Exp Mol Med.  1997 Dec;29(4):203-208.

Stimulation of c-myc protooncogene expression by transforming growth factor a in human ovarian cancer cells

Affiliations
  • 1EWHA WOMANS UNIV,COLL MED, EWHA MED RES CTR, DEPT BIOCHEM, SEOUL 158056, SOUTH KOREA.

Abstract

To investigate whether transforming growth factor alpha (TGF alpha) treatment of human ovarian cancer cells was associated with the induction of c-myc protooncogene, the expression of this gene in NIH:OVCAR-3 cells was examined. TGF alpha induced increase in c-myc mRNA level, with a peak after 1 h of treatment; this stimulation was dose-dependent, with an optimal concentration of 5 ng/ml TGF alpha. Its primary action is probably at the transcription level since the half-life of c-myc mRNA measured in the presence of actinomycin D was not modified by TGF alpha treatment. In addition, TGF alpha stimulation of c-myc mRNA did not require protein synthesis since it was not suppressed by cycloheximide treatment. Antisense phosphorothioate oligonucleotide to c-myc specifically inhibited the TGF alpha-stimulated c-Myc protein expression and growth of NIH:OVCAR-3 cells. Our results indicate that induction of c-myc expression by TGF alpha plays an important role in the growth of NIH:OVCAR-3 cells.

Keyword

c-myc; ovarian cancer cells; TGFalpha

MeSH Terms

Cycloheximide
Dactinomycin
Half-Life
Humans*
Ovarian Neoplasms*
RNA, Messenger
Transforming Growth Factor alpha
Transforming Growth Factors*
Cycloheximide
Dactinomycin
RNA, Messenger
Transforming Growth Factor alpha
Transforming Growth Factors
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