LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells
Autor(a) principal: | |
---|---|
Data de Publicação: | 2023 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/molecules28052412 http://hdl.handle.net/11449/248507 |
Resumo: | Long non-coding RNAs are frequently found to be dysregulated and are linked to carcinogenesis, aggressiveness, and chemoresistance in a variety of tumors. As expression levels of the JHDM1D gene and lncRNA JHDM1D-AS1 are altered in bladder tumors, we sought to use their combined expression to distinguish between low-and high-grade bladder tumors by RTq-PCR. In addition, we evaluated the functional role of JHDM1D-AS1 and its association with the modulation of gemcitabine sensitivity in high-grade bladder-tumor cells. J82 and UM-UC-3 cells were treated with siRNA-JHDM1D-AS1 and/or three concentrations of gemcitabine (0.39, 0.78, and 1.56 µM), and then submitted to cytotoxicity testing (XTT), clonogenic survival, cell cycle progression, cell morphology, and cell migration assays. When JHDM1D and JHDM1D-AS1 expression levels were used in combination, our findings indicated favorable prognostic value. Furthermore, the combined treatment resulted in greater cytotoxicity, a decrease in clone formation, G0/G1 cell cycle arrest, morphological alterations, and a reduction in cell migration capacity in both lineages compared to the treatments alone. Thus, silencing of JHDM1D-AS1 reduced the growth and proliferation of high-grade bladder-tumor cells and increased their sensitivity to gemcitabine treatment. In addition, the expression of JHDM1D/JHDM1D-AS1 indicated potential prognostic value in the progression of bladder tumors. |
id |
UNSP_7a1df9381814268eab868535a2cc330f |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/248507 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cellsbladder cancerJHDM1D-AS1long non-coding RNAsLong non-coding RNAs are frequently found to be dysregulated and are linked to carcinogenesis, aggressiveness, and chemoresistance in a variety of tumors. As expression levels of the JHDM1D gene and lncRNA JHDM1D-AS1 are altered in bladder tumors, we sought to use their combined expression to distinguish between low-and high-grade bladder tumors by RTq-PCR. In addition, we evaluated the functional role of JHDM1D-AS1 and its association with the modulation of gemcitabine sensitivity in high-grade bladder-tumor cells. J82 and UM-UC-3 cells were treated with siRNA-JHDM1D-AS1 and/or three concentrations of gemcitabine (0.39, 0.78, and 1.56 µM), and then submitted to cytotoxicity testing (XTT), clonogenic survival, cell cycle progression, cell morphology, and cell migration assays. When JHDM1D and JHDM1D-AS1 expression levels were used in combination, our findings indicated favorable prognostic value. Furthermore, the combined treatment resulted in greater cytotoxicity, a decrease in clone formation, G0/G1 cell cycle arrest, morphological alterations, and a reduction in cell migration capacity in both lineages compared to the treatments alone. Thus, silencing of JHDM1D-AS1 reduced the growth and proliferation of high-grade bladder-tumor cells and increased their sensitivity to gemcitabine treatment. In addition, the expression of JHDM1D/JHDM1D-AS1 indicated potential prognostic value in the progression of bladder tumors.Pró-Reitoria de Pesquisa e Pós-Graduação, Universidade Federal de Ouro PretoUniversidade Federal de Ouro PretoDepartamento de Análises Clínicas Pharmacy School UFOP—Federal University of Ouro Preto, MGLaboratory of Pain and Signaling Butantan Institute, SPDepartamento de Odontologia Faculdade do Centro Oeste Paulista—FACOP, SPDepartamento de Ciências Médicas Universidade do Oeste Paulista—UNOESTE, SPDepartamento de Cirurgia Medical School USP—University of São Paulo, SPDepartamento de Patologia Medical School UNESP—São Paulo State University, SPDepartamento de Patologia Medical School UNESP—São Paulo State University, SPPró-Reitoria de Pesquisa e Pós-Graduação, Universidade Federal de Ouro Preto: PROPPI/UFOP Nº 03/2023Universidade Federal de Ouro Preto: PROPPI/UFOP Nº 03/2023UFOP—Federal University of Ouro PretoButantan InstituteFaculdade do Centro Oeste Paulista—FACOPUniversidade do Oeste Paulista—UNOESTEUniversidade de São Paulo (USP)Universidade Estadual Paulista (UNESP)Pereira, Isadora Oliveira Ansalonida Silva, Glenda NicioliAlmeida, Tamires CunhaLima, Ana Paula BragaSávio, André Luiz VenturaLeite, Katia Ramos MoreiraSalvadori, Daisy Maria Fávero [UNESP]2023-07-29T13:45:53Z2023-07-29T13:45:53Z2023-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/molecules28052412Molecules, v. 28, n. 5, 2023.1420-3049http://hdl.handle.net/11449/24850710.3390/molecules280524122-s2.0-85149886329Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMoleculesinfo:eu-repo/semantics/openAccess2024-09-03T13:18:43Zoai:repositorio.unesp.br:11449/248507Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:18:43Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
