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  1. H-1. がん進展制御研究所
  2. h-1 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Different histological types of non-small cell lung cancer have distinct folate and DNA methylation levels

http://hdl.handle.net/2297/20147
http://hdl.handle.net/2297/20147
add47496-26d1-4dfb-82cb-7d2817383fd6
名前 / ファイル ライセンス アクション
CA-PR-KAWAKAMI-K-2325.pdf CA-PR-KAWAKAMI-K-2325.pdf (275.2 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-05
タイトル
タイトル Different histological types of non-small cell lung cancer have distinct folate and DNA methylation levels
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
著者 Jin, Ming Ji

× Jin, Ming Ji

WEKO 47553

Jin, Ming Ji

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Kawakami, Kazuyuki

× Kawakami, Kazuyuki

WEKO 177
e-Rad 00293358
研究者番号 00293358

Kawakami, Kazuyuki

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Fukui, Yousuke

× Fukui, Yousuke

WEKO 47554

Fukui, Yousuke

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Tsukioka, Sayaka

× Tsukioka, Sayaka

WEKO 47555

Tsukioka, Sayaka

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Oda, Makoto

× Oda, Makoto

WEKO 186
e-Rad 50224241
研究者番号 50224241

Oda, Makoto

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Watanabe, Go

× Watanabe, Go

WEKO 10713
研究者番号 60242492

Watanabe, Go

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Takechi, Teiji

× Takechi, Teiji

WEKO 47556

Takechi, Teiji

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Oka, Toshinori

× Oka, Toshinori

WEKO 47557

Oka, Toshinori

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Minamoto, Toshinari

× Minamoto, Toshinari

WEKO 65
e-Rad 50239323
金沢大学研究者情報 50239323
研究者番号 50239323

Minamoto, Toshinari

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提供者所属
内容記述タイプ Other
内容記述 金沢大学がん研究所分子標的がん医療研究開発センター
書誌情報 Cancer Science

巻 100, 号 12, p. 2325-2330, 発行日 2009-12-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 1347-9032
NCID
収録物識別子タイプ NCID
収録物識別子 AA11808050
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1111/j.1349-7006.2009.01321.x
出版者
出版者 Japanese Cancer Association = 日本癌学会
抄録
内容記述タイプ Abstract
内容記述 Aberrant DNA methylation is a commonly observed epigenetic change in lung cancer. Folate has been suggested to play a role in the homeostasis of DNA methylation and has also been implicated in cancer chemotherapy. We investigated a possible role for folate in DNA methylation by measuring folate concentrations in tumors and adjacent normal tissues from 72 non-small cell lung cancer (NSCLC) patients. These were compared to DNA methylation levels and to clinicopathological features. Folate concentrations were determined as the sum of 5,10-methylenetetrahydrofolate and tetrahydrofolate. The MethyLight assay was used to quantitate methylation in promoter regions of P16(CDKN2A), APC, CDH13, RARB, RASSF1, RUNX3, and MYOD1. Methylation of LINE-1 repeats was used as a surrogate for global methylation. Folate levels in tumors correlated positively with LINE-1, CDH13, and RUNX3 methylation. Folate concentrations and methylation of LINE-1, RASSF1, and RUNX3 were significantly higher in adenocarcinoma compared to squamous cell carcinoma (SCC). Two sets of array-based data retrieved from the Gene Expression Omnibus consistently showed that expression of FOLR1, a folate transport enzyme, and GGH, an enzyme that prevents folate retention, were higher and lower, respectively, in adenocarcinomas compared to SCC. This was independently validated by quantitative RT-PCR in 26 adenocarcinomas and 13 SCC. Our results suggest that folate metabolism plays a role in aberrant DNA methylation in NSCLC. The histological subtype differences in folate concentration and DNA methylation observed here were associated with distinct expression patterns for folate metabolizing enzymes. These findings may have clinical applications for histology-directed chemotherapy with fluoropyrimidine and anti-folates in NSCLC. © 2009 Japanese Cancer Association.
権利
権利情報 The definitive version is available at www.blackwell-synergy.com
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
関連URI
識別子タイプ URI
関連識別子 http://www3.interscience.wiley.com/journal/122577084/abstract
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