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Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets
AIM: The purpose of this study was to investigate the possible mechanisms of genistein (GEN) and daidzein (DAI) in inducing apoptosis of colon cancer cells by inhibition of lipid droplets (LDs) accumulation. METHODS: HT-29 cells were used and treated by GEN or DAI in this paper. LDs accumulation was...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Open Academia
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5965345/ https://www.ncbi.nlm.nih.gov/pubmed/29849534 http://dx.doi.org/10.29219/fnr.v62.1384 |
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author | Liang, Yu-Si Qi, Wen-Tao Guo, Weiqun Wang, Chun-Ling Hu, Ze-Bin Li, Ai-Ke |
author_facet | Liang, Yu-Si Qi, Wen-Tao Guo, Weiqun Wang, Chun-Ling Hu, Ze-Bin Li, Ai-Ke |
author_sort | Liang, Yu-Si |
collection | PubMed |
description | AIM: The purpose of this study was to investigate the possible mechanisms of genistein (GEN) and daidzein (DAI) in inducing apoptosis of colon cancer cells by inhibition of lipid droplets (LDs) accumulation. METHODS: HT-29 cells were used and treated by GEN or DAI in this paper. LDs accumulation was induced and inhibited by oleic acid (OA) and C75, respectively. The expression changes of LDs-related markers were confirmed by semiquantitative real time-PCR (RT–PCR), Western blotting, and immunofluorescence staining. RESULTS: GEN and DAI effectively reduced the LDs accumulation and downregulated the expression of Perilipin-1, ADRP and Tip-47 family proteins and vimentin levels. GEN and DAI significantly induced the mRNA expression of PPAR-γ, Fas, FABP, glycerol-3-phosphate acyltransferase (GPAT3), and microsomal TG transfer protein (MTTP), and reduced the mRNA expression of UCP2. Furthermore, the results showed a decrease of PI3K expression by GEN and DAI when compared with OA treatment, and both GEN and DAI can increase the expression of FOXO3a and caspase-8 significantly when these proteins were decreased by OA treatment. GEN is more effective than DAI in inducing cell apoptosis. CONCLUSION: Our results demonstrated that GEN and DAI inhibit the accumulation of LDs by regulating LDs-related factors and lead to a final apoptosis of colon cancer cells. These results may provide important new insights into the possible molecular mechanisms of isoflavones in anti-obesity and anti-tumor functions. |
format | Online Article Text |
id | pubmed-5965345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Open Academia |
record_format | MEDLINE/PubMed |
spelling | pubmed-59653452018-05-30 Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets Liang, Yu-Si Qi, Wen-Tao Guo, Weiqun Wang, Chun-Ling Hu, Ze-Bin Li, Ai-Ke Food Nutr Res Original Article AIM: The purpose of this study was to investigate the possible mechanisms of genistein (GEN) and daidzein (DAI) in inducing apoptosis of colon cancer cells by inhibition of lipid droplets (LDs) accumulation. METHODS: HT-29 cells were used and treated by GEN or DAI in this paper. LDs accumulation was induced and inhibited by oleic acid (OA) and C75, respectively. The expression changes of LDs-related markers were confirmed by semiquantitative real time-PCR (RT–PCR), Western blotting, and immunofluorescence staining. RESULTS: GEN and DAI effectively reduced the LDs accumulation and downregulated the expression of Perilipin-1, ADRP and Tip-47 family proteins and vimentin levels. GEN and DAI significantly induced the mRNA expression of PPAR-γ, Fas, FABP, glycerol-3-phosphate acyltransferase (GPAT3), and microsomal TG transfer protein (MTTP), and reduced the mRNA expression of UCP2. Furthermore, the results showed a decrease of PI3K expression by GEN and DAI when compared with OA treatment, and both GEN and DAI can increase the expression of FOXO3a and caspase-8 significantly when these proteins were decreased by OA treatment. GEN is more effective than DAI in inducing cell apoptosis. CONCLUSION: Our results demonstrated that GEN and DAI inhibit the accumulation of LDs by regulating LDs-related factors and lead to a final apoptosis of colon cancer cells. These results may provide important new insights into the possible molecular mechanisms of isoflavones in anti-obesity and anti-tumor functions. Open Academia 2018-05-11 /pmc/articles/PMC5965345/ /pubmed/29849534 http://dx.doi.org/10.29219/fnr.v62.1384 Text en © 2018 Yu-Si Liang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license. |
spellingShingle | Original Article Liang, Yu-Si Qi, Wen-Tao Guo, Weiqun Wang, Chun-Ling Hu, Ze-Bin Li, Ai-Ke Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
title | Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
title_full | Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
title_fullStr | Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
title_full_unstemmed | Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
title_short | Genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
title_sort | genistein and daidzein induce apoptosis of colon cancer cells by inhibiting the accumulation of lipid droplets |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5965345/ https://www.ncbi.nlm.nih.gov/pubmed/29849534 http://dx.doi.org/10.29219/fnr.v62.1384 |
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