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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Expression and regulatory effects on cancer cell behavior of NELL1 and NELL2 in human renal cell carcinoma

http://hdl.handle.net/2297/43216
http://hdl.handle.net/2297/43216
e0fad183-32e0-49ed-8889-e01bc22e9051
名前 / ファイル ライセンス アクション
ME-PR-NAKAMURA-R-656.pdf ME-PR-NAKAMURA-R-656.pdf (2.0 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Expression and regulatory effects on cancer cell behavior of NELL1 and NELL2 in human renal cell carcinoma
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 Nakamura, Ritsuko

× Nakamura, Ritsuko

WEKO 24254
金沢大学研究者情報 20632657
研究者番号 20632657

Nakamura, Ritsuko

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Oyama, Takeru

× Oyama, Takeru

WEKO 406
金沢大学研究者情報 00515314
研究者番号 00515314

Oyama, Takeru

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Tajiri, Ryosuke

× Tajiri, Ryosuke

WEKO 914
研究者番号 10402059

Tajiri, Ryosuke

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Mizokami, Atsushi

× Mizokami, Atsushi

WEKO 97
e-Rad 50248580
金沢大学研究者情報 50248580
研究者番号 50248580

Mizokami, Atsushi

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Namiki, Mikio

× Namiki, Mikio

WEKO 20454
e-Rad 70155985
研究者番号 70155985

Namiki, Mikio

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Nakamoto, Masaru

× Nakamoto, Masaru

WEKO 24255

Nakamoto, Masaru

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Ooi, Akishi

× Ooi, Akishi

WEKO 245
e-Rad 50160411
金沢大学研究者情報 50160411
研究者番号 50160411

Ooi, Akishi

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書誌情報 Cancer Science

巻 106, 号 5, p. 656-664, 発行日 2015-05-01
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/cas.12649
出版者
出版者 日本癌学会 = Japanese Cancer Association / Wiley
抄録
内容記述タイプ Abstract
内容記述 Neural epidermal growth factor-like like (NELL) 1 and 2 constitute a family of multimeric and multimodular extracellular glycoproteins. Although the osteogenic effects of NELL1 and functions of NELL2 in neural development have been reported, their expression and functions in cancer are largely unknown. In this study, we examined expression of NELL1 and NELL2 in renal cell carcinoma (RCC) using clinical specimens and cell lines. We show that, whereas NELL1 and NELL2 proteins are strongly expressed in renal tubules in non-cancerous areas of RCC specimens, their expression is significantly downregulated in cancerous areas. Silencing of NELL1 and NELL2 mRNA expression was also detected in RCC cell lines. Analysis of NELL1/2 promoter methylation status indicated that the CpG islands in the NELL1 and NELL2 genes are hypermethylated in RCC cell lines. NELL1 and NELL2 bind to RCC cells, suggesting that these cells express a receptor for NELL1 and NELL2 that can transduce signals. Furthermore, we found that both NELL1 and NELL2 inhibit RCC cell migration, and NELL1 further inhibits RCC cell adhesion. These results suggest that silencing of NELL gene expression by promoter hypermethylation plays roles in RCC progression by affecting cancer cell behavior. We found that the down-regulation of NELL1 and NELL2 in renal cell carcinoma (RCC) is in part due to the hypermethylation of CpG islands in their putative promoter regions. Furthermore, we found that NELL1 suppresses and NELL2 partially suppresses RCC cell migration, and NELL1 further inhibits RCC cell adhesion. © 2015 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association.
権利
権利情報 © 2015 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association. | The definitive version is available at www.wileyonlinelibrary.com/journal/cas
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
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