Genetic susceptibility to thymic lymphomas and K-ras gene mutation in mice after exposure to X-rays and N-ethyl-N-nitrosourea

Y. Shimada, M. Nishimura, S. Kakinuma, T. Ogiu, H. Fujimoto, A. Kubo, J. Nagai, K. Kobayash, K. Tano, S. Yoshinaga, K. K. Bhakat

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Abstract

Purpose: Ras activation is one of the major mechanisms for the development of murine thymic lymphomas by radiation and chemical carcinogens. To gain insight into the relationship between genetic susceptibility, and ras gene mutation, the frequency and spectrum of ras gene mutation was examined in thymic lymphomas from susceptible and resistant mice. Materials and methods: K- and N-ras mutations in thymic lymphomas that arose in X-ray-irradiated and N-ethyl-N-nitrosourea (ENU)-treated mice of susceptible C57BL/6, rather resistant C3H and their hybrid B6C3F1 were analysed by polymerase chain reaction-single-strand conformation polymorphism and subsequent DNA sequencing. Results: C57BL/6 exhibited a higher incidence of thymic lymphomas after exposure to X-rays and ENU than C3H, with B6C3F1 being intermediate. K-ras gene mutations occurred frequently in the pathogenesis of ENU-induced thymic lymphomas in susceptible C57BL/6 as opposed to resistant C3H. The ras mutations were more frequent in ENU-induced thymic lymphomas than X-ray-induced thymic lymphomas, and with the latter, there was no clear evidence for strain differences, suggesting that the genetic susceptibility, to X-rays was independent of ras activation. The mutations of K-ras in thymic lymphomas from C57BL/6 were predominantly GGT to GAT in codon 12, whereas this mutation type was never found in those from C3H. No strain difference was observed in the nucleotide sequence or expression levels of O6-alkylguanine alkyltransferase, indicating that this enzyme did not account for the genetic susceptibility to ras activation. Conclusions: The results indicate that there is a clear strain and carcinogen dependency of K-ras mutation and that the frequency of ras mutation might determine the genetic susceptibility to ENU-induced lymphomagenesis, whereas pathways independent of ras activation might determine the susceptibility to X-ray-induced lymphomagenesis.

Original languageEnglish (US)
Pages (from-to)423-430
Number of pages8
JournalInternational Journal of Radiation Biology
Volume79
Issue number6
DOIs
StatePublished - Jun 1 2003

Fingerprint

N-ethyl-N-nitrosourea
Ethylnitrosourea
ras Genes
Genetic Predisposition to Disease
mutations
lymphoma
genes
mice
Lymphoma
X-radiation
Genes
X-Rays
magnetic permeability
mutation
X rays
Mutation
Chemical activation
Carcinogens
x rays
activation

ASJC Scopus subject areas

  • Radiological and Ultrasound Technology
  • Radiology Nuclear Medicine and imaging

Cite this

Genetic susceptibility to thymic lymphomas and K-ras gene mutation in mice after exposure to X-rays and N-ethyl-N-nitrosourea. / Shimada, Y.; Nishimura, M.; Kakinuma, S.; Ogiu, T.; Fujimoto, H.; Kubo, A.; Nagai, J.; Kobayash, K.; Tano, K.; Yoshinaga, S.; Bhakat, K. K.

In: International Journal of Radiation Biology, Vol. 79, No. 6, 01.06.2003, p. 423-430.

Research output: Contribution to journalArticle

Shimada, Y, Nishimura, M, Kakinuma, S, Ogiu, T, Fujimoto, H, Kubo, A, Nagai, J, Kobayash, K, Tano, K, Yoshinaga, S & Bhakat, KK 2003, 'Genetic susceptibility to thymic lymphomas and K-ras gene mutation in mice after exposure to X-rays and N-ethyl-N-nitrosourea', International Journal of Radiation Biology, vol. 79, no. 6, pp. 423-430. https://doi.org/10.1080/0955300031000139371
Shimada, Y. ; Nishimura, M. ; Kakinuma, S. ; Ogiu, T. ; Fujimoto, H. ; Kubo, A. ; Nagai, J. ; Kobayash, K. ; Tano, K. ; Yoshinaga, S. ; Bhakat, K. K. / Genetic susceptibility to thymic lymphomas and K-ras gene mutation in mice after exposure to X-rays and N-ethyl-N-nitrosourea. In: International Journal of Radiation Biology. 2003 ; Vol. 79, No. 6. pp. 423-430.
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abstract = "Purpose: Ras activation is one of the major mechanisms for the development of murine thymic lymphomas by radiation and chemical carcinogens. To gain insight into the relationship between genetic susceptibility, and ras gene mutation, the frequency and spectrum of ras gene mutation was examined in thymic lymphomas from susceptible and resistant mice. Materials and methods: K- and N-ras mutations in thymic lymphomas that arose in X-ray-irradiated and N-ethyl-N-nitrosourea (ENU)-treated mice of susceptible C57BL/6, rather resistant C3H and their hybrid B6C3F1 were analysed by polymerase chain reaction-single-strand conformation polymorphism and subsequent DNA sequencing. Results: C57BL/6 exhibited a higher incidence of thymic lymphomas after exposure to X-rays and ENU than C3H, with B6C3F1 being intermediate. K-ras gene mutations occurred frequently in the pathogenesis of ENU-induced thymic lymphomas in susceptible C57BL/6 as opposed to resistant C3H. The ras mutations were more frequent in ENU-induced thymic lymphomas than X-ray-induced thymic lymphomas, and with the latter, there was no clear evidence for strain differences, suggesting that the genetic susceptibility, to X-rays was independent of ras activation. The mutations of K-ras in thymic lymphomas from C57BL/6 were predominantly GGT to GAT in codon 12, whereas this mutation type was never found in those from C3H. No strain difference was observed in the nucleotide sequence or expression levels of O6-alkylguanine alkyltransferase, indicating that this enzyme did not account for the genetic susceptibility to ras activation. Conclusions: The results indicate that there is a clear strain and carcinogen dependency of K-ras mutation and that the frequency of ras mutation might determine the genetic susceptibility to ENU-induced lymphomagenesis, whereas pathways independent of ras activation might determine the susceptibility to X-ray-induced lymphomagenesis.",
author = "Y. Shimada and M. Nishimura and S. Kakinuma and T. Ogiu and H. Fujimoto and A. Kubo and J. Nagai and K. Kobayash and K. Tano and S. Yoshinaga and Bhakat, {K. K.}",
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T1 - Genetic susceptibility to thymic lymphomas and K-ras gene mutation in mice after exposure to X-rays and N-ethyl-N-nitrosourea

AU - Shimada, Y.

AU - Nishimura, M.

AU - Kakinuma, S.

AU - Ogiu, T.

AU - Fujimoto, H.

AU - Kubo, A.

AU - Nagai, J.

AU - Kobayash, K.

AU - Tano, K.

AU - Yoshinaga, S.

AU - Bhakat, K. K.

PY - 2003/6/1

Y1 - 2003/6/1

N2 - Purpose: Ras activation is one of the major mechanisms for the development of murine thymic lymphomas by radiation and chemical carcinogens. To gain insight into the relationship between genetic susceptibility, and ras gene mutation, the frequency and spectrum of ras gene mutation was examined in thymic lymphomas from susceptible and resistant mice. Materials and methods: K- and N-ras mutations in thymic lymphomas that arose in X-ray-irradiated and N-ethyl-N-nitrosourea (ENU)-treated mice of susceptible C57BL/6, rather resistant C3H and their hybrid B6C3F1 were analysed by polymerase chain reaction-single-strand conformation polymorphism and subsequent DNA sequencing. Results: C57BL/6 exhibited a higher incidence of thymic lymphomas after exposure to X-rays and ENU than C3H, with B6C3F1 being intermediate. K-ras gene mutations occurred frequently in the pathogenesis of ENU-induced thymic lymphomas in susceptible C57BL/6 as opposed to resistant C3H. The ras mutations were more frequent in ENU-induced thymic lymphomas than X-ray-induced thymic lymphomas, and with the latter, there was no clear evidence for strain differences, suggesting that the genetic susceptibility, to X-rays was independent of ras activation. The mutations of K-ras in thymic lymphomas from C57BL/6 were predominantly GGT to GAT in codon 12, whereas this mutation type was never found in those from C3H. No strain difference was observed in the nucleotide sequence or expression levels of O6-alkylguanine alkyltransferase, indicating that this enzyme did not account for the genetic susceptibility to ras activation. Conclusions: The results indicate that there is a clear strain and carcinogen dependency of K-ras mutation and that the frequency of ras mutation might determine the genetic susceptibility to ENU-induced lymphomagenesis, whereas pathways independent of ras activation might determine the susceptibility to X-ray-induced lymphomagenesis.

AB - Purpose: Ras activation is one of the major mechanisms for the development of murine thymic lymphomas by radiation and chemical carcinogens. To gain insight into the relationship between genetic susceptibility, and ras gene mutation, the frequency and spectrum of ras gene mutation was examined in thymic lymphomas from susceptible and resistant mice. Materials and methods: K- and N-ras mutations in thymic lymphomas that arose in X-ray-irradiated and N-ethyl-N-nitrosourea (ENU)-treated mice of susceptible C57BL/6, rather resistant C3H and their hybrid B6C3F1 were analysed by polymerase chain reaction-single-strand conformation polymorphism and subsequent DNA sequencing. Results: C57BL/6 exhibited a higher incidence of thymic lymphomas after exposure to X-rays and ENU than C3H, with B6C3F1 being intermediate. K-ras gene mutations occurred frequently in the pathogenesis of ENU-induced thymic lymphomas in susceptible C57BL/6 as opposed to resistant C3H. The ras mutations were more frequent in ENU-induced thymic lymphomas than X-ray-induced thymic lymphomas, and with the latter, there was no clear evidence for strain differences, suggesting that the genetic susceptibility, to X-rays was independent of ras activation. The mutations of K-ras in thymic lymphomas from C57BL/6 were predominantly GGT to GAT in codon 12, whereas this mutation type was never found in those from C3H. No strain difference was observed in the nucleotide sequence or expression levels of O6-alkylguanine alkyltransferase, indicating that this enzyme did not account for the genetic susceptibility to ras activation. Conclusions: The results indicate that there is a clear strain and carcinogen dependency of K-ras mutation and that the frequency of ras mutation might determine the genetic susceptibility to ENU-induced lymphomagenesis, whereas pathways independent of ras activation might determine the susceptibility to X-ray-induced lymphomagenesis.

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