1996, Cancer treatment and research, ISBN 9780792341642, vi, 272
Book
BJU International, ISSN 1464-4096, 11/2017, Volume 120, Issue 5B, pp. E4 - E4
Journal Article
Molecular Imaging and Biology, ISSN 1536-1632, 12/2019, Volume 21, Issue 6, pp. 1054 - 1063
Prostate carcinoma consists of tumor epithelium and malignant stroma. Until recently, diagnostic and therapeutic efforts have focused exclusively on targeting...
Prognosis | Fluorescence imaging | NIRF | Medicine & Public Health | Imaging / Radiology | DPA-713 | Prostate carcinoma | Phenotypes | Animal models | Medical imaging | Xenotransplantation | Stroma | Fluorescence | Cytotoxicity | Inflammation | Macrophages | Epithelium | Sectioning | Genotype & phenotype | Infrared imaging | Xenografts | Extracellular matrix | Mice | Diagnostic systems | Prostate cancer | Prostate | Cancer | Tumors | Antigens
Prognosis | Fluorescence imaging | NIRF | Medicine & Public Health | Imaging / Radiology | DPA-713 | Prostate carcinoma | Phenotypes | Animal models | Medical imaging | Xenotransplantation | Stroma | Fluorescence | Cytotoxicity | Inflammation | Macrophages | Epithelium | Sectioning | Genotype & phenotype | Infrared imaging | Xenografts | Extracellular matrix | Mice | Diagnostic systems | Prostate cancer | Prostate | Cancer | Tumors | Antigens
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2011, Volume 121, Issue 4, pp. 1298 - 1312
HSC homing, quiescence, and self-renewal depend on the bone marrow HSC niche. A large proportion of solid tumor metastases are bone metastases, known to usurp...
PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | ADHESION | MOBILIZATION | GROWTH | MICE | INDUCTION | IDENTIFICATION | RECEPTORS | EXPRESSION | LINEAGE | Neoplasm Transplantation | Prostatic Neoplasms - pathology | Humans | Hematopoietic Stem Cells - pathology | Male | Transplantation, Heterologous | Mice, SCID | Bone Marrow Neoplasms - secondary | Osteoblasts - pathology | Animals | Bone Marrow Neoplasms - pathology | Models, Biological | Bone Marrow Transplantation | Cell Line, Tumor | Mice, Inbred NOD | Mice | Tissue Donors | Bone marrow | Genetic aspects | Metastasis | Research | Properties | Health aspects | Prostate cancer | Hematopoietic stem cells
PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | ADHESION | MOBILIZATION | GROWTH | MICE | INDUCTION | IDENTIFICATION | RECEPTORS | EXPRESSION | LINEAGE | Neoplasm Transplantation | Prostatic Neoplasms - pathology | Humans | Hematopoietic Stem Cells - pathology | Male | Transplantation, Heterologous | Mice, SCID | Bone Marrow Neoplasms - secondary | Osteoblasts - pathology | Animals | Bone Marrow Neoplasms - pathology | Models, Biological | Bone Marrow Transplantation | Cell Line, Tumor | Mice, Inbred NOD | Mice | Tissue Donors | Bone marrow | Genetic aspects | Metastasis | Research | Properties | Health aspects | Prostate cancer | Hematopoietic stem cells
Journal Article
Nature Reviews Clinical Oncology, ISSN 1759-4774, 06/2018, Volume 15, Issue 6, pp. 366 - 381
Cancers are not composed merely of cancer cells alone; instead, they are complex 'ecosystems' comprising many different cell types and noncellular factors. The...
GENE-EXPRESSION SIGNATURE | GROWTH-FACTOR-BETA | PANCREATIC STELLATE CELLS | CARCINOMA-ASSOCIATED FIBROBLASTS | RESISTANCE CAM-DR | ONCOLOGY | PROSTATE-CANCER | ADULT HUMAN FIBROBLASTS | FIBROBLAST ACTIVATION PROTEIN | MESENCHYMAL STEM-CELLS | METASTATIC COLON-CANCER | Care and treatment | Research | Gene mutations | Analysis | Cancer cells | Cancer | Stroma | Metastasis | Patients | Clinical outcomes | Metastases
GENE-EXPRESSION SIGNATURE | GROWTH-FACTOR-BETA | PANCREATIC STELLATE CELLS | CARCINOMA-ASSOCIATED FIBROBLASTS | RESISTANCE CAM-DR | ONCOLOGY | PROSTATE-CANCER | ADULT HUMAN FIBROBLASTS | FIBROBLAST ACTIVATION PROTEIN | MESENCHYMAL STEM-CELLS | METASTATIC COLON-CANCER | Care and treatment | Research | Gene mutations | Analysis | Cancer cells | Cancer | Stroma | Metastasis | Patients | Clinical outcomes | Metastases
Journal Article
The Journal of Nuclear Medicine, ISSN 0161-5505, 03/2018, Volume 59, Issue 3, p. 479
As medical imaging has grown progressively more complicated and subspecialized in recent decades, several standardized reporting systems have been proposed for...
Antigens | Relaying | Medical imaging | Standardization | Positron emission | Reporting | Studies | Urea | Reporting requirements | Data collection | Tomography | Lesions | Prostate cancer | Prostate
Antigens | Relaying | Medical imaging | Standardization | Positron emission | Reporting | Studies | Urea | Reporting requirements | Data collection | Tomography | Lesions | Prostate cancer | Prostate
Journal Article
Nature Reviews Cancer, ISSN 1474-175X, 02/2019, Volume 19, Issue 2, pp. 110 - 117
Cell cooperation promotes many of the hallmarks of cancer via the secretion of diffusible factors that can affect cancer cells or stromal cells in the tumour...
PUBLIC-GOODS | EVOLUTIONARY-GAME | ONCOLOGY | NATURAL-SELECTION | SOCIAL DILEMMAS | MICROENVIRONMENTAL REGULATION | GROWTH-FACTOR PRODUCTION | CLONAL EVOLUTION | DRUG-RESISTANCE | TUMOR-GROWTH | VOLUNTEERS DILEMMA | Cell interaction | Care and treatment | Research | Health aspects | Oncology, Experimental | Cancer | Secretion | Game theory | Cooperation | Stromal cells | Tumors
PUBLIC-GOODS | EVOLUTIONARY-GAME | ONCOLOGY | NATURAL-SELECTION | SOCIAL DILEMMAS | MICROENVIRONMENTAL REGULATION | GROWTH-FACTOR PRODUCTION | CLONAL EVOLUTION | DRUG-RESISTANCE | TUMOR-GROWTH | VOLUNTEERS DILEMMA | Cell interaction | Care and treatment | Research | Health aspects | Oncology, Experimental | Cancer | Secretion | Game theory | Cooperation | Stromal cells | Tumors
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 10/2008, Volume 14, Issue 19, pp. 6302 - 6309
Purpose: A method for enumerating circulating tumor cells (CTC) has received regulatory clearance. The primary objective of this prospective study was to...
circulating tumor cells | prostate cancer | METIS-251923 | BREAST-CANCER | SURROGATE END-POINT | ONCOLOGY | DISEASE | RECEPTOR | PROGRESSION | ANTIGEN | Prostatic Neoplasms - pathology | Prognosis | Humans | Middle Aged | Proportional Hazards Models | Neoplastic Cells, Circulating - metabolism | Drug Resistance, Neoplasm | Male | Treatment Outcome | Disease Progression | Prostatic Neoplasms - mortality | Neoplasm Metastasis | Algorithms | Castration | Time Factors | Aged, 80 and over | Prostatic Neoplasms - blood | Aged
circulating tumor cells | prostate cancer | METIS-251923 | BREAST-CANCER | SURROGATE END-POINT | ONCOLOGY | DISEASE | RECEPTOR | PROGRESSION | ANTIGEN | Prostatic Neoplasms - pathology | Prognosis | Humans | Middle Aged | Proportional Hazards Models | Neoplastic Cells, Circulating - metabolism | Drug Resistance, Neoplasm | Male | Treatment Outcome | Disease Progression | Prostatic Neoplasms - mortality | Neoplasm Metastasis | Algorithms | Castration | Time Factors | Aged, 80 and over | Prostatic Neoplasms - blood | Aged
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2016, Volume 113, Issue 7, pp. E854 - E863
Recent genomic studies challenge the conventional model that each metastasis must arise from a single tumor cell and instead reveal that metastases can be...
Keratin 14 | Breast cancer | Collective dissemination | Polyclonal metastasis | Collective invasion | MIGRATION | MATRIX | MULTIDISCIPLINARY SCIENCES | breast cancer | MODEL | CLUMPS | INVASION | keratin 14 | MICROENVIRONMENT | polyclonal metastasis | collective invasion | EXPRESSION | PROGRESSION | collective dissemination | STEPS | Neoplasm Metastasis - genetics | Animals | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Humans | Mice | Keratin-14 - genetics | Disease Models, Animal | Keratin | Genetic aspects | Metastasis | Gene expression | Observations | Health aspects | Biological Sciences | PNAS Plus
Keratin 14 | Breast cancer | Collective dissemination | Polyclonal metastasis | Collective invasion | MIGRATION | MATRIX | MULTIDISCIPLINARY SCIENCES | breast cancer | MODEL | CLUMPS | INVASION | keratin 14 | MICROENVIRONMENT | polyclonal metastasis | collective invasion | EXPRESSION | PROGRESSION | collective dissemination | STEPS | Neoplasm Metastasis - genetics | Animals | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Humans | Mice | Keratin-14 - genetics | Disease Models, Animal | Keratin | Genetic aspects | Metastasis | Gene expression | Observations | Health aspects | Biological Sciences | PNAS Plus
Journal Article
Nature, ISSN 0028-0836, 07/2012, Volume 487, Issue 7406, pp. 239 - 243
Characterization of the prostate cancer transcriptome and genome has identified chromosomal rearrangements and copy number gains and losses, including ETS gene...
