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Cellular and molecular mechanisms of hepatocellular carcinoma: an update
被引:185
|作者:
Aravalli, Rajagopal N.
[1
]
Cressman, Erik N. K.
[1
]
Steer, Clifford J.
[2
,3
]
机构:
[1] Univ Minnesota, Dept Radiol, Sch Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Med, Sch Med, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Genet Cell Biol & Dev, Sch Med, Minneapolis, MN 55455 USA
关键词:
Hepatocellular carcinoma;
Cancer stem cell;
Liver cancer;
Targeted therapy;
microRNA;
CANCER STEM-CELLS;
EPITHELIAL-MESENCHYMAL TRANSITION;
CHRONIC HEPATITIS-C;
MICRORNA REPLACEMENT THERAPY;
TUMOR-ASSOCIATED MACROPHAGES;
OXIDATIVE DNA-DAMAGE;
REGULATORY T-CELLS;
LIVER-CANCER;
UP-REGULATION;
BETA-CATENIN;
D O I:
10.1007/s00204-012-0931-2
中图分类号:
R99 [毒物学(毒理学)];
学科分类号:
100405 ;
摘要:
Hepatocellular carcinoma (HCC) is the most common primary malignant tumor that accounts for similar to 80 % of all liver cancer cases worldwide. It is a multifactorial disease caused by a variety of risk factors and often develops in the background of underlying cirrhosis. A number of cellular phenomena, such as tumor microenvironment, inflammation, oxidative stress, and hypoxia act in concert with various molecular events to facilitate tumor initiation, progression, and metastasis. The emergence of microRNAs and molecular-targeted therapies adds a new dimension in our efforts to combat this deadly disease. Intense research in this multitude of areas has led to significant progress in our understanding of cellular processes and molecular mechanisms that occur during multistage events that lead to hepatocarcinogenesis. In this review, we discuss the current knowledge of HCC, focusing mainly on advances that have occurred during the past 5 years and on the development of novel therapeutics for liver cancer.
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页码:227 / 247
页数:21
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