Pró-fármaco ativado por enzima, uma estratégia promissora na quimioterapia


Autoria(s): Blau, Lorena; Menegon, Renato Farina; Chin, Chung Man
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

01/11/2006

Resumo

Strategies that promote selective activation of prodrugs by enzymes can be divided into two major classes: 1) deliver of a monoclonal antibody-enzyme immunoconjugate that can recognize a specific antigen and promote the prodrug to a citotoxic drug, with a high selectivity for the target cells, and 2) selective gene delivery encoding an enzyme that can promote the prodrug to a citotoxic drug for the target cells. In this article are discussed ADEPT (antibody-directed enzyme prodrug therapy), GDEPT (gene-directed enzyme prodrug therapy), VDEPT (virus-directed enzyme prodrug therapy), GPAT (genetic prodrug activation therapy) and PDEPT (polymer-directed enzyme prodrug therapy) approaches, their clinical trials, advantages, disadvantages and perspectives.

Formato

1307-1316

Identificador

http://dx.doi.org/10.1590/S0100-40422006000600028

Quimica Nova, v. 29, n. 6, p. 1307-1316, 2006.

0100-4042

1678-7064

http://hdl.handle.net/11449/69198

10.1590/S0100-40422006000600028

S0100-40422006000600028

WOS:000242341600028

2-s2.0-33845716527

2-s2.0-33845716527.pdf

Idioma(s)

por

Relação

Química Nova

Direitos

openAccess

Palavras-Chave #Cancer #Enzymes #Prodrugs
Tipo

info:eu-repo/semantics/article