Uro-News, ISSN 1432-9026, 09/2018, Volume 22, Issue 9, pp. 28 - 32
Journal Article
Aktuelle Urologie, ISSN 0001-7868, 08/2017, Volume 48, Issue 4, pp. 340 - 349
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2017, Volume 12, Issue 4, p. e0176287
Many long noncoding RNAs (lncRNAs) are deregulated in cancer and contribute to oncogenesis. In urothelial carcinoma (UC), several lncRNAs have been reported to...
ANRIL | BLADDER-CANCER | METASTASIS | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | IDENTIFICATION | TUG1 | UP-REGULATION | CONTRIBUTES | SIGNATURE | CANCER CELL-PROLIFERATION | Cell Line, Tumor | Biomarkers, Tumor - genetics | RNA, Long Noncoding - genetics | Urinary Bladder Neoplasms - genetics | Humans | Urinary Bladder Neoplasms - pathology | Carcinoma | Prognosis | MicroRNA | Physiological aspects | Genetic aspects | Diagnosis | Research | Biological markers | Cancer | Urine | Deregulation | Statistical analysis | Invasiveness | Colorectal cancer | Muscles | Gene expression | Tissues | Medical diagnosis | Patients | Survival | Bladder cancer | Urology | Cell adhesion & migration | Studies | Cell growth | Medical prognosis | Cell lines | Biomarkers | Tumorigenesis | Diagnostic systems | Urothelial carcinoma | Tumors
ANRIL | BLADDER-CANCER | METASTASIS | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | IDENTIFICATION | TUG1 | UP-REGULATION | CONTRIBUTES | SIGNATURE | CANCER CELL-PROLIFERATION | Cell Line, Tumor | Biomarkers, Tumor - genetics | RNA, Long Noncoding - genetics | Urinary Bladder Neoplasms - genetics | Humans | Urinary Bladder Neoplasms - pathology | Carcinoma | Prognosis | MicroRNA | Physiological aspects | Genetic aspects | Diagnosis | Research | Biological markers | Cancer | Urine | Deregulation | Statistical analysis | Invasiveness | Colorectal cancer | Muscles | Gene expression | Tissues | Medical diagnosis | Patients | Survival | Bladder cancer | Urology | Cell adhesion & migration | Studies | Cell growth | Medical prognosis | Cell lines | Biomarkers | Tumorigenesis | Diagnostic systems | Urothelial carcinoma | Tumors
Journal Article
AKTUELLE UROLOGIE, ISSN 0001-7868, 08/2017, Volume 48, Issue 4, pp. 340 - 349
Perioperative chemotherapy is likely to improve survival in both the neoadjuvant and the adjuvant setting. Therefore, it is an integral part of the modern...
targeted therapy | MULTICENTER | PHASE-III | RANDOMIZED-TRIAL | urothelial cancer | prognostic factors | OPEN-LABEL | chemotherapy | immune checkpoint inhibition | PEMBROLIZUMAB | CISPLATIN | UROLOGY & NEPHROLOGY | CARCINOMA | T-CELLS | PLUS
targeted therapy | MULTICENTER | PHASE-III | RANDOMIZED-TRIAL | urothelial cancer | prognostic factors | OPEN-LABEL | chemotherapy | immune checkpoint inhibition | PEMBROLIZUMAB | CISPLATIN | UROLOGY & NEPHROLOGY | CARCINOMA | T-CELLS | PLUS
Journal Article
2018, Methods in Molecular Biology, ISBN 9781493972333, Volume 1655
eBook
Translational Cancer Research, ISSN 2218-676X, 2017, Volume 6, pp. S221 - S225
Radical cystectomy is the mainstay of surgical treatment in muscle invasive bladder cancer (BC). With the advent of minimally invasive surgical approaches...
