ACTIVE COMPOUNDS FROM SAUSSUREA-LAPPA CLARKS THAT SUPPRESS HEPATITIS-B VIRUS SURFACE-ANTIGEN GENE-EXPRESSION IN HUMAN HEPATOMA-CELLS

被引:152
作者
CHEN, HC
CHOU, CK
LEE, SD
WANG, JC
YEH, SF
机构
[1] NATL YANG MING MED COLL,INST BIOCHEM,TAIPEI 11221,TAIWAN
[2] VET GEN HOSP,DEPT MED RES,TAIPEI,TAIWAN
[3] VET GEN HOSP,DEPT MED,DIV GASTROENTEROL,TAIPEI,TAIWAN
[4] SOOCHOW UNIV,DEPT CHEM,TAIPEI,TAIWAN
关键词
SAUSSUREA LAPPA CLARKS; SESQUITERPENE LACTONE; ANTIVIRAL AGENT; GENE REGULATION;
D O I
10.1016/0166-3542(94)00083-K
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have examined the antiviral activity of the crude extract prepared from the root of Saussurea lappa Clarks, a Chinese medicinal herb which is widely used for many illneses including cancer. Two active components, costunolide and dehydrocostus lactone, were identified which show strong suppressive effect on the expression of the hepatitis B surface antigen (HBsAg) in human hepatoma Hep3B cells, but have little effect on the viability of the cells. Both costunolide and dehydrocostus lactone suppress the HBsAg production by Hep3B cells in a dose-dependent manner with IC(50)s of 1.0 and 2.0 mu M, respectively. Northern blotting analysis shows that the suppression of HBsAg gene expression by both costunolide and dehydrocostus lactone were mainly at the mRNA level. Furthermore, the suppressive effect of costunolide and dehydrocostus lactone on HBsAg and hepatitis B e antigen (HBeAg), a marker for hepatitis B viral genome replication in human liver cells, was also observed in another human hepatoma cell line HepA(2) which was derived from HepG(2) cells by transfecting a tandemly repeat hepatitis B virus (HBV) DNA. Similarly, the mRNA of HBsAg in HepA(2) cells was also suppressed by these two compounds. Our findings suggest that costunolide and dehydrocostus lactone may have potential to develop as specific anti-HBV drugs in the future.
引用
收藏
页码:99 / 109
页数:11
相关论文
共 26 条
  • [1] CONTROLLED SYNTHESIS OF HBSAG IN A DIFFERENTIATED HUMAN-LIVER CARCINOMA-DERIVED CELL-LINE
    ADEN, DP
    FOGEL, A
    PLOTKIN, S
    DAMJANOV, I
    KNOWLES, BB
    [J]. NATURE, 1979, 282 (5739) : 615 - 616
  • [2] GUAIANOLIDES FROM VENIDIUM-FASTUOSUM
    ALI, AA
    ELEMARY, NA
    KHALIFA, AA
    FRAHM, AW
    [J]. PHYTOCHEMISTRY, 1992, 31 (08) : 2781 - 2784
  • [3] BEASLEY RP, 1981, LANCET, V2, P1129
  • [4] BLUMBERG BS, 1989, CANCER DETECT PREV, V14, P195
  • [5] PRESENCE OF INTEGRATED HEPATITIS-B VIRUS-DNA SEQUENCES IN CELLULAR DNA OF HUMAN HEPATOCELLULAR-CARCINOMA
    BRECHOT, C
    POURCEL, C
    LOUISE, A
    RAIN, B
    TIOLLAIS, P
    [J]. NATURE, 1980, 286 (5772) : 533 - 535
  • [6] THE ENHANCER SEQUENCE OF HUMAN HEPATITIS-B VIRUS CAN ENHANCE THE ACTIVITY OF ITS SURFACE GENE PROMOTER
    CHANG, HK
    CHOU, CK
    CHANG, CM
    SU, TS
    HU, CP
    YOSHIDA, M
    TING, LP
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (05) : 2261 - 2268
  • [7] CHOU CK, 1989, J BIOL CHEM, V264, P15304
  • [8] THE MOLECULAR-BIOLOGY OF THE HEPATITIS-B VIRUSES
    GANEM, D
    VARMUS, HE
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 : 651 - 693
  • [9] RIBONUCLEIC-ACID ISOLATED BY CESIUM-CHLORIDE CENTRIFUGATION
    GLISIN, V
    CRKVENJAKOV, R
    BYUS, C
    [J]. BIOCHEMISTRY, 1974, 13 (12) : 2633 - 2637
  • [10] SESQUITERPENE LACTONES FROM ARTEMISIA-RUTIFOLIA
    JAKUPOVIC, J
    TAN, RX
    BOHLMANN, F
    JIA, ZJ
    HUNECK, S
    [J]. PHYTOCHEMISTRY, 1991, 30 (05) : 1714 - 1716