MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , , |
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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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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1814268364276629504 |