Nature Reviews Gastroenterology and Hepatology, ISSN 1759-5045, 08/2012, Volume 9, Issue 8, pp. 454 - 467
Pancreatic ductal adenocarcinoma (PDAC) is one of the five most lethal malignancies worldwide and survival has not improved substantially in the past 30 years....
PAPILLARY MUCINOUS NEOPLASMS | PHASE-III TRIAL | MATRIX METALLOPROTEINASES | RECEPTOR ANTAGONISTS | RENIN-ANGIOTENSIN SYSTEM | DUCTAL ADENOCARCINOMA | STELLATE CELLS | ELLAGIC ACID | GASTROENTEROLOGY & HEPATOLOGY | FIBROBLAST ACTIVATION PROTEIN | TUMOR MICROENVIRONMENT | Immunohistochemistry | Adenocarcinoma - pathology | Humans | Pancreatic Neoplasms - pathology | Stromal Cells - metabolism | Tomography, X-Ray Computed | Pancreatic Stellate Cells - physiology | Adenocarcinoma - drug therapy | Carcinoma, Pancreatic Ductal - pathology | Carcinoma, Pancreatic Ductal - diagnostic imaging | Pancreatic Neoplasms - drug therapy | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Adenocarcinoma - physiopathology | Stromal Cells - drug effects | Renin-Angiotensin System - drug effects | Carcinoma, Pancreatic Ductal - physiopathology | Adenocarcinoma - diagnostic imaging | Pancreatic Neoplasms - physiopathology | Stromal Cells - physiology | Pancreatic Neoplasms - diagnostic imaging | Care and treatment | Diagnosis | Research | Carcinogenesis | Pancreatic cancer | Index Medicus
PAPILLARY MUCINOUS NEOPLASMS | PHASE-III TRIAL | MATRIX METALLOPROTEINASES | RECEPTOR ANTAGONISTS | RENIN-ANGIOTENSIN SYSTEM | DUCTAL ADENOCARCINOMA | STELLATE CELLS | ELLAGIC ACID | GASTROENTEROLOGY & HEPATOLOGY | FIBROBLAST ACTIVATION PROTEIN | TUMOR MICROENVIRONMENT | Immunohistochemistry | Adenocarcinoma - pathology | Humans | Pancreatic Neoplasms - pathology | Stromal Cells - metabolism | Tomography, X-Ray Computed | Pancreatic Stellate Cells - physiology | Adenocarcinoma - drug therapy | Carcinoma, Pancreatic Ductal - pathology | Carcinoma, Pancreatic Ductal - diagnostic imaging | Pancreatic Neoplasms - drug therapy | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Adenocarcinoma - physiopathology | Stromal Cells - drug effects | Renin-Angiotensin System - drug effects | Carcinoma, Pancreatic Ductal - physiopathology | Adenocarcinoma - diagnostic imaging | Pancreatic Neoplasms - physiopathology | Stromal Cells - physiology | Pancreatic Neoplasms - diagnostic imaging | Care and treatment | Diagnosis | Research | Carcinogenesis | Pancreatic cancer | Index Medicus
Journal Article
Pancreatology, ISSN 1424-3903, 06/2018, Volume 18, Issue 4, p. S89
Journal Article
Nature Medicine, ISSN 1078-8956, 10/2015, Volume 21, Issue 10, pp. 1163 - 1171
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal human cancers and shows resistance to any therapeutic strategy used. Here we tested...
SELECTIVE-INHIBITION | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-MYC | INTRAEPITHELIAL NEOPLASIA | CELL BIOLOGY | ENGINEERED MOUSE MODELS | LUNG-CANCER | IN-VIVO | BROMODOMAIN INHIBITION | KRAS | DRUG-COMBINATION | PROGRESSION | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Adenocarcinoma - therapy | Epigenesis, Genetic | Humans | Clustered Regularly Interspaced Short Palindromic Repeats | Carcinoma, Pancreatic Ductal - therapy | Histone Deacetylase Inhibitors - therapeutic use | Mice | Adenocarcinoma - drug therapy | Proteins - antagonists & inhibitors | Adenocarcinoma | Proteins | Physiological aspects | Care and treatment | Research | Pancreatic cancer | Clinical trials | Cancer therapies | Tumors
SELECTIVE-INHIBITION | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-MYC | INTRAEPITHELIAL NEOPLASIA | CELL BIOLOGY | ENGINEERED MOUSE MODELS | LUNG-CANCER | IN-VIVO | BROMODOMAIN INHIBITION | KRAS | DRUG-COMBINATION | PROGRESSION | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Adenocarcinoma - therapy | Epigenesis, Genetic | Humans | Clustered Regularly Interspaced Short Palindromic Repeats | Carcinoma, Pancreatic Ductal - therapy | Histone Deacetylase Inhibitors - therapeutic use | Mice | Adenocarcinoma - drug therapy | Proteins - antagonists & inhibitors | Adenocarcinoma | Proteins | Physiological aspects | Care and treatment | Research | Pancreatic cancer | Clinical trials | Cancer therapies | Tumors
Journal Article
Pancreatology, ISSN 1424-3903, 2015, Volume 15, Issue 3, pp. S2 - S2
[...]isolated pancreatic fibroblasts from cerulein-treated mice show an elevated number of Wt1 positive cells compared to untreated control mice and a strong...
