Melatonin activates endoplasmic reticulum stress and apoptosis in rats with diethylnitrosamine-induced hepatocarcinogenesis

Detalhes bibliográficos
Autor(a) principal: Moreira, Andréa Janz
Data de Publicação: 2015
Outros Autores: Ordóñez, Raquel, Cerski, Carlos Thadeu Schmidt, Picada, Jaqueline Nascimento, García-Palomo, Andrés, Marroni, Norma Anair Possa, Mauriz, José Luiz, González-Gallego, Javier
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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spelling 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
dc.date.accessioned.fl_str_mv 2018-07-10T02:33:08Z
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dc.identifier.issn.pt_BR.fl_str_mv 1932-6203
dc.identifier.nrb.pt_BR.fl_str_mv 001070463
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dc.language.iso.fl_str_mv 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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