Full metadata record
DC Field | Value | Language |
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dc.contributor.author | 羅福轅 | en_US |
dc.contributor.author | Lo, Fu-Yuan | en_US |
dc.contributor.author | 梁美智 | en_US |
dc.contributor.author | Liang, Mei-Chih | en_US |
dc.date.accessioned | 2014-12-12T01:58:09Z | - |
dc.date.available | 2014-12-12T01:58:09Z | - |
dc.date.issued | 2011 | en_US |
dc.identifier.uri | http://140.113.39.130/cdrfb3/record/nctu/#GT079929522 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/49986 | - |
dc.description.abstract | 轉譯因子NF-кB (nuclear factor kappa-light-chain-enhancer of activated B cells)在許多細胞反應 (如細胞增生、細胞凋亡、免疫及發炎反應) 的調控過程中扮演重要的角色。研究顯示NF-кB調控失常與部分腫瘤細胞的增生有關,且證實透過抑制NF-кB的過度表現,能夠有效地抑制腫瘤細胞的生長,並促進細胞凋亡。因此,轉譯因子NF-кB是一個具潛力的抗癌標靶。交通大學應用化學系孫仲銘教授的實驗室,以2-aminofuran-linked-benzimidazole為核心結構,透過修飾周邊的官能基而衍生出一系列新穎的小分子化合物。經過篩選實驗,我們發現化合物 #1412 (與其衍生物# 21026),在微摩爾濃度範圍內,具有抗癌的生物活性,且能夠有效地抑制多種癌症細胞株內NF-кB的訊息活化與傳遞。例如,在人類T-淋巴癌細胞株Jurkat 與人類多發性骨髓瘤細胞株RPMI-8226,#1412 (與其衍生物# 21026)藉由抑制TNF-□所活化的IкBα 的磷酸化反應及降解反應,進而抑制NF-кB 成員p65的細胞核遷移活動 ( nuclear translocation ),使NF-кB無法從細胞質進入細胞核內進行目標基因的轉錄反應。另外,#1412 (與其衍生物# 21026)也能夠有效地抑制此二種血液癌症細胞株的增生,並誘導細胞凋亡。總結,此實驗結果建議新穎化合物#1412 (與其衍生物# 21026) 的抗癌效果與其抑制轉譯因子NF-кB訊息傳遞的能力有關。 | zh_TW |
dc.description.abstract | Transcriptional factor NF-кB plays a critical role in mediating cellular processes, including cellular growth control, apoptosis, immune and inflammatory responses. Dysregulation of the NF-кB signaling pathway has been reported in a variety of cancer types and inhibition of the constitutive NF-кB activity may have therapeutic applications. In this study, we have identified the synthetic compounds #1412 and #21026, novel derivatives of the 2-aminofuran linked benzimidazole (synthesized in the laboratory of Prof. C.M. Sun in the Department of Applied Chemistry at National Chiao Tung University), as potent NF-кB inhibitors. Compound #1412 does- and time-dependently inhibited TNF-α induced NF-кB activation in the low micromolar range in cultured cells. In the human leukemic T cell Jurkat cell line and multiple myeloma RPMI-8226 cell line, both compounds blocked TNF-α induced IкBα phosphorylation and degradation and nuclear translocation of the NF-кB subunit p65. In addition, both compounds affected cell viability and induced cell apoptosis. Taken together, these results suggest that the anticancer activity of compound #1412 and #21026 in human cancer cells is related to inhibition of the NF-кB signaling pathway. | en_US |
dc.language.iso | zh_TW | en_US |
dc.subject | small molecular inhibitors | zh_TW |
dc.subject | NF-kappa-B | zh_TW |
dc.subject | I-kappa-B-alpha | zh_TW |
dc.subject | lymphoma | zh_TW |
dc.subject | multiple myeloma | zh_TW |
dc.subject | apoptosis | zh_TW |
dc.subject | small molecular inhibitors | en_US |
dc.subject | NF-kappa-B | en_US |
dc.subject | I-kappa-B-alpha | en_US |
dc.subject | lymphoma | en_US |
dc.subject | multiple myeloma | en_US |
dc.subject | apoptosis | en_US |
dc.title | 新穎的小分子化合物之抗癌機制研究 | zh_TW |
dc.title | Synthetic small molecular inhibitors of the transcription factor NF-кB suppress cell viability and induce apoptosis in cancer cells | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | 分子醫學與生物工程研究所 | zh_TW |
Appears in Collections: | Thesis |
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