Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations

Uterine adenomyosis often co-occurs with endometriosis or leiomyoma, but little is known about its molecular underpinnings. Here, the authors show that KRAS mutations are frequent in this disease, which might reduce sensitivity to progestin treatment via epigenetic silencing of the progesterone rece...

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Autores principales: Satoshi Inoue, Yasushi Hirota, Toshihide Ueno, Yamato Fukui, Emiko Yoshida, Takuo Hayashi, Shinya Kojima, Reina Takeyama, Taiki Hashimoto, Tohru Kiyono, Masako Ikemura, Ayumi Taguchi, Tomoki Tanaka, Yosuke Tanaka, Seiji Sakata, Kengo Takeuchi, Ayako Muraoka, Satoko Osuka, Tsuyoshi Saito, Katsutoshi Oda, Yutaka Osuga, Yasuhisa Terao, Masahito Kawazu, Hiroyuki Mano
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Lenguaje:EN
Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/308ef522cafc4a86addf3079e5ad71ee
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spelling oai:doaj.org-article:308ef522cafc4a86addf3079e5ad71ee2021-12-02T15:35:37ZUterine adenomyosis is an oligoclonal disorder associated with KRAS mutations10.1038/s41467-019-13708-y2041-1723https://doaj.org/article/308ef522cafc4a86addf3079e5ad71ee2019-12-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-13708-yhttps://doaj.org/toc/2041-1723Uterine adenomyosis often co-occurs with endometriosis or leiomyoma, but little is known about its molecular underpinnings. Here, the authors show that KRAS mutations are frequent in this disease, which might reduce sensitivity to progestin treatment via epigenetic silencing of the progesterone receptor.Satoshi InoueYasushi HirotaToshihide UenoYamato FukuiEmiko YoshidaTakuo HayashiShinya KojimaReina TakeyamaTaiki HashimotoTohru KiyonoMasako IkemuraAyumi TaguchiTomoki TanakaYosuke TanakaSeiji SakataKengo TakeuchiAyako MuraokaSatoko OsukaTsuyoshi SaitoKatsutoshi OdaYutaka OsugaYasuhisa TeraoMasahito KawazuHiroyuki ManoNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Satoshi Inoue
Yasushi Hirota
Toshihide Ueno
Yamato Fukui
Emiko Yoshida
Takuo Hayashi
Shinya Kojima
Reina Takeyama
Taiki Hashimoto
Tohru Kiyono
Masako Ikemura
Ayumi Taguchi
Tomoki Tanaka
Yosuke Tanaka
Seiji Sakata
Kengo Takeuchi
Ayako Muraoka
Satoko Osuka
Tsuyoshi Saito
Katsutoshi Oda
Yutaka Osuga
Yasuhisa Terao
Masahito Kawazu
Hiroyuki Mano
Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations
description Uterine adenomyosis often co-occurs with endometriosis or leiomyoma, but little is known about its molecular underpinnings. Here, the authors show that KRAS mutations are frequent in this disease, which might reduce sensitivity to progestin treatment via epigenetic silencing of the progesterone receptor.
format article
author Satoshi Inoue
Yasushi Hirota
Toshihide Ueno
Yamato Fukui
Emiko Yoshida
Takuo Hayashi
Shinya Kojima
Reina Takeyama
Taiki Hashimoto
Tohru Kiyono
Masako Ikemura
Ayumi Taguchi
Tomoki Tanaka
Yosuke Tanaka
Seiji Sakata
Kengo Takeuchi
Ayako Muraoka
Satoko Osuka
Tsuyoshi Saito
Katsutoshi Oda
Yutaka Osuga
Yasuhisa Terao
Masahito Kawazu
Hiroyuki Mano
author_facet Satoshi Inoue
Yasushi Hirota
Toshihide Ueno
Yamato Fukui
Emiko Yoshida
Takuo Hayashi
Shinya Kojima
Reina Takeyama
Taiki Hashimoto
Tohru Kiyono
Masako Ikemura
Ayumi Taguchi
Tomoki Tanaka
Yosuke Tanaka
Seiji Sakata
Kengo Takeuchi
Ayako Muraoka
Satoko Osuka
Tsuyoshi Saito
Katsutoshi Oda
Yutaka Osuga
Yasuhisa Terao
Masahito Kawazu
Hiroyuki Mano
author_sort Satoshi Inoue
title Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations
title_short Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations
title_full Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations
title_fullStr Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations
title_full_unstemmed Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations
title_sort uterine adenomyosis is an oligoclonal disorder associated with kras mutations
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/308ef522cafc4a86addf3079e5ad71ee
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