MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression

Detalhes bibliográficos
Autor(a) principal: Maia, Beatriz de Melo
Data de Publicação: 2016
Outros Autores: Rodrigues, Iara Santana, Akagi, Erica Mie, do Amaral, Nayra Soares, Ling, Hui, Monroig, Paloma, Soares, Fernando Augusto, Calin, George Adrian, Rocha, Rafael Malagoli [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.18632/oncotarget.10247
http://repositorio.unifesp.br/handle/11600/51176
Resumo: MiR-223-5p has been previously mentioned to be associated with tumor metastasis in HPV negative vulvar carcinomas, such as in several other tumor types. In the present study, we hypothesized that this microRNA would be important in vulvar cancer carcinogenesis and progression. To investigate this, we artificially mimicked miR-223-5p expression in a cell line derived from lymph node metastasis of vulvar carcinoma (SW962) and performed in vitro assays. As results, lower cell proliferation (p < 0.01) and migration (p < 0.001) were observed when miR-223-5p was overexpressed. In contrast, increased invasive potential of these cells was verified (p < 0.004). In silico search indicated that miR-223-5p targets TP63, member of the TP53 family of proteins, largely described with importance in vulvar cancer. We experimentally demonstrated that this microRNA is capable to decrease levels of p63 at both mRNA and protein levels (p < 0.001, and p < 0.0001
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spelling MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppressionvulvar cancermicroRNAscellular assayshsa-miR-223-5pTP63MiR-223-5p has been previously mentioned to be associated with tumor metastasis in HPV negative vulvar carcinomas, such as in several other tumor types. In the present study, we hypothesized that this microRNA would be important in vulvar cancer carcinogenesis and progression. To investigate this, we artificially mimicked miR-223-5p expression in a cell line derived from lymph node metastasis of vulvar carcinoma (SW962) and performed in vitro assays. As results, lower cell proliferation (p < 0.01) and migration (p < 0.001) were observed when miR-223-5p was overexpressed. In contrast, increased invasive potential of these cells was verified (p < 0.004). In silico search indicated that miR-223-5p targets TP63, member of the TP53 family of proteins, largely described with importance in vulvar cancer. We experimentally demonstrated that this microRNA is capable to decrease levels of p63 at both mRNA and protein levels (p < 0.001, and p < 0.0001respectively). Also, a significant inverse correlation was observed between miR-223-5p and p63 expressions in tumors from patients (p = 0.0365). Furthermore, low p63 protein expression was correlated with deeper tumor invasion (p = 0.0491) and lower patient overall survival (p = 0.0494). Our study points out miR-223-5p overexpression as a putative pathological mechanism of tumor invasion and a promising therapeutic target and highlights the importance of both miR-223-5p and p63 as prognostic factors in vulvar cancer. Also, it is plausible that the evaluation of p63 expression in vulvar cancer at the biopsy level may bring important contribution on prognostic establishment and in elaborating better surgical approaches for vulvar cancer patients.AC Camargo Canc Ctr, Dept Anat Pathol, Mol Morphol Lab, Sao Paulo, BrazilUniv Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USAUniv Texas MD Anderson Canc Ctr, Ctr RNA Interference & Noncoding RNAs, Houston, TX 77030 USAUniv Fed Sao Paulo, Dept Gynecol, Gynecol Lab, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Gynecol, Gynecol Lab, Sao Paulo, BrazilWeb of ScienceSao Paulo Research Foundation (FAPESP) [2011/18065-6, 2013/04075-5]NIH/NCI [CA135444]Department of Defense Breast Cancer Idea AwardDevelopmental Research Award in Breast Cancer, Ovarian Cancer, Brain Cancer, Prostate Cancer, Multiple Myeloma, Leukemia [P50 CA100632]Developmental Research Award in Head and Neck cancer [P50 CA097007]SINF grant in colon cancerLaura and John Arnold FoundationRGK FoundationOdyssey Program in the University