Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Expression of the NEK family in normal and cancer tissue: an immunohistochemical study

Texto completo
Autor(es):
Melo-Hanchuk, Talita Diniz [1] ; Martins, Mariana Bonjiorno [1] ; Cunha, Lucas Leite [2] ; Soares, Fernando Augusto [3] ; Ward, Laura Sterian [2] ; Vassallo, Jose [4] ; Kobarg, Jorg [1, 5]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, Inst Biol, Dept Bioquim & Biol Tecidual, Campinas, SP - Brazil
[2] Univ Estadual Campinas, Fac Ciencias Med, Lab Genet Mol Canc, Campinas, SP - Brazil
[3] AC Camargo Canc Ctr, Dept Patol, Sao Paulo, SP - Brazil
[4] Univ Estadual Campinas, Fac Ciencias Med, Dept Anat Patol, Campinas, SP - Brazil
[5] Univ Estadual Campinas, UNICAMP, Fac Ciencias Farmaceut, Inst Biol, Dept Bioquim & Biol Tecidual, Rua Monteiro Lobato 255, BR-13083862 Campinas, SP - Brazil
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: BMC CANCER; v. 20, n. 1 JAN 6 2020.
Citações Web of Science: 0
Resumo

BackgroundThe NEK serine/threonine protein kinases are involved in cell cycle checkpoints, DNA damage repair, and apoptosis. Alterations in these pathways are frequently associated with cell malignant cellular transformations. Thyroid cancer is the most common malignant tumour in the endocrine system. Despite good treatment methods, the number of cases has increased significantly in recent years. Here, we studied the expression of NEK1, NEK2, NEK3, and NEK5 in different types of normal and malignant tissues, using tissue microarray analysis, and identified NEKs as potential markers in thyroid malignancy.MethodsThe studied cases comprised multiple cancer tissue microarrays, including breast, colon, esophagus, kidney, lung, pancreas, prostate, stomach, thyroid and uterine cervix, as well as 281 patients who underwent thyroid resection for thyroid cancer or thyroid nodules. The expression of NEK1, NEK2, NEK3, and NEK5 was analyzed by immunohistochemistry. The expression pattern was evaluated in terms of intensity by two methods, semiquantitative and quantitative, and was compared between normal and cancer tissue.ResultsWe analysed the expression of each member of the NEK family in a tissue-dependent manner. Compared to normal tissue, most of the evaluated proteins showed lower expression in lung tumour. However, in the thyroid, the expression was higher in malignant tissue, especially for NEK 1, NEK3 and NEK5. Concerning characteristics of the thyroid tumour, such as aggressiveness, NEK1 expression was higher in tumours with multifocality and in patients with lymph node metastasis. NEK3 expression was stronger in patients with stage II, that involved metastasis. NEK5, on the other hand, showed high expression in patients with invasion and metastasis and in patients with tumour size >4cm. Furthermore, this work, demonstrated for the first time a high specificity and sensitivity of over-expression of NEK1 in classical and follicular variants of papillary thyroid cancer and NEK3 in tall-cell papillary thyroid cancer.ConclusionTaken together, the NEK protein kinases emerge as important proteins in thyroid cancer development and may help to identify malignancy and aggressiveness features during diagnosis.Trial registrationThis study was retrospectively registered. www.accamargo.org.br/cientistas-pesquisadores/comite-de-etica-em-pequisa -cep. (AU)

Processo FAPESP: 15/06458-4 - Caracterização funcional de proteínas reguladoras envolvidas no reparo de DNA
Beneficiário:Talita Diniz Melo Hanchuk
Linha de fomento: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 17/03489-1 - De estudos funcionais à busca de novos inibidores anticâncer: explorando cinases reguladores do ciclo celular da família de NEK humana
Beneficiário:Jörg Kobarg
Linha de fomento: Auxílio à Pesquisa - Temático
Processo FAPESP: 16/02040-8 - Análise funcional de mutações em NEK1 e Nek7 em câncer e identificação dos seus substratos fisiológicos
Beneficiário:Mariana Bonjiorno Martins
Linha de fomento: Bolsas no Brasil - Pós-Doutorado