博碩士論文 108223014 詳細資訊




以作者查詢圖書館館藏 以作者查詢臺灣博碩士 以作者查詢全國書目 勘誤回報 、線上人數:6 、訪客IP:3.129.57.117
姓名 陳瑋昇(Wei-Sheng Chen)  查詢紙本館藏   畢業系所 化學學系
論文名稱
(Natural amino acid conjugates of lithocholic acid as α-2,6-sialyltransferase inhibitors with antimigratory and antiangiogenic activity)
相關論文
★ Design and Synthesis of Mono-, Di-, Tri- and Tetraindoles Derivatives as Novel Histone Deacetylase Inhibitors★ Synthesis and biological evaluation of pyrazole derivatives as antitumor agents
檔案 [Endnote RIS 格式]    [Bibtex 格式]    [相關文章]   [文章引用]   [完整記錄]   [館藏目錄]   [檢視]  [下載]
  1. 本電子論文使用權限為同意立即開放。
  2. 已達開放權限電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。
  3. 請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。

摘要(中) 在這項工作中,石膽酸的氨基酸錯合物被設計、合成並評估了它們的細胞毒性、α-2,6-唾液酸轉移酶抑制、抗遷移和抗血管生成作用。 在該系列中,具有色氨酸部分的 S1047 顯示可抑制 ST6GalI 活性(IC50 26.5 ± 1.2 μM)、抑制腫瘤生長、延遲癌細胞遷移並減少動物模型(生物體外)中的血管生成以及腫瘤生長。 正在進行進一步研究以尋求石膽酸的氨基酸錯合物的臨床應用。
摘要(英) In this work, the amino acid conjugates of lithocholic acid were designed, synthesized and evaluated their cytotoxicity, α-2,6-sialyltransferase inhibition, antimigratory and antiangiogenic effects. Among the series, S1047, possessing the tryptophan moiety, were shown to inhibit ST6GalI activity (IC50 26.5 ± 1.2 μM), suppress tumor growth, delay cancer cell migration, and reduce angiogenesis and tumor growth in animal model (ex vivo). Further study to pursue clinical application of amino acid conjugates of lithocholic acid is in progress.
關鍵字(中) ★ 唾液酸
★ 唾液酸轉移酶
★ 癌症轉移
★ 石膽酸
關鍵字(英) ★ sialic acid
★ sialyltransferase
★ metastasis
★ lithocholic acid
論文目次 摘要 I
Abstract II
Table of Contents III
List of Tables VI
List of Schemes VII
List of Abbreviation VIII
I. Introduction 1
1.1 Metastatic Process 1
1.2 The Correlation between Metastasis and Glycoconjugates 1
1.3 The Biosynthetic Process of Sialylation 2
1.4 Sialyltransferase 3
1.5 Sialyltransferase Inhibitors 4
1.6 Previous Works 6
1.7 Research Motivation 7
II. Results and Discussion 8
2.1 Chemistry 8
2.2 Cytotoxicity for LCA Derivatives 9
2.3 The Inhibition of ST3Gal I and ST6Gal 10
2.4 Anti-migration Effects 11
2.5 Anti-angiogenic Properties of S1047 14
2.6 Antiangiogenic Properties of S1047 on Mice Aortic Ring Assay 15
2.7 Animal Study 17
Ⅲ. Conclusions 20
Ⅳ. Materials and Methods 21
4.1 General Information 21
4.2 Experimental Method 22
4.2.1 Preparation of PEG linker 22
4.2.2 Synthesis of S1046 23
4.2.3 Synthesis of S1047 24
4.2.4 Synthesis of S1050 25
4.2.5 Synthesis of S1051 26
4.2.6 Synthesis of S1069 27
4.2.7 Synthesis of S1070 28
4.2.8 Synthesis of S1071 29
4.2.9 Synthesis of S1072 30
4.2.10 Synthesis of S1075 31
4.2.11 Synthesis of S1076 32
4.3 Cell Line Used and Cell Culture 34
4.4 MTT Cytotoxicity Analysis 34
V. References 35
VI. Spectra Appendix 38
參考文獻 Fu, C.-W.; Tsai, H.-E.; Chen, W.-S.; Chang, T.-T.; Chen, C.-L.; Hsiao, P.-W.; Li, W.-S., Sialyltransferase Inhibitors Suppress Breast Cancer Metastasis. J. Med. Chem. 2020, 64 (1), 527-542.
2. Vajaria, B. N.; Patel, P. S., Glycosylation: a hallmark of cancer? Glycoconj. J. 2017, 34 (2), 147-156.
3. Rodrigues, J. G.; Balmaña, M.; Macedo, J. A.; Poças, J.; Fernandes, Â.; de-Freitas-Junior, J. C. M.; Pinho, S. S.; Gomes, J.; Magalhães, A.; Gomes, C., Glycosylation in cancer: Selected roles in tumour progression, immune modulation and metastasis. Cell. Immunol. 2018, 333, 46-57.
4. Jacobs, C. L.;Goon, S.; Yarema, K. J.; Hinderlich, S.; Hang, H. C.; Chai, D. H.; Bertozzi, C. R., Substrate specificity of the sialic acid biosynthetic pathway. Biochemistry 2001, 40 (43), 12864-12874.
5. Wang, L.; Liu, Y.; Wu, L.; Sun, X.-L., Sialyltransferase inhibition and recent advances. Biochimica Et Biophysica Acta (BBA)-Proteins and Proteomics 2016, 1864 (1), 143-153.
