Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Revista Brasileira de Cancerologia (Online) |
Texto Completo: | https://rbc.inca.gov.br/index.php/revista/article/view/2945 |
Resumo: | In order to explaín the biological basis of the adult gerbil skin relative resistance to chemical carcinogenesis it was characterized the effect of cróton oil and benzoyl peroxide tumor promoters by studying the morphologicàl changès related to promotion and induced in adult gerbil skin accordingto dífferent doses, treatment frequencies, and associated pretreatment with the tumor initiator methylcholanthrene, through biphasic and triphasic carcinogenesis protocols. Similar degree of hyperkeratosis and dose-dependent hyperplasia were induced in the interfollicular epidermis after one topical application of croton oll (0.94 mg and 1.88 mg) or benzoyl peroxide (20 mg and 40 mg). Epidermal enlargment, cellular hypertrophy and inflammation were more pronnounced with croton oil treatment. Proliferative stimulus and imbalance between epidermal proliferation and differentiation could be responsible for the hyperplasia, which was more intense with croton oil treatment. The initial proliferative stimulus was reduced after repeated topical treatment with croton oll (1.41 mg) or benzoyl peroxide (30 mg). Croton oll also induced intense hyperkeratosis and regression of initial hyperplasia, which could be related to imbalance between proliferation and differentiation in favour of cellular loss. Twice or thrice a week treatment with benzoyl peroxide induced discrete progression of initial hyperplasia, which could be related to imbalance between proliferation and differentiation predominating a discrete celiular gain. Both substances determined different inflammatory effect, since there was regression with croton oll and progression with benzoyl peroxide. Divergent hyperplastic and inflammatory responses could be reflecting different mechanisms of action of these two com pounds. When croton oil and benzoyl peroxide were administered after methylcholanthrene (0.2 mg) through biphasic or triphasic carcinogenesis protocois, only benzoyl peroxide showed discrete and transitory promotion - propagation - of papiliomas in adult gerbil skin. Taking into account the regression of the proliferative stimulus registered during repeated treatment with both promoters and the response associated to cellular differentiation - hyperkeratosis - it was concluded that those effects interfered in the selective donal expansion of epidermal celis, mainly with croton oll treatment, and could be related to the biological basis of adult gerbil skin relative resistance to chemical epidermal carcinogenesis. |
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Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatusCarcinogêneseIniciaçãoPromoçãoPeleGerbilCarcinogenesisInitiationPromotionSkinGerbilIn order to explaín the biological basis of the adult gerbil skin relative resistance to chemical carcinogenesis it was characterized the effect of cróton oil and benzoyl peroxide tumor promoters by studying the morphologicàl changès related to promotion and induced in adult gerbil skin accordingto dífferent doses, treatment frequencies, and associated pretreatment with the tumor initiator methylcholanthrene, through biphasic and triphasic carcinogenesis protocols. Similar degree of hyperkeratosis and dose-dependent hyperplasia were induced in the interfollicular epidermis after one topical application of croton oll (0.94 mg and 1.88 mg) or benzoyl peroxide (20 mg and 40 mg). Epidermal enlargment, cellular hypertrophy and inflammation were more pronnounced with croton oil treatment. Proliferative stimulus and imbalance between epidermal proliferation and differentiation could be responsible for the hyperplasia, which was more intense with croton oil treatment. The initial proliferative stimulus was reduced after repeated topical treatment with croton oll (1.41 mg) or benzoyl peroxide (30 mg). Croton oll also induced intense hyperkeratosis and regression of initial hyperplasia, which could be related to imbalance between proliferation and differentiation in favour of cellular loss. Twice or thrice a week treatment with benzoyl peroxide induced discrete progression of initial hyperplasia, which could be related to imbalance between proliferation and differentiation predominating a discrete celiular gain. Both substances determined different inflammatory effect, since there was regression with croton oll and progression with benzoyl peroxide. Divergent hyperplastic and inflammatory responses could be reflecting different mechanisms of action of these two com pounds. When croton oil and benzoyl