Endocrinology & Metabolism | Gastroenterology and Hepatology | Fibroblasts | Pancreas | Rodents
Endocrinology & Metabolism | Gastroenterology and Hepatology | Fibroblasts | Pancreas | Rodents
Journal Article
5.
Full Text
Cellulose‐Based Microparticles for Magnetically Controlled Optical Modulation and Sensing
Small, ISSN 1613-6810, 12/2019, p. 1904251
Journal Article
Expert Review of Anticancer Therapy, ISSN 1473-7140, 02/2016, Volume 16, Issue 2, pp. 219 - 227
Although the concept of tumor heterogeneity was established several decades ago, the interest in this topic is still unbroken. With the identification of...
combination therapy | epigenetic alterations | cancer stem cells | tumor microenvironment | Pancreatic cancer | tumor heterogeneity | INITIATING CELLS | STEM-CELLS | SIGNALING PATHWAYS | TARGETING NOTCH | K-RAS | ONCOLOGY | GENE-EXPRESSION | FOCAL ADHESION KINASE | DUCTAL ADENOCARCINORNA | TUMOR-GROWTH | CLINICAL-SIGNIFICANCE | Epigenesis, Genetic | Humans | Pancreatic Neoplasms - pathology | Tumor Microenvironment | Drug Resistance, Neoplasm | Pancreatic Neoplasms - genetics | Antineoplastic Agents - administration & dosage | Molecular Targeted Therapy | Animals | Neoplastic Stem Cells - metabolism | Gene Rearrangement | Antineoplastic Agents - pharmacology | Pancreatic Neoplasms - therapy
combination therapy | epigenetic alterations | cancer stem cells | tumor microenvironment | Pancreatic cancer | tumor heterogeneity | INITIATING CELLS | STEM-CELLS | SIGNALING PATHWAYS | TARGETING NOTCH | K-RAS | ONCOLOGY | GENE-EXPRESSION | FOCAL ADHESION KINASE | DUCTAL ADENOCARCINORNA | TUMOR-GROWTH | CLINICAL-SIGNIFICANCE | Epigenesis, Genetic | Humans | Pancreatic Neoplasms - pathology | Tumor Microenvironment | Drug Resistance, Neoplasm | Pancreatic Neoplasms - genetics | Antineoplastic Agents - administration & dosage | Molecular Targeted Therapy | Animals | Neoplastic Stem Cells - metabolism | Gene Rearrangement | Antineoplastic Agents - pharmacology | Pancreatic Neoplasms - therapy
Journal Article
Molecular Metabolism, ISSN 2212-8778, 2016, Volume 5, Issue 4, pp. 253 - 254
Journal Article
Diabetes Care, ISSN 0149-5992, 2014, Volume 37, Issue 6, pp. 1675 - 1680
OBJECTIVE Patients with latent autoimmune diabetes in adults (LADA) express autoantibodies against the 65-kDa isoform of GAD (GADA). Intervention with...
