CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma
Autor(a) principal: | |
---|---|
Data de Publicação: | 2021 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/212785 |
Resumo: | OBJECTIVES: Malignant melanoma (MM) is an invasive tumor that poses a threat to patient health. Circular RNAs (circRNAs) are important regulators of MM carcinogenesis. In this study, we investigated the expression characteristics and biological functions of, and mechanism underlying, circ_0119872 expression in MM. METHODS: Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was employed to examine the circ_0119872, microRNA (miR)-582-3p, and E2F transcription factor 3 (E2F3) mRNA expression levels in MM tissues and cell lines. Western blotting was performed to quantify E2F3 protein expression. MM cells with circ_0119872 knockdown were established, and cell counting kit 8 (CCK-8) and transwell assays were utilized to examine the function of circ_0119872 and its effects on the malignant characteristics of MM cells. The MiRDB and TargetScan databases were used to predict the target genes of miR-582-3p. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was used to explore the biological functions of the target genes of miR582-3p. Additionally, a dual-luciferase reporter gene experiment was performed to verify the targeting relationship between circ_0119872 and miR-582-3p as well as that between miR-582-3p and E2F3. RESULTS: Circ_0119872 was remarkably upregulated in MM tissues and cell lines. Circ_0119872 knockdown suppressed the cell proliferation and metastasis In addition, miR-582-3p was identified as a downstream target of circ_0119872. The target genes of miR-193a-3p are involved in melanogenesis and cancer-related signaling pathways. Mechanistically, circ_0119872 facilitated MM progression by adsorbing miR-582-3p and upregulating E2F3 expression. CONCLUSION: Circ_0119872 is an oncogenic circRNA that participates in the promotion of MM progression by regulating the miR-582-3p/E2F3 axis. |
id |
USP-19_964ddf629ef6b459facb326339dd90f9 |
---|---|
oai_identifier_str |
oai:revistas.usp.br:article/212785 |
network_acronym_str |
USP-19 |
network_name_str |
Clinics |
repository_id_str |
|
spelling |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanomaMelanomaCirc_0119872miR-582-3pE2F3OBJECTIVES: Malignant melanoma (MM) is an invasive tumor that poses a threat to patient health. Circular RNAs (circRNAs) are important regulators of MM carcinogenesis. In this study, we investigated the expression characteristics and biological functions of, and mechanism underlying, circ_0119872 expression in MM. METHODS: Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was employed to examine the circ_0119872, microRNA (miR)-582-3p, and E2F transcription factor 3 (E2F3) mRNA expression levels in MM tissues and cell lines. Western blotting was performed to quantify E2F3 protein expression. MM cells with circ_0119872 knockdown were established, and cell counting kit 8 (CCK-8) and transwell assays were utilized to examine the function of circ_0119872 and its effects on the malignant characteristics of MM cells. The MiRDB and TargetScan databases were used to predict the target genes of miR-582-3p. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was used to explore the biological functions of the target genes of miR582-3p. Additionally, a dual-luciferase reporter gene experiment was performed to verify the targeting relationship between circ_0119872 and miR-582-3p as well as that between miR-582-3p and E2F3. RESULTS: Circ_0119872 was remarkably upregulated in MM tissues and cell lines. Circ_0119872 knockdown suppressed the cell proliferation and metastasis In addition, miR-582-3p was identified as a downstream target of circ_0119872. The target genes of miR-193a-3p are involved in melanogenesis and cancer-related signaling pathways. Mechanistically, circ_0119872 facilitated MM progression by adsorbing miR-582-3p and upregulating E2F3 expression. CONCLUSION: Circ_0119872 is an oncogenic circRNA that participates in the promotion of MM progression by regulating the miR-582-3p/E2F3 axis.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2021-10-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/21278510.6061/clinics/2021/e3036Clinics; Vol. 76 (2021); e3036Clinics; v. 76 (2021); e3036Clinics; Vol. 76 (2021); e30361980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/212785/194756Copyright (c) 2023 Clinicsinfo:eu-repo/semantics/openAccessQu, JinlongYuan, ChunyingJia, QiSun, MengweiJiang, MinZuo, Fuguang2023-07-06T13:04:04Zoai:revistas.usp.br:article/212785Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2023-07-06T13:04:04Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
title |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
spellingShingle |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma Qu, Jinlong Melanoma Circ_0119872 miR-582-3p E2F3 |
title_short |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
title_full |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
title_fullStr |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
title_full_unstemmed |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
title_sort |
CircularRNA_0119872 regulates the microRNA-582- 3p/E2F transcription factor 3 pathway to promote the progression of malignant melanoma |
author |
Qu, Jinlong |
author_facet |
Qu, Jinlong Yuan, Chunying Jia, Qi Sun, Mengwei Jiang, Min Zuo, Fuguang |
author_role |
author |
author2 |
Yuan, Chunying Jia, Qi Sun, Mengwei Jiang, Min Zuo, Fuguang |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Qu, Jinlong Yuan, Chunying Jia, Qi Sun, Mengwei Jiang, Min Zuo, Fuguang |
dc.subject.por.fl_str_mv |
Melanoma Circ_0119872 miR-582-3p E2F3 |
topic |
Melanoma Circ_0119872 miR-582-3p E2F3 |
description |
OBJECTIVES: Malignant melanoma (MM) is an invasive tumor that poses a threat to patient health. Circular RNAs (circRNAs) are important regulators of MM carcinogenesis. In this study, we investigated the expression characteristics and biological functions of, and mechanism underlying, circ_0119872 expression in MM. METHODS: Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was employed to examine the circ_0119872, microRNA (miR)-582-3p, and E2F transcription factor 3 (E2F3) mRNA expression levels in MM tissues and cell lines. Western blotting was performed to quantify E2F3 protein expression. MM cells with circ_0119872 knockdown were established, and cell counting kit 8 (CCK-8) and transwell assays were utilized to examine the function of circ_0119872 and its effects on the malignant characteristics of MM cells. The MiRDB and TargetScan databases were used to predict the target genes of miR-582-3p. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was used to explore the biological functions of the target genes of miR582-3p. Additionally, a dual-luciferase reporter gene experiment was performed to verify the targeting relationship between circ_0119872 and miR-582-3p as well as that between miR-582-3p and E2F3. RESULTS: Circ_0119872 was remarkably upregulated in MM tissues and cell lines. Circ_0119872 knockdown suppressed the cell proliferation and metastasis In addition, miR-582-3p was identified as a downstream target of circ_0119872. The target genes of miR-193a-3p are involved in melanogenesis and cancer-related signaling pathways. Mechanistically, circ_0119872 facilitated MM progression by adsorbing miR-582-3p and upregulating E2F3 expression. CONCLUSION: Circ_0119872 is an oncogenic circRNA that participates in the promotion of MM progression by regulating the miR-582-3p/E2F3 axis. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-10-11 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/212785 10.6061/clinics/2021/e3036 |
url |
https://www.revistas.usp.br/clinics/article/view/212785 |
identifier_str_mv |
10.6061/clinics/2021/e3036 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/212785/194756 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2023 Clinics info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2023 Clinics |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 76 (2021); e3036 Clinics; v. 76 (2021); e3036 Clinics; Vol. 76 (2021); e3036 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222766077575168 |