INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 TRANSCRIPTION AND REPLICATION BY DNA SEQUENCE-SELECTIVE PLANT LIGNANS

被引:83
作者
GNABRE, JN
BRADY, JN
CLANTON, DJ
ITO, Y
DITTMER, J
BATES, RB
HUANG, RCC
机构
[1] JOHNS HOPKINS UNIV,DEPT BIOL,BALTIMORE,MD 21218
[2] NCI,MOLEC VIROL LAB,BETHESDA,MD 20892
[3] NCI,FREDERICK CANC RES & DEV CTR,PROGRAM RESOURCES INC,FREDERICK,MD 21702
[4] NHLBI,BIOPHYS CHEM LAB,BETHESDA,MD 20892
[5] UNIV ARIZONA,DEPT CHEM,TUCSON,AZ 85721
关键词
ANTI-HUMAN IMMUNODEFICIENCY VIRUS; SP1; SITE-SPECIFIC; 3'-O-METHYLNORDIHYDROGUAIARETIC ACID;
D O I
10.1073/pnas.92.24.11239
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A plant lignan, 3'-O-methyl nordihydroguaiaretic acid (3'-O-methyl NDGA, denoted Malachi 4:5-6 or Mal.4; molecular weight 316), was isolated from Larrea tridentata and found to be able to inhibit human immunodeficiency virus (HIV) Tat-regulated transactivation in vivo, induce protection of lymphoblastoid CEM-SS cells from HIV (strain IIIB) killing, and suppress the replication of five HIV-1 strains (WM, MN, VS, JR-CSF, and IlI(B)) in mitogen-stimulated peripheral blood mononuclear cells, all in a dose-dependent manner. Mal.4 inhibits both basal transcription and Tat-regulated transactivation in vitro. The target of Mal.4 has been localized to nucleotides -87 to -40 of the HIV long terminal repeat, Mal.4 directly and specifically interferes with the binding of Spl to Spl sites in the HIV long terminal repeat, By inhibiting proviral expression, Mal.4 may be able to interrupt the life cycles of both wild-type and reverse transcriptase or protease mutant viruses in HIV-infected patients.
引用
收藏
页码:11239 / 11243
页数:5
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