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Characterization of the epithelial cell adhesion molecule (EpCAM)^+ cell population in hepatocellular carcinoma cell lines
by
UENO Yoshiyuki
, ISHII Naoto
, FUKUSHIMA Koji
, KONDO Yasuteru
, KAKAZU Eiji
, INOUE Yuki
, TAKAHASHI Takeshi
, SHIINA Masaaki
, KIMURA Osamu
, YAMAGIWA Yoko
, INOUE Jun
, IWASAKI Takao
, KOGURE Takayuki
, KAWAGISHI Naoki
, SHIMOSEGAWA Tooru
, SUGAMURA Kazuo
in
Animals
/ Antigens, Neoplasm - analysis
/ Antigens, Neoplasm - chemistry
/ Antigens, Neoplasm - genetics
/ Antigens, Neoplasm - physiology
/ Biological and medical sciences
/ Carcinoma, Hepatocellular - chemistry
/ Carcinoma, Hepatocellular - pathology
/ Cell Adhesion Molecules - analysis
/ Cell Adhesion Molecules - chemistry
/ Cell Adhesion Molecules - genetics
/ Cell Adhesion Molecules - physiology
/ Cell Line, Tumor
/ Epithelial Cell Adhesion Molecule
/ Gastroenterology. Liver. Pancreas. Abdomen
/ Humans
/ Liver Neoplasms - chemistry
/ Liver Neoplasms - pathology
/ Liver. Biliary tract. Portal circulation. Exocrine pancreas
/ Medical sciences
/ Mice
/ Neoplastic Stem Cells - physiology
/ Original
/ Protein Structure, Tertiary
/ Tumors
2010
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Characterization of the epithelial cell adhesion molecule (EpCAM)^+ cell population in hepatocellular carcinoma cell lines
by
UENO Yoshiyuki
, ISHII Naoto
, FUKUSHIMA Koji
, KONDO Yasuteru
, KAKAZU Eiji
, INOUE Yuki
, TAKAHASHI Takeshi
, SHIINA Masaaki
, KIMURA Osamu
, YAMAGIWA Yoko
, INOUE Jun
, IWASAKI Takao
, KOGURE Takayuki
, KAWAGISHI Naoki
, SHIMOSEGAWA Tooru
, SUGAMURA Kazuo
in
Animals
/ Antigens, Neoplasm - analysis
/ Antigens, Neoplasm - chemistry
/ Antigens, Neoplasm - genetics
/ Antigens, Neoplasm - physiology
/ Biological and medical sciences
/ Carcinoma, Hepatocellular - chemistry
/ Carcinoma, Hepatocellular - pathology
/ Cell Adhesion Molecules - analysis
/ Cell Adhesion Molecules - chemistry
/ Cell Adhesion Molecules - genetics
/ Cell Adhesion Molecules - physiology
/ Cell Line, Tumor
/ Epithelial Cell Adhesion Molecule
/ Gastroenterology. Liver. Pancreas. Abdomen
/ Humans
/ Liver Neoplasms - chemistry
/ Liver Neoplasms - pathology
/ Liver. Biliary tract. Portal circulation. Exocrine pancreas
/ Medical sciences
/ Mice
/ Neoplastic Stem Cells - physiology
/ Original
/ Protein Structure, Tertiary
/ Tumors
2010
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Characterization of the epithelial cell adhesion molecule (EpCAM)^+ cell population in hepatocellular carcinoma cell lines
by
UENO Yoshiyuki
, ISHII Naoto
, FUKUSHIMA Koji
, KONDO Yasuteru
, KAKAZU Eiji
, INOUE Yuki
, TAKAHASHI Takeshi
, SHIINA Masaaki
, KIMURA Osamu
, YAMAGIWA Yoko
, INOUE Jun
, IWASAKI Takao
, KOGURE Takayuki
, KAWAGISHI Naoki
, SHIMOSEGAWA Tooru
, SUGAMURA Kazuo
in
Animals
/ Antigens, Neoplasm - analysis
/ Antigens, Neoplasm - chemistry
/ Antigens, Neoplasm - genetics
/ Antigens, Neoplasm - physiology
/ Biological and medical sciences
/ Carcinoma, Hepatocellular - chemistry
/ Carcinoma, Hepatocellular - pathology
/ Cell Adhesion Molecules - analysis
/ Cell Adhesion Molecules - chemistry
/ Cell Adhesion Molecules - genetics
/ Cell Adhesion Molecules - physiology
/ Cell Line, Tumor
/ Epithelial Cell Adhesion Molecule
/ Gastroenterology. Liver. Pancreas. Abdomen
/ Humans
/ Liver Neoplasms - chemistry
/ Liver Neoplasms - pathology
/ Liver. Biliary tract. Portal circulation. Exocrine pancreas
/ Medical sciences
/ Mice
/ Neoplastic Stem Cells - physiology
/ Original
/ Protein Structure, Tertiary
/ Tumors
2010
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Characterization of the epithelial cell adhesion molecule (EpCAM)^+ cell population in hepatocellular carcinoma cell lines
Journal Article
Characterization of the epithelial cell adhesion molecule (EpCAM)^+ cell population in hepatocellular carcinoma cell lines
2010
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Overview
Accumulating evidence suggests that cancer stem cells (CSC) play an important role in tumorigenicity. Epithelial cell adhesion molecule (EpCAM) is one of the markers that identifies tumor cells with high tumorigenicity. The expression of EpCAM in liver progenitor cells prompted us to investigate whether CSC could be identified in hepatocellular carcinoma (HCC) cell lines. The sorted EpCAM+ subpopulation from HCC cell lines showed a greater colony formation rate than the sorted EpCAM− subpopulation from the same cell lines, although cell proliferation was comparable between the two subpopulations. The in vivo evaluation of tumorigenicity, using supra‐immunodeficient NOD/scid/γcnull (NOG) mice, revealed that a smaller number of EpCAM+ cells (minimum 100) than EpCAM− cells was necessary for tumor formation. The bifurcated differentiation of EpCAM+ cell clones into both EpCAM+ and EpCAM− cells was obvious both in vitro and in vivo, but EpCAM− clones sustained their phenotype. These clonal analyses suggested that EpCAM+ cells may contain a multipotent cell population. Interestingly, the introduction of exogenous EpCAM into EpCAM+ clones, but not into EpCAM− clones, markedly enhanced their tumor‐forming ability, even though both transfectants expressed a similar level of EpCAM. Therefore, the difference in the tumor‐forming ability between EpCAM+ and EpCAM− cells is probably due to the intrinsic biological differences between them. Collectively, our results suggest that the EpCAM+ population is biologically quite different from the EpCAM− population in HCC cell lines, and preferentially contains a highly tumorigenic cell population with the characteristics of CSC. (Cancer Sci 2010)
Publisher
Blackwell Publishing Ltd,Blackwell
Subject
/ Antigens, Neoplasm - analysis
/ Antigens, Neoplasm - chemistry
/ Antigens, Neoplasm - genetics
/ Antigens, Neoplasm - physiology
/ Biological and medical sciences
/ Carcinoma, Hepatocellular - chemistry
/ Carcinoma, Hepatocellular - pathology
/ Cell Adhesion Molecules - analysis
/ Cell Adhesion Molecules - chemistry
/ Cell Adhesion Molecules - genetics
/ Cell Adhesion Molecules - physiology
/ Epithelial Cell Adhesion Molecule
/ Gastroenterology. Liver. Pancreas. Abdomen
/ Humans
/ Liver. Biliary tract. Portal circulation. Exocrine pancreas
/ Mice
/ Neoplastic Stem Cells - physiology
/ Original
/ Tumors
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