In the last decade, basic cancer research has produced remarkable advances
in our understanding of cancer biology and cancer genetics, Among the most
important of these advances is the realization that apoptosis and the genes
that control it have a profound effect on the malignant phenotype. For exa
mple, it is now clear that some oncogenic mutations disrupt apoptosis, lead
ing to tumor initiation, progression or metastasis. Conversely, compelling
evidence indicates that other oncogenic changes promote apoptosis, thereby
producing selective pressure to override apoptosis during multistage carcin
ogenesis. Finally, it is now well documented that most cytotoxic anticancer
agents induce apoptosis, raising the intriguing possibility that defects i
n apoptotic programs contribute to treatment failure, Because the same muta
tions that suppress apoptosis during tumor development also reduce treatmen
t sensitivity, apoptosis provides a conceptual framework to link cancer gen
etics with cancer therapy. An intense research effort is uncovering the und
erlying mechanisms of apoptosis such that, in the nest decade, one envision
s that this information will produce new strategies to exploit apoptosis fo
r therapeutic benefit.