Published online Jul 7, 2018. doi: 10.3748/wjg.v24.i25.2647
Peer-review started: March 29, 2018
First decision: May 9, 2018
Revised: May 18, 2018
Accepted: June 16, 2018
Article in press: June 16, 2018
Published online: July 7, 2018
Processing time: 98 Days and 17.4 Hours
Hepatocellular carcinoma (HCC) is the most common primary liver malignant neoplasia. HCC is characterized by a poor prognosis. The need to find new molecular markers for its diagnosis and prognosis has led to a progressive increase in the number of scientific studies on this topic. MicroRNAs (miRNAs) are small non-coding RNA that play a role in almost all main cellular pathways. miRNAs are involved in the regulation of expression of the major tumor-related genes in carcinogenesis, acting as oncogenes or tumor suppressor genes. The aim of this review was to identify papers published in 2017 investigating the role of miRNAs in HCC tumorigenesis. miRNAs were classified according to their role in the main molecular pathways involved in HCC tumorigenesis: (1) mTOR; (2) Wnt; (3) JAK/STAT; (4) apoptosis; and (5) MAPK. The role of miRNAs in prognosis/response prediction was taken into consideration. Bearing in mind that the analysis of miRNAs in serum and other body fluids would be crucial for clinical management, the role of circulating miRNAs in HCC patients was also investigated. The most represented miRNA-regulated pathway in HCC is mTOR, but apoptosis, Wnt, JAK/STAT or MAPK pathways are also influenced by miRNA expression levels. These miRNAs could thus be used in clinical practice as diagnostic, prognostic or therapeutic targets for HCC treatment.
Core tip: Hepatocellular carcinoma (HCC) is the most common primary liver neoplasia and is characterized by a poor prognosis. MicroRNAs (miRNAs) are involved in the regulation of expression of the major tumor-related pathways in carcinogenesis and may act as oncogenes or tumor suppressor genes. mTOR is the most represented miRNA-regulated pathway in HCC. miRNAs found to be deregulated in HCC could be used in clinical practice as diagnostic, prognostic or therapeutic targets.