of Texas MD Anderson Cancer CenterFAPESP:2011/18065-62013/04075-5NIH/NCI:CA135444BCRP:P50 CA100632P50 CA097007]Impact Journals Llc2019-07-22T15:46:55Z2019-07-22T15:46:55Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion49217-49231http://dx.doi.org/10.18632/oncotarget.10247Oncotarget. Orchard Park, v. 7, n. 31, p. 49217-49231, 2016.10.18632/oncotarget.10247WOS000385422000031.pdf1949-2553http://repositorio.unifesp.br/handle/11600/51176WOS:000385422000031enginfo:eu-repo/semantics/openAccessMaia, Beatriz de MeloRodrigues, Iara SantanaAkagi, Erica Miedo Amaral, Nayra SoaresLing, HuiMonroig, PalomaSoares, Fernando AugustoCalin, George AdrianRocha, Rafael Malagoli [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2021-10-05T15:45:57Zoai:repositorio.unifesp.br/:11600/51176Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652021-10-05T15:45:57Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
title MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
spellingShingle MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
Maia, Beatriz de Melo
vulvar cancer
microRNAs
cellular assays
hsa-miR-223-5p
TP63
title_short MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
title_full MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
title_fullStr MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
title_full_unstemmed MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
title_sort MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
author Maia, Beatriz de Melo
author_facet Maia, Beatriz de Melo
Rodrigues, Iara Santana
Akagi, Erica Mie
do Amaral, Nayra Soares
Ling, Hui
Monroig, Paloma
Soares, Fernando Augusto
Calin, George Adrian
Rocha, Rafael Malagoli [UNIFESP]
author_role author
author2 Rodrigues, Iara Santana
Akagi, Erica Mie
do Amaral, Nayra Soares
Ling, Hui
Monroig, Paloma
Soares, Fernando Augusto
Calin, George Adrian
Rocha, Rafael Malagoli [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Maia, Beatriz de Melo
Rodrigues, Iara Santana
Akagi, Erica Mie
do Amaral, Nayra Soares
Ling, Hui
Monroig, Paloma
Soares, Fernando Augusto
Calin, George Adrian
Rocha, Rafael Malagoli [UNIFESP]
dc.subject.por.fl_str_mv vulvar cancer
microRNAs
cellular assays
hsa-miR-223-5p
TP63
topic vulvar cancer
microRNAs
cellular assays
hsa-miR-223-5p
TP63
description MiR-223-5p has been previously mentioned to be associated with tumor metastasis in HPV negative vulvar carcinomas, such as in several other tumor types. In the present study, we hypothesized that this microRNA would be important in vulvar cancer carcinogenesis and progression. To investigate this, we artificially mimicked miR-223-5p expression in a cell line derived from lymph node metastasis of vulvar carcinoma (SW962) and performed in vitro assays. As results, lower cell proliferation (p < 0.01) and migration (p < 0.001) were observed when miR-223-5p was overexpressed. In contrast, increased invasive potential of these cells was verified (p < 0.004). In silico search indicated that miR-223-5p targets TP63, member of the TP53 family of proteins, largely described with importance in vulvar cancer. We experimentally demonstrated that this microRNA is capable to decrease levels of p63 at both mRNA and protein levels (p < 0.001, and p < 0.0001
publishDate 2016
dc.date.none.fl_str_mv 2016
2019-07-22T15:46:55Z
2019-07-22T15:46:55Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.18632/oncotarget.10247
Oncotarget. Orchard Park, v. 7, n. 31, p. 49217-49231, 2016.
10.18632/oncotarget.10247
WOS000385422000031.pdf
1949-2553
http://repositorio.unifesp.br/handle/11600/51176
WOS:000385422000031
url http://dx.doi.org/10.18632/oncotarget.10247
http://repositorio.unifesp.br/handle/11600/51176
identifier_str_mv Oncotarget. Orchard Park, v. 7, n. 31, p. 49217-49231, 2016.
10.18632/oncotarget.10247
WOS000385422000031.pdf
1949-2553
WOS:000385422000031
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 49217-49231
dc.publisher.none.fl_str_mv Impact Journals Llc
publisher.none.fl_str_mv Impact Journals Llc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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