DOWN-REGULATION OF C-MYC AND MAX GENES IS ASSOCIATED TO INHIBITION OF PROTEIN PHOSPHATASE 2A IN K562 HUMAN LEUKEMIA-CELLS

被引:18
作者
LERGA, A
BELANDIA, B
DELGADO, MD
CUADRADO, MA
RICHARD, C
ORTIZ, JM
MARTINPEREZ, J
LEON, J
机构
[1] UNIV CANTABRIA,FAC MED,DEPT BIOL MOLEC,E-39011 SANTANDER,SPAIN
[2] CSIC,INST INVEST BIOMED,MADRID,SPAIN
[3] HOSP UNIV MARQUES DE VALDECILLA,SERV HEMATOL,SANTANDER,SPAIN
关键词
D O I
10.1006/bbrc.1995.2547
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
Treatment of the human myeloid leukemia K562 cells with the protein phosphatase inhibitors okadaic acid or calyculin A resulted in down-regulation of both c-myc and max genes at the mRNA and protein levels. The extent of the down-regulation was similar for both genes and was dependent on the dose and on the treatment time. Interestingly, c-myc and max down-regulation was concomitant with apoptosis induced by okadaic acid and calyculin A in K562 cells. The expression of c-myc and max returned to control levels after the removal of okadaic acid from the media, although apoptosis was irreversible. These effects were observed at okadaic acid concentrations (15 nM) that inhibited the activity of protein phosphatase type 2A but not of phosphatase type 1. We conclude that the inhibition of protein phosphatase 2A is associated to decreased levels of c-Myc/Max heterodimers in K562 cells. (C) 1995 Academic Press, Inc.
引用
收藏
页码:889 / 895
页数:7
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