, the results suggested that LUM in NPs could be applied as a safer form of drug delivery for targeting cancer.https://ddj.hums.ac.ir/PDF/iejm-175.pdftargeted therapynanoparticleapoptosiscaspaseu87mg
spellingShingle Zeinolabedin Sharifian Dastjerdi
Elyas Kargar Abargouei
Salman Jafari
Ebrahim Eftekhar
Majid Pourentezari
Fahimeh Zamani Rarani
Reza Afzalipour
Javad Mohajer Ansari
Mohammad Zamani Rarani
Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line
Disease and Diagnosis
targeted therapy
nanoparticle
apoptosis
caspase
u87mg
title Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line
title_full Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line
title_fullStr Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line
title_full_unstemmed Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line
title_short Evaluation of Lomustine-Loaded Iron Nanoparticles on Caspase-6 Gene Expression and Cell Viability in U87Mg Cell Line
title_sort evaluation of lomustine loaded iron nanoparticles on caspase 6 gene expression and cell viability in u87mg cell line
topic targeted therapy
nanoparticle
apoptosis
caspase
u87mg
url https://ddj.hums.ac.ir/PDF/iejm-175.pdf
work_keys_str_mv AT zeinolabedinsharifiandastjerdi evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT elyaskargarabargouei evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT salmanjafari evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT ebrahimeftekhar evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT majidpourentezari evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT fahimehzamanirarani evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT rezaafzalipour evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT javadmohajeransari evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline
AT mohammadzamanirarani evaluationoflomustineloadedironnanoparticlesoncaspase6geneexpressionandcellviabilityinu87mgcellline