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  1. 原著論文

Tissue-specific and time-dependent clonal expansion of ENU-induced mutant cells in gpt delta mice.

https://repo.qst.go.jp/records/48441
https://repo.qst.go.jp/records/48441
0b6728df-7e33-47d3-9022-67d1ae6a339a
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-01-18
タイトル
タイトル Tissue-specific and time-dependent clonal expansion of ENU-induced mutant cells in gpt delta mice.
言語
言語 eng
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
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Nakayama, Takafumi

× Nakayama, Takafumi

WEKO 486988

Nakayama, Takafumi

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Sawai, Tomoko

× Sawai, Tomoko

WEKO 486989

Sawai, Tomoko

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Masuda, Ikuko

× Masuda, Ikuko

WEKO 486990

Masuda, Ikuko

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Kaneko, Shinya

× Kaneko, Shinya

WEKO 486991

Kaneko, Shinya

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Yamauchi, Kazumi

× Yamauchi, Kazumi

WEKO 486992

Yamauchi, Kazumi

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Blyth, Benjamin

× Blyth, Benjamin

WEKO 486993

Blyth, Benjamin

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Shimada, Yoshiya

× Shimada, Yoshiya

WEKO 486994

Shimada, Yoshiya

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Tachibana, Akira

× Tachibana, Akira

WEKO 486995

Tachibana, Akira

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Kakinuma, Shizuko

× Kakinuma, Shizuko

WEKO 486996

Kakinuma, Shizuko

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中山 貴文

× 中山 貴文

WEKO 486997

en 中山 貴文

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澤井 知子

× 澤井 知子

WEKO 486998

en 澤井 知子

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益田 郁子

× 益田 郁子

WEKO 486999

en 益田 郁子

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山内 一己

× 山内 一己

WEKO 487000

en 山内 一己

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Blyth Benjamin

× Blyth Benjamin

WEKO 487001

en Blyth Benjamin

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島田 義也

× 島田 義也

WEKO 487002

en 島田 義也

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立花 章

× 立花 章

WEKO 487003

en 立花 章

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柿沼 志津子

× 柿沼 志津子

WEKO 487004

en 柿沼 志津子

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抄録
内容記述タイプ Abstract
内容記述 DNA mutations play a crucial role in the origins of cancer, and the clonal expansion of mutant cells is one of the fundamental steps in multistage carcinogenesis. In this study, we correlated tumor incidence in B6C3F1 mice during the period after exposure to N-ethyl-N-nitrosourea (ENU) with the persistence of ENU-induced mutant clones in transgenic gpt delta B6C3F1 mice. The induced gpt mutations afforded no selective advantage in the mouse cells and could be distinguished by a mutational spectrum that is characteristic of ENU treatment. The gpt mutations were passengers of the mutant cell of origin and its daughter cells and thus could be used as neutral markers of clones that arose and persisted in the tissues. Female B6C3F1 mice exposed for 1 month to 200 ppm ENU in the drinking water developed early thymic lymphomas and late liver and lung tumors. To assay gpt mutations, we sampled the thymus, liver, lung, and small intestine of female gpt delta mice at 3 days, 4 weeks, and 8 weeks after the end of ENU exposure. Our results reveal that, in all four tissues, the ENU-induced gpt mutations persisted for weeks after the end of mutagen exposure. Clonal expansion of mutant cells was observed in the thymus and small intestine, with the thymus showing larger clone sizes. These results indicate that the clearance of mutant cells and the potential for clonal expansion during normal tissue growth depends on tissue type and that these factors may affect the sensitivity of different tissues to carcinogenesis.
書誌情報 Environmental and Molecular Mutagenesis

巻 58, 号 8, p. 592-606, 発行日 2017-10
ISSN
収録物識別子タイプ ISSN
収録物識別子 0893-6692
PubMed番号
識別子タイプ PMID
関連識別子 28921690
DOI
識別子タイプ DOI
関連識別子 10.1002/em.22132
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