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Critical Role of Estrogen Receptor Alpha O-Glycosylation by N-Acetylgalactosaminyltransferase 6 (GALNT6) in Its Nuclear Localization in Breast Cancer Cells

https://tokushima-u.repo.nii.ac.jp/records/2008569
https://tokushima-u.repo.nii.ac.jp/records/2008569
bc4758ee-b6ec-4d62-8363-b67447b301b2
名前 / ファイル ライセンス アクション
neo_20_10_1038.pdf neo_20_10_1038.pdf (1.22 MB)
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Item type 文献 / Documents(1)
公開日 2021-04-19
アクセス権
アクセス権 open access
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版社版DOI
関連識別子 https://doi.org/10.1016/j.neo.2018.08.006
関連名称 10.1016/j.neo.2018.08.006
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル Critical Role of Estrogen Receptor Alpha O-Glycosylation by N-Acetylgalactosaminyltransferase 6 (GALNT6) in Its Nuclear Localization in Breast Cancer Cells
タイトル別表記
その他のタイトル GALNT6 O-Glycosylates ER-α in Breast Cancer Cells
著者 Deng, Boya

× Deng, Boya

en Deng, Boya

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Tarhan, Yunus Emre

× Tarhan, Yunus Emre

en Tarhan, Yunus Emre

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ウエダ, コウジ

× ウエダ, コウジ

ja ウエダ, コウジ

ja-Kana ウエダ, コウジ

en Ueda, Koji

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Ren, Lili

× Ren, Lili

en Ren, Lili

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片桐, 豊雅

× 片桐, 豊雅

WEKO 316
徳島大学 教育研究者総覧 174774/profile-ja.html
e-Rad 60291895

ja 片桐, 豊雅
ISNI

ja-Kana カタギリ, トヨマサ

en Katagiri, Toyomasa

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Park, Jae-Hyun

× Park, Jae-Hyun

en Park, Jae-Hyun

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ナカムラ, ユウスケ

× ナカムラ, ユウスケ

ja ナカムラ, ユウスケ

ja-Kana ナカムラ, ユウスケ

en Nakamura, Yusuke

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抄録
内容記述 Alteration of protein O-glycosylation in various human cancers including breast cancer is well known, but molecular roles of their aberrant glycosylations on cancer have not been fully understood. We previously reported critical roles of polypeptide N-acetylgalactosaminyltransferase 6 (GALNT6 or GalNAc-T6) that was upregulated in a great majority of breast cancer tissues. Here we further report O-glycosylation of estrogen receptor alpha (ER-α) by GALNT6 and the significant role of its nuclear localization in breast cancer cells. Knockdown of GALNT6 expression in two breast cancer cell lines, T47D and MCF7, in which both ER-α and GALNT6 were highly expressed, by small interfering RNA could significantly attenuate expression of ER-α. Immunocytochemical analysis clearly demonstrated the drastic decrease of ER-α protein in the nucleus of these cancer cells. Accordingly, the downstream genes of the ER-α pathway such as MYC, CCND1, and CTSD were significantly downregulated. We confirmed GALNT6-dependent ER-α O-glycosylation and identified O-glycosylation of S573 in an F domain of ER-α by GALNT6 through LC-MS/MS analysis. We also obtained evidences showing that the glycosylation of ER-α at S573 by GALNT6 is essential for protein stability and nuclear localization of ER-α in breast cancer cells. Furthermore, we designed cell membrane–permeable peptides including the O-glycosylation site and found a significant decrease of the cell viability of breast cancer cells by treatment of these peptides in a GALNT6 expression–dependent manner. Our study suggests that targeting the GALNT6 enzymatic activity as well as the GALNT6/ER-α interaction could be a promising therapeutic approach to ER-α–positive breast cancer patients.
書誌情報 en : Neoplasia

巻 20, 号 10, p. 1038-1044, 発行日 2018-09-09
収録物ID
収録物識別子タイプ ISSN
収録物識別子 14765586
出版者
出版者 Neoplasia Press
出版者
出版者 Elsevier
権利情報
権利情報 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
EID
識別子 346450
言語
言語 eng
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