Molecular targeted therapy for hepatocellular carcinoma: Current and future

被引:72
|
作者
Shin, Jung Woo [1 ]
Chung, Young-Hwa [2 ]
机构
[1] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Internal Med, Ulsan 682714, South Korea
[2] Univ Ulsan, Coll Med, Dept Internal Med, Asan Med Ctr, Seoul 138736, South Korea
关键词
Hepatocellular carcinoma; Targeted therapy; Molecular agents; Sorafenib; ENDOTHELIAL GROWTH-FACTOR; TYROSINE KINASE INHIBITOR; MESSENGER-RNA EXPRESSION; VIRUS X-PROTEIN; PHASE-II TRIAL; FACTOR RECEPTOR; HEPATOCYTE GROWTH; HBX PROTEIN; CELL-PROLIFERATION; SIGNALING PATHWAYS;
D O I
10.3748/wjg.v19.i37.6144
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular carcinoma (HCC) is one of the most frequent tumors worldwide. The majority of HCC cases occur in patients with chronic liver disease. Despite regular surveillance to detect small HCC in these patients, HCC is often diagnosed at an advanced stage. Because HCC is highly resistant to conventional systemic therapies, the prognosis for advanced HCC patients remains poor. The introduction of sorafenib as the standard systemic therapy has unveiled a new direction for future research regarding HCC treatment. However, given the limited efficacy of the drug, a need exists to look beyond sorafenib. Many molecular targeted agents that inhibit different pathways involved in hepatocarcinogenesis are under various phases of clinical development, and novel targets are being assessed in HCC. This review aims to summarize the efforts to target molecular components of the signaling pathways that are responsible for the development and progression of HCC and to discuss perspectives on the future direction of research. (c) 2013 Baishideng. All rights reserved.
引用
收藏
页码:6144 / 6155
页数:12
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