Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 2001 May;109(5):471–479. doi: 10.1289/ehp.01109471

A rat mammary tumor model induced by the organophosphorous pesticides parathion and malathion, possibly through acetylcholinesterase inhibition.

G Cabello 1, M Valenzuela 1, A Vilaxa 1, V Durán 1, I Rudolph 1, N Hrepic 1, G Calaf 1
PMCID: PMC1240306  PMID: 11401758

Abstract

Environmental chemicals may be involved in the etiology of breast cancers. Many studies have addressed the association between cancer in humans and agricultural pesticide exposure. Organophosphorous pesticides have been used extensively to control mosquito plagues. Parathion and malathion are organophosphorous pesticides extensively used to control a wide range of sucking and chewing pests of field crops, fruits, and vegetables. They have many structural similarities with naturally occurring compounds, and their primary target of action in insects is the nervous system; they inhibit the release of the enzyme acetylcholinesterase at the synaptic junction. Eserine, parathion, and malathion are cholinesterase inhibitors responsible for the hydrolysis of body choline esters, including acetylcholine at cholinergic synapses. Atropine, a parasympatholytic alkaloid, is used as an antidote to acetylcholinesterase inhibitors. The aim of this study was to examine whether pesticides were able to induce malignant transformation of the rat mammary gland and to determine whether alterations induced by these substances increase the cholinergic activation influencing such transformation. These results showed that eserine, parathion, and malathion increased cell proliferation of terminal end buds of the 44-day-old mammary gland of rats, followed by formation of 8.6, 14.3, and 24.3% of mammary carcinomas, respectively, after about 28 months. At the same time, acetylcholinesterase activity decreased in the serum of these animals from 9.78 +/- 0.78 U/mL in the control animals to 3.05 +/- 0.06 U/mL; 2.57 +/- 0.15 U/mL; and 3.88 +/- 0.44 U/mL in the eserine-, parathion-, and malathion-treated groups, respectively. However, atropine alone induced a significant (p < 0.05) decrease in the acetylcholinesterase activity from the control value of 9.78 +/- 0.78 to 4.38 +/- 0.10 for atropine alone, to 1.32 +/- 0.06 for atropine in combination with eserine, and 2.39 +/- 0.29 for atropine with malathion, and there was no mammary tumor formation. These results indicate that organophosphorous pesticides induce changes in the epithelium of mammary gland influencing the process of carcinogenesis, and such alterations occur at the level of nervous system by increasing the cholinergic stimulation.

