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Identification of a highly effective rapamycin schedule that markedly reduces the size, multiplicity, and phenotypic progression of tobacco carcinogen-induced murine lung tumors.

Publication ,  Journal Article
Granville, CA; Warfel, N; Tsurutani, J; Hollander, MC; Robertson, M; Fox, SD; Veenstra, TD; Issaq, HJ; Linnoila, RI; Dennis, PA
Published in: Clin Cancer Res
April 1, 2007

PURPOSE: Human and murine preneoplastic lung lesions induced by tobacco exposure are characterized by increased activation of the Akt/mammalian target of rapamycin (mTOR) pathway, suggesting a role for this pathway in lung cancer development. To test this, we did studies with rapamycin, an inhibitor of mTOR, in A/J mice that had been exposed to the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). EXPERIMENTAL DESIGN: Tumorigenesis was induced by i.p. injection of NNK, and rapamycin was administered 1 or 26 weeks after NNK administration. Biomarkers associated with mTOR inhibition were assessed in lung and/or surrogate tissues using immunohistochemistry and immunoblotting. Rapamycin levels were measured using mass spectroscopy. RESULTS: Rapamycin was administered on a daily (5 of 7 days) regimen beginning 26 weeks after NNK decreased tumor size, proliferative rate, and mTOR activity. Multiplicity was not affected. Comparing this regimen with an every-other-day (qod) regimen revealed that rapamycin levels were better maintained with qod administration, reaching a nadir of 16.4 ng/mL, a level relevant in humans. When begun 1 week after NNK, this regimen was well tolerated and decreased tumor multiplicity by 90%. Tumors that did develop showed decreased phenotypic progression and a 74% decrease in size that correlated with decreased proliferation and inhibition of mTOR. CONCLUSIONS: Tobacco carcinogen-induced lung tumors in A/J mice are dependent upon mTOR activity because rapamycin markedly reduced the development and growth of tumors. Combined with the Food and Drug Administration approval of rapamycin and broad clinical experience, these studies provide a rationale to assess rapamycin in trials with smokers at high risk to develop lung cancer.

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Published In

Clin Cancer Res

DOI

ISSN

1078-0432

Publication Date

April 1, 2007

Volume

13

Issue

7

Start / End Page

2281 / 2289

Location

United States

Related Subject Headings

  • TOR Serine-Threonine Kinases
  • Sirolimus
  • Protein Kinases
  • Phenotype
  • Oncology & Carcinogenesis
  • Nitrosamines
  • Nicotiana
  • Mice
  • Lung Neoplasms
  • Immunohistochemistry
 

Citation

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Granville, C. A., Warfel, N., Tsurutani, J., Hollander, M. C., Robertson, M., Fox, S. D., … Dennis, P. A. (2007). Identification of a highly effective rapamycin schedule that markedly reduces the size, multiplicity, and phenotypic progression of tobacco carcinogen-induced murine lung tumors. Clin Cancer Res, 13(7), 2281–2289. https://doi.org/10.1158/1078-0432.CCR-06-2570
Granville, Courtney A., Noel Warfel, Junji Tsurutani, M Christine Hollander, Matthew Robertson, Stephen D. Fox, Timothy D. Veenstra, Haleem J. Issaq, R Ilona Linnoila, and Phillip A. Dennis. “Identification of a highly effective rapamycin schedule that markedly reduces the size, multiplicity, and phenotypic progression of tobacco carcinogen-induced murine lung tumors.Clin Cancer Res 13, no. 7 (April 1, 2007): 2281–89. https://doi.org/10.1158/1078-0432.CCR-06-2570.
Granville CA, Warfel N, Tsurutani J, Hollander MC, Robertson M, Fox SD, et al. Identification of a highly effective rapamycin schedule that markedly reduces the size, multiplicity, and phenotypic progression of tobacco carcinogen-induced murine lung tumors. Clin Cancer Res. 2007 Apr 1;13(7):2281–9.
Granville, Courtney A., et al. “Identification of a highly effective rapamycin schedule that markedly reduces the size, multiplicity, and phenotypic progression of tobacco carcinogen-induced murine lung tumors.Clin Cancer Res, vol. 13, no. 7, Apr. 2007, pp. 2281–89. Pubmed, doi:10.1158/1078-0432.CCR-06-2570.
Granville CA, Warfel N, Tsurutani J, Hollander MC, Robertson M, Fox SD, Veenstra TD, Issaq HJ, Linnoila RI, Dennis PA. Identification of a highly effective rapamycin schedule that markedly reduces the size, multiplicity, and phenotypic progression of tobacco carcinogen-induced murine lung tumors. Clin Cancer Res. 2007 Apr 1;13(7):2281–2289.

Published In

Clin Cancer Res

DOI

ISSN

1078-0432

Publication Date

April 1, 2007

Volume

13

Issue

7

Start / End Page

2281 / 2289

Location

United States

Related Subject Headings

  • TOR Serine-Threonine Kinases
  • Sirolimus
  • Protein Kinases
  • Phenotype
  • Oncology & Carcinogenesis
  • Nitrosamines
  • Nicotiana
  • Mice
  • Lung Neoplasms
  • Immunohistochemistry