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Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells

BACKGROUND: Capsaicin (8-methyl-N-vanillyl-6-nonenamide) is one of the main pungent components of chili peppers and has been shown to exert various effects on numerous physiological processes. Recent studies have focused on the chemopreventive effects of capsaicin, which can combat growth in various...

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Autores principales: Lin, Rong-Jaan, Wu, I-Jung, Hong, Jo-Yu, Liu, Bang-Hung, Liang, Ruei-Yue, Yuan, Tein-Ming, Chuang, Show-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177521/
https://www.ncbi.nlm.nih.gov/pubmed/30323679
http://dx.doi.org/10.2147/CMAR.S162383
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author Lin, Rong-Jaan
Wu, I-Jung
Hong, Jo-Yu
Liu, Bang-Hung
Liang, Ruei-Yue
Yuan, Tein-Ming
Chuang, Show-Mei
author_facet Lin, Rong-Jaan
Wu, I-Jung
Hong, Jo-Yu
Liu, Bang-Hung
Liang, Ruei-Yue
Yuan, Tein-Ming
Chuang, Show-Mei
author_sort Lin, Rong-Jaan
collection PubMed
description BACKGROUND: Capsaicin (8-methyl-N-vanillyl-6-nonenamide) is one of the main pungent components of chili peppers and has been shown to exert various effects on numerous physiological processes. Recent studies have focused on the chemopreventive effects of capsaicin, which can combat growth in various human cancer cell systems. The tribbles-related protein 3 (TRIB3) is evolutionarily conserved from Drosophila to humans. In the latter, TRIB3 is a key determinant in numerous cellular processes, including apoptosis. PURPOSE: The aim of this study was to examine the importance of TRIB3 in the antitumor efficacy of capsaicin in human cancer cells, and further assess potential mechanism(s) underlying the capsaicin-induced upregulation of TRIB3. METHODS: Human cancer cell lines were treated with capsaicin, then evaluated for levels of TRIB3 and molecules related to apoptosis or signaling pathways. The impact of TRIB3 on capsaicin-induced apoptosis was investigated using si-RNA or overexpression of TRIB3. RESULTS: It is the first time to show that TRIB3 is targeted by capsaicin to promote apoptosis. Capsaicin promotes apoptotic cell death by upregulating TRIB3 expression in cancer cells. Overexpression of TRIB3 enhances capsaicin-induced apoptosis, and TRIB3 knockdown experiments demonstrate that the effect of capsaicin in apoptotic cell death is correlated with the induction of TRIB3 in cancer cells. Finally, enhancements in gene expression and protein stability are involved in the capsaicin-induced upregulation of TRIB3. CONCLUSION: Our results show that the capsaicin-induced upregulation of TRIB3 triggers apoptosis and thereby contributes to the suppression of cell growth in cancer cell lines.
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spelling pubmed-61775212018-10-15 Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells Lin, Rong-Jaan Wu, I-Jung Hong, Jo-Yu Liu, Bang-Hung Liang, Ruei-Yue Yuan, Tein-Ming Chuang, Show-Mei Cancer Manag Res Original Research BACKGROUND: Capsaicin (8-methyl-N-vanillyl-6-nonenamide) is one of the main pungent components of chili peppers and has been shown to exert various effects on numerous physiological processes. Recent studies have focused on the chemopreventive effects of capsaicin, which can combat growth in various human cancer cell systems. The tribbles-related protein 3 (TRIB3) is evolutionarily conserved from Drosophila to humans. In the latter, TRIB3 is a key determinant in numerous cellular processes, including apoptosis. PURPOSE: The aim of this study was to examine the importance of TRIB3 in the antitumor efficacy of capsaicin in human cancer cells, and further assess potential mechanism(s) underlying the capsaicin-induced upregulation of TRIB3. METHODS: Human cancer cell lines were treated with capsaicin, then evaluated for levels of TRIB3 and molecules related to apoptosis or signaling pathways. The impact of TRIB3 on capsaicin-induced apoptosis was investigated using si-RNA or overexpression of TRIB3. RESULTS: It is the first time to show that TRIB3 is targeted by capsaicin to promote apoptosis. Capsaicin promotes apoptotic cell death by upregulating TRIB3 expression in cancer cells. Overexpression of TRIB3 enhances capsaicin-induced apoptosis, and TRIB3 knockdown experiments demonstrate that the effect of capsaicin in apoptotic cell death is correlated with the induction of TRIB3 in cancer cells. Finally, enhancements in gene expression and protein stability are involved in the capsaicin-induced upregulation of TRIB3. CONCLUSION: Our results show that the capsaicin-induced upregulation of TRIB3 triggers apoptosis and thereby contributes to the suppression of cell growth in cancer cell lines. Dove Medical Press 2018-10-04 /pmc/articles/PMC6177521/ /pubmed/30323679 http://dx.doi.org/10.2147/CMAR.S162383 Text en © 2018 Lin et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Lin, Rong-Jaan
Wu, I-Jung
Hong, Jo-Yu
Liu, Bang-Hung
Liang, Ruei-Yue
Yuan, Tein-Ming
Chuang, Show-Mei
Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells
title Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells
title_full Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells
title_fullStr Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells
title_full_unstemmed Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells
title_short Capsaicin-induced TRIB3 upregulation promotes apoptosis in cancer cells
title_sort capsaicin-induced trib3 upregulation promotes apoptosis in cancer cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177521/
https://www.ncbi.nlm.nih.gov/pubmed/30323679
http://dx.doi.org/10.2147/CMAR.S162383
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