Laparoscopic radical cystectomy | Robotic radical cystectomy | Bladder cancer | Radical cystectomy | SURVIVAL | METAANALYSIS | UROTHELIAL CARCINOMA | CHEMOTHERAPY | ADJUVANT | TRIAL | PERIOPERATIVE OUTCOMES | ONCOLOGY | radical cystectomy | COMPLICATIONS | robotic radical cystectomy | CYSTOPROSTATECTOMY | laparoscopic radical cystectomy | NEOADJUVANT
Laparoscopic radical cystectomy | Robotic radical cystectomy | Bladder cancer | Radical cystectomy | SURVIVAL | METAANALYSIS | UROTHELIAL CARCINOMA | CHEMOTHERAPY | ADJUVANT | TRIAL | PERIOPERATIVE OUTCOMES | ONCOLOGY | radical cystectomy | COMPLICATIONS | robotic radical cystectomy | CYSTOPROSTATECTOMY | laparoscopic radical cystectomy | NEOADJUVANT
Journal Article
International journal of molecular sciences, ISSN 1422-0067, 04/2019, Volume 20, Issue 9, p. 2135
Class I histone deacetylases (HDACs) generally promote cell proliferation and tumorigenesis, whereas class IIA HDACs like HDAC4 and HDAC5 may promote or impede...
HDAC4 | HDAC5 | TNFα | proteomics | bladder cancer | transcriptomics | TGFβ | histone deacetylase | EMT | epigenetics
HDAC4 | HDAC5 | TNFα | proteomics | bladder cancer | transcriptomics | TGFβ | histone deacetylase | EMT | epigenetics
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 09/2014, Volume 15, Issue 11, pp. 20500 - 20517
Genetic and epigenetic changes in the mitogen activated protein kinase (MAPK) signaling render urothelial cancer a potential target for tyrosine kinase...
Mitogen activated protein kinase (MAPK) signaling | Urothelial cancer | Tyrosine kinase inhibitor | Apoptosis | HDAC INHIBITORS | INDUCED APOPTOSIS | URINARY-BLADDER | BIOCHEMISTRY & MOLECULAR BIOLOGY | apoptosis | HEPATOMA-CELLS | urothelial cancer | CHEMISTRY, MULTIDISCIPLINARY | MULTIKINASE INHIBITOR | C-FLIP | tyrosine kinase inhibitor | HUMAN BLADDER-CANCER | mitogen activated protein kinase (MAPK) signaling | BCL-2 FAMILY | CELL-CARCINOMA | ENDOTHELIAL GROWTH-FACTOR | Niacinamide - analogs & derivatives | Apoptosis - drug effects | Humans | Urinary Bladder Neoplasms - enzymology | Drug Resistance, Neoplasm | Urinary Bladder - pathology | Urinary Bladder Neoplasms - drug therapy | Urothelium - pathology | MAP Kinase Signaling System - drug effects | Urinary Bladder Neoplasms - pathology | Cell Line, Tumor | Urinary Bladder - drug effects | Antineoplastic Agents - pharmacology | Phenylurea Compounds - pharmacology | Protein Kinase Inhibitors - pharmacology | Niacinamide - pharmacology | Urinary Bladder - enzymology | Urothelium - drug effects | Signal transduction | Inhibitor drugs | Kinases | Urogenital system | Cancer
Mitogen activated protein kinase (MAPK) signaling | Urothelial cancer | Tyrosine kinase inhibitor | Apoptosis | HDAC INHIBITORS | INDUCED APOPTOSIS | URINARY-BLADDER | BIOCHEMISTRY & MOLECULAR BIOLOGY | apoptosis | HEPATOMA-CELLS | urothelial cancer | CHEMISTRY, MULTIDISCIPLINARY | MULTIKINASE INHIBITOR | C-FLIP | tyrosine kinase inhibitor | HUMAN BLADDER-CANCER | mitogen activated protein kinase (MAPK) signaling | BCL-2 FAMILY | CELL-CARCINOMA | ENDOTHELIAL GROWTH-FACTOR | Niacinamide - analogs & derivatives | Apoptosis - drug effects | Humans | Urinary Bladder Neoplasms - enzymology | Drug Resistance, Neoplasm | Urinary Bladder - pathology | Urinary Bladder Neoplasms - drug therapy | Urothelium - pathology | MAP Kinase Signaling System - drug effects | Urinary Bladder Neoplasms - pathology | Cell Line, Tumor | Urinary Bladder - drug effects | Antineoplastic Agents - pharmacology | Phenylurea Compounds - pharmacology | Protein Kinase Inhibitors - pharmacology | Niacinamide - pharmacology | Urinary Bladder - enzymology | Urothelium - drug effects | Signal transduction | Inhibitor drugs | Kinases | Urogenital system | Cancer
Journal Article
Clinical Epigenetics, ISSN 1868-7075, 2018, Volume 10, Issue 1, pp. 1 - 14
Background: New efficient therapies for urothelial carcinoma (UC) are urgently required. Small-molecule drugs targeting chromatin regulators are reasonable...
