Molecular Biology of the Cell, ISSN 1059-1524, 09/2007, Volume 18, Issue 9, pp. 3533 - 3544
Epithelial-mesenchymal transition (EMT), a crucial event in cancer progression and embryonic development, is induced by transforming growth factor (TGF)-beta...
GROWTH-FACTOR-BETA | CELL-MEMBRANE | SMAD PROTEINS | ZEB PROTEINS | E-CADHERIN | TRANSCRIPTIONAL REGULATION | CANCER | PROGRESSION | TRANSDIFFERENTIATION | SNAIL | CELL BIOLOGY
GROWTH-FACTOR-BETA | CELL-MEMBRANE | SMAD PROTEINS | ZEB PROTEINS | E-CADHERIN | TRANSCRIPTIONAL REGULATION | CANCER | PROGRESSION | TRANSDIFFERENTIATION | SNAIL | CELL BIOLOGY
Journal Article
Developmental Cell, ISSN 1534-5807, 2006, Volume 11, Issue 1, pp. 93 - 104
Alteration in the differentiated state of smooth muscle cells (SMCs) is known to be integral to vascular development and the pathogenesis of vascular disease....
DNA | DEVBIO | SIGNALING | ZINC-FINGER | TRANSCRIPTION | BINDING PROTEIN DELTA-EF1 | SERUM RESPONSE FACTOR | GENE-EXPRESSION | ZEB PROTEINS | ENHANCER | MICE | DEVELOPMENTAL BIOLOGY | MYOFIBROBLAST DIFFERENTIATION | CARG ELEMENTS | CELL BIOLOGY
DNA | DEVBIO | SIGNALING | ZINC-FINGER | TRANSCRIPTION | BINDING PROTEIN DELTA-EF1 | SERUM RESPONSE FACTOR | GENE-EXPRESSION | ZEB PROTEINS | ENHANCER | MICE | DEVELOPMENTAL BIOLOGY | MYOFIBROBLAST DIFFERENTIATION | CARG ELEMENTS | CELL BIOLOGY
Journal Article
Oncogene, ISSN 0950-9232, 10/2007, Volume 26, Issue 49, pp. 6979 - 6988
Epithelial to mesenchymal transition (EMT) is implicated in the progression of primary tumours towards metastasis andis likely caused by a pathological...
Epithelial to mesenchymal transition | Transcription | Epithelial polarity | Invasion | Cell adhesion | epithelial polarity | DIFFERENTIATION PROGRAM | transcription | FACTOR SNAIL | BIOCHEMISTRY & MOLECULAR BIOLOGY | E-CADHERIN EXPRESSION | VITAMIN-D-RECEPTOR | BETA-CATENIN | CELL BIOLOGY | BREAST-CANCER | COLON-CANCER | LUNG-CANCER | invasion | ONCOLOGY | cell adhesion | MESENCHYMAL TRANSITIONS | GENETICS & HEREDITY | epithelial to mesenchymal transition | PROGRESSION | Cell Polarity | Colonic Neoplasms - genetics | Nucleoside-Phosphate Kinase - genetics | Cadherins - metabolism | Cytoskeletal Proteins - antagonists & inhibitors | Membrane Glycoproteins - metabolism | Oligonucleotide Array Sequence Analysis | Cytoskeletal Proteins - genetics | Homeodomain Proteins - metabolism | Humans | Middle Aged | Immunoblotting | Gene Expression Profiling | Colonic Neoplasms - metabolism | Breast Neoplasms - metabolism | Membrane Glycoproteins - antagonists & inhibitors | Chromatin Immunoprecipitation | Neoplasm Invasiveness - pathology | Adult | Cytoskeletal Proteins - metabolism | Cell Differentiation | Membrane Proteins - metabolism | Tumor Cells, Cultured | Snail Family Transcription Factors | Promoter Regions, Genetic | Epithelium - pathology | Epithelium - metabolism | Membrane Proteins - genetics | Down-Regulation | Nucleoside-Phosphate Kinase - antagonists & inhibitors | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Disease Progression | Homeodomain Proteins - genetics | Membrane Glycoproteins - genetics | Transcription Factors - metabolism | Breast Neoplasms - genetics | Membrane Proteins - antagonists & inhibitors | Breast Neoplasms - pathology | Colonic Neoplasms - pathology | Aged | Microscopy, Fluorescence | Nucleoside-Phosphate Kinase - metabolism | Zinc Finger E-box-Binding Homeobox 1 | Cancer cells | Physiological aspects | Genetic aspects | Research | DNA binding proteins | Health aspects | Proteins | Oncology | Gene expression | Colorectal cancer | Cell adhesion & migration | Tumors