title |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
spellingShingle |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells Pereira, Isadora Oliveira Ansaloni bladder cancer JHDM1D-AS1 long non-coding RNAs |
title_short |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
title_full |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
title_fullStr |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
title_full_unstemmed |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
title_sort |
LncRNA JHDM1D-AS1 Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells |
author |
Pereira, Isadora Oliveira Ansaloni |
author_facet |
Pereira, Isadora Oliveira Ansaloni da Silva, Glenda Nicioli Almeida, Tamires Cunha Lima, Ana Paula Braga Sávio, André Luiz Ventura Leite, Katia Ramos Moreira Salvadori, Daisy Maria Fávero [UNESP] |
author_role |
author |
author2 |
da Silva, Glenda Nicioli Almeida, Tamires Cunha Lima, Ana Paula Braga Sávio, André Luiz Ventura Leite, Katia Ramos Moreira Salvadori, Daisy Maria Fávero [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
UFOP—Federal University of Ouro Preto Butantan Institute Faculdade do Centro Oeste Paulista—FACOP Universidade do Oeste Paulista—UNOESTE Universidade de São Paulo (USP) Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Pereira, Isadora Oliveira Ansaloni da Silva, Glenda Nicioli Almeida, Tamires Cunha Lima, Ana Paula Braga Sávio, André Luiz Ventura Leite, Katia Ramos Moreira Salvadori, Daisy Maria Fávero [UNESP] |
dc.subject.por.fl_str_mv |
bladder cancer JHDM1D-AS1 long non-coding RNAs |
topic |
bladder cancer JHDM1D-AS1 long non-coding RNAs |
description |
Long non-coding RNAs are frequently found to be dysregulated and are linked to carcinogenesis, aggressiveness, and chemoresistance in a variety of tumors. As expression levels of the JHDM1D gene and lncRNA JHDM1D-AS1 are altered in bladder tumors, we sought to use their combined expression to distinguish between low-and high-grade bladder tumors by RTq-PCR. In addition, we evaluated the functional role of JHDM1D-AS1 and its association with the modulation of gemcitabine sensitivity in high-grade bladder-tumor cells. J82 and UM-UC-3 cells were treated with siRNA-JHDM1D-AS1 and/or three concentrations of gemcitabine (0.39, 0.78, and 1.56 µM), and then submitted to cytotoxicity testing (XTT), clonogenic survival, cell cycle progression, cell morphology, and cell migration assays. When JHDM1D and JHDM1D-AS1 expression levels were used in combination, our findings indicated favorable prognostic value. Furthermore, the combined treatment resulted in greater cytotoxicity, a decrease in clone formation, G0/G1 cell cycle arrest, morphological alterations, and a reduction in cell migration capacity in both lineages compared to the treatments alone. Thus, silencing of JHDM1D-AS1 reduced the growth and proliferation of high-grade bladder-tumor cells and increased their sensitivity to gemcitabine treatment. In addition, the expression of JHDM1D/JHDM1D-AS1 indicated potential prognostic value in the progression of bladder tumors. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:45:53Z 2023-07-29T13:45:53Z 2023-03-01 |
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/10.3390/molecules28052412 Molecules, v. 28, n. 5, 2023. 1420-3049 http://hdl.handle.net/11449/248507 10.3390/molecules28052412 2-s2.0-85149886329 |
url |
http://dx.doi.org/10.3390/molecules28052412 http://hdl.handle.net/11449/248507 |
identifier_str_mv |
Molecules, v. 28, n. 5, 2023. 1420-3049 10.3390/molecules28052412 2-s2.0-85149886329 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Molecules |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1810021422835171328 |