RESPONSES | THERAPY | ENDOCRINOLOGY & METABOLISM | RISK | MELLITUS | ONSET | CHILDREN | Alum Compounds - chemistry | Double-Blind Method | Autoantibodies - blood | Humans | Middle Aged | Vaccination | Male | Vaccines, Synthetic - immunology | Diabetes Mellitus, Type 1 - therapy | Glucose Intolerance | Disease Progression | Insulin-Secreting Cells - immunology | Insulin-Secreting Cells - metabolism | Adult | Female | Aged | Diabetes Mellitus, Type 1 - immunology | Vaccines, Synthetic - administration & dosage | Glutamate Decarboxylase - immunology | C-Peptide - metabolism | Diabetics | Usage | Autoantibodies | Analysis | Clinical trials | Health aspects | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
RESPONSES | THERAPY | ENDOCRINOLOGY & METABOLISM | RISK | MELLITUS | ONSET | CHILDREN | Alum Compounds - chemistry | Double-Blind Method | Autoantibodies - blood | Humans | Middle Aged | Vaccination | Male | Vaccines, Synthetic - immunology | Diabetes Mellitus, Type 1 - therapy | Glucose Intolerance | Disease Progression | Insulin-Secreting Cells - immunology | Insulin-Secreting Cells - metabolism | Adult | Female | Aged | Diabetes Mellitus, Type 1 - immunology | Vaccines, Synthetic - administration & dosage | Glutamate Decarboxylase - immunology | C-Peptide - metabolism | Diabetics | Usage | Autoantibodies | Analysis | Clinical trials | Health aspects | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
Journal Article
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2014, Volume 816, pp. 129 - 151
Pancreatic ductal adenocarcinoma (PDAC) is a devastating disease with an extremely poor prognosis. Inflammatory processes have emerged as key mediators of...
Pancreatic Neoplasms - epidemiology | Pancreatic Neoplasms - etiology | Humans | Pancreatitis, Chronic - epidemiology | Carcinoma, Pancreatic Ductal - therapy | Signal Transduction - genetics | Pancreatitis, Chronic - genetics | Cytokines - physiology | Carcinoma, Pancreatic Ductal - epidemiology | Signal Transduction - immunology | Cell Transformation, Neoplastic - immunology | Animals | Cell Transformation, Neoplastic - genetics | Pancreatitis, Chronic - complications | Pancreatitis, Chronic - therapy | Mice | Carcinoma, Pancreatic Ductal - etiology | Pancreatic Neoplasms - therapy
Pancreatic Neoplasms - epidemiology | Pancreatic Neoplasms - etiology | Humans | Pancreatitis, Chronic - epidemiology | Carcinoma, Pancreatic Ductal - therapy | Signal Transduction - genetics | Pancreatitis, Chronic - genetics | Cytokines - physiology | Carcinoma, Pancreatic Ductal - epidemiology | Signal Transduction - immunology | Cell Transformation, Neoplastic - immunology | Animals | Cell Transformation, Neoplastic - genetics | Pancreatitis, Chronic - complications | Pancreatitis, Chronic - therapy | Mice | Carcinoma, Pancreatic Ductal - etiology | Pancreatic Neoplasms - therapy
Conference Proceeding
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2014, Volume 816, pp. 129 - 151
Conference Proceeding
Frontiers in Physiology, ISSN 1664-042X, 2012, Volume 3, p. 389
Our understanding of pancreatic ductal adenocarcinoma (PDAC) is shifting away from a disease of malignant ductal cells-only, toward a complex system where...
Angiogenesis | Stellate cells | Molecular diagnostics | Desmoplasia | Periostin | Microenvironment | Cystic pancreatic tumors | molecular diagnostics | PHYSIOLOGY | RISK-FACTORS | desmoplasia | periostin | DUCTAL ADENOCARCINOMA | angiogenesis | stellate cells | CYSTIC NEOPLASMS | ALPHA-V-BETA-6 INTEGRIN | INTERNATIONAL CONSENSUS GUIDELINES | microenvironment | PAPILLARY MUCINOUS NEOPLASMS | POSITRON-EMISSION-TOMOGRAPHY | DISTAL PANCREATECTOMY | IN-VIVO | cystic pancreatic tumors
Angiogenesis | Stellate cells | Molecular diagnostics | Desmoplasia | Periostin | Microenvironment | Cystic pancreatic tumors | molecular diagnostics | PHYSIOLOGY | RISK-FACTORS | desmoplasia | periostin | DUCTAL ADENOCARCINOMA | angiogenesis | stellate cells | CYSTIC NEOPLASMS | ALPHA-V-BETA-6 INTEGRIN | INTERNATIONAL CONSENSUS GUIDELINES | microenvironment | PAPILLARY MUCINOUS NEOPLASMS | POSITRON-EMISSION-TOMOGRAPHY | DISTAL PANCREATECTOMY | IN-VIVO | cystic pancreatic tumors
Journal Article
Pancreatology, ISSN 1424-3903, 2015, Volume 15, Issue 3, pp. S33 - S33
[...]the development of therapeutic drugs directed against periostin and its downstream targets might be a promising approach to inhibit pancreatic...
