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[Comparison of therapeutic peptides targeting pancreatic cancer]. / Hasnyálmirigytumort célzó terápiás irányítópeptidek összehasonlítása.
Mezõ, Gábor; Dókus, Levente; Schlosser, Gitta; Lajkó, Eszter; Szász, Zsófia; Randelovic, Ivan; Biri-Kovács, Beáta; Tóvári, József; Kõhidai, László.
Afiliação
  • Mezõ G; Eötvös Loránd Tudományegyetem, Magyar Tudományos Akadémia, MTA-ELTE Peptidkémiai Kutatócsoport, Budapest, Hungary. gmezo@caesar.elte.hu.
  • Dókus L; Kémiai Intézet, Eötvös Loránd Tudományegyetem, Budapest, Hungary.
  • Schlosser G; Eötvös Loránd Tudományegyetem, Magyar Tudományos Akadémia, MTA-ELTE Peptidkémiai Kutatócsoport, Budapest, Hungary. gmezo@caesar.elte.hu.
  • Lajkó E; Genetikai, Sejt- és Immunbiológiai Intézet, Semmelweis Egyetem, Budapest, Hungary.
  • Szász Z; Genetikai, Sejt- és Immunbiológiai Intézet, Semmelweis Egyetem, Budapest, Hungary.
  • Randelovic I; Kísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.
  • Biri-Kovács B; Kémiai Intézet, Eötvös Loránd Tudományegyetem, Budapest, Hungary.
  • Tóvári J; Kísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.
  • Kõhidai L; Genetikai, Sejt- és Immunbiológiai Intézet, Semmelweis Egyetem, Budapest, Hungary.
Magy Onkol ; 63(4): 301-308, 2019 12 09.
Article em Hu | MEDLINE | ID: mdl-31821385
ABSTRACT
Despite the small number of cases, pancreatic cancer is one of the biggest challenges in tumor therapy as its treatment is not yet resolved and the expected 5-year survival rate is only 5%. Therefore, innovative solutions for pancreatic cancer are of great importance. Targeted tumor therapy might provide new possibilities in this field. In our research, we focused on finding peptide-based homing molecules and modified their structure to achieve better targeting properties. We compared several peptides that efficiently recognize receptors that are specific for or overexpressed by pancreatic cancer cells. Their structure-effect relationship was determined that can be useful during drug designing in the future. The antitumor effect of Dau=Aoa-GFLG-K(Dau=Aoa) SKAAKN-OH conjugate, which turned out to be the most efficient one during in vitro studies, were analyzed in vivo in female SCID mice. The obtained 30% inhibition, beside the low toxic side effects, might be a good starting point to develop further, more powerful conjugates.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: Hu Revista: Magy Onkol Assunto da revista: NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Hungria
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: Hu Revista: Magy Onkol Assunto da revista: NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Hungria
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