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PI3K Signaling Pathways as a Molecular Target for Glioblastoma Multiforme.
da Silva, Andressa Letícia Lopes; de Araújo, Thiago Pina Goes; de Albuquerque Ferreira, Shakira Cavalcante; Leite, Anderson Brandão; da Silva, João Kaycke Sarmento; Albuquerque, Lilyana Waleska Nunes; de Lima, Ana Rachel Vasconcelos; Barros, Herbert Charles Silva; Silva, Leandro Rocha; da Silva-Júnior, Edeildo Ferreira; de Araújo-Júnior, João Xavier; Neto, Vivaldo Moura; de Queiroz, Aline Cavalcanti; Alexandre-Moreira, Magna Suzana.
Afiliação
  • da Silva ALL; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • de Araújo TPG; Laboratory of Medicinal Chemistry, Institute of Pharmaceutical Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • de Albuquerque Ferreira SC; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • Leite AB; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • da Silva JKS; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • Albuquerque LWN; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • de Lima ARV; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • Barros HCS; Laboratory of Pharmacology and Immunity, Institute of Biological and Health Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • Silva LR; Municipal Secretary of Health of Maceio, Governo do estado de Alagoas, Brazil.
  • da Silva-Júnior EF; Biological and Molecular Chemistry Research Group, Institute of Chemistry and Biotechnology, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • de Araújo-Júnior JX; Biological and Molecular Chemistry Research Group, Institute of Chemistry and Biotechnology, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • Neto VM; Laboratory of Medicinal Chemistry, Institute of Pharmaceutical Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • de Queiroz AC; Laboratory of Medicinal Chemistry, Institute of Pharmaceutical Sciences, Federal University of Alagoas, AC. Simões campus, Maceió, 57072-900, Brazil.
  • Alexandre-Moreira MS; Paulo Niemeyer State Brain Institute, Study and Research Center, Brain Biomedicine Laboratory, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Curr Protein Pept Sci ; 25(1): 12-26, 2024.
Article em En | MEDLINE | ID: mdl-37653631
ABSTRACT
Glioblastoma multiforme (GBM) is the most common type of cancer that affects the central nervous system (CNS). It currently accounts for about 2% of diagnosed malignant tumors worldwide, with 296,000 new cases reported per year. The first-choice treatment consists of surgical resection, radiotherapy, and adjuvant chemotherapy, which increases patients' survival by 15 months. New clinical and pre-clinical research aims to improve this prognosis by proposing the search for new drugs that effectively eliminate cancer cells, circumventing problems such as resistance to treatment. One of the promising therapeutic strategies in the treatment of GBM is the inhibition of the phosphatidylinositol 3-kinase (PI3K) pathway, which is closely related to the process of tumor carcinogenesis. This review sought to address the main scientific studies of synthetic or natural drug prototypes that target specific therapy co-directed via the PI3K pathway, against human glioblastoma.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article