| Literature DB >> 27900050 |
Yoshikuni Inokawa1, Kenichi Inaoka1, Fuminori Sonohara1, Masamichi Hayashi2, Mitsuro Kanda2, Shuji Nomoto1.
Abstract
Although hepatocellular carcinoma (HCC) is associated with poor prognosis worldwide, the molecular mechanisms underlying the carcinogenesis and progression of this disease remain unclear. Several tumor characteristics have previously been demonstrated to be prognostic factors of survival following hepatic resection, or the recurrence of HCC or other types of cancer. Comparisons of normal tissues and HCC tumor tissues have revealed the presence of numerous molecular alterations in HCC, including genetic and epigenetic mechanisms, particularly mutations in certain genes and DNA methylation in the promoter regions of tumor-suppressor genes. A number of studies have previously used array analysis to detect variations in the expression levels of cancer-associated genes and microRNAs, and in DNA methylation. However, an investigation of HCC tumor tissues may not determine the effect of noncancerous liver tissues (background liver) in patients with HCC. As HCC may recur multicentrically following resection, a damaged or chronically diseased HCC background liver may be considered as a pre-cancerous organ. Therefore, the influence of the background liver on HCC requires further study. Detailed studies regarding the background liver may be essential for the improved understanding of the carcinogenesis and progression of this malignancy; however only a few studies have investigated the microenvironment of the HCC background liver. The present review discusses prior molecular studies of hepatocarcinogenesis that focus on HCC and background liver tissues.Entities:
Keywords: background liver factors; hepatocellular carcinoma; intrahepatic metastases; molecular alterations; multicentric occurrence
Year: 2016 PMID: 27900050 PMCID: PMC5104146 DOI: 10.3892/ol.2016.5141
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967