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Effects of Toxoplasma gondii and Toxocara canis Antigens on WEHI-164 Fibrosarcoma Growth in a Mouse Model

  • Published : 2009.06.30

Abstract

Cancer is the main cause of death in developed countries. However, in underdeveloped countries infections and parasitic diseases are the main causes of death. There are raising scientific evidences indicating that parasitic infections induce antitumor activity against certain types of cancers. In this study, the effects of Toxoplasma gondii and Toxocara canis egg antigens in comparison with Bacillus Calmette Guerin (BCG) (known to have anticancer distinctive) on WEHI-164 fibosarcoma transplanted to BALB/c mice was investigated. Groups of 6 male BALB/c mice injected with T. gondii antigen, BCG, or T. canis egg antigen as case groups and alum alone as control groups. All mice were then challenged with WEHI-164 fibrosarcoma cells. The mice were examined for growth of the solid tumor and the tumor sizes were measured every other day up to 4wk. The mean tumor area in T. gondii, BCG, or alum alone injected mice in 4 different days of measurements was $25\;mm^2$, $23\;mm^2$, and $186\;mm^2$ respectively, Also the mean tumor area in T. canis injected mice in 4 different days was $25.5\;mm^2$ compared to the control group (alum treated) which was $155\;mm^2$. T. gondii parasites and T. canis egg antigens induced inhibition of the tumor growth in the fibrosarcoma mouse model. We need further study to clarify the mechanisms of anti-cancer effects.

Keywords

References

  1. World Health Organization. Data and statistics, causes of death. Table 3. Estimated deaths per 100000 population by cause and number state. 2002. (http://www.WHO.int/research/en/)
  2. Centers for Disease Control and Prevention (CDC). Cancer mortality among American Indians and Alaska Natives-United States, 1994-1998. MMWR Mob Mortal Wkly Rep 2003; 52: 704-707
  3. Kallinikova VD, Matekin PV, Ogloblina TA, Leikina MI, Kononenko AF, Sokolova NM, Pogodina LS. Anticancer properties of flagellate protozoan Trypanosoma cruzi Chagas. Izv Akad Nauk Ser Biol 2001; 3: 299-311
  4. Atayde VD, Jasiulionis MG, Cortez M, Yoshida N. A recombinant protein based on Trypanosoma cruzi surface molecule gp82 induces apoptotic cell death in melanoma cells. Melanoma Res 2008; 18: 172-183 https://doi.org/10.1097/CMR.0b013e3282feeaab
  5. Kim JO, Jung SS, Kim SY, Kim TY, Shin DW, Lee JH, Lee YH. Inhibition of Lewis lung carcinoma growth by Toxoplasma gondii through induction of Th1 immune responses and inhibition of angiogenesis. J Korean Med Sci 2007; 22 (Suppl): S38-S46 https://doi.org/10.3346/jkms.2007.22.S.S38
  6. Plumelle Y, Gonin C, Edouard A, Bucher BJ, Thomas L, Brebion A, Panelatti G. Effect of Strongyloides stercoralis infection and eosinophilia on age at onset and prognosis of adult T cell leukemia. Am J Clin Pathol 1997; 107: 81-87 https://doi.org/10.1093/ajcp/107.1.81
  7. Pidherney MS, Alizadeh H, Stewart GL, McCulley JP, Niederkorn JY. In vitro and in vivo tumoricidal properties of a pathogenic/freeliving amoeba. Cancer Lett 1993; 72 (1-2): 91-98 https://doi.org/10.1016/0304-3835(93)90016-3
  8. Herr HW, Morales A. History of Bacillus Calmette-Guerin and bladder cancer: an immunotherapy success story. J Urol 2008; 179: 53-56
  9. Mungadi IA, Malami SA. Urinary bladder cancer and schistosomiasis in Northen-Western Nigeria. West Afr J Med 2007; 26: 226-229
  10. Sayed el-Ahl SA, el-Wakil HS, Kamel NM, Mahmoud MS. A preliminary study on the relationship between Trichomonas vaginalis and cervical cancer in Egyptian women. J Egypt Soc Parasitol 2002; 32: 167-178
  11. Watanapa P, Watanapa WB. Liver fluke-associated cholangiocarcinoma. Br J Surg 2002; 89: 962-970 https://doi.org/10.1046/j.1365-2168.2002.02143.x
  12. Ju YH, Oh JK, Kong HJ, Sohn WM, Kim JI, Jung KY, Kim YG, Shin HR. Epidemiological study of Clonorchis sinensis infestation in a rural area of Kyongsangnam-do, South Korea. J Prev Med Public Health 2005; 38: 425-430
  13. Abdel-Rahim AY. Parasitic infections and hepatic neoplasia. Dig Dis 2002; 19: 288-291 https://doi.org/10.1159/000050695
  14. Korbel DS. Finney OC, Riley EM. Natural killer cells and innate immunity to protozoan pathogens. Int J Parasitol 2004; 34 (13-14): 1517-1528 https://doi.org/10.1016/j.ijpara.2004.10.006
  15. Lodoen MB, Lanier LL. Natural killer cells as an initial defense against pathogens. Curr Opin Immunol 2006; 18: 391-398 https://doi.org/10.1016/j.coi.2006.05.002
  16. Kodama N, Asakawa A, Inui A, Masuda Y, Nanba H. Enhancement of cytotoxicity of NK cells by D-fraction, a polysaccharide from Grifola frondosa. Onco Res 2005; 13: 497-502
  17. Lanier LL. Evolutionary struggles between NK cells and viruses. Nat Rev Immunol 2008; 8: 259-268 https://doi.org/10.1038/nri2276
  18. Papazahariadou M, Athanasiadis GI, Papadopoulos E, Symeonidou I, Hatzistilianou M, Castellani ML, Bhattacharya K, Shanmugham LN, Conti P, Frydas S. Involvement of NK cells against tumors and parasites. Int J Biol Marker 2007; 22: 144-153 https://doi.org/10.1177/172460080702200208

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