The suppression of tumor formation, first demonstrated by somatic cell
hybrid and microcell fusion experiments, suggests the existence of a
class of genes that selectively suppress the growth of tumor cells but
not normal cells. The reintroduction of these genes into tumor cells
presumably renders the cells responsive to in vivo growth inhibitory e
nvironment. As the inheritance of a defective retinoblastoma gene (Rb-
1) allele results in a predisposition to the development of various ca
ncers, and since inactivation of both alleles are observed in tumor ce
lls, the Rb gene has been suspected to have the ability to suppress tu
mor growth. Data presented here demonstrated that different types of n
ormal cells, which have a limited life span, were also growth arrested
by a transfected Rb gene. Cell lines which are resistant to the growt
h suppression effect of the Rb gene in vitro, retain the ability to fo
rm tumors in nude mice even in the presence of a stable and highly exp
ressed wild type Rb protein. We conclude that while the Rb gene can su
ppress the growth of many tumor cell lines, its growth suppression eff
ect is not tumor specific.