BET inhibitor | JQ1 | Romidepsin | Bladder cancer | HDACi | Apoptosis | HISTONE DEACETYLASE INHIBITOR | ACTIVATION | MECHANISMS | DEATH | BROMODOMAIN | BREAST-CANCER | ONCOLOGY | BLADDER | EXPRESSION | BRD4 | Cyclin-Dependent Kinase Inhibitor p57 - metabolism | Cell Survival - drug effects | Cyclin-Dependent Kinase Inhibitor p57 - genetics | Humans | Histone Deacetylases - metabolism | Nuclear Proteins - metabolism | Carcinoma, Transitional Cell - metabolism | Depsipeptides - pharmacology | Transcription Factors - genetics | Urinary Bladder Neoplasms - drug therapy | Azepines - pharmacology | Dose-Response Relationship, Drug | Drug Synergism | Transcription Factors - metabolism | Triazoles - pharmacology | Cell Cycle Checkpoints | Carcinoma, Transitional Cell - drug therapy | Cell Line, Tumor | Cell Proliferation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Nuclear Proteins - genetics | Urinary Bladder Neoplasms - metabolism | Care and treatment | Carcinoma | Development and progression | Genetic aspects | Genetic transcription | Research | Health aspects | Cancer
BET inhibitor | JQ1 | Romidepsin | Bladder cancer | HDACi | Apoptosis | HISTONE DEACETYLASE INHIBITOR | ACTIVATION | MECHANISMS | DEATH | BROMODOMAIN | BREAST-CANCER | ONCOLOGY | BLADDER | EXPRESSION | BRD4 | Cyclin-Dependent Kinase Inhibitor p57 - metabolism | Cell Survival - drug effects | Cyclin-Dependent Kinase Inhibitor p57 - genetics | Humans | Histone Deacetylases - metabolism | Nuclear Proteins - metabolism | Carcinoma, Transitional Cell - metabolism | Depsipeptides - pharmacology | Transcription Factors - genetics | Urinary Bladder Neoplasms - drug therapy | Azepines - pharmacology | Dose-Response Relationship, Drug | Drug Synergism | Transcription Factors - metabolism | Triazoles - pharmacology | Cell Cycle Checkpoints | Carcinoma, Transitional Cell - drug therapy | Cell Line, Tumor | Cell Proliferation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Nuclear Proteins - genetics | Urinary Bladder Neoplasms - metabolism | Care and treatment | Carcinoma | Development and progression | Genetic aspects | Genetic transcription | Research | Health aspects | Cancer
Journal Article
Targeted Oncology, ISSN 1776-2596, 12/2016, Volume 11, Issue 6, pp. 783 - 798
Targeting of class I histone deacetylases (HDACs) exerts antineoplastic actions in various cancer types by modulation of transcription, upregulation of tumor...
