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  • 學位論文

新穎的小分子化合物之抗癌機制研究

Synthetic small molecular inhibitors of the transcription factor NF-кB suppress cell viability and induce apoptosis in cancer cells

指導教授 : 梁美智

摘要


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。

並列摘要


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.

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