Isoform switch of CD44 induces different chemotactic and tumorigenic ability in gallbladder cancer

Keyphrases

• Cluster of Differentiation 44 (CD44) 100%
• Gallbladder Cancer 100%
• Isoform Switching 100%
• CD44v9 100%
• Epithelial-mesenchymal Transition 26%
• Tumorigenicity 26%
• Chemotaxis 26%
• Invasiveness 20%
• Poor Prognosis 13%
• Metastasis 13%
• Distant Metastasis 13%
• CD44 Isoforms 13%
• Tumor 6%
• E-cadherin 6%
• Tumor Growth 6%
• Transcription Factor 6%
• Immunohistochemical Analysis 6%
• Cancer Cell Lines 6%
• Tumor Metastasis 6%
• Cell Invasion Assay 6%
• Cell Migration Assays 6%
• In Vivo Mice 6%
• Xenotransplantation 6%
• Tissue Microarray 6%
• Vimentin 6%
• Epithelial Phenotype 6%
• Zinc Finger E-box Binding Homeobox 1 (ZEB1) 6%
• Poorly Differentiated Tumor 6%
• In Vitro Cells 6%
• Mesenchymal Phenotype 6%
• Splicing Factor 6%
• CD44 Expression 6%
• Variant Isoform 6%
• Gallbladder Cancer Cells 6%
• ZEB2 6%
• ESRP1 6%

Biochemistry, Genetics and Molecular Biology

• CD44 100%
• Isoform 100%
• Mesenchymal-Epithelial Transition 80%
• Chemotaxis 80%
• Cancer Cell 20%
• Cell Migration 20%
• Tumor Progression 20%
• Cell Invasion 20%
• Tissue Microarray 20%
• Vimentin 20%
• Splicing Factor 20%
• Transcription Factor ZEB1 20%
• ZEB2 20%
• Cadherin 20%

Immunology and Microbiology

• CD44 100%
• Gall Bladder 100%
• Epithelial Mesenchymal Transition 80%
• Chemotaxis 80%
• Cell Migration 20%
• Cell Invasion 20%
• Cadherin 20%
• Xenotransplantation 20%
• Gallbladder Cancer Cell Line 20%
• Transcription Factor ZEB1 20%