Biomedicine, general | Medicine & Public Health | Oncology | PHASE-III TRIAL | MITOSIS | BLADDER-CANCER | CISPLATIN | EFFICACY | ONCOLOGY | ACETYLATION | MECHANISMS | HISTONE DEACETYLASE INHIBITORS | EXPRESSION | CHEMOTHERAPY | Cell Line, Tumor | Histone Deacetylase Inhibitors - pharmacology | Urinary Bladder Neoplasms - drug therapy | Humans | Immunoglobulin Isotypes - genetics | Carcinoma | Cell death | Health aspects | Analysis | Cancer | Original
Biomedicine, general | Medicine & Public Health | Oncology | PHASE-III TRIAL | MITOSIS | BLADDER-CANCER | CISPLATIN | EFFICACY | ONCOLOGY | ACETYLATION | MECHANISMS | HISTONE DEACETYLASE INHIBITORS | EXPRESSION | CHEMOTHERAPY | Cell Line, Tumor | Histone Deacetylase Inhibitors - pharmacology | Urinary Bladder Neoplasms - drug therapy | Humans | Immunoglobulin Isotypes - genetics | Carcinoma | Cell death | Health aspects | Analysis | Cancer | Original
Journal Article
Urologic Oncology: Seminars and Original Investigations, ISSN 1078-1439, 10/2017, Volume 35, Issue 10, pp. 600 - 601
Journal Article
Journal of Experimental and Clinical Cancer Research, ISSN 1756-9966, 07/2014, Volume 33, Issue 1
Background: Previous studies have shown that class-I histone deacetylase (HDAC) 8 mRNA is upregulated in urothelial cancer tissues and urothelial cancer cell...
Cell cycle arrest | Histone deacetylase inhibitor | Histone deacetylase 8 | Urothelial bladder cancer | BLADDER-CANCER | CELLS | APOPTOSIS | HDAC EXPRESSION | ACETYLATION | ONCOLOGY | GASTRIC-CANCER | CLONING | PROSTATE-CANCER | INHIBITORS | CARCINOMA | Research | Comparative analysis | Health aspects | Oncology, Experimental | Cancer | Breast cancer | Kinases | Experiments | Cancer therapies | Bladder cancer | Proteins | Liver cancer | Cell growth | Rodents | Medical prognosis | Cell cycle | Protein expression | Apoptosis
Cell cycle arrest | Histone deacetylase inhibitor | Histone deacetylase 8 | Urothelial bladder cancer | BLADDER-CANCER | CELLS | APOPTOSIS | HDAC EXPRESSION | ACETYLATION | ONCOLOGY | GASTRIC-CANCER | CLONING | PROSTATE-CANCER | INHIBITORS | CARCINOMA | Research | Comparative analysis | Health aspects | Oncology, Experimental | Cancer | Breast cancer | Kinases | Experiments | Cancer therapies | Bladder cancer | Proteins | Liver cancer | Cell growth | Rodents | Medical prognosis | Cell cycle | Protein expression | Apoptosis
Journal Article
BMC cancer, ISSN 1471-2407, 2014, Volume 14, Issue 1, pp. 628 - 628
Background: Notch signalling regulates cell fate in most tissues, promoting precursor cell proliferation in some, but differentiation in others. Accordingly,...
Notch pathway | γ-secretase inhibitors | NOTCH1 | Urothelial carcinoma | Bladder cancer | BLADDER-CANCER | MECHANISM | HES-1 EXPRESSION | gamma-secretase inhibitors | MOLECULAR PATHWAYS | THERAPY | ONCOLOGY | EAU INTERNATIONAL CONSULTATION | SQUAMOUS-CELL CARCINOMA | POLYPLOIDY | LIGAND | MUTATIONS | Cell Proliferation | Receptors, Notch - metabolism | Humans | Middle Aged | Male | Receptors, Notch - genetics | Intercellular Signaling Peptides and Proteins - metabolism | Urinary Bladder Neoplasms - genetics | Serrate-Jagged Proteins | Urinary Bladder Neoplasms - pathology | Aged, 80 and over | Female | Membrane Proteins - metabolism | Carcinoma - pathology | Urinary Bladder Neoplasms - metabolism | Calcium-Binding Proteins - metabolism | Tumor Stem Cell Assay | Gene Expression | Signal Transduction | Urinary Bladder - metabolism | Membrane Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Receptor, Notch1 - metabolism | Protein Transport | Cell Line, Tumor | Carcinoma - genetics | Ligands | Aged | Carcinoma - metabolism | Receptor, Notch1 - genetics | Calcium-Binding Proteins - genetics | Cellular signal transduction | Carcinoma | Research | Analysis | Cancer | Urothelium
Notch pathway | γ-secretase inhibitors | NOTCH1 | Urothelial carcinoma | Bladder cancer | BLADDER-CANCER | MECHANISM | HES-1 EXPRESSION | gamma-secretase inhibitors | MOLECULAR PATHWAYS | THERAPY | ONCOLOGY | EAU INTERNATIONAL CONSULTATION | SQUAMOUS-CELL CARCINOMA | POLYPLOIDY | LIGAND | MUTATIONS | Cell Proliferation | Receptors, Notch - metabolism | Humans | Middle Aged | Male | Receptors, Notch - genetics | Intercellular Signaling Peptides and Proteins - metabolism | Urinary Bladder Neoplasms - genetics | Serrate-Jagged Proteins | Urinary Bladder Neoplasms - pathology | Aged, 80 and over | Female | Membrane Proteins - metabolism | Carcinoma - pathology | Urinary Bladder Neoplasms - metabolism | Calcium-Binding Proteins - metabolism | Tumor Stem Cell Assay | Gene Expression | Signal Transduction | Urinary Bladder - metabolism | Membrane Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Receptor, Notch1 - metabolism | Protein Transport | Cell Line, Tumor | Carcinoma - genetics | Ligands | Aged | Carcinoma - metabolism | Receptor, Notch1 - genetics | Calcium-Binding Proteins - genetics | Cellular signal transduction | Carcinoma | Research | Analysis | Cancer | Urothelium
Journal Article
The Journal of Urology, ISSN 0022-5347, 04/2018, Volume 199, Issue 4, pp. e697 - e698
Journal Article
Molecular Cancer, ISSN 1476-4598, 05/2015, Volume 14, Issue 1, p. 108
Background: Urothelial carcinoma (UC) is the fifth most common cancer in the developed world. Delineation of differentiation subtypes in UC highlighted the...
HOTAIR | HOX gene | Long noncoding RNA | Bladder cancer | PROSTATE | STEM-CELLS | METASTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | LUNG-CANCER | ONCOLOGY | POOR-PROGNOSIS | RECURRENCE | DIFFERENTIATION | HUMAN BLADDER-CANCER | UP-REGULATION | CARCINOMA | Multivariate Analysis | Cell Proliferation | Urothelium - metabolism | Oligonucleotide Array Sequence Analysis | Homeodomain Proteins - metabolism | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Male | Gene Expression Profiling | Urothelium - pathology | Urinary Bladder Neoplasms - genetics | Urinary Bladder Neoplasms - pathology | Aged, 80 and over | Female | Clone Cells | Neoplasm Invasiveness | Kaplan-Meier Estimate | RNA, Long Noncoding - genetics | Organ Specificity | Homeodomain Proteins - genetics | Phenotype | Cell Line, Tumor | Aged | RNA, Long Noncoding - metabolism | Epigenetic inheritance | Stem cells | Antisense RNA | Genetic aspects | DNA binding proteins | Gene expression | Cell differentiation
HOTAIR | HOX gene | Long noncoding RNA | Bladder cancer | PROSTATE | STEM-CELLS | METASTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | LUNG-CANCER | ONCOLOGY | POOR-PROGNOSIS | RECURRENCE | DIFFERENTIATION | HUMAN BLADDER-CANCER | UP-REGULATION | CARCINOMA | Multivariate Analysis | Cell Proliferation | Urothelium - metabolism | Oligonucleotide Array Sequence Analysis | Homeodomain Proteins - metabolism | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Male | Gene Expression Profiling | Urothelium - pathology | Urinary Bladder Neoplasms - genetics | Urinary Bladder Neoplasms - pathology | Aged, 80 and over | Female | Clone Cells | Neoplasm Invasiveness | Kaplan-Meier Estimate | RNA, Long Noncoding - genetics | Organ Specificity | Homeodomain Proteins - genetics | Phenotype | Cell Line, Tumor | Aged | RNA, Long Noncoding - metabolism | Epigenetic inheritance | Stem cells | Antisense RNA | Genetic aspects | DNA binding proteins | Gene expression | Cell differentiation
Journal Article
Oncology, ISSN 0030-2414, 07/2015, Volume 89, Issue 2, pp. 70 - 78
Objective: The efficacy of second-line treatment after failure of platinum-based chemotherapy in patients with advanced urothelial cancer is limited. Based on...
