Fluorescent taxoids

被引:58
作者
Guy, RK
Scott, ZA
Sloboda, RD
Nicolaou, KC
机构
[1] Scripps Res Inst, DEPT CHEM, LA JOLLA, CA 92037 USA
[2] Scripps Res Inst, SKAGGS INST CHEM BIOL, LA JOLLA, CA 92037 USA
[3] UNIV CALIF SAN DIEGO, DEPT CHEM & BIOCHEM, LA JOLLA, CA 92093 USA
[4] DARTMOUTH COLL, DEPT BIOL SCI, HANOVER, NH 03755 USA
来源
CHEMISTRY & BIOLOGY | 1996年 / 3卷 / 12期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
fluorescence; localization; microscopy; taxol;
D O I
10.1016/S1074-5521(96)90168-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Taxol* is a natural product produced by the Pacific Yew, Taxus brevifolia, that has emerged as a prominent chemotherapeutic agent for the treatment of solid tumors. Taxol's biochemical mode of action has been well studied: it binds to microtubules, stabilizing them and preventing their depolymerization to tubulin subunits. At lower dosage levels, taxol also interferes with the normal dynamics of the tubulin-microtubule equilibrium. This biochemical effect causes taxol's ultimate physiological effect, cell cycle arrest; taxol is thought to block anaphase A of mitosis. Taxol also causes a number of intriguing secondary effects on interphase cells that are poorly understood. We believed that a bio-active fluorescent taxol derivative could be a useful tool in the study of these cellular mechanisms, especially in interphase cells. Results: We have synthesized and characterized a series of stable, fluorescently labeled derivatives of taxol that bind to microtubules and have cytotoxicities similar to that of taxol. Fluorescence microscopy experiments in interphase human foreskin fibroblast (HFF) cells indicate that one of these, a sulforhodamine taxoid, is particularly well suited for optical microscopy. The use of this taxoid in HFF cells revealed a previously undetected localization of taxoids to the nucleolus during interphase. Conclusion: The production of a new fluorescent derivative of taxol provides a useful tool, enabling cellular biologists to study taxol's mechanism of action. It is hoped that this material will prove particularly useful for the study of taxol's effects upon interphase cells. (C) Current Biology Ltd.
引用
收藏
页码:1021 / 1031
页数:11
相关论文
共 47 条
[1]  
[Anonymous], ANN PHARMACOTHER
[2]  
ARBUCK SG, 1993, SEMIN ONCOL, V20, P31
[3]  
CAMERON MR, 1995, ONCOL RES, V7, P145
[4]   REGULATION OF MICROTUBULE DYNAMIC INSTABILITY [J].
CASSIMERIS, L .
CELL MOTILITY AND THE CYTOSKELETON, 1993, 26 (04) :275-281
[5]   TAXOL(R) STRUCTURE-ACTIVITY-RELATIONSHIPS - SYNTHESIS AND BIOLOGICAL EVALUATION OF TAXOL ANALOGS MODIFIED AT C-7 [J].
CHEN, SH ;
KANT, J ;
MAMBER, SW ;
ROTH, GP ;
WEI, JM ;
MARSHALL, D ;
VYAS, DM ;
FARINA, V ;
CASAZZA, A ;
LONG, BH ;
ROSE, WC ;
JOHNSTON, K ;
FAIRCHILD, C .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (18) :2223-2228
[6]   SUBSTOICHIOMETRIC BINDING OF TAXOL SUPPRESSES MICROTUBULE DYNAMICS [J].
DERRY, WB ;
WILSON, L ;
JORDAN, MA .
BIOCHEMISTRY, 1995, 34 (07) :2203-2211
[7]   SYNTHESIS OF CONGENERS AND PRODRUGS .3. WATER-SOLUBLE PRODRUGS OF TAXOL WITH POTENT ANTITUMOR-ACTIVITY [J].
DEUTSCH, HM ;
GLINSKI, JA ;
HERNANDEZ, M ;
HAUGWITZ, RD ;
NARAYANAN, VL ;
SUFFNESS, M ;
ZALKOW, LH .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (04) :788-792
[8]   FLUORESCENT AND BIOTINYLATED ANALOGS OF DOCETAXEL - SYNTHESIS AND BIOLOGICAL EVALUATION [J].
DUBOIS, J ;
LEGOFF, MT ;
GUERITTEVOEGELEIN, F ;
GUENARD, D ;
TOLLON, Y ;
WRIGHT, M .
BIOORGANIC & MEDICINAL CHEMISTRY, 1995, 3 (10) :1357-1368
[9]  
GASKIN F, 1982, METHOD ENZYMOL, V85, P433
[10]   INVITRO MICROTUBULE ASSEMBLY REGULATION BY DIVALENT-CATIONS AND NUCLEOTIDES [J].
GASKIN, F .
BIOCHEMISTRY, 1981, 20 (05) :1318-1322