Lin Che-Pin, Liu Chien-Ru, Lee Chun-Nin, Chan Tze-Sian, Liu H Eugene
Che-Pin Lin, Chien-Ru Liu, Department of Medicine, Taipei City Hospital, Ren-Ai Branch, Taipei 106, Taiwan.
World J Hepatol. 2010 Jan 27;2(1):16-20. doi: 10.4254/wjh.v2.i1.16.
Hepatocelluar carcinoma (HCC) is the most lethal cancer in the world. Most HCC over-express c-Myc, which plays a critical role in regulating cellular growth, differentiation and apoptosis in both normal and neoplastic cells. c-Myc is among the most frequently overexpressed genes in human cancers. Overexpression of c-Myc in hepatic cells leads to development of hepatocellular carcinoma. Here, we review the current progress in understanding physiologic function and regulation of c-Myc as well as its role in hepatic carcinogenesis and discuss the association of c-Myc activation in chronic hepatitis B infection and the upregulation of HIF-1/VEGF. We also explore the possibility of treating HCC by inhibiting c-Myc and examine the pros and cons of such an approach. Although this strategy is currently not available in clinics, with recent advances in better drug design, pharmacokinetics and pharmacogenetics, inhibition of c-Myc might become a novel therapy for HCC in the future.
肝细胞癌(HCC)是全球致死率最高的癌症。大多数HCC过度表达c-Myc,c-Myc在正常细胞和肿瘤细胞中对调节细胞生长、分化及凋亡起着关键作用。c-Myc是人类癌症中最常过度表达的基因之一。肝细胞中c-Myc的过度表达会导致肝细胞癌的发生。在此,我们综述了目前在理解c-Myc的生理功能、调控及其在肝癌发生中的作用方面取得的进展,并讨论了慢性乙型肝炎感染中c-Myc激活与HIF-1/VEGF上调之间的关联。我们还探讨了通过抑制c-Myc治疗HCC的可能性,并审视了这种方法的利弊。尽管目前该策略尚未应用于临床,但随着药物设计、药代动力学和药物遗传学方面的最新进展,抑制c-Myc未来可能会成为治疗HCC的一种新疗法。