Understanding the Integrated Gene Regulatory Networks for Hepatocellular Carcinoma

Long Gao
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Abstract

Hepatic cancer is a malignant tumor that begins in the cells of the liver. The leading cause is a viral infection with hepatitis B and hepatitis C. Hepatocellular carcinoma (HCC) has become the most common form of hepatic cancer. It is the fastest-growing cause of cancer deaths in the United States. HCC is also found to be associated with obesity, type 2 diabetes and fatty liver disease. To understand the gene expression regulation during HCC development, scientists have identified a few related transcription factors (TFs) and characterize their roles such as E2F1[1], Foxm1b [2] and hepatic nuclear factors [3]. However, these findings still cannot fully explain the underlying molecular mechanism during liver tumorigenesis. It is necessary to systematically study the global gene regulatory network (GRN) during HCC development.
了解肝癌的整合基因调控网络
肝癌是一种恶性肿瘤,起源于肝脏细胞。主要原因是乙型肝炎和丙型肝炎的病毒感染。肝细胞癌(HCC)已成为最常见的肝癌形式。它是美国癌症死亡人数增长最快的原因。HCC还被发现与肥胖、2型糖尿病和脂肪肝疾病有关。为了了解HCC发展过程中的基因表达调控,科学家们确定了一些相关的转录因子(TFs),并表征了它们的作用,如E2F1[1]、Foxm1b[2]和肝核因子[3]。然而,这些发现仍不能完全解释肝脏肿瘤发生的潜在分子机制。有必要系统地研究HCC发展过程中的全球基因调控网络(GRN)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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