Clinical Study | Urothelial cancer | Chemotherapy | Platinum failure | Everolimus | Paclitaxel | BLADDER-CANCER | DOXORUBICIN | METHOTREXATE | GEMCITABINE | CISPLATIN | ONCOLOGY | TRANSITIONAL-CELL CARCINOMA | EUROPEAN-ORGANIZATION | TRACT TUMORS | PLUS | Humans | Middle Aged | Paclitaxel - adverse effects | Male | Treatment Outcome | Everolimus - administration & dosage | Antineoplastic Agents - administration & dosage | Urothelium - pathology | Urologic Neoplasms - pathology | Urologic Neoplasms - drug therapy | Antineoplastic Agents - adverse effects | Everolimus - adverse effects | Quality of Life | Adult | Female | Aged | Paclitaxel - administration & dosage | Urothelium - drug effects | Germany | Clinical trials | Urogenital system | Clinical outcomes | Cancer
Clinical Study | Urothelial cancer | Chemotherapy | Platinum failure | Everolimus | Paclitaxel | BLADDER-CANCER | DOXORUBICIN | METHOTREXATE | GEMCITABINE | CISPLATIN | ONCOLOGY | TRANSITIONAL-CELL CARCINOMA | EUROPEAN-ORGANIZATION | TRACT TUMORS | PLUS | Humans | Middle Aged | Paclitaxel - adverse effects | Male | Treatment Outcome | Everolimus - administration & dosage | Antineoplastic Agents - administration & dosage | Urothelium - pathology | Urologic Neoplasms - pathology | Urologic Neoplasms - drug therapy | Antineoplastic Agents - adverse effects | Everolimus - adverse effects | Quality of Life | Adult | Female | Aged | Paclitaxel - administration & dosage | Urothelium - drug effects | Germany | Clinical trials | Urogenital system | Clinical outcomes | Cancer
Journal Article
International Journal of Molecular Sciences, ISSN 1422-0067, 02/2018, Volume 19, Issue 2, p. 590
Therapeutic efficacy of cisplatin-based treatment of late stage urothelial carcinoma (UC) is limited by chemoresistance. To elucidate underlying mechanisms and...
MOLECULAR CHARACTERIZATION | BLADDER-CANCER | BIOMARKER | INDUCED APOPTOSIS | metallothionein | Survivin | resistance mechanisms | CHEMOTHERAPY | CANCER STEM-CELLS | urothelial carcinoma | ENHANCED EXPRESSION | YM155 | cisplatin | DNA-REPAIR | Urothelial carcinoma | Cisplatin | Metallothionein | Resistance mechanisms | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, MULTIDISCIPLINARY | Metallothionein - metabolism | Urothelium - metabolism | Humans | Drug Resistance, Neoplasm | Cisplatin - pharmacology | Cell Cycle | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Carcinoma - metabolism | DNA Damage | Urothelium - drug effects | Urinary Bladder Neoplasms - metabolism | Apoptosis | DNA repair | DNA damage | Deoxyribonucleic acid--DNA | Cell cycle
MOLECULAR CHARACTERIZATION | BLADDER-CANCER | BIOMARKER | INDUCED APOPTOSIS | metallothionein | Survivin | resistance mechanisms | CHEMOTHERAPY | CANCER STEM-CELLS | urothelial carcinoma | ENHANCED EXPRESSION | YM155 | cisplatin | DNA-REPAIR | Urothelial carcinoma | Cisplatin | Metallothionein | Resistance mechanisms | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, MULTIDISCIPLINARY | Metallothionein - metabolism | Urothelium - metabolism | Humans | Drug Resistance, Neoplasm | Cisplatin - pharmacology | Cell Cycle | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Carcinoma - metabolism | DNA Damage | Urothelium - drug effects | Urinary Bladder Neoplasms - metabolism | Apoptosis | DNA repair | DNA damage | Deoxyribonucleic acid--DNA | Cell cycle
Journal Article
Clinical Epigenetics, ISSN 1868-7075, 07/2018, Volume 10, Issue 1, pp. 100 - 18
Background: Histone deacetylase inhibitors (HDACi) are promising anti-cancer drugs that could also be employed for urothelial carcinoma (UC) therapy. It is...
