Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model

Detalhes bibliográficos
Autor(a) principal: Morgan, Henrique Jorge Novaes
Data de Publicação: 2021
Outros Autores: Delgado, Aislan Quintiliano [UNESP], Saldanha, Luiz Leonardo [UNESP], Camaforte, Nathalia Aparecida De Paula [UNESP], Dokkedal, Anne Ligia [UNESP], Bosqueiro, Jose Roberto [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/s12906-020-03190-1
http://hdl.handle.net/11449/209948
Resumo: Background Cancer is a multifactorial disease caused by uncontrolled proliferation of cells. About 50-80% of cancer patients develop cachexia, a complex metabolic syndrome associated with an increase of mortality and morbidity. However, there are no effective therapies in medical clinic for cancer cachexia. Vochysia tucanorum Mart. is a common three of the Brazilian Cerrado. The butanolic fraction of V. tucanorum (Fr-BuVt), very rich in triterpenes with various biological activities, might be interesting in being tested in cancer cachexia syndrome. Hence, the present study was undertaken to investigate the antitumoral activity of Fr-BuVt and its potential against cachexia development. Methods Ehrlich tumor was used as model of cancer cachexia. Ascitic Ehrlich tumor cells were collected, processed and inoculated subcutaneously in saline solution (1 x 10(7)/100 mu l; >= 95% viability) for the obtention of solid Ehrlich carcinoma. After inoculation, solid Ehrlich carcinoma-bearing mice were treated by 14 consecutive days by gavage with Fr-BuVt (200 mg/kg). Body weight and tumor volume were measure during the treatment period. Tumors were removed, weighed and properly processed to measure the content and phosphorylation levels of key-proteins involved to apoptotic and proliferation process by Western Blot. Muscles and adipose tissues were removed for weighed. Serum was collected to cytokines levels and energetic blood markers measurements. Results The treatment with the Fr-BuVt (200 mg/kg, 14 days) decreased the solid Ehrlich tumor volume and weight besides increased the expression of the pro-apoptotic proteins caspase-3 and BAX, but also decreased the expression of the proteins involved in proliferation NF kappa B, mTOR and ERK. In addition, our data shows that the administration of Fr-BuVt was able to prevent the installation of cancer cachexia in Ehrlich carcinoma-bearing mice, since prevented the loss of body weight, as well as the loss of muscle and adipose tissue. Moreover, an improvement in some blood parameters such as decrease in cytokines TNF-alpha and IL-6 levels is observed. Conclusions The study revealed that Fr-BuVt has antitumoral activity and prevent installation of cancer cachexia in Ehrlich model. Therefore, Fr-BuVt may represent an alternative treatment for cancer cachexia.
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spelling Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor modelAnti-apoptoticAnti-proliferationCancer cachexiaMetabolic syndromeTriterpenesBackground Cancer is a multifactorial disease caused by uncontrolled proliferation of cells. About 50-80% of cancer patients develop cachexia, a complex metabolic syndrome associated with an increase of mortality and morbidity. However, there are no effective therapies in medical clinic for cancer cachexia. Vochysia tucanorum Mart. is a common three of the Brazilian Cerrado. The butanolic fraction of V. tucanorum (Fr-BuVt), very rich in triterpenes with various biological activities, might be interesting in being tested in cancer cachexia syndrome. Hence, the present study was undertaken to investigate the antitumoral activity of Fr-BuVt and its potential against cachexia development. Methods Ehrlich tumor was used as model of cancer cachexia. Ascitic Ehrlich tumor cells were collected, processed and inoculated subcutaneously in saline solution (1 x 10(7)/100 mu l; >= 95% viability) for the obtention of solid Ehrlich carcinoma. After inoculation, solid Ehrlich carcinoma-bearing mice were treated by 14 consecutive days by gavage with Fr-BuVt (200 mg/kg). Body weight and tumor volume were measure during the treatment period. Tumors were removed, weighed and properly processed to measure the content and phosphorylation levels of key-proteins involved to apoptotic and proliferation process by Western Blot. Muscles and adipose tissues were removed for weighed. Serum was collected to cytokines levels and energetic blood markers measurements. Results The treatment with the Fr-BuVt (200 mg/kg, 14 days) decreased the solid Ehrlich tumor volume and weight besides increased the expression of the pro-apoptotic proteins caspase-3 and BAX, but also decreased the expression of the proteins involved in proliferation NF kappa B, mTOR and ERK. In addition, our data shows that the administration of Fr-BuVt was able to prevent the installation of cancer cachexia in Ehrlich carcinoma-bearing mice, since prevented the loss of body weight, as well as the loss of muscle and adipose tissue. Moreover, an improvement in some blood parameters such as decrease in cytokines TNF-alpha and IL-6 levels is observed. Conclusions The study revealed that Fr-BuVt has antitumoral activity and prevent installation of cancer cachexia in Ehrlich model. Therefore, Fr-BuVt may represent an alternative treatment for cancer cachexia.