Chlorophylls, chlorins, and other porphyrins have been used clinically
for many years, including photodynamic therapy of tumors. More recent
ly, the cancer chemopreventive properties of chlorophylls have come to
be recognized. Chlorophylls exhibit anti-mutagenic activity in short-
term genotoxicity assays, and protect against various intermediate bio
markers of cancer in vivo. The anticarcinogenic activity of sodium-cop
per chlorophyllin (CHL), a clinically-used water soluble salt of chlor
ophyll, has been studied in several species. Collectively, the results
from these studies support a chemopreventive role for CHL against aro
matic carcinogens (aflatoxins, polycyclic aromatic hydrocarbons, heter
ocyclic amines) in various target organs of rats, mice, and rainbow tr
out. In vivo mechanism studies indicate that inhibition is most effect
ive when CHL is administered simultaneously with the carcinogen, there
by allowing direct interaction (molecular complex formation) between C
HL and the carcinogen. Studies of post-initiation treatment with CHL h
ave provided conflicting results, with evidence for inhibition or prom
otion of carcinogenesis. These findings are discussed in terms of the
inhibitory and promotional mechanisms of CHL, the relevance of such me
chanisms to natural chlorophylls present in the diet, and the current
use of CHL as a health supplement.