peroxide were administered after methylcholanthrene (0.2 mg) through biphasic or triphasic carcinogenesis protocois, only benzoyl peroxide showed discrete and transitory promotion - propagation - of papiliomas in adult gerbil skin. Taking into account the regression of the proliferative stimulus registered during repeated treatment with both promoters and the response associated to cellular differentiation - hyperkeratosis - it was concluded that those effects interfered in the selective donal expansion of epidermal celis, mainly with croton oll treatment, and could be related to the biological basis of adult gerbil skin relative resistance to chemical epidermal carcinogenesis.Supondo que a resistência relativa da pele de gerbil adulto à carcinogênese química estaria relacionada a um fenômeno de adaptação ao processo de promoção tumoral, foi caracterizado o efeito de óleo de cróton (OC) e peróxido de benzoíla (PB) sobre a pele de gerbil, através do estudo das alterações morfológicas, correlatas à atividade promotora e induzidas em função da dose administrada, da freqüência do tratamento e da associação ao iniciador metilcolantreno (MC) em modelos bifásicos e trifásicos de carcinogênese. Verificou-se que uma única aplicação tópica de 00 (0,94 mg e 1,88 mg) ou PB (20 mg e 40 mg) induz, na epiderme interfolicular, grau similar de hiperceratose e hiperplasia dose-dependente; outros efeitos, como espessamento da epiderme, hipertrofia celular e inflamação, eram mais acentuados pelo tratamento com OC. O efeito hiperplásico, também mais acentuado com OC, decorreria do estímulo proliferativo e do desequilíbrio entre proliferação e diferenciação epidérmica. O tratamento tópico repetido, com OC (1,41 mg) ou PB (30 mg), independente da freqüência semanal, bi-semanal ou tri-semanal, determinou diminuição do estímulo proliferativo inicial, além de intensa hiperceratose e regressão da hiperplasia, no caso do OC conseqüente ao desequilíbrio entre proliferação e diferenciação, favorecendo a perda celular. Entretanto, o PB, quando aplicado 2 ou 3 vezes/semana, determinou discreta progressão da hiperplasia inicial, decorrente de ligeiro desequilíbrio entre proliferação e diferenciação, prevalecendo discreto ganho celular. Ambas substâncias diferiram também no efeito inflamatório, ocorrendo regressão com OC e progressão com PB. A divergência nos efeitos hiperplásico e inflamatório estaria refletindo mecanismos de ação distintos destas duas substâncias. Ao ser aplicado OC ou PB após MC (0,2 mg), segundo protocolos de carcinogênese bifásica ou trifásica, comprovou-se que apenas o PB tem discreto efeito promotor - propagador – de papilomas na pele de gerbil adulto. Considerando a diminuição do estímulo proliferativo, que ocorre durante o tratamento repetido com OC e PB, associada ao efeito destas substâncias sobre a diferenciação celular - hiperceratose - entende-se que a expansão clonal seletiva de células epidérmicas estaria prejudicada, principalmente com OC, sendo talvez esta a base biológica da resistência relativa da pele de gerbil adulto à indução química de tumores de linhagem epidérmica.INCA2022-10-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArtigos, Avaliado pelos paresapplication/pdfhttps://rbc.inca.gov.br/index.php/revista/article/view/294510.32635/2176-9745.RBC.1995v41n3.2945Revista Brasileira de Cancerologia; Vol. 41 No. 3 (1995): July/Aug./Sept.; 167-183Revista Brasileira de Cancerologia; Vol. 41 Núm. 3 (1995): jul./ago./sept.; 167-183Revista Brasileira de Cancerologia; v. 41 n. 3 (1995): jul./ago./set.; 167-1832176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporhttps://rbc.inca.gov.br/index.php/revista/article/view/2945/1818https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessGuzmán-Silva, Maria Angélica2023-06-19T13:19:56Zoai:rbc.inca.gov.br:article/2945Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2023-06-19T13:19:56Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false |
dc.title.none.fl_str_mv |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
title |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
spellingShingle |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus Guzmán-Silva, Maria Angélica Carcinogênese Iniciação Promoção Pele Gerbil Carcinogenesis Initiation Promotion Skin Gerbil |
title_short |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
title_full |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
title_fullStr |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
title_full_unstemmed |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
title_sort |
Efeito de promotores tumorais em pele de gerbil, Meriones unguiculatus |
author |
Guzmán-Silva, Maria Angélica |
