Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/180290 |
Resumo: | Abstract Hepatocellular carcinoma (HCC) is one of the most lethal human cancers worldwide because of its high incidence, its metastatic potential and the low efficacy of conventional treatment. Inactivation of apoptosis is implicated in tumour progression and chemotherapy resistance, and has been linked to the presence of endoplasmic reticulum stress. Melatonin, the main product of the pineal gland, exerts anti-proliferative, pro-apoptotic and antiangiogenic effects in HCC cells, but these effects still need to be confirmed in animal models. Male Wistar rats in treatment groups received diethylnitrosamine (DEN) 50 mg/kg intraperitoneally twice/once a week for 18 weeks. Melatonin was given in drinking water at 1 mg/ kg/d, beginning 5 or 12 weeks after the start of DEN administration. Melatonin improved survival rates and successfully attenuated liver injury, as shown by histopathology, decreased levels of serum transaminases and reduced expression of placental glutathione S-transferase. Furthermore, melatonin treatment resulted in a significant increase of caspase 3, 8 and 9 activities, polyadenosine diphosphate (ADP) ribose polymerase (PARP) cleavage, and Bcl-associated X protein (Bax)/Bcl-2 ratio. Cytochrome c, p53 and Fas-L protein concentration were also significantly enhanced by melatonin. Melatonin induced an increased expression of activating transcription factor 6 (ATF6), C/EBP-homologous protein (CHOP) and immunoglobulin heavy chain-binding protein (BiP), while cyclooxygenase (COX)-2 expression decreased. Data obtained suggest that induction of apoptosis and ER stress contribute to the beneficial effects of melatonin in rats with DEN-induced HCC. |
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Moreira, Andréa JanzOrdóñez, RaquelCerski, Carlos Thadeu SchmidtPicada, Jaqueline NascimentoGarcía-Palomo, AndrésMarroni, Norma Anair PossaMauriz, José LuizGonzález-Gallego, Javier2018-07-10T02:33:08Z20151932-6203http://hdl.handle.net/10183/180290001070463Abstract Hepatocellular carcinoma (HCC) is one of the most lethal human cancers worldwide because of its high incidence, its metastatic potential and the low efficacy of conventional treatment. Inactivation of apoptosis is implicated in tumour progression and chemotherapy resistance, and has been linked to the presence of endoplasmic reticulum stress. Melatonin, the main product of the pineal gland, exerts anti-proliferative, pro-apoptotic and antiangiogenic effects in HCC cells, but these effects still need to be confirmed in animal models. Male Wistar rats in treatment groups received diethylnitrosamine (DEN) 50 mg/kg intraperitoneally twice/once a week for 18 weeks. Melatonin was given in drinking water at 1 mg/ kg/d, beginning 5 or 12 weeks after the start of DEN administration. Melatonin improved survival rates and successfully attenuated liver injury, as shown by histopathology, decreased levels of serum transaminases and reduced expression of placental glutathione S-transferase. Furthermore, melatonin treatment resulted in a significant increase of caspase 3, 8 and 9 activities, polyadenosine diphosphate (ADP) ribose polymerase (PARP) cleavage, and Bcl-associated X protein (Bax)/Bcl-2 ratio. Cytochrome c, p53 and Fas-L protein concentration were also significantly enhanced by melatonin. Melatonin induced an increased expression of activating transcription factor 6 (ATF6), C/EBP-homologous protein (CHOP) and immunoglobulin heavy chain-binding protein (BiP), while cyclooxygenase (COX)-2 expression decreased. Data obtained suggest that induction of apoptosis and ER stress contribute to the beneficial effects of melatonin in rats with DEN-induced HCC.application/pdfengPLoS ONE. San Francisco. Vol. 10, no. 12 (Dec. 2015), e0144517, 17 p.Carcinoma hepatocelularCarcinogeneseMelatoninaBiomarcadores tumoraisAnimaisRatos WistarMelatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesisEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001070463.pdf001070463.pdfTexto completo (inglês)application/pdf3644424http://www.lume.ufrgs.br/bitstream/10183/180290/1/001070463.pdf0beb2c75c9bcb1b19bc3d8abfcdfd376MD51TEXT001070463.pdf.txt001070463.pdf.txtExtracted Texttext/plain57591http://www.lume.ufrgs.br/bitstream/10183/180290/2/001070463.pdf.txt90ee11e1a2e16ca6c1c39c40b937f4e4MD5210183/1802902018-07-11 02:31:26.279792oai:www.lume.ufrgs.br:10183/180290Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-07-11T05:31:26Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