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Physiol, Lab Metab Control, Ribeirao Preto, SP, BrazilSao Paulo State Univ, Dept Phys Educ, Lab Endocrine Pancreas Physiol, Fac Sci, Av Eng Luiz Edmundo Carrijo Coube 14-01, BR-17033360 Bauru, SP, BrazilSao Paulo State Univ, Dept Biol Sci, Lab Nat Prod Chem, Fac Sci, Bauru, SP, BrazilSao Paulo State Univ, Dept Phys Educ, Lab Endocrine Pancreas Physiol, Fac Sci, Av Eng Luiz Edmundo Carrijo Coube 14-01, BR-17033360 Bauru, SP, BrazilSao Paulo State Univ, Dept Biol Sci, Lab Nat Prod Chem, Fac Sci, Bauru, SP, BrazilFAPESP: FAPESP -2016/07866-1BmcUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Morgan, Henrique Jorge NovaesDelgado, Aislan Quintiliano [UNESP]Saldanha, Luiz Leonardo [UNESP]Camaforte, Nathalia Aparecida De Paula [UNESP]Dokkedal, Anne Ligia [UNESP]Bosqueiro, Jose Roberto [UNESP]2021-06-25T12:34:34Z2021-06-25T12:34:34Z2021-01-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article13http://dx.doi.org/10.1186/s12906-020-03190-1Bmc Complementary Medicine And Therapies. London: Bmc, v. 21, n. 1, 13 p., 2021.http://hdl.handle.net/11449/20994810.1186/s12906-020-03190-1WOS:000610409300004Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBmc Complementary Medicine And Therapiesinfo:eu-repo/semantics/openAccess2024-04-24T18:53:11Zoai:repositorio.unesp.br:11449/209948Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-04-24T18:53:11Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
title Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
spellingShingle Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
Morgan, Henrique Jorge Novaes
Anti-apoptotic
Anti-proliferation
Cancer cachexia
Metabolic syndrome
Triterpenes
title_short Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
title_full Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
title_fullStr Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
title_full_unstemmed Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
title_sort Vochysia tucanorum Mart. butanol fraction presents antitumoral activity in vivo and prevents the installation of cachexia in solid Ehrlich tumor model
author Morgan, Henrique Jorge Novaes
author_facet Morgan, Henrique Jorge Novaes
Delgado, Aislan Quintiliano [UNESP]
Saldanha, Luiz Leonardo [UNESP]
Camaforte, Nathalia Aparecida De Paula [UNESP]
Dokkedal, Anne Ligia [UNESP]
Bosqueiro, Jose Roberto [UNESP]
author_role author
author2 Delgado, Aislan Quintiliano [UNESP]
Saldanha, Luiz Leonardo [UNESP]
Camaforte, Nathalia Aparecida De Paula [UNESP]
Dokkedal, Anne Ligia [UNESP]
Bosqueiro, Jose Roberto [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Morgan, Henrique Jorge Novaes
Delgado, Aislan Quintiliano [UNESP]
Saldanha, Luiz Leonardo [UNESP]
Camaforte, Nathalia Aparecida De Paula [UNESP]
Dokkedal, Anne Ligia [UNESP]
Bosqueiro, Jose Roberto [UNESP]
dc.subject.por.fl_str_mv Anti-apoptotic
Anti-proliferation
Cancer cachexia
Metabolic syndrome
Triterpenes
topic Anti-apoptotic
Anti-proliferation
Cancer cachexia
Metabolic syndrome
Triterpenes
description Background Cancer is a multifactorial disease caused by uncontrolled proliferation of cells. About 50-80% of cancer patients develop cachexia, a complex metabolic syndrome associated with an increase of mortality and morbidity. However, there are no effective therapies in medical clinic for cancer cachexia. Vochysia tucanorum Mart. is a common three of the Brazilian Cerrado. The butanolic fraction of V. tucanorum (Fr-BuVt), very rich in triterpenes with various biological activities, might be interesting in being tested in cancer cachexia syndrome. Hence, the present study was undertaken to investigate the antitumoral activity of Fr-BuVt and its potential against cachexia development. Methods Ehrlich tumor was used as model of cancer cachexia. Ascitic Ehrlich tumor cells were collected, processed and inoculated subcutaneously in saline solution (1 x 10(7)/100 mu l; >= 95% viability) for the obtention of solid Ehrlich carcinoma. After inoculation, solid Ehrlich carcinoma-bearing mice were treated by 14 consecutive days by gavage with Fr-BuVt (200 mg/kg). Body weight and tumor volume were measure during the treatment period. Tumors were removed, weighed and properly processed to measure the content and phosphorylation levels of key-proteins involved to apoptotic and proliferation process by Western Blot. Muscles and adipose tissues were removed for weighed. Serum was collected to cytokines levels and energetic blood markers measurements. Results The treatment with the Fr-BuVt (200 mg/kg, 14 days) decreased the solid Ehrlich tumor volume and weight besides increased the expression of the pro-apoptotic proteins caspase-3 and BAX, but also decreased the expression of the proteins involved in proliferation NF kappa B, mTOR and ERK. In addition, our data shows that the administration of Fr-BuVt was able to prevent the installation of cancer cachexia in Ehrlich carcinoma-bearing mice, since prevented the loss of body weight, as well as the loss of muscle and adipose tissue. Moreover, an improvement in some blood parameters such as decrease in cytokines TNF-alpha and IL-6 levels is observed. Conclusions The study revealed that Fr-BuVt has antitumoral activity and prevent installation of cancer cachexia in Ehrlich model. Therefore, Fr-BuVt may represent an alternative treatment for cancer cachexia.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T12:34:34Z
2021-06-25T12:34:34Z
2021-01-07
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/s12906-020-03190-1
Bmc Complementary Medicine And Therapies. London: Bmc, v. 21, n. 1, 13 p., 2021.
http://hdl.handle.net/11449/209948
10.1186/s12906-020-03190-1
WOS:000610409300004
url http://dx.doi.org/10.1186/s12906-020-03190-1
http://hdl.handle.net/11449/209948
identifier_str_mv Bmc Complementary Medicine And Therapies. London: Bmc, v. 21, n. 1, 13 p., 2021.
10.1186/s12906-020-03190-1
WOS:000610409300004
dc.language.iso.fl_str_mv eng
language eng
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dc.publisher.none.fl_str_mv Bmc
publisher.none.fl_str_mv Bmc
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
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