A functional switch from lung cancer resistance to susceptibility at the Pas1 locus in Kras2LA2 mice

Abstract

Pulmonary adenoma susceptibility 1 (Pas1) is the major mouse lung cancer susceptibility locus on chromosome 6 (ref. 1). Kras2 is a common target of somatic mutation in chemically induced mouse lung tumors2,3 and is a candidate Pas1 gene4. M. spretus mice (SPRET/Ei) carry a Pas1 resistance haplotype for chemically induced lung tumors5. We demonstrate that the SPRET/Ei Pas1 allele is switched from resistance to susceptibility by fixation of the parental origin of the mutant Kras2 allele. This switch correlates with low expression of endogenous Kras2 in SPRET/Ei. We propose that the Pas1 modifier effect is due to Kras2, and that a sensitive balance between the expression levels of wild-type and mutant alleles determines lung tumor susceptibility. These data demonstrate that cancer predisposition should also be considered in the context of somatic events and could have major implications for the design of human association studies to identify cancer susceptibility genes.

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Figure 1: Lung tumor multiplicity.
Figure 2: Expression of the Pas1 candidate genes in normal lungs of different strains of mice.
Figure 3: Proposed model for the role of Kras2 in lung tumor susceptibility.

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References

  1. 1

    Gariboldi, M. et al. A major susceptibility locus to murine lung carcinogenesis maps on chromosome 6. Nat. Genet. 3, 132–136 (1993).

    CAS  Article  Google Scholar 

  2. 2

    You, M., Candrian, U., Maronpot, R.R., Stoner, G.D. & Anderson, M.W. Activation of the Ki-ras protooncogene in spontaneously occurring and chemically induced lung tumors of the strain A mouse. Proc. Natl. Acad. Sci. USA 86, 3070–3074 (1989).

    CAS  Article  Google Scholar 

  3. 3

    You, M. et al. Mutagenesis of the K-ras protooncogene in mouse lung tumors induced by N-ethyl-N-nitrosourea or N-nitrosodiethylamine. Carcinogenesis 13, 1583–1586 (1992).

    CAS  Article  Google Scholar 

  4. 4

    Ryan, J., Barker, P.E., Nesbitt, M.N. & Ruddle, F.H. KRAS2 as a genetic marker for lung tumor susceptibility in inbred mice. J. Natl. Cancer Inst. 79, 1351–1357 (1987).

    CAS  PubMed  Google Scholar 

  5. 5

    Wang, M. et al. Fine mapping and identification of candidate pulmonary adenoma susceptibility 1 genes using advanced intercross lines. Cancer Res. 63, 3317–3324 (2003).

    CAS  PubMed  Google Scholar 

  6. 6

    Manenti, G. et al. Haplotype sharing suggests that a genomic segment containing six genes accounts for the pulmonary adenoma susceptibility 1 (Pas1) locus activity in mice. Oncogene 23, 4495–4504 (2004).

    CAS  Article  Google Scholar 

  7. 7

    Johnson, L. et al. Somatic activation of the K-ras oncogene causes early onset lung cancer in mice. Nature 410, 1111–1116 (2001).

    CAS  Article  Google Scholar 

  8. 8

    Jackson, E.L. et al. Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras. Genes Dev. 15, 3243–3248 (2001).

    CAS  Article  Google Scholar 

  9. 9

    You, M. et al. Parental bias of Ki-ras oncogenes detected in lung tumors from mouse hybrids. Proc. Natl. Acad. Sci. USA 89, 5804–5808 (1992).

    CAS  Article  Google Scholar 

  10. 10

    Zhang, Z. et al. Positional cloning of the major quantitative trait locus underlying lung tumor susceptibility in mice. Proc. Natl. Acad. Sci. USA 100, 12642–12647 (2003).

    CAS  Article  Google Scholar 

  11. 11

    Wang, M., Futamura, M., Wang, Y. & You, M. Pas1c1 is a candidate for the mouse pulmonary adenoma susceptibility 1 locus. Oncogene 24, 1958–1963 (2005).

    CAS  Article  Google Scholar 

  12. 12

    Maria, D.A. et al. Pulmonary adenoma susceptibility 1 (Pas1) locus affects inflammatory response. Oncogene 22, 426–432 (2003).

    CAS  Article  Google Scholar 

  13. 13

    Hennings, H. et al. FVB/N mice: an inbred strain sensitive to the chemical induction of squamous cell carcinomas in the skin. Carcinogenesis 14, 2353–2358 (1993).

    CAS  Article  Google Scholar 

  14. 14

    Nagase, H. et al. Distinct genetic loci control development of benign and malignant skin tumours in mice. Nat. Genet. 10, 424–429 (1995).

    CAS  Article  Google Scholar 

  15. 15

    Demant, P. Cancer susceptibility in the mouse: genetics, biology and implications for human cancer. Nat. Rev. Genet. 4, 721–734 (2003).

