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      Chemopreventive effects of deguelin, a novel Akt inhibitor, on tobacco-induced lung tumorigenesis.

      JNCI Journal of the National Cancer Institute
      Animals, Anticarcinogenic Agents, pharmacology, Antineoplastic Agents, Benzo(a)pyrene, Bronchial Neoplasms, drug therapy, enzymology, etiology, prevention & control, Carcinogens, Cell Transformation, Neoplastic, drug effects, Enzyme Activation, Immunoblotting, Immunohistochemistry, Lung Neoplasms, Mice, Mice, Transgenic, Nitrosamines, Proto-Oncogene Proteins c-akt, antagonists & inhibitors, metabolism, Respiratory Mucosa, pathology, Rotenone, analogs & derivatives, Smoking, adverse effects, Tobacco Smoke Pollution

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          Abstract

          Tobacco carcinogens induce Akt activation and lung carcinogenesis. We previously demonstrated that deguelin, a natural plant product, specifically inhibits the proliferation of premalignant and malignant human bronchial epithelial cells by blocking Akt activation. To evaluate the ability of deguelin to block tobacco carcinogen-induced lung tumorigenesis, we evaluated the in vivo effects of deguelin on Akt activation and lung tumorigenesis in transgenic mice in which Akt expression was induced by tamoxifen and in 4-(methylnitrosoamino)-1-(3-pyridyl)-1-butanone (NNK)/benzo(a)pyrene (BaP)-treated A/J mice. Deguelin suppressed Akt activation in vivo, as measured by immunohistochemistry and immunoblotting, and statistically significantly reduced NNK/BaP-induced lung tumor multiplicity, volume, and load in A/J mice, as monitored by microcomputed tomography image analysis, with no detectable toxicity. These results indicate that deguelin warrants consideration as a chemopreventive agent for early-stage lung carcinogenesis in a clinical lung cancer chemoprevention trial.

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