Hui Kam M
Bek Chai Heah Laboratory of Cancer Genomics, Division of Cellular and Molecular Research, Humphrey Oei Institute of Cancer Research National Cancer Centre, 11 Hospital Drive, Singapore 169610, Singapore.
Cancer Lett. 2009 Dec 1;286(1):96-102. doi: 10.1016/j.canlet.2008.11.005. Epub 2008 Dec 17.
Primary liver cancer is the fifth most common cancer worldwide and hepatocellular carcinoma (HCC) accounts for over 85% of all primary liver cancers. The clinical management of advanced and metastatic HCC is challenging on many counts. Besides largely occurs within a background of underlying chronic liver disease and cirrhosis, HCC is a phenotypically and genetically heterogeneous polyclonal disease and resistant to most conventional chemotherapy. Early manifestation of HCC is characteristically slow growing with few symptoms, and HCC is therefore often diagnosed at an advanced stage when potentially curative surgical or local ablative therapy is not feasible. In this review, I have summarized my presentation at the recent HCC workshop at IARC, Lyon, on our knowledge generated from comprehensive molecular studies of primary liver cancer tissues and attempt to translate these results to gain molecular insights, especially on identification of biomarkers that could confer pathological and functional changes associated with the pathogenesis and progression of HCC, hoping to provide important molecular basis for the development of novel diagnosis and treatments to alter clinical outcomes of this disease.
原发性肝癌是全球第五大常见癌症,肝细胞癌(HCC)占所有原发性肝癌的85%以上。晚期和转移性HCC的临床管理在很多方面都具有挑战性。除了大多发生在潜在的慢性肝病和肝硬化背景下,HCC是一种表型和基因异质性的多克隆疾病,对大多数传统化疗耐药。HCC的早期表现特征是生长缓慢,症状较少,因此HCC常常在晚期才被诊断出来,此时潜在的根治性手术或局部消融治疗已不可行。在这篇综述中,我总结了我在近期于里昂国际癌症研究机构(IARC)举办的HCC研讨会上的发言内容,这些内容基于我们对原发性肝癌组织进行全面分子研究所获得的知识,并试图转化这些结果以获得分子层面的见解,尤其是关于识别那些可能导致与HCC发病机制和进展相关的病理和功能变化的生物标志物,希望为开发新的诊断方法和治疗手段以改变这种疾病的临床结局提供重要的分子基础。