LUNG tissue is unsuitable for direct injection of carcinogens, consequently pulmonary tumours in laboratory animals have hitherto been induced by applying the carcinogen at some remote site, by injecting it subcutaneously, intratracheally, intravascularly, intraperitoneally, or by including it in the diet. These indirect methods are often laborious, and tumour induction may take a considerable time.Recently the author (Horning, 1947) reported the induction of pulmonary tumours after relatively short periods of treatment by the direct application of carcinogens to adult lung tissue growing as subcutaneous homologous grafts in host animals. Further experiments have shown that success with this technique depends upon several factors, and the object of this paper is to describe additional observations.
TECHNIQUE.The method of tumour induction consists in isolating small strips of lung from 6-12 weeks Strain A mice, impregnating the grafts with crystals of a carcinogen (2-acetylaminofluorene, 2-aminofluorene, or 20-methylcholanthrene) prior to implanting them subcutaneously into host mice of similar age and strain in a manner which has been described elswhere (Horning, 1947). Usually 4 subcutaneous grafts were made on each side of the abdomen of a single host mouse in order to have the implants growing under identical conditions. Small palpable tumours were obtained at intervals ranging from 6-12 weeks following grafting, but in order to examine the differences between the responses to individual carcinogens, grafts were fixed before tumours developed at intervals ranging from 1-5 weeks after implantation.Lung fragments from 61 weeks old Strain A mice were grafted, in some instances without the carcinogen, into host mice of similar age, and also into mice of 15 months age which were selected from stock mice of undetermined ancestry. This was done to find out if the survival of homologous grafts was dependent on employing a closely inbred strain, or whether it might be influenced by the age of the host.In another series of experiments a number of lung grafts were treated with 20-methylcholanthrene, half being implanted into the superficial fascia, and the remainder placed as usual between the skin and the abdominal wall. The host mice were again of the same age and strain, and it was thought that some information might be obtained as to whether rapid vascularization played any role in successful survival of the grafts.