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TCTP as a therapeutic target in melanoma treatment
BACKGROUND: Translationally controlled tumour protein (TCTP) is an antiapoptotic protein highly conserved through phylogeny. Translationally controlled tumour protein overexpression was detected in several tumour types. Silencing TCTP was shown to induce tumour reversion. There is a reciprocal repre...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572181/ https://www.ncbi.nlm.nih.gov/pubmed/28751755 http://dx.doi.org/10.1038/bjc.2017.230 |
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author | Boia-Ferreira, M Basílio, A B Hamasaki, A E Matsubara, F H Appel, M H Da Costa, C R V Amson, R Telerman, A Chaim, O M Veiga, S S Senff-Ribeiro, A |
author_facet | Boia-Ferreira, M Basílio, A B Hamasaki, A E Matsubara, F H Appel, M H Da Costa, C R V Amson, R Telerman, A Chaim, O M Veiga, S S Senff-Ribeiro, A |
author_sort | Boia-Ferreira, M |
collection | PubMed |
description | BACKGROUND: Translationally controlled tumour protein (TCTP) is an antiapoptotic protein highly conserved through phylogeny. Translationally controlled tumour protein overexpression was detected in several tumour types. Silencing TCTP was shown to induce tumour reversion. There is a reciprocal repression between TCTP and P53. Sertraline interacts with TCTP and decreases its cellular levels. METHODS: We evaluate the role of TCTP in melanoma using sertraline and siRNA. Cell viability, migration, and clonogenicity were assessed in human and murine melanoma cells in vitro. Sertraline was evaluated in a murine melanoma model and was compared with dacarbazine, a major chemotherapeutic agent used in melanoma treatment. RESULTS: Inhibition of TCTP levels decreases melanoma cell viability, migration, clonogenicity, and in vivo tumour growth. Human melanoma cells treated with sertraline show diminished migration properties and capacity to form colonies. Sertraline was effective in inhibiting tumour growth in a murine melanoma model; its effect was stronger when compared with dacarbazine. CONCLUSIONS: Altogether, these results indicate that sertraline could be effective against melanoma and TCTP can be a target for melanoma therapy. |
format | Online Article Text |
id | pubmed-5572181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55721812018-08-22 TCTP as a therapeutic target in melanoma treatment Boia-Ferreira, M Basílio, A B Hamasaki, A E Matsubara, F H Appel, M H Da Costa, C R V Amson, R Telerman, A Chaim, O M Veiga, S S Senff-Ribeiro, A Br J Cancer Translational Therapeutics BACKGROUND: Translationally controlled tumour protein (TCTP) is an antiapoptotic protein highly conserved through phylogeny. Translationally controlled tumour protein overexpression was detected in several tumour types. Silencing TCTP was shown to induce tumour reversion. There is a reciprocal repression between TCTP and P53. Sertraline interacts with TCTP and decreases its cellular levels. METHODS: We evaluate the role of TCTP in melanoma using sertraline and siRNA. Cell viability, migration, and clonogenicity were assessed in human and murine melanoma cells in vitro. Sertraline was evaluated in a murine melanoma model and was compared with dacarbazine, a major chemotherapeutic agent used in melanoma treatment. RESULTS: Inhibition of TCTP levels decreases melanoma cell viability, migration, clonogenicity, and in vivo tumour growth. Human melanoma cells treated with sertraline show diminished migration properties and capacity to form colonies. Sertraline was effective in inhibiting tumour growth in a murine melanoma model; its effect was stronger when compared with dacarbazine. CONCLUSIONS: Altogether, these results indicate that sertraline could be effective against melanoma and TCTP can be a target for melanoma therapy. Nature Publishing Group 2017-08-22 2017-07-27 /pmc/articles/PMC5572181/ /pubmed/28751755 http://dx.doi.org/10.1038/bjc.2017.230 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Translational Therapeutics Boia-Ferreira, M Basílio, A B Hamasaki, A E Matsubara, F H Appel, M H Da Costa, C R V Amson, R Telerman, A Chaim, O M Veiga, S S Senff-Ribeiro, A TCTP as a therapeutic target in melanoma treatment |
title | TCTP as a therapeutic target in melanoma treatment |
title_full | TCTP as a therapeutic target in melanoma treatment |
title_fullStr | TCTP as a therapeutic target in melanoma treatment |
title_full_unstemmed | TCTP as a therapeutic target in melanoma treatment |
title_short | TCTP as a therapeutic target in melanoma treatment |
title_sort | tctp as a therapeutic target in melanoma treatment |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572181/ https://www.ncbi.nlm.nih.gov/pubmed/28751755 http://dx.doi.org/10.1038/bjc.2017.230 |
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