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人类肝细胞癌肿瘤标志物的最新进展

Recent advances in tumor markers of human hepatocellular carcinoma.

作者信息

Yoon Seung Kew

机构信息

Department of Internal Medicine and WHO Collaborating Center for Reference and Research on Viral Hepatitis, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

出版信息

Intervirology. 2008;51 Suppl 1:34-41. doi: 10.1159/000122596. Epub 2008 Jun 10.

Abstract

Hepatocellular carcinoma (HCC) is one of the most devastating malignancies in the world and is the third most common cause of cancer-related death in Korea. Because most HCC are accompanied by chronic liver disease that results from hepatitis B or C viruses, prognosis is still poor even after surgical resection of the tumor. Moreover, diagnosis of advanced HCC still leads to an extremely bleak prognosis. Earlier detection of HCC, therefore, could improve patient survival. Accordingly, the development of tumor markers that can detect HCC at even earlier stages is essential. The functions of tumor markers include prediction of prognosis or therapeutic response as well as diagnosis or screening of cancer. Possible candidate tumor markers may be quantitative alterations in DNA-, RNA- or protein-based molecules in tumorous conditions assessed by various technologies, e.g. serological assays, microarrays, mass spectrometry and proteomics. However, validation and clinical implementation is needed after the discovery of novel genes. An ideal tumor marker for HCC would be sensitive and specific enabling to differentiate it at an early stage from premalignant lesions like dysplastic nodules. In addition, the marker should be easily measurable, reproducible and minimally invasive. Although it is important to identify new biomarkers for HCC, the validation and cost-effectiveness of those markers as diagnostic or prognostic tools need confirmation in large-scale studies in clinical practice.

摘要

肝细胞癌(HCC)是全球最具毁灭性的恶性肿瘤之一,在韩国是癌症相关死亡的第三大常见原因。由于大多数HCC都伴有由乙型或丙型肝炎病毒引起的慢性肝病,即使在肿瘤手术切除后预后仍然很差。此外,晚期HCC的诊断仍然导致极其黯淡的预后。因此,早期检测HCC可以提高患者生存率。相应地,开发能够在更早阶段检测HCC的肿瘤标志物至关重要。肿瘤标志物的功能包括预测预后或治疗反应以及癌症的诊断或筛查。可能的候选肿瘤标志物可能是通过各种技术(如血清学检测、微阵列、质谱和蛋白质组学)评估的肿瘤状态下基于DNA、RNA或蛋白质的分子的定量改变。然而,发现新基因后需要进行验证和临床应用。理想的HCC肿瘤标志物应敏感且特异,能够在早期将其与发育异常结节等癌前病变区分开来。此外,该标志物应易于测量、可重复且微创。虽然识别HCC的新生物标志物很重要,但这些标志物作为诊断或预后工具的验证和成本效益需要在临床实践的大规模研究中得到证实。

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