Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types
Breast cancer (BC) is the most common cause of cancer-related death worldwide. Although platinum-based drugs (PBDs) are effective anticancer agents, responsive patients eventually become resistant. While resistance of some cancers to PBDs has been explored, the cellular responses of BC cells are not...
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doaj-4ab497235142405080b17c2ffaaaedd62020-11-24T23:08:56ZengHindawi LimitedBioMed Research International2314-61332314-61412017-01-01201710.1155/2017/31787943178794Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell TypesShadia Al-Bahlani0Buthaina Al-Dhahli1Kawther Al-Adawi2Abdurahman Al-Nabhani3Mohamed Al-Kindi4Department of Allied Health Sciences, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, OmanDepartment of Allied Health Sciences, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, OmanDepartment of Pathology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, OmanDepartment of Pathology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, OmanDepartment of Pathology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, OmanBreast cancer (BC) is the most common cause of cancer-related death worldwide. Although platinum-based drugs (PBDs) are effective anticancer agents, responsive patients eventually become resistant. While resistance of some cancers to PBDs has been explored, the cellular responses of BC cells are not studied yet. Therefore, we aim to assess the differential effects of PBDs on BC ultrastructure. Three representative cells were treated with different concentrations and timing of Cisplatin, Carboplatin, and Oxaliplatin. Changes on cell surface and ultrastructure were detected by scanning (SEM) and transmission electron microscope (TEM). In SEM, control cells were semiflattened containing microvilli with extending lamellipodia while treated ones were round with irregular surface and several pores, indicating drug entry. Prolonged treatment resembled distinct apoptotic features such as shrinkage, membrane blebs, and narrowing of lamellipodia with blunt microvilli. TEM detected PBDs’ deposits that scattered among cellular organelles inducing structural distortion, lumen swelling, chromatin condensation, and nuclear fragmentation. Deposits were attracted to fat droplets, explained by drug hydrophobic properties, while later they were located close to cell membrane, suggesting drug efflux. Phagosomes with destructed organelles and deposits were detected as defending mechanism. Understanding BC cells response to PBDs might provide new insight for an effective treatment.http://dx.doi.org/10.1155/2017/3178794 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shadia Al-Bahlani Buthaina Al-Dhahli Kawther Al-Adawi Abdurahman Al-Nabhani Mohamed Al-Kindi |
spellingShingle |
Shadia Al-Bahlani Buthaina Al-Dhahli Kawther Al-Adawi Abdurahman Al-Nabhani Mohamed Al-Kindi Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types BioMed Research International |
author_facet |
Shadia Al-Bahlani Buthaina Al-Dhahli Kawther Al-Adawi Abdurahman Al-Nabhani Mohamed Al-Kindi |
author_sort |
Shadia Al-Bahlani |
title |
Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types |
title_short |
Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types |
title_full |
Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types |
title_fullStr |
Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types |
title_full_unstemmed |
Platinum-Based Drugs Differentially Affect the Ultrastructure of Breast Cancer Cell Types |
title_sort |
platinum-based drugs differentially affect the ultrastructure of breast cancer cell types |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2017-01-01 |
description |
Breast cancer (BC) is the most common cause of cancer-related death worldwide. Although platinum-based drugs (PBDs) are effective anticancer agents, responsive patients eventually become resistant. While resistance of some cancers to PBDs has been explored, the cellular responses of BC cells are not studied yet. Therefore, we aim to assess the differential effects of PBDs on BC ultrastructure. Three representative cells were treated with different concentrations and timing of Cisplatin, Carboplatin, and Oxaliplatin. Changes on cell surface and ultrastructure were detected by scanning (SEM) and transmission electron microscope (TEM). In SEM, control cells were semiflattened containing microvilli with extending lamellipodia while treated ones were round with irregular surface and several pores, indicating drug entry. Prolonged treatment resembled distinct apoptotic features such as shrinkage, membrane blebs, and narrowing of lamellipodia with blunt microvilli. TEM detected PBDs’ deposits that scattered among cellular organelles inducing structural distortion, lumen swelling, chromatin condensation, and nuclear fragmentation. Deposits were attracted to fat droplets, explained by drug hydrophobic properties, while later they were located close to cell membrane, suggesting drug efflux. Phagosomes with destructed organelles and deposits were detected as defending mechanism. Understanding BC cells response to PBDs might provide new insight for an effective treatment. |
url |
http://dx.doi.org/10.1155/2017/3178794 |
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