Full Text

The Full Text of this article is available as a PDF (232.4 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BRODEUR J., DUBOIS K. P. COMPARISON OF ACUTE TOXICITY OF ANTICHOLINESTERASE INSECTICIDES TO WEANLING AND ADULT MALE RATS. Proc Soc Exp Biol Med. 1963 Nov;114:509–511. doi: 10.3181/00379727-114-28716. [DOI] [PubMed] [Google Scholar]
  2. Benke G. M., Murphy S. D. The influence of age on the toxicity and metabolism of methyl parathion and parathion in male and female rats. Toxicol Appl Pharmacol. 1975 Feb;31(2):254–269. doi: 10.1016/0041-008x(75)90161-1. [DOI] [PubMed] [Google Scholar]
  3. Blair A., Dosemeci M., Heineman E. F. Cancer and other causes of death among male and female farmers from twenty-three states. Am J Ind Med. 1993 May;23(5):729–742. doi: 10.1002/ajim.4700230507. [DOI] [PubMed] [Google Scholar]
  4. Calaf G., Russo J. Transformation of human breast epithelial cells by chemical carcinogens. Carcinogenesis. 1993 Mar;14(3):483–492. doi: 10.1093/carcin/14.3.483. [DOI] [PubMed] [Google Scholar]
  5. Dauterman W. C. Biological and nonbiological modifications of organophosphorus compounds. Bull World Health Organ. 1971;44(1-3):133–150. [PMC free article] [PubMed] [Google Scholar]
  6. DuBois K. P., Kinoshita F. K. Influence of induction of hepatic microsomal enzymes by phenobarbital on toxicity of organic phosphate insecticides. Proc Soc Exp Biol Med. 1968 Dec;129(3):699–702. doi: 10.3181/00379727-129-33402. [DOI] [PubMed] [Google Scholar]
  7. Falck F., Jr, Ricci A., Jr, Wolff M. S., Godbold J., Deckers P. Pesticides and polychlorinated biphenyl residues in human breast lipids and their relation to breast cancer. Arch Environ Health. 1992 Mar-Apr;47(2):143–146. [PubMed] [Google Scholar]
  8. Gaines T. B. Acute toxicity of pesticides. Toxicol Appl Pharmacol. 1969 May;14(3):515–534. doi: 10.1016/0041-008x(69)90013-1. [DOI] [PubMed] [Google Scholar]
  9. Gullino P. M., Pettigrew H. M., Grantham F. H. N-nitrosomethylurea as mammary gland carcinogen in rats. J Natl Cancer Inst. 1975 Feb;54(2):401–414. [PubMed] [Google Scholar]
  10. HUGGINS C., YANG N. C. Induction and extinction of mammary cancer. A striking effect of hydrocarbons permits analysis of mechanisms of causes and cure of breast cancer. Science. 1962 Jul 27;137(3526):257–262. doi: 10.1126/science.137.3526.257. [DOI] [PubMed] [Google Scholar]
  11. Huggins C., Grand L. C., Brillantes F. P. CRITICAL SIGNIFICANCE OF BREAST STRUCTURE IN THE INDUCTION OF MAMMARY CANCER IN THE RAT. Proc Natl Acad Sci U S A. 1959 Aug;45(8):1294–1300. doi: 10.1073/pnas.45.8.1294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Martinez J. R., Adelstein E., Quissel D., Barbero G. J. The chronically reserpinized rat as a possible model for cystic fibrosis. I. Submaxillary gland morphology and ultrastructure. Pediatr Res. 1975 May;9(5):463–469. doi: 10.1203/00006450-197505000-00001. [DOI] [PubMed] [Google Scholar]
  13. McCormick D. L., Adamowski C. B., Fiks A., Moon R. C. Lifetime dose-response relationships for mammary tumor induction by a single administration of N-methyl-N-nitrosourea. Cancer Res. 1981 May;41(5):1690–1694. [PubMed] [Google Scholar]
  14. McDuffie H. H. Women at work: agriculture and pesticides. J Occup Med. 1994 Nov;36(11):1240–1246. doi: 10.1097/00043764-199411000-00012. [DOI] [PubMed] [Google Scholar]
  15. Miyamoto S., Guzman R. C., Osborn R. C., Nandi S. Neoplastic transformation of mouse mammary epithelial cells by in vitro exposure to N-methyl-N-nitrosourea. Proc Natl Acad Sci U S A. 1988 Jan;85(2):477–481. doi: 10.1073/pnas.85.2.477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Novi A. M., Baserga R. Association of hypertrophy and DNA synthesis in mouse salivary glands after chronic administration of isoproterenol. Am J Pathol. 1971 Mar;62(3):295–308. [PMC free article] [PubMed] [Google Scholar]
  17. Perelman A., Abeijon C., Hirschberg C. B., Inestrosa N. C., Brandan E. Differential association and distribution of acetyl- and butyrylcholinesterases within rat liver subcellular organelles. J Biol Chem. 1990 Jan 5;265(1):214–220. [PubMed] [Google Scholar]
  18. Perera F. P. Environment and cancer: who are susceptible? Science. 1997 Nov 7;278(5340):1068–1073. doi: 10.1126/science.278.5340.1068. [DOI] [PubMed] [Google Scholar]
  19. Russo J., Calaf G., Roi L., Russo I. H. Influence of age and gland topography on cell kinetics of normal human breast tissue. J Natl Cancer Inst. 1987 Mar;78(3):413–418. [PubMed] [Google Scholar]
  20. Russo J., Calaf G., Russo I. H. A critical approach to the malignant transformation of human breast epithelial cells with chemical carcinogens. Crit Rev Oncog. 1993;4(4):403–417. [PubMed] [Google Scholar]
  21. Russo J., Russo I. H. DNA labeling index and structure of the rat mammary gland as determinants of its susceptibility to carcinogenesis. J Natl Cancer Inst. 1978 Dec;61(6):1451–1459. [PubMed] [Google Scholar]
  22. Russo J., Russo I. H. Influence of differentiation and cell kinetics on the susceptibility of the rat mammary gland to carcinogenesis. Cancer Res. 1980 Aug;40(8 Pt 1):2677–2687. [PubMed] [Google Scholar]
  23. Russo J., Russo I. H. Mammary tumorigenesis. Prog Exp Tumor Res. 1991;33:175–191. [PubMed] [Google Scholar]
  24. Russo J., Russo I. H. The etiopathogenesis of breast cancer prevention. Cancer Lett. 1995 Mar 23;90(1):81–89. doi: 10.1016/0304-3835(94)03681-8. [DOI] [PubMed] [Google Scholar]
  25. Russo J., Tay L. K., Russo I. H. Differentiation of the mammary gland and susceptibility to carcinogenesis. Breast Cancer Res Treat. 1982;2(1):5–73. doi: 10.1007/BF01805718. [DOI] [PubMed] [Google Scholar]
  26. Silman I., Futerman A. H. Modes of attachment of acetylcholinesterase to the surface membrane. Eur J Biochem. 1987 Dec 30;170(1-2):11–22. doi: 10.1111/j.1432-1033.1987.tb13662.x. [DOI] [PubMed] [Google Scholar]
  27. Wellings S. R., Jensen H. M., Marcum R. G. An atlas of subgross pathology of the human breast with special reference to possible precancerous lesions. J Natl Cancer Inst. 1975 Aug;55(2):231–273. [PubMed] [Google Scholar]
  28. Welsch C. W. Host factors affecting the growth of carcinogen-induced rat mammary carcinomas: a review and tribute to Charles Brenton Huggins. Cancer Res. 1985 Aug;45(8):3415–3443. [PubMed] [Google Scholar]
  29. Wolff M. S., Toniolo P. G., Lee E. W., Rivera M., Dubin N. Blood levels of organochlorine residues and risk of breast cancer. J Natl Cancer Inst. 1993 Apr 21;85(8):648–652. doi: 10.1093/jnci/85.8.648. [DOI] [PubMed] [Google Scholar]
  30. Young S., Hallowes R. C. Tumours of the mammary gland. IARC Sci Publ. 1973;(5):31–73. [PubMed] [Google Scholar]
  31. Zahm S. H., Ward M. H., Blair A. Pesticides and cancer. Occup Med. 1997 Apr-Jun;12(2):269–289. [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES