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We began analyzing https://link.springer.com/article/10.1007/BF01637081, but it redirected us to https://link.springer.com/article/10.1007/BF01637081. The analysis below is for the second page.

Title[redir]:
Comparative carcinogenicity of cigarette mainstream and sidestream smoke condensates on the mouse skin | Journal of Cancer Research and Clinical Oncology
Description:
The direct carcinogenic effects of sidestream (SS) and mainstream (MS) smoke condensates of a filtered commercial brand of blond cigarettes were compared using a lifetime mouse skin tumorigenicity assay on female NMRI mice. Each cigarette was smoked by a smoking machine under the standard conditions, and the separately collected SS and MS smoke condensates were extracted with acetone/methanol as described elsewhere. These were tested for carcinogenicity on an area of 1–1.5 cm shaved skin of mice on the lower back. The mice were treated with half of each dose (5, 10 or 15 mg) twice a week, for only 3 months. No substance was used as promoter or as an additional initiator of carcinogenicity. No statistically significant difference was found when the life spans of MS-treated and untreated animals were compared. In contrast, the life spans of SS-treated mice were significantly (P<0.01) shorter than those of MS-treated animals or those of all three negative control groups together. The observed carcinogenic effects were based on tumours and lesions found only on the site of application of the test material. Of 210 mice (effective number, 129) serving as the negative controls, 3 developed skin lesions but no tumours. Of 210 MS-treated mice (effective number, 177), 7 developed tumours (4 malignant and 3 benign) and 35 had a uniform type of precancerous skin lesions. The numbers of tumours or lesions were not increased dose-dependently. Of 210 SS-treated animals (effective number, 182), 30 developed tumours (16 malignant and 14 benign) and 56 had a uniform type of precancerous skin lesion. The initiation of these latter lesions was found to be dose-dependent (P<0.001).The SS-treated animals developed two to six times more skin tumours than the MS-treated mice. Comparing the negative controls with the MS- or SS-treated animals, the overall carcinogenic effect observed was statistically significant. Comparing the MS- with SS-treated animals, the overall carcinogenic effect of SS was much higher than that of MS (P<0.001).

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google, scholar, smoke, tobacco, cigarette, cancer, mice, article, skin, mainstream, sidestream, mouse, mohtashamipur, carcinogenic, research, carcinogenicity, untersuchungen, res, condensates, smoking, animals, tumours, access, experimentelle, krebsforsch, hoffmann, wynder, privacy, cookies, content, journal, comparative, effects, sstreated, lesions, carcinogenesis, publish, search, experimental, norpoth, cigarettes, mstreated, developed, effect, tumors, exp, pathol, environ, study, dontenwill,

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month download article/chapter chronic cigarette-smoke inhalation paul-georg germann cigarette smoke-induced micronuclei cigarette smoke condensate mouse-skin painting hannover medical school clinical oncology aims privacy choices/manage cookies environmental tobacco smoke ss-treated animals developed related subjects passive smoking university medical center full article pdf sidestream smoke condensates syrian golden hamsters mainstream cigarette smoke precancerous skin lesion recombined smoke condensates ames/salmonella assay ms smoke condensates experimental tobacco carcinogenesis comparative carcinogenic effect mouse skin carcinogenic effect observed precancerous skin lesions check access instant access filtered commercial brand connarus ruber cortex 2-bromo-6-hydroxy-4-methoxyphenyl internal combustion engines selenium-mediated reduction age-adjusted tests condensate fractions la voie ej anti-angiogenic activity polycyclic aromatic hydrocarbons carcinogenic agents present ms-treated animals separately collected ss animal carcinogenicity experiments tumor promoting activity negative control groups 210 ss-treated animals ss-treated animals tobacco smoke increased dose-dependently dose-response studies

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