Tumors are known to produce factors suppressing immune functions. We p
reviously showed that a murine renal cell carcinoma (Renca) suppressed
macrophage function in vitro and that this suppression was abolished
by co-incubation with extracts of two Chinese medicinal herbs. We now
report that these phytochemicals are capable of inhibiting growth of R
enca in vivo. BALB/c mice were transplanted intraperitoneally (IP) wit
h 1-2 x 10(5) Renca cells. One day after tumor transplant, mice were r
andomized into two groups. One group was treated IP, daily for 10 days
, with 100 mul of phytochemicals containing 500 mug each of Astragalus
membranaceus and Ligustrum lucidum, while the other group received sa
line as controls. A cure rate of 57% was obtained with these phytochem
icals when the initial tumor load was 2 x 10(5) and 100% when the init
ial tumor load was 1 x 10(5). Additional experiments were performed to
investigate the mechanisms involved in this protection. Splenic macro
phages from tumor-bearing mice were shown to have depressed chemilumin
escent oxidative burst activity, and this depression was restored with
phytochemical treatment. Splenocytes from mice transplanted with Renc
a responded less favorably to interleukin-2 (IL-2) in generating lymph
okine-activated killer (LAK) cells, again this depression was restored
with phytochemical treatment. Our data suggest that these phytochemic
als may have exerted their antitumor effects via augmentation of phago
cyte and LAK cell activities.