徳島大学 教育・研究者情報データベース(EDB)

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著作: Kinouchi Makoto/[内田 大亮]/[栗林 伸行]/[玉谷 哲也]/[永井 宏和]/[宮本 洋二]/Involvement of miR-518c-5p to Growth and Metastasis in Oral Cancer/[PLoS ONE]

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EID
289422
EOID
782679
Map
0
LastModified
2015年7月4日(土) 21:21:39
Operator
大家 隆弘
Avail
TRUE
Censor
承認済
Owner
宮本 洋二
Read
継承
Write
継承
Delete
継承
種別 必須 学術論文(審査論文)
言語 必須 英語
招待 推奨
審査 推奨
カテゴリ 推奨
共著種別 推奨
学究種別 推奨
組織 推奨
著者 必須
  1. (英) Kinouchi Makoto
    役割 任意
    貢献度 任意
    学籍番号 推奨
  2. 内田 大亮
    役割 任意
    貢献度 任意
    学籍番号 推奨
  3. 栗林 伸行
    役割 任意
    貢献度 任意
    学籍番号 推奨
  4. 玉谷 哲也
    役割 任意
    貢献度 任意
    学籍番号 推奨
  5. 永井 宏和
    役割 任意
    貢献度 任意
    学籍番号 推奨
  6. 宮本 洋二
    役割 任意
    貢献度 任意
    学籍番号 推奨
題名 必須

(英) Involvement of miR-518c-5p to Growth and Metastasis in Oral Cancer

副題 任意
要約 任意

(英) We have previously demonstrated that a stromal cell-derived factor-1 (SDF-1; CXCL12)/CXCR4 system is involved in the establishment of metastasis in oral cancer. Recently, small non coding RNAs, microRNAs (miRNAs) have been shown to be involved in the metastatic process of several types of cancers. However, the miRNAs that contribute to metastases induced by the SDF-1/CXCR4 system in oral cancer are largely unknown. In this study, we examined the metastasis-related miRNAs induced by the SDF-1/CXCR4 system using B88-SDF-1 oral cancer cells, which exhibit functional CXCR4 and distant metastatic potential in vivo. Through miRNA microarray analysis, we identified the upregulation of miR-518c-5p in B88-SDF-1 cells, and confirmed the induction by real-time PCR analysis. Although an LNA-based miR-518c-5p inhibitor did not affect cell growth of B88-SDF-1 cells, it did significantly inhibit the migration of the cells. Next, we transfected a miR-518c expression vector into parental B88 cells and CAL27 oral cancer cells and isolated stable transfectants, B88-518c and CAL27-518c cells, respectively. The anchorage-dependent and -independent growth of miR-518c transfectants was significantly enhanced compared with the growth of mock cells. Moreover, we detected the enhanced migration of these cells. The LNA-based miR-518c-5p inhibitor significantly impaired the enhanced cell growth and migration of miR-518c transfectants, indicating that these phenomena were mainly dependent on the expression of miR-518c-5p. Next, we examined the function of miR-518c-5p in vivo. miR-518c transfectants or mock transfectants were inoculated into the masseter muscle or the blood vessels of nude mice. Tumor volume, lymph nodes metastasis, and lung metastasis were significantly increased in the mice inoculated with the miR-518c transfectants. These results indicated that miR-518c-5p regulates the growth and metastasis of oral cancer as a downstream target of the SDF-1/CXCR4 system.

キーワード 推奨
発行所 推奨
誌名 必須 PLoS ONE(Public Library of Science)
(eISSN: 1932-6203)
ISSN 任意 1932-6203
ISSN: 1932-6203 (eISSN: 1932-6203)
Title: PloS one
Title(ISO): PLoS One
Publisher: PLOS
 (NLM Catalog  (Scopus  (CrossRef (Scopus information is found. [need login])
必須 9
必須 12
必須 e115936 e115936
都市 任意
年月日 必須 2014年 12月 23日
URL 任意
DOI 任意 10.1371/journal.pone.0115936    (→Scopusで検索)
PMID 任意 25536052    (→Scopusで検索)
CRID 任意
WOS 任意 000348563300089
Scopus 任意 2-s2.0-84919809244
評価値 任意
被引用数 任意
指導教員 推奨
備考 任意
  1. (英) Article.ELocationID: 10.1371/journal.pone.0115936

  2. (英) Article.PublicationTypeList.PublicationType: Journal Article

  3. (英) Article.PublicationTypeList.PublicationType: Research Support, Non-U.S. Gov't

  4. (英) OtherID: PMC4275267