Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1

Detalhes bibliográficos
Autor(a) principal: Sabrina Ferreira de Jesus
Data de Publicação: 2023
Outros Autores: Marcela Gonçalves de Souza, Lorena dos Reis Pereira Queiroz, Daniela Paola Santos de Paula, Angeliny Tamiarana Lima Tabosa, Wislene Sarajane Moreira Alves, Luiz Henrique da Silveira, André Teixeira da Silva Ferreira, Ozires José Dutra Martuscelli, Lucyana Conceição Farias, Alfredo Maurício Batista de Paula, Sérgio Henrique Sousa Santos, André Luiz Sena Guimarães
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFMG
Texto Completo: https://doi.org/10.1016/j.gene.2022.147041
http://hdl.handle.net/1843/77342
Resumo: Differences in the features of aggressiveness of non-melanoma skin cancer (NMSC) subtypes, between basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) are relevant characteristics. Comparing the characteristics between NMSC subtypes might help identify molecules associated with cancer metastasis and invasion. Considering these facts, the current study aimed to identify a molecular target for inhibiting skin cancer metastasis and invasion. Proteomic analysis suggested that heat shock protein 90 kDa, alpha, class B member 1 (HSP90AB1), pentaxin (PTX3), caspase-14 (CASP14), S100, actin-1, and profilin were the primary targets related to metastasis and invasion. However, after a differential expression comparison between BCC and SCC, HSP90AB1 was identified as the best target to repress metastasis and invasion. Based on molecular docking results, gallic acid (GA) was selected to inhibit HSP90AB1. A specific Hsp90ab1 siRNA targeting was designed and compared to GA. Interestingly, GA was more efficient in silencing HSP90AB1 than siRNAhsp90ab1. Hence, our data suggest that HSP90AB1 is a crucial biomarker for identifying invasion and metastasis and that its inhibition may be a viable strategy for treating skin cancer.
id UFMG_f058966820955453ecf0402574458d31
oai_identifier_str oai:repositorio.ufmg.br:1843/77342
network_acronym_str UFMG
network_name_str Repositório Institucional da UFMG
repository_id_str
spelling Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1Pele - CâncerCarcinoma de células escamosasMetástaseÁcido gálicoBioinformáticaDifferences in the features of aggressiveness of non-melanoma skin cancer (NMSC) subtypes, between basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) are relevant characteristics. Comparing the characteristics between NMSC subtypes might help identify molecules associated with cancer metastasis and invasion. Considering these facts, the current study aimed to identify a molecular target for inhibiting skin cancer metastasis and invasion. Proteomic analysis suggested that heat shock protein 90 kDa, alpha, class B member 1 (HSP90AB1), pentaxin (PTX3), caspase-14 (CASP14), S100, actin-1, and profilin were the primary targets related to metastasis and invasion. However, after a differential expression comparison between BCC and SCC, HSP90AB1 was identified as the best target to repress metastasis and invasion. Based on molecular docking results, gallic acid (GA) was selected to inhibit HSP90AB1. A specific Hsp90ab1 siRNA targeting was designed and compared to GA. Interestingly, GA was more efficient in silencing HSP90AB1 than siRNAhsp90ab1. Hence, our data suggest that HSP90AB1 is a crucial biomarker for identifying invasion and metastasis and that its inhibition may be a viable strategy for treating skin cancer.CNPq - Conselho Nacional de Desenvolvimento Científico e TecnológicoFAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas GeraisCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorUniversidade Federal de Minas GeraisBrasilICA - INSTITUTO DE CIÊNCIAS AGRÁRIASUFMG2024-10-09T19:16:10Z2024-10-09T19:16:10Z2023-01-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.1016/j.gene.2022.1470411879-0038http://hdl.handle.net/1843/77342engGeneSabrina Ferreira de JesusMarcela Gonçalves de SouzaLorena dos Reis Pereira QueirozDaniela Paola Santos de PaulaAngeliny Tamiarana Lima TabosaWislene Sarajane Moreira AlvesLuiz Henrique da SilveiraAndré Teixeira da Silva FerreiraOzires José Dutra MartuscelliLucyana Conceição FariasAlfredo Maurício Batista de PaulaSérgio Henrique Sousa SantosAndré Luiz Sena Guimarãesinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2024-10-09T19:59:58Zoai:repositorio.ufmg.br:1843/77342Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2024-10-09T19:59:58Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.none.fl_str_mv Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
title Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
spellingShingle Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
Sabrina Ferreira de Jesus
Pele - Câncer
Carcinoma de células escamosas
Metástase
Ácido gálico
Bioinformática
title_short Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
title_full Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
title_fullStr Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
title_full_unstemmed Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
title_sort Gallic acid has an inhibitory effect on skin squamous cell carcinoma and acts on the heat shock protein HSP90AB1
author Sabrina Ferreira de Jesus
author_facet Sabrina Ferreira de Jesus
Marcela Gonçalves de Souza
Lorena dos Reis Pereira Queiroz
Daniela Paola Santos de Paula
Angeliny Tamiarana Lima Tabosa
Wislene Sarajane Moreira Alves
Luiz Henrique da Silveira
André Teixeira da Silva Ferreira
Ozires José Dutra Martuscelli
Lucyana Conceição Farias
Alfredo Maurício Batista de Paula
Sérgio Henrique Sousa Santos
André Luiz Sena Guimarães
author_role author
author2 Marcela Gonçalves de Souza
Lorena dos Reis Pereira Queiroz
Daniela Paola Santos de Paula
Angeliny Tamiarana Lima Tabosa
Wislene Sarajane Moreira Alves
Luiz Henrique da Silveira
André Teixeira da Silva Ferreira
Ozires José Dutra Martuscelli
Lucyana Conceição Farias
Alfredo Maurício Batista de Paula
Sérgio Henrique Sousa Santos
André Luiz Sena Guimarães
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sabrina Ferreira de Jesus
Marcela Gonçalves de Souza
Lorena dos Reis Pereira Queiroz
Daniela Paola Santos de Paula
Angeliny Tamiarana Lima Tabosa
Wislene Sarajane Moreira Alves
Luiz Henrique da Silveira
André Teixeira da Silva Ferreira
Ozires José Dutra Martuscelli
Lucyana Conceição Farias
Alfredo Maurício Batista de Paula
Sérgio Henrique Sousa Santos
André Luiz Sena Guimarães
dc.subject.por.fl_str_mv Pele - Câncer
Carcinoma de células escamosas
Metástase
Ácido gálico
Bioinformática
topic Pele - Câncer
Carcinoma de células escamosas
Metástase
Ácido gálico
Bioinformática
description Differences in the features of aggressiveness of non-melanoma skin cancer (NMSC) subtypes, between basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) are relevant characteristics. Comparing the characteristics between NMSC subtypes might help identify molecules associated with cancer metastasis and invasion. Considering these facts, the current study aimed to identify a molecular target for inhibiting skin cancer metastasis and invasion. Proteomic analysis suggested that heat shock protein 90 kDa, alpha, class B member 1 (HSP90AB1), pentaxin (PTX3), caspase-14 (CASP14), S100, actin-1, and profilin were the primary targets related to metastasis and invasion. However, after a differential expression comparison between BCC and SCC, HSP90AB1 was identified as the best target to repress metastasis and invasion. Based on molecular docking results, gallic acid (GA) was selected to inhibit HSP90AB1. A specific Hsp90ab1 siRNA targeting was designed and compared to GA. Interestingly, GA was more efficient in silencing HSP90AB1 than siRNAhsp90ab1. Hence, our data suggest that HSP90AB1 is a crucial biomarker for identifying invasion and metastasis and that its inhibition may be a viable strategy for treating skin cancer.
publishDate 2023
dc.date.none.fl_str_mv 2023-01-30
2024-10-09T19:16:10Z
2024-10-09T19:16:10Z
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 https://doi.org/10.1016/j.gene.2022.147041
1879-0038
http://hdl.handle.net/1843/77342
url https://doi.org/10.1016/j.gene.2022.147041
http://hdl.handle.net/1843/77342
identifier_str_mv 1879-0038
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Gene
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
Brasil
ICA - INSTITUTO DE CIÊNCIAS AGRÁRIAS
UFMG
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
Brasil
ICA - INSTITUTO DE CIÊNCIAS AGRÁRIAS
UFMG
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
instname_str Universidade Federal de Minas Gerais (UFMG)
instacron_str UFMG
institution UFMG
reponame_str Repositório Institucional da UFMG
collection Repositório Institucional da UFMG
repository.name.fl_str_mv Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)
repository.mail.fl_str_mv repositorio@ufmg.br
_version_ 1816829552422289408