Ultrastructural aspects of melatonin cytotoxicity on Caco-2 cells in vitro
Colon adenocarcinoma is a disease expanding worldwide. Cancer of colon and rectum are among the top ten most insidious types in Brazil. In vitro and in vivo studies have demonstrated the efficacy of the hormone melatonin to prevent and reduce tumor growth. However, there are only few studies address...
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Published in | Micron (Oxford, England : 1993) Vol. 59; pp. 17 - 23 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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England
Elsevier Ltd
01.04.2014
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Abstract | Colon adenocarcinoma is a disease expanding worldwide. Cancer of colon and rectum are among the top ten most insidious types in Brazil. In vitro and in vivo studies have demonstrated the efficacy of the hormone melatonin to prevent and reduce tumor growth. However, there are only few studies addressing the action of melatonin on Caco-2 cells. Thus, the cytotoxic effect of melatonin on the ultrastructure of Caco-2 cells was investigated. The MTT colorimetric method was used to assess the cytotoxicity. A total of 2×106cells/mL were seeded in microplates and incubated at 50, 25, 12.5, 6.25, 3.125, 1.56, 0.78 and 0.0 (control) μg/mL of melatonin. For ultrastructural analysis concentrations with low, medium and high cytotoxicity plus the control were used for ultrastructural analysis. The concentrations 50, 1.56 and 0.78μg/mL of melatonin showed low, medium and high cytotoxicity, respectively. Ultrastructurally, the control tumor cells were shown to be preserved. Caco-2 cells showed morphological changes at 50μg/mL of melatonin, with numerous vacuoles, mitochondrial degeneration and reduced glycogen. However, Caco-2 cells also showed altered morphology in treatments at 1.56 and 0.78μg/mL of melatonin with characteristics of cells in degeneration by the presence of numerous vacuoles, absence of microvilli, mitochondrial degeneration and nuclear fragmentation. Thus, one can infer that concentrations of 1.56 and 0.78μg/mL of melatonin promote cytotoxicity in Caco-2 cells, which can probably be related to the generation of reactive oxygen species (ROS). |
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AbstractList | Colon adenocarcinoma is a disease expanding worldwide. Cancer of colon and rectum are among the top ten most insidious types in Brazil. In vitro and in vivo studies have demonstrated the efficacy of the hormone melatonin to prevent and reduce tumor growth. However, there are only few studies addressing the action of melatonin on Caco-2 cells. Thus, the cytotoxic effect of melatonin on the ultrastructure of Caco-2 cells was investigated. The MTT colorimetric method was used to assess the cytotoxicity. A total of 2×10(6)cells/mL were seeded in microplates and incubated at 50, 25, 12.5, 6.25, 3.125, 1.56, 0.78 and 0.0 (control) μg/mL of melatonin. For ultrastructural analysis concentrations with low, medium and high cytotoxicity plus the control were used for ultrastructural analysis. The concentrations 50, 1.56 and 0.78 μg/mL of melatonin showed low, medium and high cytotoxicity, respectively. Ultrastructurally, the control tumor cells were shown to be preserved. Caco-2 cells showed morphological changes at 50 μg/mL of melatonin, with numerous vacuoles, mitochondrial degeneration and reduced glycogen. However, Caco-2 cells also showed altered morphology in treatments at 1.56 and 0.78 μg/mL of melatonin with characteristics of cells in degeneration by the presence of numerous vacuoles, absence of microvilli, mitochondrial degeneration and nuclear fragmentation. Thus, one can infer that concentrations of 1.56 and 0.78 μg/mL of melatonin promote cytotoxicity in Caco-2 cells, which can probably be related to the generation of reactive oxygen species (ROS). Colon adenocarcinoma is a disease expanding worldwide. Cancer of colon and rectum are among the top ten most insidious types in Brazil. In vitro and in vivo studies have demonstrated the efficacy of the hormone melatonin to prevent and reduce tumor growth. However, there are only few studies addressing the action of melatonin on Caco-2 cells. Thus, the cytotoxic effect of melatonin on the ultrastructure of Caco-2 cells was investigated. The MTT colorimetric method was used to assess the cytotoxicity. A total of 2 106 cells/mL were seeded in microplates and incubated at 50, 25, 12.5, 6.25, 3.125, 1.56, 0.78 and 0.0 (control) mu g/mL of melatonin. For ultrastructural analysis concentrations with low, medium and high cytotoxicity plus the control were used for ultrastructural analysis. The concentrations 50, 1.56 and 0.78 mu g/mL of melatonin showed low, medium and high cytotoxicity, respectively. Ultrastructurally, the control tumor cells were shown to be preserved. Caco-2 cells showed morphological changes at 50 mu g/mL of melatonin, with numerous vacuoles, mitochondrial degeneration and reduced glycogen. However, Caco-2 cells also showed altered morphology in treatments at 1.56 and 0.78 mu g/mL of