Endocrinology & Metabolism | Gastroenterology and Hepatology | Pancreas | Rodents | Metastasis
Endocrinology & Metabolism | Gastroenterology and Hepatology | Pancreas | Rodents | Metastasis
Journal Article
13.
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Abstract B08: The role of periostin in pancreatic carcinogenesis and metastatic spread
Cancer Research, ISSN 0008-5472, 07/2015, Volume 75, Issue 13 Supplement, pp. B08 - B08
Journal Article
14.
Full Text
Analysis of the extracellular matrix protein periostin in early pancreatic carcinogenesis
Pancreatology, ISSN 1424-3903, 2013, Volume 13, Issue 3, pp. S14 - S15
Conclusion: The lack of periostin promotes a worse pancreatic regeneration after cerulein induced pancreatic injury. [...]periostin affects the development...
Endocrinology & Metabolism | Gastroenterology and Hepatology | Cell culture | Extracellular matrix | Pancreas | Experiments | Rodents
Endocrinology & Metabolism | Gastroenterology and Hepatology | Cell culture | Extracellular matrix | Pancreas | Experiments | Rodents
Journal Article
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2014, Volume 816, pp. 129 - 151
Pancreatic ductal adenocarcinoma (PDAC) is a devastating disease with an extremely poor prognosis. Inflammatory processes have emerged as key mediators of...
PHASE-II TRIAL | ENHANCED EXPRESSION | ONCOLOGY | UROKINASE PLASMINOGEN-ACTIVATOR | DUCTAL ADENOCARCINOMA | EPIDERMAL-GROWTH-FACTOR | BETA SIGNALING PATHWAYS | MATRIX METALLOPROTEINASE-2 | IMMUNOLOGY | CELL-LINES | INTRAEPITHELIAL NEOPLASIA | NF-KAPPA-B
PHASE-II TRIAL | ENHANCED EXPRESSION | ONCOLOGY | UROKINASE PLASMINOGEN-ACTIVATOR | DUCTAL ADENOCARCINOMA | EPIDERMAL-GROWTH-FACTOR | BETA SIGNALING PATHWAYS | MATRIX METALLOPROTEINASE-2 | IMMUNOLOGY | CELL-LINES | INTRAEPITHELIAL NEOPLASIA | NF-KAPPA-B
Conference Proceeding
Molecular Metabolism, ISSN 2212-8778, 10/2018, Volume 16, pp. 191 - 202
The metabolic role of -serine, a non-proteinogenic NMDA receptor co-agonist, is poorly understood. Conversely, inhibition of pancreatic NMDA receptors as well...
Obesity | Diabetes | d-serine | Insulin secretion | D-serine | NMDA RECEPTORS | SEQUENCES | SUSCEPTIBILITY | SCHIZOPHRENIA | RISK | METABOLOMICS | ANTIPSYCHOTICS | ENDOCRINOLOGY & METABOLISM | DOUBLE-BLIND | EXPRESSION | CONTRIBUTES
Obesity | Diabetes | d-serine | Insulin secretion | D-serine | NMDA RECEPTORS | SEQUENCES | SUSCEPTIBILITY | SCHIZOPHRENIA | RISK | METABOLOMICS | ANTIPSYCHOTICS | ENDOCRINOLOGY & METABOLISM | DOUBLE-BLIND | EXPRESSION | CONTRIBUTES
Journal Article
Cell, ISSN 0092-8674, 01/2019, Volume 176, Issue 3, pp. 491 - 504.e21
Increased protein synthesis plays an etiologic role in diverse cancers. Here, we demonstrate that METTL13 (methyltransferase-like 13) dimethylation of eEF1A...
lung cancer | pancreatic cancer | METTL13 | RAS | protein methylation | translation | eEF1A | lysine methylation | translation elongation | PROTEIN METHYLATION | INHIBITION | K-RAS ONCOGENE | ADENOCARCINOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | PANCREATIC-CANCER | CARCINOMAS | VECTORS | PROGRESSION | CELL BIOLOGY | Medical colleges | Lysine | Analysis | Pancreatic cancer | Lung cancer | Transferases | Protein biosynthesis | Methylation | Statistics
lung cancer | pancreatic cancer | METTL13 | RAS | protein methylation | translation | eEF1A | lysine methylation | translation elongation | PROTEIN METHYLATION | INHIBITION | K-RAS ONCOGENE | ADENOCARCINOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | PANCREATIC-CANCER | CARCINOMAS | VECTORS | PROGRESSION | CELL BIOLOGY | Medical colleges | Lysine | Analysis | Pancreatic cancer | Lung cancer | Transferases | Protein biosynthesis | Methylation | Statistics
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2016, Volume 186, Issue 1, pp. 24 - 31
The extracellular matrix molecule periostin (POSTN, encoded by POSTN ), which is secreted by activated pancreatic stellate cells, has important functions in...
