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Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA

Long-term estrogen deprivation (LTED) of an estrogen receptor (ER) α-positive breast cancer cell line recapitulates cancer cells that have acquired estrogen-independent cell proliferation and endocrine therapy resistance. Previously, we have shown that a cluster of non-coding RNAs, Eleanors (ESR1 lo...

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Autores principales: Yamamoto, Tatsuro, Sakamoto, Chiyomi, Tachiwana, Hiroaki, Kumabe, Mitsuru, Matsui, Toshiro, Yamashita, Tadatoshi, Shinagawa, Masatoshi, Ochiai, Koji, Saitoh, Noriko, Nakao, Mitsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185934/
https://www.ncbi.nlm.nih.gov/pubmed/30315184
http://dx.doi.org/10.1038/s41598-018-33227-y
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author Yamamoto, Tatsuro
Sakamoto, Chiyomi
Tachiwana, Hiroaki
Kumabe, Mitsuru
Matsui, Toshiro
Yamashita, Tadatoshi
Shinagawa, Masatoshi
Ochiai, Koji
Saitoh, Noriko
Nakao, Mitsuyoshi
author_facet Yamamoto, Tatsuro
Sakamoto, Chiyomi
Tachiwana, Hiroaki
Kumabe, Mitsuru
Matsui, Toshiro
Yamashita, Tadatoshi
Shinagawa, Masatoshi
Ochiai, Koji
Saitoh, Noriko
Nakao, Mitsuyoshi
author_sort Yamamoto, Tatsuro
collection PubMed
description Long-term estrogen deprivation (LTED) of an estrogen receptor (ER) α-positive breast cancer cell line recapitulates cancer cells that have acquired estrogen-independent cell proliferation and endocrine therapy resistance. Previously, we have shown that a cluster of non-coding RNAs, Eleanors (ESR1 locus enhancing and activating non-coding RNAs) formed RNA cloud and upregulated the ESR1 gene in the nuclei of LTED cells. Eleanors were inhibited by resveratrol through ER. Here we prepared another polyphenol, glyceollin I from stressed soybeans, and identified it as a major inhibitor of the Eleanor RNA cloud and ESR1 mRNA transcription. The inhibition was independent of ER, unlike one by resveratrol. This was consistent with a distinct tertiary structure of glyceollin I for ER binding. Glyceollin I preferentially inhibited the growth of LTED cells and induced apoptosis. Our results suggest that glyceollin I has a novel role in LTED cell inhibition through Eleanors. In other words, LTED cells or endocrine therapy-resistant breast cancer cells may be ready for apoptosis, which can be triggered with polyphenols both in ER-dependent and ER-independent manners.
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spelling pubmed-61859342018-10-15 Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA Yamamoto, Tatsuro Sakamoto, Chiyomi Tachiwana, Hiroaki Kumabe, Mitsuru Matsui, Toshiro Yamashita, Tadatoshi Shinagawa, Masatoshi Ochiai, Koji Saitoh, Noriko Nakao, Mitsuyoshi Sci Rep Article Long-term estrogen deprivation (LTED) of an estrogen receptor (ER) α-positive breast cancer cell line recapitulates cancer cells that have acquired estrogen-independent cell proliferation and endocrine therapy resistance. Previously, we have shown that a cluster of non-coding RNAs, Eleanors (ESR1 locus enhancing and activating non-coding RNAs) formed RNA cloud and upregulated the ESR1 gene in the nuclei of LTED cells. Eleanors were inhibited by resveratrol through ER. Here we prepared another polyphenol, glyceollin I from stressed soybeans, and identified it as a major inhibitor of the Eleanor RNA cloud and ESR1 mRNA transcription. The inhibition was independent of ER, unlike one by resveratrol. This was consistent with a distinct tertiary structure of glyceollin I for ER binding. Glyceollin I preferentially inhibited the growth of LTED cells and induced apoptosis. Our results suggest that glyceollin I has a novel role in LTED cell inhibition through Eleanors. In other words, LTED cells or endocrine therapy-resistant breast cancer cells may be ready for apoptosis, which can be triggered with polyphenols both in ER-dependent and ER-independent manners. Nature Publishing Group UK 2018-10-12 /pmc/articles/PMC6185934/ /pubmed/30315184 http://dx.doi.org/10.1038/s41598-018-33227-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yamamoto, Tatsuro
Sakamoto, Chiyomi
Tachiwana, Hiroaki
Kumabe, Mitsuru
Matsui, Toshiro
Yamashita, Tadatoshi
Shinagawa, Masatoshi
Ochiai, Koji
Saitoh, Noriko
Nakao, Mitsuyoshi
Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA
title Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA
title_full Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA
title_fullStr Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA
title_full_unstemmed Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA
title_short Endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin I through Eleanor non-coding RNA
title_sort endocrine therapy-resistant breast cancer model cells are inhibited by soybean glyceollin i through eleanor non-coding rna
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185934/
https://www.ncbi.nlm.nih.gov/pubmed/30315184
http://dx.doi.org/10.1038/s41598-018-33227-y
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