Epithelial to mesenchymal transition | Transcription | Epithelial polarity | Invasion | Cell adhesion | epithelial polarity | DIFFERENTIATION PROGRAM | transcription | FACTOR SNAIL | BIOCHEMISTRY & MOLECULAR BIOLOGY | E-CADHERIN EXPRESSION | VITAMIN-D-RECEPTOR | BETA-CATENIN | CELL BIOLOGY | BREAST-CANCER | COLON-CANCER | LUNG-CANCER | invasion | ONCOLOGY | cell adhesion | MESENCHYMAL TRANSITIONS | GENETICS & HEREDITY | epithelial to mesenchymal transition | PROGRESSION | Cell Polarity | Colonic Neoplasms - genetics | Nucleoside-Phosphate Kinase - genetics | Cadherins - metabolism | Cytoskeletal Proteins - antagonists & inhibitors | Membrane Glycoproteins - metabolism | Oligonucleotide Array Sequence Analysis | Cytoskeletal Proteins - genetics | Homeodomain Proteins - metabolism | Humans | Middle Aged | Immunoblotting | Gene Expression Profiling | Colonic Neoplasms - metabolism | Breast Neoplasms - metabolism | Membrane Glycoproteins - antagonists & inhibitors | Chromatin Immunoprecipitation | Neoplasm Invasiveness - pathology | Adult | Cytoskeletal Proteins - metabolism | Cell Differentiation | Membrane Proteins - metabolism | Tumor Cells, Cultured | Snail Family Transcription Factors | Promoter Regions, Genetic | Epithelium - pathology | Epithelium - metabolism | Membrane Proteins - genetics | Down-Regulation | Nucleoside-Phosphate Kinase - antagonists & inhibitors | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Disease Progression | Homeodomain Proteins - genetics | Membrane Glycoproteins - genetics | Transcription Factors - metabolism | Breast Neoplasms - genetics | Membrane Proteins - antagonists & inhibitors | Breast Neoplasms - pathology | Colonic Neoplasms - pathology | Aged | Microscopy, Fluorescence | Nucleoside-Phosphate Kinase - metabolism | Zinc Finger E-box-Binding Homeobox 1 | Cancer cells | Physiological aspects | Genetic aspects | Research | DNA binding proteins | Health aspects | Proteins | Oncology | Gene expression | Colorectal cancer | Cell adhesion & migration | Tumors
Journal Article
FEBS JOURNAL, ISSN 1742-464X, 05/2016, Volume 283, Issue 9, pp. 1767 - 1781
The objective of this study was to determine the role of transforming growth factor beta 1 (TGF-beta 1) in transcriptional regulation and function of the...
TGF-BETA | ATRIAL-NATRIURETIC-PEPTIDE | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOWN-REGULATION | chromatin immunoprecipitation | EPITHELIAL-MESENCHYMAL TRANSITION | particulate guanylyl cyclase A | CARDIAC FIBROBLASTS | MESANGIAL CELLS | Smad | SMOOTH-MUSCLE-CELLS | EXTRACELLULAR-MATRIX | A GENE | atrial natriuretic peptide | gene expression
TGF-BETA | ATRIAL-NATRIURETIC-PEPTIDE | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOWN-REGULATION | chromatin immunoprecipitation | EPITHELIAL-MESENCHYMAL TRANSITION | particulate guanylyl cyclase A | CARDIAC FIBROBLASTS | MESANGIAL CELLS | Smad | SMOOTH-MUSCLE-CELLS | EXTRACELLULAR-MATRIX | A GENE | atrial natriuretic peptide | gene expression
Journal Article
The FEBS Journal, ISSN 1742-464X, 05/2016, Volume 283, Issue 9, p. 1767
The objective of this study was to determine the role of transforming growth factor [beta]1 (TGF-[beta]1) in transcriptional regulation and function of the...
Enzymes | Smooth muscle | Peptides | Cellular biology | Growth factors | Rodents | Phosphorylation | Smad protein | Collagen (type I) | Gene regulation | Homeostasis | Atrial natriuretic peptide | Gene deletion | Remodeling | Blood | Deltas | Signal transduction | Control | Pathways | Clonal deletion | Protein folding | Actin | Deletion | Mesangial cells | Aorta | Attenuation | Blood pressure | Crystal structure | Binding | Kidneys | Thorax | Gene silencing | Overexpression | Crystallin | Mutagenesis | Site-directed mutagenesis
Enzymes | Smooth muscle | Peptides | Cellular biology | Growth factors | Rodents | Phosphorylation | Smad protein | Collagen (type I) | Gene regulation | Homeostasis | Atrial natriuretic peptide | Gene deletion | Remodeling | Blood | Deltas | Signal transduction | Control | Pathways | Clonal deletion | Protein folding | Actin | Deletion | Mesangial cells | Aorta | Attenuation | Blood pressure | Crystal structure | Binding | Kidneys | Thorax | Gene silencing | Overexpression | Crystallin | Mutagenesis | Site-directed mutagenesis
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2012, Volume 7, Issue 12, p. e52380
Resistance to tamoxifen therapy represents a major barrier to the successful treatment of breast cancer, where a loss of or reduced ER-alpha level is...
CELLS | GENE | PROTEIN DELTA-EF1 | MULTIDISCIPLINARY SCIENCES | ESTROGEN-RECEPTOR-ALPHA | ZINC-FINGER | TRANSCRIPTION FACTOR ZEB1 | ENDOCRINE THERAPY RESISTANCE | MECHANISMS | E-CADHERIN | MESENCHYMAL TRANSITION | Transcription, Genetic - drug effects | Homeodomain Proteins - metabolism | Humans | NF-kappa B - metabolism | Phosphatidylinositol 3-Kinases - metabolism | Down-Regulation - drug effects | Breast Neoplasms - drug therapy | Down-Regulation - genetics | Transcription Factors - metabolism | Up-Regulation - drug effects | Breast Neoplasms - enzymology | Breast Neoplasms - genetics | Estrogen Receptor alpha - genetics | MCF-7 Cells | Signal Transduction - drug effects | Breast Neoplasms - pathology | Tamoxifen - pharmacology | Estrogen Receptor alpha - metabolism | Female | Gene Expression Regulation, Neoplastic - drug effects | Estradiol - pharmacology | Drug Resistance, Neoplasm - drug effects | Zinc Finger E-box-Binding Homeobox 1 | NF-κB protein | Immunoglobulins | Transcription factors | Transcription | RNA-mediated interference | Estrogen | Estrogen receptors | Endocrine therapy | 17β-Estradiol | Breast cancer | Kinases | Tamoxifen | Gene expression | 1-Phosphatidylinositol 3-kinase | Sex hormones | Sensitivity | Ribonucleic acids | Mutagenesis | Breast | Cancer | Tumors
CELLS | GENE | PROTEIN DELTA-EF1 | MULTIDISCIPLINARY SCIENCES | ESTROGEN-RECEPTOR-ALPHA | ZINC-FINGER | TRANSCRIPTION FACTOR ZEB1 | ENDOCRINE THERAPY RESISTANCE | MECHANISMS | E-CADHERIN | MESENCHYMAL TRANSITION | Transcription, Genetic - drug effects | Homeodomain Proteins - metabolism | Humans | NF-kappa B - metabolism | Phosphatidylinositol 3-Kinases - metabolism | Down-Regulation - drug effects | Breast Neoplasms - drug therapy | Down-Regulation - genetics | Transcription Factors - metabolism | Up-Regulation - drug effects | Breast Neoplasms - enzymology | Breast Neoplasms - genetics | Estrogen Receptor alpha - genetics | MCF-7 Cells | Signal Transduction - drug effects | Breast Neoplasms - pathology | Tamoxifen - pharmacology | Estrogen Receptor alpha - metabolism | Female | Gene Expression Regulation, Neoplastic - drug effects | Estradiol - pharmacology | Drug Resistance, Neoplasm - drug effects | Zinc Finger E-box-Binding Homeobox 1 | NF-κB protein | Immunoglobulins | Transcription factors | Transcription | RNA-mediated interference | Estrogen | Estrogen receptors | Endocrine therapy | 17β-Estradiol | Breast cancer | Kinases | Tamoxifen | Gene expression | 1-Phosphatidylinositol 3-kinase | Sex hormones | Sensitivity | Ribonucleic acids | Mutagenesis | Breast | Cancer | Tumors
Journal Article
FEBS Letters, ISSN 0014-5793, 01/2016, Volume 590, Issue 2, pp. 270 - 278
The epithelial–mesenchymal transition (EMT) is associated with tumor progression. We reported previously that expression of the δEF1 family proteins (δEF1/ZEB1...
epithelial–mesenchymal transition | δEF1 | smad‐interacting protein 1 | regulator of G‐protein signaling 16 | δEF1 family proteins | smad-interacting protein 1 | epithelial-mesenchymal transition | regulator of G-protein signaling 16 | CANCER-CELLS | delta EF1 | TGF-BETA | TUMOR PROGRESSION | RGS16 | BIOCHEMISTRY & MOLECULAR BIOLOGY | MARKERS | LINES | CELL BIOLOGY | BIOPHYSICS | delta EF1 family proteins | GROWTH | Repressor Proteins - physiology | Transcription Factors - physiology | Breast Neoplasms - pathology | Epithelial-Mesenchymal Transition - physiology | Humans | Cell Line, Tumor | RGS Proteins - physiology | Homeodomain Proteins - physiology | Zinc Finger E-box Binding Homeobox 2 | Cell Movement - physiology | Zinc Finger E-box-Binding Homeobox 1 | Research Letters | Research Letter
epithelial–mesenchymal transition | δEF1 | smad‐interacting protein 1 | regulator of G‐protein signaling 16 | δEF1 family proteins | smad-interacting protein 1 | epithelial-mesenchymal transition | regulator of G-protein signaling 16 | CANCER-CELLS | delta EF1 | TGF-BETA | TUMOR PROGRESSION | RGS16 | BIOCHEMISTRY & MOLECULAR BIOLOGY | MARKERS | LINES | CELL BIOLOGY | BIOPHYSICS | delta EF1 family proteins | GROWTH | Repressor Proteins - physiology | Transcription Factors - physiology | Breast Neoplasms - pathology | Epithelial-Mesenchymal Transition - physiology | Humans | Cell Line, Tumor | RGS Proteins - physiology | Homeodomain Proteins - physiology | Zinc Finger E-box Binding Homeobox 2 | Cell Movement - physiology | Zinc Finger E-box-Binding Homeobox 1 | Research Letters | Research Letter
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 2014, Volume 55, Issue 8, pp. 5445 - 5455
PURPOSE. Posterior capsular opacification (PCO), the most prevalent side effect of cataract surgery, occurs when residual lens epithelial cells (LECs) undergo...
lens regeneration | ZINC-FINGER | MESENCHYMAL TRANSITION | cataract surgery | epithelial-to-mesenchymal transition | mouse disease model | Zeb | posterior capsular opacification | CHICKEN | OPHTHALMOLOGY | MOUSE LENS | POSTERIOR CAPSULE OPACIFICATION | DIFFERENTIATION | BETA-CRYSTALLIN | DUAL ROLES | EXPRESSION | TRANSCRIPTIONAL REPRESSOR | Nerve Tissue Proteins - physiology | Transcription Factors - physiology | Animals | Cataract - pathology | Cataract Extraction - adverse effects | Lens, Crystalline - metabolism | Cataract - metabolism | Homeodomain Proteins - physiology | RNA, Messenger - metabolism | Postoperative Complications | Disease Models, Animal | Mice, Knockout
lens regeneration | ZINC-FINGER | MESENCHYMAL TRANSITION | cataract surgery | epithelial-to-mesenchymal transition | mouse disease model | Zeb | posterior capsular opacification | CHICKEN | OPHTHALMOLOGY | MOUSE LENS | POSTERIOR CAPSULE OPACIFICATION | DIFFERENTIATION | BETA-CRYSTALLIN | DUAL ROLES | EXPRESSION | TRANSCRIPTIONAL REPRESSOR | Nerve Tissue Proteins - physiology | Transcription Factors - physiology | Animals | Cataract - pathology | Cataract Extraction - adverse effects | Lens, Crystalline - metabolism | Cataract - metabolism | Homeodomain Proteins - physiology | RNA, Messenger - metabolism | Postoperative Complications | Disease Models, Animal | Mice, Knockout
Journal Article
Cancer Medicine, ISSN 2045-7634, 01/2015, Volume 4, Issue 1, pp. 125 - 135
Abnormal DNA methylation at the C‐5 position of cytosine (5mC) of CpG dinucleotides is a well‐known epigenetic feature of cancer. Levels of E‐cadherin, which...
DNA methylation | δEF1 | EMT | E‐cadherin | Cancer cells | E-cadherin | EPITHELIAL-MESENCHYMAL TRANSITION | COMPLEX | delta EF1 | ONCOLOGY | BINDING | LINES | RNA, Small Interfering - genetics | RNA-Binding Proteins - genetics | Cadherins - metabolism | Homeodomain Proteins - metabolism | Humans | Gene Expression Regulation, Neoplastic | Gene Expression Profiling | Breast Neoplasms - metabolism | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA Methylation | RNA Interference | Female | Cadherins - genetics | Promoter Regions, Genetic | DNA (Cytosine-5-)-Methyltransferase 1 | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Breast Neoplasms - genetics | Cell Line, Tumor | CpG Islands | Protein Binding | RNA-Binding Proteins - metabolism | Zinc Finger E-box-Binding Homeobox 1 | Smad protein | Immunoglobulins | Mesenchyme | DNMT1 protein | Breast cancer | Metastasis | Gene expression | Proteins | Gene silencing | Plasmids | Epigenetics | DNA methyltransferase | Cytosine | Scientific imaging | Deoxyribonucleic acid--DNA | CpG islands | Tumors | Cancer Biology
DNA methylation | δEF1 | EMT | E‐cadherin | Cancer cells | E-cadherin | EPITHELIAL-MESENCHYMAL TRANSITION | COMPLEX | delta EF1 | ONCOLOGY | BINDING | LINES | RNA, Small Interfering - genetics | RNA-Binding Proteins - genetics | Cadherins - metabolism | Homeodomain Proteins - metabolism | Humans | Gene Expression Regulation, Neoplastic | Gene Expression Profiling | Breast Neoplasms - metabolism | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA Methylation | RNA Interference | Female | Cadherins - genetics | Promoter Regions, Genetic | DNA (Cytosine-5-)-Methyltransferase 1 | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Breast Neoplasms - genetics | Cell Line, Tumor | CpG Islands | Protein Binding | RNA-Binding Proteins - metabolism | Zinc Finger E-box-Binding Homeobox 1 | Smad protein | Immunoglobulins | Mesenchyme | DNMT1 protein | Breast cancer | Metastasis | Gene expression | Proteins | Gene silencing | Plasmids | Epigenetics | DNA methyltransferase | Cytosine | Scientific imaging | Deoxyribonucleic acid--DNA | CpG islands | Tumors | Cancer Biology
Journal Article
DEVELOPMENT GROWTH & DIFFERENTIATION, ISSN 0012-1592, 02/2016, Volume 58, Issue 2, pp. 205 - 214
The vertebrate Zfhx1 transcription factor family comprises EF1 and Sip1, which bind to CACCT-containing sequences and act as transcriptional repressors. It has...
SYSTEM | COMPLEX | shRNA-mediated knockdown | ZINC-FINGER | TRANSCRIPTION | BINDING PROTEIN DELTA-EF1 | DEVELOPMENTAL BIOLOGY | GENETIC INTERACTION | E-CADHERIN | MOUSE EMBRYO | CELL BIOLOGY | Zfhx1 transcription factors | chicken neural crest | REPRESSOR | ZFHX1B | Sox10
SYSTEM | COMPLEX | shRNA-mediated knockdown | ZINC-FINGER | TRANSCRIPTION | BINDING PROTEIN DELTA-EF1 | DEVELOPMENTAL BIOLOGY | GENETIC INTERACTION | E-CADHERIN | MOUSE EMBRYO | CELL BIOLOGY | Zfhx1 transcription factors | chicken neural crest | REPRESSOR | ZFHX1B | Sox10
Journal Article
Oncogene, ISSN 0950-9232, 11/2005, Volume 24, Issue 49, pp. 7273 - 7280
The discovery of two new p53 homologs, p73 and p63, has defined a family of transcription factors heavily involved in the control of growth suppression,...
p63 | p73 | δEF1 transcriptional repressor | p53 family | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | KERATINOCYTES | PROLIFERATION | HOMOLOG | DROSOPHILA ZFH-1 | CELL BIOLOGY | REGULATOR | ONCOLOGY | GENETICS & HEREDITY | delta EF1 transcriptional repressor | PROTEINS | EXPRESSION
p63 | p73 | δEF1 transcriptional repressor | p53 family | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | KERATINOCYTES | PROLIFERATION | HOMOLOG | DROSOPHILA ZFH-1 | CELL BIOLOGY | REGULATOR | ONCOLOGY | GENETICS & HEREDITY | delta EF1 transcriptional repressor | PROTEINS | EXPRESSION
Journal Article
BBA - Gene Regulatory Mechanisms, ISSN 1874-9399, 2011, Volume 1809, Issue 3, pp. 200 - 210
Breast cancer metastasis is supposed to involve several stages in which epithelial–mesenchymal transition (EMT) is regarded as the mechanistic basis for the...
Bone metastasis | Breast cancer | δEF1 | MMP-1 | AP-1 | delta EF1 | DUAL MECHANISM | TGF-BETA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | LINES | BIOPHYSICS | GENE | MATRIX METALLOPROTEINASE-1 | PROSTATE-CANCER | BONE MORPHOGENETIC PROTEIN-6 | TRANSCRIPTIONAL REGULATION | Transcription factors | Regulatory sequences | Matrix metalloproteinase | Osteolysis | Metastases | Signal transduction | Bone growth | Mineralization | Growth factors | c-Fos protein | Interstitial collagenase | Bone remodelling | Secretion | Activator protein 1 | c-Jun protein | MAP kinase | Gene expression | Promoters | Zinc | Bone cancer | Osteoblastogenesis | Osteoclasts | Microenvironments | Tumors
Bone metastasis | Breast cancer | δEF1 | MMP-1 | AP-1 | delta EF1 | DUAL MECHANISM | TGF-BETA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | LINES | BIOPHYSICS | GENE | MATRIX METALLOPROTEINASE-1 | PROSTATE-CANCER | BONE MORPHOGENETIC PROTEIN-6 | TRANSCRIPTIONAL REGULATION | Transcription factors | Regulatory sequences | Matrix metalloproteinase | Osteolysis | Metastases | Signal transduction | Bone growth | Mineralization | Growth factors | c-Fos protein | Interstitial collagenase | Bone remodelling | Secretion | Activator protein 1 | c-Jun protein | MAP kinase | Gene expression | Promoters | Zinc | Bone cancer | Osteoblastogenesis | Osteoclasts | Microenvironments | Tumors
Journal Article
Journal of Immunology, ISSN 0022-1767, 03/2006, Volume 176, Issue 5, pp. 2711 - 2721
Forkhead transcription factors regulate many aspects of lymphocyte development and function. The FOXO subgroup of Forkhead factors opposes proliferation and...
TRANSFORMATION | ZEB | FACTOR FKHR | CELL-CYCLE | PROLIFERATION | MICE | DIFFERENTIATION | IMMUNOLOGY | FORKHEAD | PHOSPHOINOSITIDE 3-KINASE | EXPRESSION | Up-Regulation | Protein Binding - genetics | Homeodomain Proteins - metabolism | Cyclins - genetics | Cercopithecus aethiops | Molecular Sequence Data | Forkhead Transcription Factors - physiology | RNA, Messenger - metabolism | Cyclins - metabolism | Retinoblastoma-Like Protein p130 - metabolism | Base Sequence | Genes, Tumor Suppressor - physiology | Tumor Suppressor Proteins - genetics | B-Lymphocytes - metabolism | Promoter Regions, Genetic | Cyclin G2 | Transcription Factors - physiology | Tumor Suppressor Proteins - metabolism | Gene Expression Regulation - immunology | Down-Regulation | Protein Binding - immunology | Transcription Factors - metabolism | Animals | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Homeodomain Proteins - physiology | COS Cells | Retinoblastoma-Like Protein p130 - genetics
TRANSFORMATION | ZEB | FACTOR FKHR | CELL-CYCLE | PROLIFERATION | MICE | DIFFERENTIATION | IMMUNOLOGY | FORKHEAD | PHOSPHOINOSITIDE 3-KINASE | EXPRESSION | Up-Regulation | Protein Binding - genetics | Homeodomain Proteins - metabolism | Cyclins - genetics | Cercopithecus aethiops | Molecular Sequence Data | Forkhead Transcription Factors - physiology | RNA, Messenger - metabolism | Cyclins - metabolism | Retinoblastoma-Like Protein p130 - metabolism | Base Sequence | Genes, Tumor Suppressor - physiology | Tumor Suppressor Proteins - genetics | B-Lymphocytes - metabolism | Promoter Regions, Genetic | Cyclin G2 | Transcription Factors - physiology | Tumor Suppressor Proteins - metabolism | Gene Expression Regulation - immunology | Down-Regulation | Protein Binding - immunology | Transcription Factors - metabolism | Animals | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Homeodomain Proteins - physiology | COS Cells | Retinoblastoma-Like Protein p130 - genetics
Journal Article
Developmental Dynamics, ISSN 1058-8388, 06/2006, Volume 235, Issue 6, pp. 1491 - 1500
The zinc finger/homeodomain transcription factor (zfhx1) family in vertebrates consists of two members, δEF1 and SIP1. They have been proposed to display...
SIP1 | Sox2 | Zfhx1 | δEF1 | ZEB | neural induction | Neural induction | δef1 | ACTIVE REPRESSION | delta EF1 | COREPRESSOR CTBP | ANATOMY & MORPHOLOGY | ZINC-FINGER PROTEINS | SMAD-INTERACTING PROTEIN-1 | BINDING-PROTEIN | DEVELOPMENTAL BIOLOGY | HIRSCHSPRUNG-DISEASE | GROWTH-FACTOR | TRANSCRIPTION FACTOR | BMP INHIBITION
SIP1 | Sox2 | Zfhx1 | δEF1 | ZEB | neural induction | Neural induction | δef1 | ACTIVE REPRESSION | delta EF1 | COREPRESSOR CTBP | ANATOMY & MORPHOLOGY | ZINC-FINGER PROTEINS | SMAD-INTERACTING PROTEIN-1 | BINDING-PROTEIN | DEVELOPMENTAL BIOLOGY | HIRSCHSPRUNG-DISEASE | GROWTH-FACTOR | TRANSCRIPTION FACTOR | BMP INHIBITION
Journal Article
FEBS Letters, ISSN 0014-5793, 2007, Volume 581, Issue 8, pp. 1617 - 1624
Plakophilin 3 (PKP3) belongs to the p120ctn family of armadillo-related proteins predominantly functioning in desmosome formation. Here we report that PKP3 is...
