The c-myc gene and the expression of the c-Myc protein are frequently alter
ed in human cancers. The c-myc gene encodes the transcription factor c-Myc,
which heterodimerizes with a partner protein, termed Max, to regulate gene
expression. Max also heterodimerizes with the Mad family of proteins to re
press transcription, antagonize c-Myc, and promote cellular differentiation
The constitutive activation of c-myc expression is key to the genesis of m
any cancers, and hence the understanding of c-Myc function depends on our u
nderstanding of its target genes. In this review, we attempt to place the p
utative target genes of c-Myc in the context of c-Myc-mediated phenotypes.
From this perspective, c-Myc emerges as an oncogenic transcription factor t
hat integrates the cell cycle machinery with cell adhesion, cellular metabo
lism, and the apoptotic pathways. (C) 1999 Academic Press.