Chemical Carcinogenesis by Franz Oesch (auth.), Claudio Nicolini (eds.)

By Franz Oesch (auth.), Claudio Nicolini (eds.)

During October 18-30, 1981, the second one process the overseas college of natural and utilized Biostructure, a NATO complex examine Institute, used to be held on the Ettore Majorana heart for clinical tradition in Erice, Italy, co-sponsored through the foreign Union opposed to melanoma, the Italian League opposed to melanoma, the Italian Ministry of Public schooling, the Italian Ministry of clinical and Technological examine, the North Atlantic Treaty association, the Italian nationwide learn Council, the Sicilian neighborhood executive and pharmaceutical businesses (Zambeletti and Farmitalia). the topic of the direction used to be "Chemical Carcino­ genesis" with individuals chosen world-wide from 18 diverse international locations. it's now eminently transparent that.the bulk of human cancers are regarding one of the different types of environmental publicity. Of the environmental risks, chemical substances are one of the best characterised cancer causing agents. despite the fact that, how chemical substances result in melanoma remains to be poorly understood. as a result of importance of the matter and the ob­ vious desire for a way more severe clinical research of the method through which melanoma is caused (carcinogenesis), it used to be hugely fascinating to show a better variety of scientists with various heritage to a couple of the newest considering in chemical carcino­ genesis. The path had this as its significant goal and the re­ sulting booklet does replicate it.

Show description

Read Online or Download Chemical Carcinogenesis PDF

Best chemical books

Extra info for Chemical Carcinogenesis

Example text

Oesch, F. (1981) Methods Enzymol. 77, 344-349. Bentley, ~ & Oesch, F. (1975) FEBS Lett. 59, 296-299. 23 24 31. 32. 33. 34. 35. 36. 37. 38. 39. 40. 41. 42. 43. 44. 45. 46. 47. 48. 49. 50. F. , Yamasaki, E. N. (1975) Proc. Nat. Acad. Sci. USA 21, 5135-5139. C. & Oesch, F. (1978) Mutat. Res. 66, 307-328. R. & Oesch, F. (1977) Arch. Toxicol. ~, 87-96. , Nakajima, M. & Tomida, I. (1959) Biochim. Biophys. Acta 33, 111-119. L. & Oesch, F. (1980) J. BioI. Chern. 255, 9621-9625. , Bentley, P. & Oesch, F.

KING Structure OQ-NH OONH2 Name 2 Use/Occurrence 4-Aminobiphenyl Antioxidant Benzidine Dye Intermediate 2-Naphthylamine Antioxidant Ch lornaphazi n Pharmacological Agent Phenacetin Analgesic 2-Acetylaminofluorene Insectide (Never marketed) 1-N itropyrene 8 Combustion Product "Trp-P-2" Food Pyrolysis a The carcinogenic potential of this potent mutagen is now being determined. Fig. 1. Representative carcinogenic N-substituted aromatic compounds. g. , 1980). A second more indirect mechanism for the production of amines is seen in the formation of nitroaromatic compounds as a consequence of combustion processes.

Oesch, F. (1980) in Quantitative Aspects of Risk Assessment in Chemical Carcinogenesis, eds. , Henschler, D. & Oesch, F. (Springer Verlag, Heidelberg), pp. 179-194. M. & Oesch, F. (1981) in Polycyclic Hydrocarbons and Cancer, eds. Gelboin, H. P. (Academic Press, New York), pp. 183-212. M. & Oesch, F. (1981) TIPS 2, 129-132. R. & Oesch, F. (1981) Mutat. Res. 81, 11-19. D. W. (1980) Eur. J. Cell BioI. 21, 79-92. Oesch, F. (1979) in Progress in Drug Metabolism, eds. W. F. (John Wiley, Chichester, England), Vol.

Download PDF sample

Rated 4.89 of 5 – based on 24 votes