title |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
spellingShingle |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis Moreira, Andréa Janz Carcinoma hepatocelular Carcinogenese Melatonina Biomarcadores tumorais Animais Ratos Wistar |
title_short |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
title_full |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
title_fullStr |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
title_full_unstemmed |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
title_sort |
Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis |
author |
Moreira, Andréa Janz |
author_facet |
Moreira, Andréa Janz Ordóñez, Raquel Cerski, Carlos Thadeu Schmidt Picada, Jaqueline Nascimento García-Palomo, Andrés Marroni, Norma Anair Possa Mauriz, José Luiz González-Gallego, Javier |
author_role |
author |
author2 |
Ordóñez, Raquel Cerski, Carlos Thadeu Schmidt Picada, Jaqueline Nascimento García-Palomo, Andrés Marroni, Norma Anair Possa Mauriz, José Luiz González-Gallego, Javier |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Moreira, Andréa Janz Ordóñez, Raquel Cerski, Carlos Thadeu Schmidt Picada, Jaqueline Nascimento García-Palomo, Andrés Marroni, Norma Anair Possa Mauriz, José Luiz González-Gallego, Javier |
dc.subject.por.fl_str_mv |
Carcinoma hepatocelular Carcinogenese Melatonina Biomarcadores tumorais Animais Ratos Wistar |
topic |
Carcinoma hepatocelular Carcinogenese Melatonina Biomarcadores tumorais Animais Ratos Wistar |
description |
Abstract Hepatocellular carcinoma (HCC) is one of the most lethal human cancers worldwide because of its high incidence, its metastatic potential and the low efficacy of conventional treatment. Inactivation of apoptosis is implicated in tumour progression and chemotherapy resistance, and has been linked to the presence of endoplasmic reticulum stress. Melatonin, the main product of the pineal gland, exerts anti-proliferative, pro-apoptotic and antiangiogenic effects in HCC cells, but these effects still need to be confirmed in animal models. Male Wistar rats in treatment groups received diethylnitrosamine (DEN) 50 mg/kg intraperitoneally twice/once a week for 18 weeks. Melatonin was given in drinking water at 1 mg/ kg/d, beginning 5 or 12 weeks after the start of DEN administration. Melatonin improved survival rates and successfully attenuated liver injury, as shown by histopathology, decreased levels of serum transaminases and reduced expression of placental glutathione S-transferase. Furthermore, melatonin treatment resulted in a significant increase of caspase 3, 8 and 9 activities, polyadenosine diphosphate (ADP) ribose polymerase (PARP) cleavage, and Bcl-associated X protein (Bax)/Bcl-2 ratio. Cytochrome c, p53 and Fas-L protein concentration were also significantly enhanced by melatonin. Melatonin induced an increased expression of activating transcription factor 6 (ATF6), C/EBP-homologous protein (CHOP) and immunoglobulin heavy chain-binding protein (BiP), while cyclooxygenase (COX)-2 expression decreased. Data obtained suggest that induction of apoptosis and ER stress contribute to the beneficial effects of melatonin in rats with DEN-induced HCC. |
publishDate |
2015 |
dc.date.issued.fl_str_mv |
2015 |
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2018-07-10T02:33:08Z |
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1932-6203 |
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001070463 |
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http://hdl.handle.net/10183/180290 |
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eng |
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dc.relation.ispartof.pt_BR.fl_str_mv |
PLoS ONE. San Francisco. Vol. 10, no. 12 (Dec. 2015), e0144517, 17 p. |
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