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Current Status of Molecular Targeted Therapies in Hepatocellular Carcinoma / 대한소화기학회지
The Korean Journal of Gastroenterology ; : 136-146, 2013.
Artigo em Coreano | WPRIM | ID: wpr-143716
ABSTRACT
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer death in Korea. Curative treatment is only possible when the disease is diagnosed at the early stage. The prognosis of patients with HCC is even dismal in advanced stages. No systemic cytotoxic chemotherapy has proven to be beneficial in overall survival. Recently, the understanding of the molecular pathogenesis led to the development of new therapies. With the evidence of dysregulation of critical genes associated with cellular proliferation, growth factor signaling, cell cycling, apoptosis, and angiogenesis in HCC, a number of molecular target agents are under clinical trials. Sorafenib is the first systemic anticancer drug which has proven to gain survival benefit in the global as well as Asia-Pacific trials. However, the survival gain is still modest, and further efforts to improve outcomes in patients with HCC are necessary by developing novel drugs or combining other forms of therapies. This article will review signaling pathways in HCC and introduce molecular target agents under investigation currently.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Compostos de Fenilureia / Transdução de Sinais / Receptor IGF Tipo 1 / Niacinamida / Carcinoma Hepatocelular / Quinases de Proteína Quinase Ativadas por Mitógeno / Inibidores de Proteínas Quinases / Proteínas Proto-Oncogênicas c-akt / Proteínas Wnt / Serina-Treonina Quinases TOR Tipo de estudo: Estudo prognóstico Limite: Humanos Idioma: Coreano Revista: The Korean Journal of Gastroenterology Ano de publicação: 2013 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Compostos de Fenilureia / Transdução de Sinais / Receptor IGF Tipo 1 / Niacinamida / Carcinoma Hepatocelular / Quinases de Proteína Quinase Ativadas por Mitógeno / Inibidores de Proteínas Quinases / Proteínas Proto-Oncogênicas c-akt / Proteínas Wnt / Serina-Treonina Quinases TOR Tipo de estudo: Estudo prognóstico Limite: Humanos Idioma: Coreano Revista: The Korean Journal of Gastroenterology Ano de publicação: 2013 Tipo de documento: Artigo