    CAS  Article  Google Scholar 

  16. 16

    Dragani, T.A. 10 years of mouse cancer modifier loci: human relevance. Cancer Res. 63, 3011–3018 (2003).

    CAS  PubMed  Google Scholar 

  17. 17

    Manenti, G., Falvella, F.S., Gariboldi, M., Dragani, T.A. & Pierotti, M.A. Different susceptibility to lung tumorigenesis in mice with an identical Kras2 intron 2. Genomics 29, 438–444 (1995).

    CAS  Article  Google Scholar 

  18. 18

    Manenti, G. et al. Genetic mapping of lung cancer modifier loci specifically affecting tumor initiation and progression. Cancer Res. 57, 4164–4166 (1997).

    CAS  PubMed  Google Scholar 

  19. 19

    Czarnomska, A. et al. Opposite effects of modifiers of the ApcMin mutation in intestine and mammary gland. Cancer Res. 63, 4533–4537 (2003).

    CAS  PubMed  Google Scholar 

  20. 20

    Quintanilla, M., Brown, K., Ramsden, M. & Balmain, A. Carcinogen-specific mutation and amplification of Ha-ras during mouse skin carcinogenesis. Nature 322, 78–80 (1986).

    CAS  Article  Google Scholar 

  21. 21

    Guerrero, I., Villasante, A., Corces, V. & Pellicer, A. Loss of the normal N-ras allele in a mouse thymic lymphoma induced by a chemical carcinogen. Proc. Natl. Acad. Sci. USA 82, 7810–7814 (1985).

    CAS  Article  Google Scholar 

  22. 22

    Li, J. et al. LOH of chromosome 12p correlates with Kras2 mutation in non-small cell lung cancer. Oncogene 22, 1243–1246 (2003).

    CAS  Article  Google Scholar 

  23. 23

    Diaz, R. et al. Inhibition of Ras oncogenic activity by Ras protooncogenes. Int. J. Cancer 113, 241–248 (2005).

    CAS  Article  Google Scholar 

  24. 24

    Zhang, Z. et al. Wildtype Kras2 can inhibit lung carcinogenesis in mice. Nat. Genet. 29, 25–33 (2001).

    CAS  Article  Google Scholar 

  25. 25

    Wang, Y. & You, M. Alternative splicing of the K-ras gene in mouse tissues and cell lines. Exp. Lung Res. 27, 255–267 (2001).

    Article  Google Scholar 

  26. 26

    Bystrykh, L. et al. Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'. Nat. Genet. 37, 225–232 (2005).

    CAS  Article  Google Scholar 

  27. 27

    Schadt, E.E. et al. Genetics of gene expression surveyed in maize, mouse and man. Nature 422, 297–302 (2003).

    CAS  Article  Google Scholar 

  28. 28

    Dragani, T.A. et al. Population-based mapping of pulmonary adenoma susceptibility 1 locus. Cancer Res. 60, 5017–5020 (2000).

    CAS  PubMed  Google Scholar 

  29. 29

    Yanagitani, N. et al. Localization of a human lung adenocarcinoma susceptibility locus, possibly syntenic to the mouse Pas1 locus, in the vicinity of the D12S1034 locus on chromosome 12p11. Carcinogenesis 23, 1177–1183 (2002).

    CAS  Article  Google Scholar 

  30. 30

    Beck, J.A. et al. Genealogies of mouse inbred strains. Nat. Genet. 24, 23–25 (2000).

    CAS  Article  Google Scholar 

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Acknowledgements

We are grateful to R. Del Rosario and B. Sails for technical assistance with mouse breeding and genotyping and to CIDR for genotyping of mice. This work was supported by National Cancer Institute grant U01CA84244 (A.B.) and a supplement to U01CA84306 (T.J.). A.B. acknowledges support from the Bruce and Davina Isackson Foundation and from the Barbara Bass Bakar Chair of Cancer Genetics.

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The study was designed by M.D.T., J.P.L., J.H.M. and A.B.; phenotype assessment and genotyping were performed by M.D.T. and J.P.-L..; mutational and gene expression analyses were performed by M.D.T.; J.H. was involved in mouse breeding; statistical analysis was performed by J.-H.M.; T.J. provided the Kras2LA2 mice and was involved in study design and discussion of results; M.D.T. and A.B. wrote the paper.

Corresponding author

Correspondence to Allan Balmain.

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The authors declare no competing financial interests.

Supplementary information

Supplementary Fig. 1

Kras2 expression in lungs of wild-type untreated (FVBSPRETF1)FVB mice. (PDF 21 kb)

Supplementary Table 1

Kras2 status in urethane-induced lung tumors. (PDF 8 kb)

Supplementary Table 2

Oligonucleotide sequences (PDF 6 kb)

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To, M., Perez-Losada, J., Mao, JH. et al. A functional switch from lung cancer resistance to susceptibility at the Pas1 locus in Kras2LA2 mice. Nat Genet 38, 926–930 (2006). https://doi.org/10.1038/ng1836

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