VARIATIONS IN AMPLIFICATION AND EXPRESSION OF THE ORNITHINE DECARBOXYLASE GENE IN HUMAN BREAST-CANCER CELLS

被引:24
|
作者
THOMAS, T
KIANG, DT
JANNE, OA
THOMAS, TJ
机构
[1] UNIV MED & DENT NEW JERSEY,ROBERT WOOD JOHNSON MED SCH,CLIN RES CTR,PISCATAWAY,NJ 08854
[2] UNIV MED & DENT NEW JERSEY,ROBERT WOOD JOHNSON MED SCH,DEPT MED,DIV RHEUMATOL,PISCATAWAY,NJ 08854
[3] UNIV MINNESOTA,DEPT MED,DIV ONCOL,MINNEAPOLIS,MN 55455
[4] ROCKEFELLER UNIV,POPULAT COUNCIL,NEW YORK,NY 10021
关键词
BREAST CANCER; DIFLUOROMETHYLORNITHINE; ORNITHINE DECARBOXYLASE; POLYAMINES;
D O I
10.1007/BF01961162
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The polyamine biosynthetic pathway plays a critical role in the growth of human breast cancer cells. Ornithine decarboxylase (ODC) is a key enzyme in polyamine biosynthesis. To understand the regulation of ODC activity and polyamine accumulation in breast cancer cells, we studied amplification and expression of the ODC gene in four breast cancer cell lines. ODC gene dosage was analyzed by Southern blot hybridization and was 4- to 12-fold higher in T-47D, MDA-MB-231, and BT-20 cell lines than in the MCF-7 cell line. ODC mRNA level was 2- to 3-fold higher in BT-20 and MDA-MB-231 cell lines than in the other two lines. We also measured ODC activity and polyamine concentration in these cell lines, and determined their sensitivity to an ODC inhibitor, difluoromethylornithine (DFMO). BT-20 cells showed significantly higher ODC activity and polyamine concentrations than the other three cell lines. BT-20 cells were resistant to the growth inhibitory effect of DFMO even at 4 mM concentration, whereas the proliferation of MCF-7, T47D, and MDA-MB-231 cells was inhibited by this drug. These results suggest that different transcriptional and post-transcriptional mechanisms control the regulation of ODC gene expression in breast cancer cell lines.
引用
收藏
页码:257 / 267
页数:11
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