一般注記type:text
Tumor or cancer immunology is a new and fast growing field where the interactions of the inherent immune system with malignant cancers have shown the suppression of disease progression. In this field, systems biology approach is required to understand and control the cellular response, since cellular behaviors are highly dynamic, complex and well orchestrated. This thesis describes the current understanding of the systems biology approach and addresses the connectivity between immunology and systems biology. The main aims of this research are i) to regulate the proinflammatory response in Tumor necrosis factor (TNF) signaling pathway and ii) to understand the resistance mechanisms for cancer treatment in TNF related apoptosis inducing ligand (TRAIL) signaling pathway. Therefore dynamical computational models were developed using the well-established perturbation response approach, and analyzed the dynamics of key signaling molecules and gene expressions were analyzed. Using this systems biology approach, a key molecule was identified to effectively regulate, but not abolish, the proinflammatory response in TNF signaling and we also found a target to enhance cell death in TRAIL resistant cancer cells. This work shows systems biology approach integrating computational approaches and wet bench experiments shed light on the drug development for the regulation of the immune-mediated diseases.
慶應義塾大学湘南藤沢キャンパス先端生命科学研究会 2014年度学生論文集
博士論文ダイジェスト
identifier:SFC-RM2014-003
identifier:請求記号:
一次資料へのリンクURLhttps://koara.lib.keio.ac.jp/xoonips/modules/xoonips/download.php?koara_id=KO92001004-00000021-0011
連携機関・データベース国立情報学研究所 : 学術機関リポジトリデータベース(IRDB)(機関リポジトリ)