FOXA1 | ANDROGEN RECEPTOR | NETWORK | FUSIONS | BINDING | MULTIDISCIPLINARY SCIENCES | Prostatic Neoplasms - pathology | Cell Proliferation | Signal Transduction | Humans | Receptors, Androgen - metabolism | Cells, Cultured | Molecular Sequence Data | Male | Hepatocyte Nuclear Factor 3-alpha - genetics | Orchiectomy | Sequence Alignment | Prostatic Neoplasms - genetics | Mutation | Development and progression | Genetic aspects | Research | Gene mutations | Health aspects | Prostate cancer | Genetics | Kinases | Genomics | Deoxyribonucleic acid--DNA
FOXA1 | ANDROGEN RECEPTOR | NETWORK | FUSIONS | BINDING | MULTIDISCIPLINARY SCIENCES | Prostatic Neoplasms - pathology | Cell Proliferation | Signal Transduction | Humans | Receptors, Androgen - metabolism | Cells, Cultured | Molecular Sequence Data | Male | Hepatocyte Nuclear Factor 3-alpha - genetics | Orchiectomy | Sequence Alignment | Prostatic Neoplasms - genetics | Mutation | Development and progression | Genetic aspects | Research | Gene mutations | Health aspects | Prostate cancer | Genetics | Kinases | Genomics | Deoxyribonucleic acid--DNA
Journal Article
Frontiers in Oncology, ISSN 2234-943X, 2019, Volume 9, p. 10
Tumor microenvironments contain multiple cell types interacting among one another via different signaling pathways. Furthermore, both cancer cells and...
M1-/M2-polarized macrophages | Multi-stability | EMT-epithelial-to-mesenchymal transition | Interaction network | MET-mesenchymal-to-epithelial transition | CANCER-CELLS | STATES | multi-stability | PHENOTYPE | EMT | interaction network | ZEB1 | ONCOLOGY | PROGRESSION | PARACRINE | Cancer cells | Physiological aspects | Models | Cellular signal transduction | Macrophages | Carcinogenesis | Health aspects | MET–mesenchymal-to-epithelial transition | EMT–epithelial-to-mesenchymal transition
M1-/M2-polarized macrophages | Multi-stability | EMT-epithelial-to-mesenchymal transition | Interaction network | MET-mesenchymal-to-epithelial transition | CANCER-CELLS | STATES | multi-stability | PHENOTYPE | EMT | interaction network | ZEB1 | ONCOLOGY | PROGRESSION | PARACRINE | Cancer cells | Physiological aspects | Models | Cellular signal transduction | Macrophages | Carcinogenesis | Health aspects | MET–mesenchymal-to-epithelial transition | EMT–epithelial-to-mesenchymal transition
Journal Article
Cancer Research, ISSN 0008-5472, 08/2018, Volume 78, Issue 16 Supplement, pp. IA15 - IA15
Journal Article
Cancer and Metastasis Reviews, ISSN 0167-7659, 12/2010, Volume 29, Issue 4, pp. 709 - 722
Chemokines, small pro-inflammatory chemoattractant cytokines that bind to specific G-protein-coupled seven-span transmembrane receptors, are major regulators...
Biomedicine | Oncology | Cancer Research | Cancer progression | CXCL12 / CXCR4 / CXCR7 chemokine axis | Biomedicine general | Chemokines | PROTEIN COUPLED RECEPTOR | STEM-CELLS | CXCR4 EXPRESSION | TRANSENDOTHELIAL MIGRATION | FACTOR-I | COMPLEMENT COMPONENT C3 | BREAST-CANCER | chemokine axis | CELL-DERIVED FACTOR-1 | ONCOLOGY | RHABDOMYOSARCOMA CELLS | CXCL12 / CXCR4 / CXCR7 | TUMOR-GROWTH | Neoplasms - metabolism | Animals | Chemokine CXCL12 - metabolism | Receptors, CXCR - metabolism | Humans | Neoplasms - pathology | Disease Progression | Neoplasms - drug therapy | Receptors, CXCR4 - metabolism | Development and progression | Care and treatment | Metastasis | Cancer
Biomedicine | Oncology | Cancer Research | Cancer progression | CXCL12 / CXCR4 / CXCR7 chemokine axis | Biomedicine general | Chemokines | PROTEIN COUPLED RECEPTOR | STEM-CELLS | CXCR4 EXPRESSION | TRANSENDOTHELIAL MIGRATION | FACTOR-I | COMPLEMENT COMPONENT C3 | BREAST-CANCER | chemokine axis | CELL-DERIVED FACTOR-1 | ONCOLOGY | RHABDOMYOSARCOMA CELLS | CXCL12 / CXCR4 / CXCR7 | TUMOR-GROWTH | Neoplasms - metabolism | Animals | Chemokine CXCL12 - metabolism | Receptors, CXCR - metabolism | Humans | Neoplasms - pathology | Disease Progression | Neoplasms - drug therapy | Receptors, CXCR4 - metabolism | Development and progression | Care and treatment | Metastasis | Cancer
Journal Article