Protein A (PA) is an immunostimulating glycoprotein (mel. wt. 43 000 k
Da) obtained from Staphylococcus aureus cowan I. The antitumour proper
ty of PA is well documented in the literature in various transplantabl
e rumours of rats and mice. In the present set of investigations, the
antitumour property of PA was tested in Swiss albino mice in a two-sta
ge initiation-promotion mouse skin carcinogenesis model. The animals w
ere initiated topically with a single subcarcinogenic dose (52 mu g) o
f 7,12-dimethylbenzanthracene (DMBA). PA was administered intraperiton
eally (1 mu g/animal), twice weekly for 2 weeks. Promotion was perform
ed by twice weekly applications of 12-O-tetradecanoyl phorbol-13-aceta
te (TPA) at a dose of 5 mu g/animal for 32 weeks. The result showed th
at the treatment schedule can effectively check the onset of tumorigen
esis, the cumulative number of tumours and the average number of tumou
rs per mouse. In the PA administered group, 30% of the animals remaine
d tumour free until the termination of the experiments (i.e. 32 weeks
of promotion). Thus the present study proves that protein A can effect
ively inhibit DMBA initiated and TPA promoted mouse skin carcinogenesi
s.