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博士論文
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Gene analysis of ameloblastoma-derived cells treated with retinoic acid
- 国立国会図書館永続的識別子
- info:ndljp/pid/12071502
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- Ameloblastoma is one of the most common odontogenic benign tumors in the jawbone, and may recur because it grows in a locally invasive manner. Althoug...
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デジタル
- 資料種別
- 博士論文
- 著者・編者
- 宮, 由紀子
- 著者標目
- 出版年月日等
- 2020-03-06
- 出版年(W3CDTF)
- 2020-03-06
- 並列タイトル等
- エナメル上皮腫由来細胞の レチノイン酸作用時における遺伝子解析
- 授与機関名
- 大阪歯科大学
- 授与年月日
- 2020-03-06
- 授与年月日(W3CDTF)
- 2020-03-06
- 報告番号
- 甲第875号
- 学位
- 博士(歯学)
- 博論授与番号
- 甲第875号
- 本文の言語コード
- eng
- 対象利用者
- 一般
- 一般注記
- Ameloblastoma is one of the most common odontogenic benign tumors in the jawbone, and may recur because it grows in a locally invasive manner. Although many studies have been performed on ameloblastoma, its bioactive characteristics remain unclear.Retinoic acid, a metabolite of fat-soluble vitamin A used as a leukemia drug, has been demonstrated to have antitumor effects on some tumor types. The present study examined whether retinoic acid has potential as a new therapeutic drug for ameloblastoma. We found that retinoic acid 1) inhibited the proliferation of cells derived from ameloblastoma and 2) induced differentiation. However, its intracellular signaling and regulatory mechanisms remain unclear. In this study, we primarily cultured cells from ameloblastoma to elucidate signal transduction, and examined the differences in gene expression levels due to retinoic acid action by microarray analysis.Surgically removed specimens were obtained with consent from the Second Department of Oral and Maxillofacial Surgery, Osaka Dental University Hospital. Primary culture was started with medium for the epithelium, followed by cloning to be used as ameloblastoma cells. Subsequently, retinoic acid was added at a final concentration of 10-6 to 10-7 M and incubated for 6 hours to prepare an experimental group. A control group was also prepared without its addition. After culturing, the cells were collected to extract RNA from each group for microarray analysis.In the experimental group, the expression of the EDF1 gene was most strongly increased, whereas that of the TM4SF10 gene was mostly markedly suppressed. Furthermore, the expression levels of the MMP3 and FGF2 genes were suppressed by 0.37- and 0.48-fold, respectively.The regulation of cell growth and differentiation comprises comprehensive regulatory mechanisms, such as protein synthesis, degradation, complex formation, and phosphorylation, in addition to gene expression. Our study suggested that changes in the expression of FGF2 and MMP3 genes are partly involved in the inhibition of growth and promotion of differentiation by retinoic acid in ameloblastoma-derived cells.2019年度
- 国立国会図書館永続的識別子
- info:ndljp/pid/12071502
- コレクション(共通)
- コレクション(障害者向け資料:レベル1)
- コレクション(個別)
- 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文
- 収集根拠
- 博士論文(自動収集)
- 受理日(W3CDTF)
- 2022-02-06T04:33:19+09:00
- 作成日(W3CDTF)
- 2020-04-28
- 記録形式(IMT)
- application/pdf
- オンライン閲覧公開範囲
- 国立国会図書館内限定公開
- デジタル化資料送信
- 図書館・個人送信対象外
- 遠隔複写可否(NDL)
- 可
- 連携機関・データベース
- 国立国会図書館 : 国立国会図書館デジタルコレクション