Epithelial to mesenchymal transition | Desmosomes | Transcription | Invasion | Cell adhesion | DNA-BINDING | PROTEIN | transcription | TUMOR PROGRESSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | EPITHELIAL-MESENCHYMAL TRANSITIONS | E-CADHERIN | BETA-CATENIN | CELL BIOLOGY | BREAST-CANCER | ADHESION | BIOPHYSICS | invasion | cell adhesion | epithelial to mesenchymal transition | CELL DIFFERENTIATION | DESMOSOMAL PLAQUE | desmosomes | Cadherins - metabolism | Homeodomain Proteins - metabolism | Humans | Gene Expression Regulation, Neoplastic | Plakophilins - analysis | Repressor Proteins - analysis | Neoplasms - chemistry | Neoplasms - genetics | Base Sequence | Tumor Cells, Cultured | Repressor Proteins - metabolism | Promoter Regions, Genetic | Neoplasm Invasiveness | Plakophilins - genetics | Repressor Proteins - genetics | Transcription Factors - genetics | Disease Progression | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Animals | Homeodomain Proteins - analysis | Mice | Transcription Factors - analysis | Neoplasms - pathology | Zinc Finger E-box-Binding Homeobox 1
Epithelial to mesenchymal transition | Desmosomes | Transcription | Invasion | Cell adhesion | DNA-BINDING | PROTEIN | transcription | TUMOR PROGRESSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | EPITHELIAL-MESENCHYMAL TRANSITIONS | E-CADHERIN | BETA-CATENIN | CELL BIOLOGY | BREAST-CANCER | ADHESION | BIOPHYSICS | invasion | cell adhesion | epithelial to mesenchymal transition | CELL DIFFERENTIATION | DESMOSOMAL PLAQUE | desmosomes | Cadherins - metabolism | Homeodomain Proteins - metabolism | Humans | Gene Expression Regulation, Neoplastic | Plakophilins - analysis | Repressor Proteins - analysis | Neoplasms - chemistry | Neoplasms - genetics | Base Sequence | Tumor Cells, Cultured | Repressor Proteins - metabolism | Promoter Regions, Genetic | Neoplasm Invasiveness | Plakophilins - genetics | Repressor Proteins - genetics | Transcription Factors - genetics | Disease Progression | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Animals | Homeodomain Proteins - analysis | Mice | Transcription Factors - analysis | Neoplasms - pathology | Zinc Finger E-box-Binding Homeobox 1
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 2010, Volume 1802, Issue 2, pp. 301 - 312
Although the zinc finger-homeodomain transcription factor δEF1 is implied as a regulatory factor at the crossroad between proliferation and differentiation in...
δEF1 | CDK | Breast cancer proliferation | p21 | Cell cycle | delta EF1 | TGF-BETA | PROTEIN DELTA-EF1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | E-CADHERIN | GROWTH-FACTOR RECEPTOR | CDK INHIBITORS | CYCLE CONTROL | BIOPHYSICS | ESTROGEN-RECEPTOR-ALPHA | P53 FAMILY | TRANSCRIPTION FACTOR
δEF1 | CDK | Breast cancer proliferation | p21 | Cell cycle | delta EF1 | TGF-BETA | PROTEIN DELTA-EF1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | E-CADHERIN | GROWTH-FACTOR RECEPTOR | CDK INHIBITORS | CYCLE CONTROL | BIOPHYSICS | ESTROGEN-RECEPTOR-ALPHA | P53 FAMILY | TRANSCRIPTION FACTOR
Journal Article