TY - JOUR
T1 - Mechanisms of hepatocellular carcinoma progression
AU - Ogunwobi, Olorunseun O.
AU - Harricharran, Trisheena
AU - Huaman, Jeannette
AU - Galuza, Anna
AU - Odumuwagun, Oluwatoyin
AU - Tan, Yin
AU - Ma, Grace X.
AU - Nguyen, Minhhuyen T.
N1 - Publisher Copyright:
© 2019 Baishideng Publishing Group Inc. All rights reserved.
PY - 2019
Y1 - 2019
N2 - Hepatocellular carcinoma (HCC) is the most common primary malignancy of the liver. It is the second leading cause of cancer-related deaths worldwide, with a very poor prognosis. In the United States, there has been only minimal improvement in the prognosis for HCC patients over the past 15 years. Details of the molecular mechanisms and other mechanisms of HCC progression remain unclear. Consequently, there is an urgent need for better understanding of these mechanisms. HCC is often diagnosed at advanced stages, and most patients will therefore need systemic therapy, with sorafenib being the most common at the present time. However, sorafenib therapy only minimally enhances patient survival. This review provides a summary of some of the known mechanisms that either cause HCC or contribute to its progression. Included in this review are the roles of viral hepatitis, non-viral hepatitis, chronic alcohol intake, genetic predisposition and congenital abnormalities, toxic exposures, and autoimmune diseases of the liver. Well-established molecular mechanisms of HCC progression such as epithelial-mesenchymal transition, tumor-stromal interactions and the tumor microenvironment, cancer stem cells, and senescence bypass are also discussed. Additionally, we discuss the roles of circulating tumor cells, immunomodulation, and neural regulation as potential new mechanisms of HCC progression. A better understanding of these mechanisms could have implications for the development of novel and more effective therapeutic and prognostic strategies, which are critically needed.
AB - Hepatocellular carcinoma (HCC) is the most common primary malignancy of the liver. It is the second leading cause of cancer-related deaths worldwide, with a very poor prognosis. In the United States, there has been only minimal improvement in the prognosis for HCC patients over the past 15 years. Details of the molecular mechanisms and other mechanisms of HCC progression remain unclear. Consequently, there is an urgent need for better understanding of these mechanisms. HCC is often diagnosed at advanced stages, and most patients will therefore need systemic therapy, with sorafenib being the most common at the present time. However, sorafenib therapy only minimally enhances patient survival. This review provides a summary of some of the known mechanisms that either cause HCC or contribute to its progression. Included in this review are the roles of viral hepatitis, non-viral hepatitis, chronic alcohol intake, genetic predisposition and congenital abnormalities, toxic exposures, and autoimmune diseases of the liver. Well-established molecular mechanisms of HCC progression such as epithelial-mesenchymal transition, tumor-stromal interactions and the tumor microenvironment, cancer stem cells, and senescence bypass are also discussed. Additionally, we discuss the roles of circulating tumor cells, immunomodulation, and neural regulation as potential new mechanisms of HCC progression. A better understanding of these mechanisms could have implications for the development of novel and more effective therapeutic and prognostic strategies, which are critically needed.
KW - Alcohol consumption
KW - Cancer stem cells
KW - Circulating tumor cells
KW - Epithelial-mesenchymal transition
KW - Hepatocellular carcinoma
KW - Immunomodulation
KW - Neural regulation
KW - Tumor microenvironment
KW - Tumor-stromal interactions
KW - Viral/non-viral hepatitis
UR - http://www.scopus.com/inward/record.url?scp=85065882494&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000468329900002&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.3748/wjg.v25.i19.2279
DO - 10.3748/wjg.v25.i19.2279
M3 - Review article
C2 - 31148900
SN - 1007-9327
VL - 25
SP - 2279
EP - 2293
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 19
ER -