Radiobiological data and measurements with O2 microelectrodes show tha
t EMT6 tumors implanted into aged mice have a higher proportion of rad
ioresistant, hypoxic cells than do tumors implanted into young adult a
nimals; radiation is less effective in killing cells in tumors in old
mice than in tumors in young adult mice. The studies reported here exa
mine the effects of porfiromycin (POR), a bioreductive alkylating agen
t shown previously to be preferentially toxic to hypoxic EMT6 cells in
vitro and in solid tumors in young adult mice. POR was effective in a
ttacking the hypoxic cells of tumors in aged mice; regimens combining
POR with x-rays overcame the radioresistance of tumors in the old anim
als. Comparisons of the distribution of H-3-labeled POR in young and o
ld mice showed that tumors in aged mice had a slightly larger proporti
on of areas with necrotic features, which bound higher levels of triti
ated POR than did healthy tumor regions without necrotic features. Stu
dies of histology, lissamine green distributions, binding of tritiated
POR, and radiation and POR cytotoxicity suggested that tumors in old
mice contained a larger proportion of poorly perfused tumor cells, and
that cells in these regions were resistant to radiation and sensitive
to POR. Studies of the distribution of POR in normal tissues and of t
he toxicity of POR to bone marrow progenitor cells (CFU-GM) revealed n
o differences between young and old animals, showing that the differen
ces observed in tumors reflected differences in the microenvironments
within the tumors, rather than differences in the processing of drug i
n young and old animals.