腫瘍抑制性micraRNA-29ファミリーは肺扁平上皮癌においてLOXL2を直接標的として癌細胞の遊走と浸潤を阻害する

• Material Type: 博士論文
• Title: 腫瘍抑制性micraRNA-29ファミリーは肺扁平上皮癌においてLOXL2を直接標的として癌細胞の遊走と浸潤を阻害する
• Author/Editor: 水野, 圭子
• Author Heading: 水野, 圭子
• Publication, Distribution, etc.: Spandidos Publications
• Publication Date: 2015
• Publication Date (W3CDTF): 2015
• Alternative Title: Tumor-suppressive microRNA-29 family inhibits cancer cell migration and invasion directly targeting LOXL2 in lung squamous cell carcinoma
• Periodical title: International Journal of Oncology
• Degree grantor/type: 鹿児島大学
• Date Granted: 2019-05-31
• Date Granted (W3CDTF): 2019-05-31
• Dissertation Number: 乙総論第37号
• Degree Type: 博士(医学); Doctor of Philosophy in Medical Science
• Conferring No. (Dissertation): 乙総論第37号
• Text Language Code: eng
• Subject Heading: lung squamous cell carcinoma; microRNA; miR-29a; miR-29b; miR-29c; lysyl oxidase-like 2
• NDC: 490
• Target Audience: 一般
• Note (General): 博士論文全文, 博士論文要旨, 最終試験結果の要旨, 論文審査の要旨; Lung cancer remains the most frequent cause of cancer-related death in developed countries. A recent molecular-targeted strategy has contributed to improvement of the remarkable effect of adenocarcinoma of the lung. However, such treatment has not been developed for squamous cell carcinoma (SCC) of the disease. Our recent studies of microRNA (miRNA) expression signatures of human cancers showed that the microRNA-29 family (miR‑29a, miR‑29b and miR‑29c) significantly reduced cancer tissues compared to normal tissues. These findings suggest that miR‑29s act as tumor-suppressors by targeting several oncogenic genes. The aim of the study was to investigate the functional significance of miR‑29s in lung SCC and to identify miR‑29s modulating molecular targets in lung SCC cells. Restoration of all mature members of the miR‑29s inhibited cancer cell migration and invasion. Gene expression data combined in silico analysis and luciferase reporter assays demonstrated that the lysyl oxidase-like 2 (LOXL2) gene was a direct regulator of tumor‑suppressive miR‑29s. Moreover, overexpressed LOXL2 was confirmed in lung SCC clinical specimens, and silencing of LOXL2 inhibited cancer cell migration and invasion in lung SCC cell lines. Our present data suggested that loss of tumor-suppressive miR‑29s enhanced cancer cell invasion in lung SCC through direct regulation of oncogenic LOXL2. Elucidation of the novel lung SCC molecular pathways and targets regulated by tumor-suppressive miR‑29s will provide new insights into the potential mechanisms of oncogenesis and metastasis of the disease.
• DOI: info:doi/10.3892/ijo.2015.3289; https://doi.org/info:doi/10.3892/ijo.2015.3289
• Persistent ID (NDL): info:ndljp/pid/11378026; https://dl.ndl.go.jp/pid/11378026
• Collection: 障害者向け資料
• Collection (Materials For Handicapped People:1): テキストデータ
• Collection (particular): 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; https://dl.ndl.go.jp/collections/A00014
• Acquisition Basis: 博士論文（自動収集）
• Date Accepted (W3CDTF): 2019-11-04T14:30:53+09:00
• Date Created (W3CDTF): 2019-07-23
• Format (IMT): PDF; application/pdf
• Access Restrictions: 国立国会図書館内限定公開
• Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
• Availability of remote photoduplication service: 可
• Original Material (URI): https://www.spandidos-publications.com/ijo/48/2/450
• Periodical Title (URI): http://hdl.handle.net/10232/00030745
• Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

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