author_facet |
Guzmán-Silva, Maria Angélica |
author_role |
author |
dc.contributor.author.fl_str_mv |
Guzmán-Silva, Maria Angélica |
dc.subject.por.fl_str_mv |
Carcinogênese Iniciação Promoção Pele Gerbil Carcinogenesis Initiation Promotion Skin Gerbil |
topic |
Carcinogênese Iniciação Promoção Pele Gerbil Carcinogenesis Initiation Promotion Skin Gerbil |
description |
In order to explaín the biological basis of the adult gerbil skin relative resistance to chemical carcinogenesis it was characterized the effect of cróton oil and benzoyl peroxide tumor promoters by studying the morphologicàl changès related to promotion and induced in adult gerbil skin accordingto dífferent doses, treatment frequencies, and associated pretreatment with the tumor initiator methylcholanthrene, through biphasic and triphasic carcinogenesis protocols. Similar degree of hyperkeratosis and dose-dependent hyperplasia were induced in the interfollicular epidermis after one topical application of croton oll (0.94 mg and 1.88 mg) or benzoyl peroxide (20 mg and 40 mg). Epidermal enlargment, cellular hypertrophy and inflammation were more pronnounced with croton oil treatment. Proliferative stimulus and imbalance between epidermal proliferation and differentiation could be responsible for the hyperplasia, which was more intense with croton oil treatment. The initial proliferative stimulus was reduced after repeated topical treatment with croton oll (1.41 mg) or benzoyl peroxide (30 mg). Croton oll also induced intense hyperkeratosis and regression of initial hyperplasia, which could be related to imbalance between proliferation and differentiation in favour of cellular loss. Twice or thrice a week treatment with benzoyl peroxide induced discrete progression of initial hyperplasia, which could be related to imbalance between proliferation and differentiation predominating a discrete celiular gain. Both substances determined different inflammatory effect, since there was regression with croton oll and progression with benzoyl peroxide. Divergent hyperplastic and inflammatory responses could be reflecting different mechanisms of action of these two com pounds. When croton oil and benzoyl peroxide were administered after methylcholanthrene (0.2 mg) through biphasic or triphasic carcinogenesis protocois, only benzoyl peroxide showed discrete and transitory promotion - propagation - of papiliomas in adult gerbil skin. Taking into account the regression of the proliferative stimulus registered during repeated treatment with both promoters and the response associated to cellular differentiation - hyperkeratosis - it was concluded that those effects interfered in the selective donal expansion of epidermal celis, mainly with croton oll treatment, and could be related to the biological basis of adult gerbil skin relative resistance to chemical epidermal carcinogenesis. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-10-05 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Artigos, Avaliado pelos pares |
format |
article |
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publishedVersion |
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https://rbc.inca.gov.br/index.php/revista/article/view/2945 10.32635/2176-9745.RBC.1995v41n3.2945 |
url |
https://rbc.inca.gov.br/index.php/revista/article/view/2945 |
identifier_str_mv |
10.32635/2176-9745.RBC.1995v41n3.2945 |
dc.language.iso.fl_str_mv |
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language |
por |
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https://rbc.inca.gov.br/index.php/revista/article/view/2945/1818 |
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https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0 |
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INCA |
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INCA |
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Revista Brasileira de Cancerologia; Vol. 41 No. 3 (1995): July/Aug./Sept.; 167-183 Revista Brasileira de Cancerologia; Vol. 41 Núm. 3 (1995): jul./ago./sept.; 167-183 Revista Brasileira de Cancerologia; v. 41 n. 3 (1995): jul./ago./set.; 167-183 2176-9745 reponame:Revista Brasileira de Cancerologia (Online) instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) instacron:INCA |
instname_str |
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
instacron_str |
INCA |
institution |
INCA |
reponame_str |
Revista Brasileira de Cancerologia (Online) |
collection |
Revista Brasileira de Cancerologia (Online) |
repository.name.fl_str_mv |
Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
repository.mail.fl_str_mv |
rbc@inca.gov.br |
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1797042233409536000 |