melatonin with characteristics of cells in degeneration by the presence of numerous vacuoles, absence of microvilli, mitochondrial degeneration and nuclear fragmentation. Thus, one can infer that concentrations of 1.56 and 0.78 mu g/mL of melatonin promote cytotoxicity in Caco-2 cells, which can probably be related to the generation of reactive oxygen species (ROS). Colon adenocarcinoma is a disease expanding worldwide. Cancer of colon and rectum are among the top ten most insidious types in Brazil. In vitro and in vivo studies have demonstrated the efficacy of the hormone melatonin to prevent and reduce tumor growth. However, there are only few studies addressing the action of melatonin on Caco-2 cells. Thus, the cytotoxic effect of melatonin on the ultrastructure of Caco-2 cells was investigated. The MTT colorimetric method was used to assess the cytotoxicity. A total of 2×106cells/mL were seeded in microplates and incubated at 50, 25, 12.5, 6.25, 3.125, 1.56, 0.78 and 0.0 (control) μg/mL of melatonin. For ultrastructural analysis concentrations with low, medium and high cytotoxicity plus the control were used for ultrastructural analysis. The concentrations 50, 1.56 and 0.78μg/mL of melatonin showed low, medium and high cytotoxicity, respectively. Ultrastructurally, the control tumor cells were shown to be preserved. Caco-2 cells showed morphological changes at 50μg/mL of melatonin, with numerous vacuoles, mitochondrial degeneration and reduced glycogen. However, Caco-2 cells also showed altered morphology in treatments at 1.56 and 0.78μg/mL of melatonin with characteristics of cells in degeneration by the presence of numerous vacuoles, absence of microvilli, mitochondrial degeneration and nuclear fragmentation. Thus, one can infer that concentrations of 1.56 and 0.78μg/mL of melatonin promote cytotoxicity in Caco-2 cells, which can probably be related to the generation of reactive oxygen species (ROS). |
Author | Silva, Eliete C. Batista, Ana Paula C. Teixeira, Álvaro A.C. de Medeiros, Paloma L. dos Santos, Fábio A.B. Teixeira, Valeria W. Alves, Luiz C. da Silva, Terezinha G. |
Author_xml | – sequence: 1 givenname: Ana Paula C. surname: Batista fullname: Batista, Ana Paula C. organization: Department of Animal Morphology and Physiology, University Federal Rural of Pernambuco, Rua Dom Manoel de Medeiros, s/n, 52171-900 Recife, PE, Brazil – sequence: 2 givenname: Terezinha G. surname: da Silva fullname: da Silva, Terezinha G. organization: Department of Antibiotics, University Federal Rural of Pernambuco, Av. Prof. Moraes Rego, 1235, 50670-901 Recife, PE, Brazil – sequence: 3 givenname: Álvaro A.C. surname: Teixeira fullname: Teixeira, Álvaro A.C. email: alvaro@dmfa.ufrpe.br organization: Department of Animal Morphology and Physiology, University Federal Rural of Pernambuco, Rua Dom Manoel de Medeiros, s/n, 52171-900 Recife, PE, Brazil – sequence: 4 givenname: Paloma L. surname: de Medeiros fullname: de Medeiros, Paloma L. organization: Department of Histology and Embryology, University Federal Rural of Pernambuco, Av. Prof. Moraes Rego, 1235, 50670-901 Recife, PE, Brazil – sequence: 5 givenname: Valeria W. surname: Teixeira fullname: Teixeira, Valeria W. organization: Department of Animal Morphology and Physiology, University Federal Rural of Pernambuco, Rua Dom Manoel de Medeiros, s/n, 52171-900 Recife, PE, Brazil – sequence: 6 givenname: Luiz C. surname: Alves fullname: Alves, Luiz C. organization: Laboratory of Immunopathology Keizo Asami (LIKA), and Research Center Aggeu Magalhães, CPqAM/Fiocruz, University Federal of Pernambuco, Av. Prof. Moraes Rego, 1235, 50670-901 Recife, PE, Brazil – sequence: 7 givenname: Fábio A.B. surname: dos Santos fullname: dos Santos, Fábio A.B. organization: Laboratory of Immunopathology Keizo Asami (LIKA), and Research Center Aggeu Magalhães, CPqAM/Fiocruz, University Federal of Pernambuco, Av. Prof. Moraes Rego, 1235, 50670-901 Recife, PE, Brazil – sequence: 8 givenname: Eliete C. surname: Silva fullname: Silva, Eliete C. organization: Department of Histology and Embryology, University Federal Rural of Pernambuco, Av. Prof. Moraes Rego, 1235, 50670-901 Recife, PE, Brazil |
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Keywords | Adenocarcinoma Cytotoxicity Melatonin Ultrastructure Caco-2 |
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Snippet | Colon adenocarcinoma is a disease expanding worldwide. Cancer of colon and rectum are among the top ten most insidious types in Brazil. In vitro and in vivo... |
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SubjectTerms | Adenocarcinoma Apoptosis - drug effects Caco-2 Caco-2 Cells - drug effects Caco-2 Cells - ultrastructure Colon Colorimetry Cytotoxicity Degeneration Effectiveness Humans In vitro testing In vivo methods and tests Melatonin Melatonin - pharmacology Microscopy, Electron, Transmission Mitochondria - drug effects Mitochondria - metabolism Reactive Oxygen Species - metabolism Tumors Ultrastructure |
Title | Ultrastructural aspects of melatonin cytotoxicity on Caco-2 cells in vitro |
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