Pathology | FIBROSIS | CELLS | PROTEIN | RESECTION | INFLAMMATION | STROMA | MODEL | PATHOLOGY | EXPRESSION | Immunohistochemistry | Ceruletide - toxicity | Pancreas, Exocrine - pathology | Pancreatitis - chemically induced | Cell Adhesion Molecules - metabolism | Mice, Knockout | Pancreas, Exocrine - physiology | Atrophy | Regeneration | Animals | Pancreatitis - pathology | Mice | Pancreatitis - metabolism | Real-Time Polymerase Chain Reaction | Disease Models, Animal
Pathology | FIBROSIS | CELLS | PROTEIN | RESECTION | INFLAMMATION | STROMA | MODEL | PATHOLOGY | EXPRESSION | Immunohistochemistry | Ceruletide - toxicity | Pancreas, Exocrine - pathology | Pancreatitis - chemically induced | Cell Adhesion Molecules - metabolism | Mice, Knockout | Pancreas, Exocrine - physiology | Atrophy | Regeneration | Animals | Pancreatitis - pathology | Mice | Pancreatitis - metabolism | Real-Time Polymerase Chain Reaction | Disease Models, Animal
Journal Article
Molecular Cancer Research, ISSN 1541-7786, 02/2013, Volume 11, Issue 2, pp. 161 - 172
Human lung cancer is a disease with high incidence and accounts for most cancer-related deaths in both men and women. Metastasis is a common event in non-small...
TRANSCRIPTION FACTORS | METHYLATION | PROTEIN | REPRESSION | ONCOLOGY | GENE-EXPRESSION | BINDING DOMAIN | GRANULOSA-CELL TUMORS | PROMOTER | CANCER | FAMILY | CELL BIOLOGY | Mucin-2 - genetics | ras Proteins - genetics | Proto-Oncogene Proteins p21(ras) | Adenocarcinoma - pathology | Adenocarcinoma of Lung | Epigenesis, Genetic | Humans | Lung Neoplasms - metabolism | Gene Expression Regulation, Neoplastic | Cell Growth Processes - physiology | Lung Neoplasms - pathology | Male | Genes, myc | DNA Methylation | Proto-Oncogene Proteins c-myc - biosynthesis | Adenocarcinoma - metabolism | Female | Adenocarcinoma - genetics | GATA4 Transcription Factor - biosynthesis | Lung Neoplasms - genetics | Promoter Regions, Genetic | GATA4 Transcription Factor - genetics | Proto-Oncogene Proteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Cell Adhesion - physiology | Cell Line, Tumor | Proto-Oncogene Proteins c-myc - genetics
TRANSCRIPTION FACTORS | METHYLATION | PROTEIN | REPRESSION | ONCOLOGY | GENE-EXPRESSION | BINDING DOMAIN | GRANULOSA-CELL TUMORS | PROMOTER | CANCER | FAMILY | CELL BIOLOGY | Mucin-2 - genetics | ras Proteins - genetics | Proto-Oncogene Proteins p21(ras) | Adenocarcinoma - pathology | Adenocarcinoma of Lung | Epigenesis, Genetic | Humans | Lung Neoplasms - metabolism | Gene Expression Regulation, Neoplastic | Cell Growth Processes - physiology | Lung Neoplasms - pathology | Male | Genes, myc | DNA Methylation | Proto-Oncogene Proteins c-myc - biosynthesis | Adenocarcinoma - metabolism | Female | Adenocarcinoma - genetics | GATA4 Transcription Factor - biosynthesis | Lung Neoplasms - genetics | Promoter Regions, Genetic | GATA4 Transcription Factor - genetics | Proto-Oncogene Proteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Cell Adhesion - physiology | Cell Line, Tumor | Proto-Oncogene Proteins c-myc - genetics
Journal Article
PEDIATRIC RHEUMATOLOGY, ISSN 1546-0096, 05/2017, Volume 15, Issue S1, pp. 105 - 201
Journal Article