Akt activation and localisation correlate with tumour invasion and oncogene expression in thyroid cancer
Autor: | M Miyakawa, O. Isozaki, Victoria Savchenko, Vasily Vasko, C De Micco, Kenneth D. Burman, Motoyasu Saji, T Tsushima, Matthew D. Ringel, A Larin, Elena Hardy, H Murakami, M Kruhlak |
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Předmět: |
Adenoma
medicine.medical_specialty endocrine system Cytoplasm endocrine system diseases Retroviridae Proteins Oncogenic Thyroid Gland Cell Cycle Proteins Biology Protein Serine-Threonine Kinases Phosphatidylinositol 3-Kinases Cell Movement Internal medicine Proto-Oncogene Proteins Genetics medicine Humans Neoplasm Invasiveness Thyroid Neoplasms Thyroid cancer Protein kinase B Genetics (clinical) Cell Nucleus Oncogene Tumor Suppressor Proteins Thyroid Cell migration medicine.disease Immunohistochemistry Enzyme Activation Isoenzymes Oncogene Protein v-akt Protein Transport Endocrinology medicine.anatomical_structure Cancer cell Cancer research Disease Progression Original Article Proto-Oncogene Proteins c-akt Cyclin-Dependent Kinase Inhibitor p27 |
Zdroj: | Scopus-Elsevier |
Popis: | Introduction: Akt activation is involved in the pathogenesis of inherited thyroid cancer in Cowden's syndrome and in sporadic thyroid cancers. In cell culture, Akt regulates thyroid cell growth and survival; but recent data suggest that Akt also regulates cell motility in non-thyroid cell lines. We therefore sought to evaluate the role of Akt in thyroid cancer progression. Methods: We evaluated 46 thyroid cancer, 20 thyroid follicular adenoma, and adjacent normal tissues samples by immunohistochemistry for activated Akt (pAkt), Akt 1, 2, and 3, and p27 expression. Immunoblots were performed in 14 samples. Results: Akt activation was identified in 10/10 follicular cancers, 26/26 papillary cancers, and 2/10 follicular variant of papillary cancers, but in only 4/66 normal tissue samples and 2/10 typical benign follicular adenomas. Immunoactive pAkt was greatest in regions of capsular invasion; and was localised to the nucleus in follicular cancers and the cytoplasm in papillary cancers, except for invasive regions of papillary cancers where it localised to both compartments. Immunoactive Akt 1, but not Akt 2 or Akt 3, correlated with pAkt localisation, and nuclear pAkt was associated with cytoplasmic expression of p27. In vitro studies using human thyroid cancer cells demonstrated that nuclear translocation of Akt 1 and pAkt were associated with cytoplasmic p27 and cell invasion and migration. Cell migration and the localisation of Akt 1, pAkt, and p27 were inhibited by PI3 kinase, but not MEK inhibition. Discussion: These data suggest an important role for nuclear activation of Akt 1 in thyroid cancer progression. |
Databáze: | OpenAIRE |
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