Skip to main content
Log in

Effect of vasopressin gene expression on the growth of walker 256 carcinosarcoma in rats

  • Short Communications
  • Published:
Russian Journal of Genetics Aims and scope Submit manuscript

Abstract

The growth pattern of the Walker 256 solid tumor has been studied in rats with different doses of the mutant vasopressin gene. In contrast to the vasopressin gene of normal WAG rats, that of mutant Brattleboro rats has a deletion in the coding region that blocks expression at the translation level. The mutation is inherited as a recessive character and is expressed in homozygous Brattleboro rats as diabetes insipidus with an increased water consumption because of the absence of vasopressin in the blood. (WAG × Brattleboro) F1 hybrids have the same normal phenotype as WAG rats, including a low water consumption. Walker 256 carcinosarcoma, which is not strain-specific, intensely grows only in WAG and (WAG × Brattleboro) F1 rats. In these groups, the growth of the tumor leads to the animal death within approximately 30 days after the inoculation of tumor cells. In Brattleboro rats, the carcinosarcoma grows less intensely: the tumor node somewhat increases only within the first two weeks, after which the tumor began to decrease and eventually disappears altogether. Both characters exhibit a 100% concordance at the individual level.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Schmale, H. and Richter, D., Single Base Deletion in the Vasopressin Gene is the Cause of Diabetes Insipidus in Brattleboro Rats, Nature, 1984, vol. 308, pp. 705–709.

    Article  PubMed  CAS  Google Scholar 

  2. Khegai, I.I., Specific Expression of Gene di (diabetes insiridus) in Homologous Inbred Rat Lines, Rus. J. Genet., 2002, vol. 38, no. 12, pp. 1424–1427.

    Article  CAS  Google Scholar 

  3. Valtin, H., The Discovery of the Brattleboro Rat, Recommended Nomenclature, and the Question of Proper Controls, Annals, New York Acad. Sci., 1982, vol. 394, pp. 1–9.

    CAS  Google Scholar 

  4. Khegai, I.I., Voitenko, N.N., and Tinnikov, A.A., Pleiotropic Physiological Effects of the di Mutation Determining Diabetes Insiridus in Rat, Rus. J. Genet., 1996, vol. 32, no. 10, pp. 1190–1193.

    CAS  Google Scholar 

  5. Khegai, I.I., Phenotypic Expression of the Mutant Gene diabetes insiridus in Rats and Nriteria of Genotyping by Phenotype, Rus. J. Genet., 2003, vol. 39, no. 1, pp. 57–60.

    Article  CAS  Google Scholar 

  6. Zakharova, L.A., Karyagina, A.Yu., Popova, N.A., et al., Humoral Immune Response in Ontogeny of Brattleboro Rats with Inherited Deficiency of Vasopressin Synthesis, Dokl. Akad. Nauk, 2001, vol. 376, pp. 283–285.

    CAS  Google Scholar 

  7. Khegai, I.I., Gulyaeva, M.A., Popova, N.A., et al., Characteristics of the Immune System in Ontogeny of the Rats with the Inherited Deficiency of Vasopressin Synthesis, Byull. Eksp. Biol. Med., 2003, vol. 136, pp. 505–508.

    Google Scholar 

  8. Bender, K., Adams, M., Baverstock, P.R., et al., Biochemical Markers in Inbred Strains of the Rat (Rattus norvegicus), Immunogenetics, 1984, vol. 19, pp. 257–266.

    Article  PubMed  CAS  Google Scholar 

  9. Vrionis, F.D., Wu, J.K., Qi, P., et al., Tumor Cells Expressing the Herpes Simplex Virus-Thymidine Kinase Gene in the Treatment of Walker 256 Meningeal Neoplasia in Rats, J. Neurosurg., 1996, vol. 84, pp. 250–257.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Original Russian Text © I.I. Khegai, N.A. Popova, L.N. Ivanova, 2006, published in Genetika, 2006, Vol. 42, No. 7, pp. 993–995.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Khegai, I.I., Popova, N.A. & Ivanova, L.N. Effect of vasopressin gene expression on the growth of walker 256 carcinosarcoma in rats. Russ J Genet 42, 818–820 (2006). https://doi.org/10.1134/S1022795406070180

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1022795406070180

Keywords

Navigation