Changes in expression of protooncogenes and tumor suppressor genes play a k
ey role in oncogenesis. Dysfunction of their protein products leads to abno
rmal regulation of signaling pathways, which control the cell cycle, apopto
sis, genetic stability, cell differentiation, and morphogenetic reactions.
Changes in these important physiological processes are obviously responsibl
e both for initial steps of neoplastic cell transformation and for determin
ation of subsequent tumor progression resulting in the development of malig
nant tumors.