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Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer
PURPOSE: Leptin is a potent adipokine that plays a significant role in tumor development and the progression of breast cancer. The aim of this study was to evaluate whether leptin affects the response to tamoxifen treatment in estrogen receptor (ER)-positive breast cancer cells. METHODS: Leptin, lep...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Breast Cancer Society
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706857/ https://www.ncbi.nlm.nih.gov/pubmed/23843844 http://dx.doi.org/10.4048/jbc.2013.16.2.138 |
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author | Yom, Cha Kyong Lee, Kyung-Min Han, Wonshik Kim, Sung-Won Kim, Hee Sung Moon, Byung In Jeong, Ku-Young Im, Seock-Ah Noh, Dong-Young |
author_facet | Yom, Cha Kyong Lee, Kyung-Min Han, Wonshik Kim, Sung-Won Kim, Hee Sung Moon, Byung In Jeong, Ku-Young Im, Seock-Ah Noh, Dong-Young |
author_sort | Yom, Cha Kyong |
collection | PubMed |
description | PURPOSE: Leptin is a potent adipokine that plays a significant role in tumor development and the progression of breast cancer. The aim of this study was to evaluate whether leptin affects the response to tamoxifen treatment in estrogen receptor (ER)-positive breast cancer cells. METHODS: Leptin, leptin receptor (Ob-R), and activation of signaling pathways were studied by Western immunoblotting. The effects of leptin on tamoxifen-dependent growth inhibition were studied in MCF-7 and T-47D cells. RESULTS: Leptin was expressed in MCF-7 and T-47D and had a proliferative effect on MCF-7 cells. Leptin significantly inhibited the antiestrogenic effect of tamoxifen in both cells only under β-estradiol (E2) (20 nM) conditions. In MCF-7, the inhibitory effect against tamoxifen was a result from the activation of the ERK1/2 and STAT3 signal transduction pathway. CONCLUSION: Leptin interferes with the effects of tamoxifen under E2 stimulated conditions in ER-positive breast cancer cells. These results imply that inhibition of leptin is expected to enhance the response to tamoxifen in ER-positive breast cancer cells, and, therefore, could be a promising way to overcome endocrine resistance. |
format | Online Article Text |
id | pubmed-3706857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Breast Cancer Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-37068572013-07-10 Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer Yom, Cha Kyong Lee, Kyung-Min Han, Wonshik Kim, Sung-Won Kim, Hee Sung Moon, Byung In Jeong, Ku-Young Im, Seock-Ah Noh, Dong-Young J Breast Cancer Original Article PURPOSE: Leptin is a potent adipokine that plays a significant role in tumor development and the progression of breast cancer. The aim of this study was to evaluate whether leptin affects the response to tamoxifen treatment in estrogen receptor (ER)-positive breast cancer cells. METHODS: Leptin, leptin receptor (Ob-R), and activation of signaling pathways were studied by Western immunoblotting. The effects of leptin on tamoxifen-dependent growth inhibition were studied in MCF-7 and T-47D cells. RESULTS: Leptin was expressed in MCF-7 and T-47D and had a proliferative effect on MCF-7 cells. Leptin significantly inhibited the antiestrogenic effect of tamoxifen in both cells only under β-estradiol (E2) (20 nM) conditions. In MCF-7, the inhibitory effect against tamoxifen was a result from the activation of the ERK1/2 and STAT3 signal transduction pathway. CONCLUSION: Leptin interferes with the effects of tamoxifen under E2 stimulated conditions in ER-positive breast cancer cells. These results imply that inhibition of leptin is expected to enhance the response to tamoxifen in ER-positive breast cancer cells, and, therefore, could be a promising way to overcome endocrine resistance. Korean Breast Cancer Society 2013-06 2013-06-28 /pmc/articles/PMC3706857/ /pubmed/23843844 http://dx.doi.org/10.4048/jbc.2013.16.2.138 Text en © 2013 Korean Breast Cancer Society. All rights reserved. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yom, Cha Kyong Lee, Kyung-Min Han, Wonshik Kim, Sung-Won Kim, Hee Sung Moon, Byung In Jeong, Ku-Young Im, Seock-Ah Noh, Dong-Young Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer |
title | Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer |
title_full | Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer |
title_fullStr | Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer |
title_full_unstemmed | Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer |
title_short | Leptin as a Potential Target for Estrogen Receptor-Positive Breast Cancer |
title_sort | leptin as a potential target for estrogen receptor-positive breast cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706857/ https://www.ncbi.nlm.nih.gov/pubmed/23843844 http://dx.doi.org/10.4048/jbc.2013.16.2.138 |
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