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Telomerase and its potential for therapeutic intervention.
Phatak, P; Burger, A M.
Afiliação
  • Phatak P; Department of Pharmacology and Experimental Therapeutics, and Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Br J Pharmacol ; 152(7): 1003-11, 2007 Dec.
Article em En | MEDLINE | ID: mdl-17603541
ABSTRACT
Telomerase and telomeres are attractive targets for anticancer therapy. This is supported by the fact that the majority of human cancers express the enzyme telomerase which is essential to maintain their telomere length and thus, to ensure indefinite cell proliferation--a hallmark of cancer. Tumours have relatively shorter telomeres compared to normal cell types, opening the possibility that human cancers may be considerably more susceptible to killing by agents that inhibit telomere replication than normal cells. Advances in the understanding of the regulation of telomerase activity and the telomere structure, as well as the identification of telomerase and telomere associated binding proteins have opened new avenues for therapeutic intervention. Here, we review telomere and telomerase biology and the various approaches which have been developed to inhibit the telomere/telomerase complex over the past decade. They include inhibitors of the enzyme catalytic subunit and RNA component, agents that target telomeres, telomerase vaccines and drugs targeting binding proteins. The emerging role of telomerase in cancer stem cells and the implications for cancer therapy are also discussed.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Telômero / Telomerase / Vacinas Anticâncer / Inibidores Enzimáticos / Neoplasias Limite: Animals / Humans Idioma: En Revista: Br J Pharmacol Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Telômero / Telomerase / Vacinas Anticâncer / Inibidores Enzimáticos / Neoplasias Limite: Animals / Humans Idioma: En Revista: Br J Pharmacol Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos