Multi parameter in vitro testing of ratjadone using flow cytometry

被引:15
作者
Burzlaff, A
Kalesse, M
Kasper, C
Scheper, T
机构
[1] Leibniz Univ Hannover, Inst Tech Chem, D-30167 Hannover, Germany
[2] Inst Chem Organ Chem, Berlin, Germany
关键词
D O I
10.1007/s00253-003-1300-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Ratjadone, isolated from the myxobacterium Sorangium cellulosum, belongs to the family of so-called orphan ligands, which includes leptomycin, callystatin and other compounds. In previous screening tests, ratjadone revealed a growth inhibitory effect against bacteria, yeast and human cancer cells. Following these first results, ratjadone was tested on several human tumour cell lines (Jurkat, HepG2, U87-MG) and, as a control, on a non-tumour cell line (RLC18) for its mode of action. The cell analysis was carried out by flow cytometry. This comprised cell density measurements, live-dead analysis, cell-cycle analysis and detection of apoptosis. First experiments confirmed the growth inhibitory effect on any chosen tumour cell line. Following these results a dose effect relationship was monitored, confirming the high effectiveness of ratjadone against cell growth at nanomolar concentration. Cell cycle analysis has shown that ratjadone intervenes in the cell cycle by arresting the cells in G1-phase. Biological testing of additional ratjadone derivatives with changed configuration and stereochemistry, identified the pharmacophoric site of the molecule.
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收藏
页码:174 / 179
页数:6
相关论文
共 21 条
[1]   CONTROLLED SYNTHESIS OF HBSAG IN A DIFFERENTIATED HUMAN-LIVER CARCINOMA-DERIVED CELL-LINE [J].
ADEN, DP ;
FOGEL, A ;
PLOTKIN, S ;
DAMJANOV, I ;
KNOWLES, BB .
NATURE, 1979, 282 (5739) :615-616
[2]  
[Anonymous], FLOW CYTOMETRY PRACT
[3]  
Darzynkiewicz Z, 2000, METHOD ENZYMOL, V322, P18
[4]  
Darzynkiewicz Z, 1997, CYTOMETRY, V27, P1
[5]  
Kalesse M, 2001, CHEMBIOCHEM, V2, P709, DOI 10.1002/1439-7633(20010903)2:9<709::AID-CBIC709>3.0.CO
[6]  
2-7
[7]  
Kaufmann SH, 2000, METHOD ENZYMOL, V322, P3
[8]   Leptomycin B inactivates CRM1/exportin 1 by covalent modification at a cysteine residue in the central conserved region [J].
Kudo, N ;
Matsumori, N ;
Taoka, H ;
Fujiwara, D ;
Schreiner, EP ;
Wolff, B ;
Yoshida, M ;
Horinouchi, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9112-9117
[9]   Participation of the conjugated diene part for potent cytotoxicity of callystatin A, a spongean polyketide [J].
Murakami, N ;
Sugimoto, M ;
Nakajima, T ;
Kawanishi, M ;
Tsutsui, Y ;
Kobayashi, M .
BIOORGANIC & MEDICINAL CHEMISTRY, 2000, 8 (11) :2651-2661
[10]   Participation of the β-hydroxyketone part for potent cytotoxicity of callystatin A, a spongean polyketide [J].
Murakami, N ;
Sugimoto, M ;
Kobayashi, M .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (01) :57-67