Cell cycle arrest | Histone deacetylase inhibitor | Histone deacetylase HDAC4 | Class IIA HDACs | Urothelial bladder cancer | CANCER-CELLS | PHYSIOLOGY | EXPORT | PROFILE | ONCOLOGY | ROLES | CLASS-I | DIFFERENTIATION | EXPRESSION | TUMORIGENESIS | IIA HISTONE DEACETYLASES | Adenocarcinoma | Histones | Care and treatment | Research | Gene expression | Cancer cells | Flow cytometry | Histone deacetylase | Enzymes | Medical research | Chromatin | Senescence | Mitosis | Cytotoxicity | Thymidylate synthase | Bladder cancer | Western blotting | Cyclin-dependent kinase inhibitor p21 | Tubulin | Cell cycle | Cell lines | Acetylation | Urothelial carcinoma | Tumors | Apoptosis | Crystal structure
Cell cycle arrest | Histone deacetylase inhibitor | Histone deacetylase HDAC4 | Class IIA HDACs | Urothelial bladder cancer | CANCER-CELLS | PHYSIOLOGY | EXPORT | PROFILE | ONCOLOGY | ROLES | CLASS-I | DIFFERENTIATION | EXPRESSION | TUMORIGENESIS | IIA HISTONE DEACETYLASES | Adenocarcinoma | Histones | Care and treatment | Research | Gene expression | Cancer cells | Flow cytometry | Histone deacetylase | Enzymes | Medical research | Chromatin | Senescence | Mitosis | Cytotoxicity | Thymidylate synthase | Bladder cancer | Western blotting | Cyclin-dependent kinase inhibitor p21 | Tubulin | Cell cycle | Cell lines | Acetylation | Urothelial carcinoma | Tumors | Apoptosis | Crystal structure
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1655, pp. 289 - 317
Mutations, dysregulation, and dysbalance of epigenetic regulators are especially frequent in urothelial carcinoma (UC) compared to other malignancies....
Epigenetics | Histone deacetylase inhibitors | Histone deacetylases | Urothelial carcinoma | Targeted therapy | RNA, Small Interfering - genetics | Urologic Neoplasms - diagnosis | Humans | Antineoplastic Agents - therapeutic use | Gene Knockdown Techniques | Dose-Response Relationship, Drug | Caspases - metabolism | Flow Cytometry | Urologic Neoplasms - drug therapy | Urologic Neoplasms - genetics | Antineoplastic Agents - pharmacology | Epigenesis, Genetic - drug effects | Cell Survival - drug effects | Tumor Stem Cell Assay | Urologic Neoplasms - metabolism | DNA Modification Methylases - metabolism | Histone Deacetylases - metabolism | Workflow | Histone Demethylases - metabolism | Fluorescent Antibody Technique | Cell Line, Tumor | Histone Deacetylase Inhibitors - pharmacology | Cell Proliferation - drug effects | Histone Deacetylase Inhibitors - therapeutic use | Histones - metabolism | DNA Methylation - drug effects
Epigenetics | Histone deacetylase inhibitors | Histone deacetylases | Urothelial carcinoma | Targeted therapy | RNA, Small Interfering - genetics | Urologic Neoplasms - diagnosis | Humans | Antineoplastic Agents - therapeutic use | Gene Knockdown Techniques | Dose-Response Relationship, Drug | Caspases - metabolism | Flow Cytometry | Urologic Neoplasms - drug therapy | Urologic Neoplasms - genetics | Antineoplastic Agents - pharmacology | Epigenesis, Genetic - drug effects | Cell Survival - drug effects | Tumor Stem Cell Assay | Urologic Neoplasms - metabolism | DNA Modification Methylases - metabolism | Histone Deacetylases - metabolism | Workflow | Histone Demethylases - metabolism | Fluorescent Antibody Technique | Cell Line, Tumor | Histone Deacetylase Inhibitors - pharmacology | Cell Proliferation - drug effects | Histone Deacetylase Inhibitors - therapeutic use | Histones - metabolism | DNA Methylation - drug effects
Journal Article