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  1. 紀要
  2. Tumor Research
  3. Vol.45

Epigenetic biomarkers for prediction of sensitivity to chemotherapeutic drugs in multiple myeloma

https://doi.org/10.15114/tr.45.21
https://doi.org/10.15114/tr.45.21
c79bc360-4a2f-4080-9a40-f5b2ec2f85dd
名前 / ファイル ライセンス アクション
n004140934521.pdf n004140934521.pdf (56.3 MB)
Item type 紀要論文 / Departmental Bulletin Paper(1)
公開日 2019-07-31
タイトル
タイトル Epigenetic biomarkers for prediction of sensitivity to chemotherapeutic drugs in multiple myeloma
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 Multiple myeloma
キーワード
言語 en
主題Scheme Other
主題 Epigenetics
キーワード
言語 en
主題Scheme Other
主題 DNA methylation
キーワード
言語 en
主題Scheme Other
主題 Biomarker
キーワード
言語 en
主題Scheme Other
主題 Multiple myeloma
キーワード
言語 en
主題Scheme Other
主題 Epigenetics
キーワード
言語 en
主題Scheme Other
主題 DNA methylation
キーワード
言語 en
主題Scheme Other
主題 Biomarker
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 departmental bulletin paper
ID登録
ID登録 10.15114/tr.45.21
ID登録タイプ JaLC
著者 Hiroshi, Yasui

× Hiroshi, Yasui

Hiroshi, Yasui

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Tadao, Ishida

× Tadao, Ishida

Tadao, Ishida

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Masanori, Nojima

× Masanori, Nojima

Masanori, Nojima

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Yuka, Aoki

× Yuka, Aoki

Yuka, Aoki

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Hiroshi, Ikeda

× Hiroshi, Ikeda

Hiroshi, Ikeda

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Hiromu, Suzuki

× Hiromu, Suzuki

Hiromu, Suzuki

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Toshiaki, Hayashi

× Toshiaki, Hayashi

Toshiaki, Hayashi

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Yasuhisa, Shinomura

× Yasuhisa, Shinomura

Yasuhisa, Shinomura

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Minoru, Toyota

× Minoru, Toyota

Minoru, Toyota

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抄録
内容記述タイプ Abstract
内容記述 Multiple myeloma continues to be a lethal malignancy despite the development of treatments such as high-dose chemotherapy combined with stem cell transplantation. Multiple myeloma arises through an accumulation of multiple genetic anges, including immunoglobulin gene rearrangements involved in Cyclin D. The main difficulties in multiple myeloma treatments are drug-resistance. DNA methylation of the5' CpG islands of genes is often found in multiple myeloma. To screen for he genes involved in tumorigenesis of multiple myeloma, which are silenced by DNA methylation, we performed cDNA microarray analysis using multiple myeloma cell lines treated with demethylating agent5-aza-2-deoxycytidine (DAC), and entified RASD1, a dexamethasone (Dex)-inducible gene, as one of the targets of epigenetic changes. Inactivation of RASD1 was found to correlate with resistance to Dex, and treatment of multiple myeloma cells with DAC restored sensitivity to Dex. These findings suggest the involvement of epigenetic gene silencing in multiple myeloma progression and drug-resistance, and the usefulness of demethylation therapy for multiple myeloma treatment. Furthermore, DNA methylation can be an epigenetic biomarker for multiple myeloma.
書誌情報 Tumor Research
en : Tumor Research

巻 45, p. 21-31, 発行日 2010
ISSN
収録物識別子タイプ ISSN
収録物識別子 0041-4093
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
出版者
出版者 Sapporo Medical University
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Cite as

Hiroshi, Yasui, Tadao, Ishida, Masanori, Nojima, Yuka, Aoki, Hiroshi, Ikeda, Hiromu, Suzuki, Toshiaki, Hayashi, Yasuhisa, Shinomura, Minoru, Toyota, 2010, Epigenetic biomarkers for prediction of sensitivity to chemotherapeutic drugs in multiple myeloma: Sapporo Medical University, 21–31 p.

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