TY - CHAP
T1 - Hepatic Stellate Cells in Liver Tumor
AU - Shiraha, Hidenori
AU - Iwamuro, Masaya
AU - Okada, Hiroyuki
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Hepatocellular carcinoma and intrahepatic cholangiocarcinoma are the most common types of primary liver cancers. Moreover, the liver is the second most frequently involved organ in cancer metastasis after lymph nodes. The tumor microenvironment is crucial for the development of both primary and secondary liver cancers. The hepatic microenvironment consists of multiple cell types, including liver sinusoidal endothelial cells, Kupffer cells, natural killer cells, liver-associated lymphocytes, and hepatic stellate cells (HSCs). The microenvironment of a normal liver changes to a tumor microenvironment when tumor cells exist or tumor cells migrate to and multiply in the liver. Interactions between tumor cells and non-transformed cells generate a tumor microenvironment that contributes significantly to tumor progression. HSCs play a central role in the tumor microenvironment crosstalk. As this crosstalk is crucial for liver carcinogenesis and liver-tumor development, elucidating the mechanism underlying the interaction of HSCs with the tumor microenvironment could provide potential therapeutic targets for liver cancer.
AB - Hepatocellular carcinoma and intrahepatic cholangiocarcinoma are the most common types of primary liver cancers. Moreover, the liver is the second most frequently involved organ in cancer metastasis after lymph nodes. The tumor microenvironment is crucial for the development of both primary and secondary liver cancers. The hepatic microenvironment consists of multiple cell types, including liver sinusoidal endothelial cells, Kupffer cells, natural killer cells, liver-associated lymphocytes, and hepatic stellate cells (HSCs). The microenvironment of a normal liver changes to a tumor microenvironment when tumor cells exist or tumor cells migrate to and multiply in the liver. Interactions between tumor cells and non-transformed cells generate a tumor microenvironment that contributes significantly to tumor progression. HSCs play a central role in the tumor microenvironment crosstalk. As this crosstalk is crucial for liver carcinogenesis and liver-tumor development, elucidating the mechanism underlying the interaction of HSCs with the tumor microenvironment could provide potential therapeutic targets for liver cancer.
KW - Angiogenesis
KW - Cancer-associated fibroblast
KW - Epithelial-mesenchymal transition
KW - Extracellular matrix
KW - Fibroblast activation protein
KW - Jagged-1
KW - Matrix metalloproteinase
KW - Myofibroblast
KW - Platelet-derived growth factor
KW - Stromal cell-derived factor-1
KW - Transforming growth factor-β
KW - Tumor stroma
KW - Tumor-associated macrophages
KW - Tumor-infiltrating leukocyte
KW - Vascular endothelial growth factor
UR - http://www.scopus.com/inward/record.url?scp=85079235940&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85079235940&partnerID=8YFLogxK
U2 - 10.1007/978-3-030-37184-5_4
DO - 10.1007/978-3-030-37184-5_4
M3 - Chapter
C2 - 32040854
AN - SCOPUS:85079235940
T3 - Advances in Experimental Medicine and Biology
SP - 43
EP - 56
BT - Advances in Experimental Medicine and Biology
PB - Springer
ER -