6. Lu, J.; Gu, J., Significance of β-galactoside α2, 6 sialyltranferase 1 in cancers. Molecules 2015, 20 (5), 7509-7527.
7. Jung, K.-H.; Schwörer, R.; Schmidt, R. R., Sialyltransferase inhibitors. Trends Glycosci. Glycotechnol. 2003, 15 (85), 275-289.
8. Wang, X.; Zhang, L. H.; Ye, X. S., Recent development in the design of sialyltransferase inhibitors. Med. Res. Rev. 2003, 23 (1), 32-47.
9. Rillahan, C. D.; Antonopoulos, A.; Lefort, C. T.; Sonon, R.; Azadi, P.; Ley, K.; Dell, A.; Haslam, S. M.; Paulson, J. C., Global metabolic inhibitors of sialyl-and fucosyltransferases remodel the glycome. Nat. Chem. Biol. 2012, 8 (7), 661-668.
10. Kajihara, Y.; Kodama, H.; Wakabayashi, T.; Sato, K.-i.; Hashimoto, H., Characterization of inhibitory activities and binding mode of synthetic 6′-modified methyl N-acetyl-β-lactosaminide toward rat liver CMP-D-Neu5Ac: d-galactoside-(2→ 6)-α-d-sialyltransferase. Carbohydr. Res. 1993, 247, 179-193.
11. Guo, J.; Li, W.; Xue, W.; Ye, X.-S., Transition state-based sialyltransferase inhibitors: mimicking oxocarbenium ion by simple amide. J. Med. Chem. 2017, 60 (5), 2135-2141.
12. Li, W.; Niu, Y.; Xiong, D.-C.; Cao, X.; Ye, X.-S., Highly substituted cyclopentane–CMP conjugates as potent sialyltransferase inhibitors. J. Med. Chem. 2015, 58 (20), 7972-7990.
13. Müller, B.; Schaub, C.; Schmidt, R. R., Efficient sialyltransferase inhibitors based on transition‐state analogues of the sialyl donor. Angew. Chem. Int. Ed. 1998, 37 (20), 2893-2897.
14. Huang, W.; Sun, L.; Wang, B.; Ma, Y.; Yao, D.; Han, W.; Wang, L., Ginsenosides, potent inhibitors of sialyltransferase. Z. Naturforsch. C 2020, 75 (1-2), 41-49.
15. Wu, C.-Y.; Hsu, C.-C.; Chen, S.-T.; Tsai, Y.-C., Soyasaponin I, a potent and specific sialyltransferase inhibitor. Biochem. Biophys. Res. Commun. 2001, 284 (2), 466-469.
16. Chang, K.-H.; Lee, L.; Chen, J.; Li, W.-S., Lithocholic acid analogues, new and potent α-2, 3-sialyltransferase inhibitors. Chem. Commun. 2006, (6), 629-631.
17. Lin, T.-W.; Chang, W.-W.; Chen, C.-C.; Tsai, Y.-C., Stachybotrydial, a potent inhibitor of fucosyltransferase and sialyltransferase. Biochem. Biophys. Res. Commun. 2005, 331 (4), 953-957.
18. Hsu, C.-C.; Lin, T.-W.; Chang, W.-W.; Wu, C.-Y.; Lo, W.-H.; Wang, P.-H.; Tsai, Y.-C., Soyasaponin-I-modified invasive behavior of cancer by changing cell surface sialic acids. Gynecol. Oncol. 2005, 96 (2), 415-422.
19. Fu, C.-W. 由自然界靈感設計及合成出抗癌症和抗癌症轉移試劑: 細胞和動物體內之活性測試評估. National Central University, 2015.
20. Zih-Fan, H., 探討雙高石膽酸衍生物對於唾液酸轉移酶及癌細胞轉移的影響. 臺灣師範大學化學系學位論文 2019, 1-96.
21. Hashimoto, M.; Liu, Y.; Fang, K.; Li, H.-y.; Campiani, G.; Nakanishi, K., Preparation and biological properties of biotinylated PhTX derivatives. Bioorg. Med. Chem. 1999, 7 (6), 1181-1194.
22. Incerti, M.; Tognolini, M.; Russo, S.; Pala, D.; Giorgio, C.; Hassan-Mohamed, I.; Noberini, R.; Pasquale, E. B.; Vicini, P.; Piersanti, S., Amino acid conjugates of lithocholic acid as antagonists of the EphA2 receptor. J. Med. Chem. 2013, 56 (7), 2936-2947.
23. Gale, N. W.; Yancopoulos, G. D., Ephrins and their receptors: a repulsive topic? Cell Tissue Res. 1997, 290 (2), 227-241.
24. Himanen, J.-P.; Saha, N.; Nikolov, D. B., Cell–cell signaling via Eph receptors and ephrins. Curr. Opin. Cell Biol. 2007, 19 (5), 534-542.
指導教授 李文山 侯敦仁(Wen-Shan Li Duen-Ren Hou) 審核日期 2021-7-29
推文 facebook   plurk   twitter   funp   google   live   udn   HD   myshare   reddit   netvibes   friend   youpush   delicious   baidu   
網路書籤 Google bookmarks   del.icio.us   hemidemi   myshare   

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明