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1. Full Text Latent TGF-β structure and activation
by Shi, Minlong and Zhu, Jianghai and Wang, Rui and Chen, Xing and Mi, Lizhi and Walz, Thomas and Springer, Timothy A
Nature, ISSN 0028-0836, 06/2011, Volume 474, Issue 7351, pp. 343 - 351
Transforming growth factor (TGF)-beta is stored in the extracellular matrix as a latent complex with its prodomain. Activation of TGF-beta 1 requires the... 
GROWTH-FACTOR-BETA | TRANSFORMING GROWTH-FACTOR-BETA-2 | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | COMPLEXES | BINDING-PROTEIN | MATURE | SUPERFAMILY | SECRETION | FACTOR-BETA-1 | TGF-BETA-1 | Latent TGF-beta Binding Proteins - chemistry | Multigene Family | Receptors, Transforming Growth Factor beta - chemistry | Humans | Transforming Growth Factor beta1 - metabolism | Integrins - chemistry | Camurati-Engelmann Syndrome - genetics | Molecular Sequence Data | Activins - metabolism | Crystallography, X-Ray | Antigens, Neoplasm - chemistry | Integrins - metabolism | Transforming Growth Factor beta1 - chemistry | Swine | HEK293 Cells | Antigens, Neoplasm - metabolism | Oligopeptides - chemistry | Transforming Growth Factor beta1 - biosynthesis | Latent TGF-beta Binding Proteins - metabolism | Protein Structure, Tertiary | Amino Acid Sequence | Cell Line | Models, Molecular | Transforming Growth Factor beta1 - genetics | Oligopeptides - metabolism | Mutation - genetics | Amino Acid Motifs | Animals | Receptors, Transforming Growth Factor beta - metabolism
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2. Full Text Fibroblast growth factor-2 and transforming growth factor-beta1 oppositely regulate miR-221 that targets thrombospondin-1 in bovine luteal endothelial cells
by Farberov, Svetlana and Meidan, Rina
Biology of Reproduction, ISSN 0006-3363, 03/2018, Volume 98, Issue 3, pp. 366 - 375
Thrombospondin-1 (THBS1) affects corpus luteum (CL) regression. Highly induced during luteolysis, it acts as a natural anti-angiogenic, proapoptotic compound.... 
Corpus luteum | Angiogenesis | Serpine1 | MicroRNA | Luteolysis | serpine1 | APOPTOSIS | angiogenesis | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | luteolysis | PROMOTES FOLLICULAR ATRESIA | IN-VITRO | REPRODUCTIVE BIOLOGY | INTEGRINS | corpus luteum | microRNA | DIFFERENTIATION | MICRORNA EXPRESSION | CORPUS-LUTEUM | MODULATION | Cell Adhesion - genetics | Luteal Cells - metabolism | Endothelial Cells - metabolism | Transforming Growth Factor beta1 - metabolism | Gene Expression Regulation | MicroRNAs - metabolism | Transforming Growth Factor beta1 - genetics | Luteal Cells - cytology | Corpus Luteum - cytology | Animals | Fibroblast Growth Factor 2 - genetics | Plasminogen Activator Inhibitor 1 - metabolism | Cattle | Corpus Luteum - metabolism | Endothelial Cells - cytology | Thrombospondin 1 - genetics | Fibroblast Growth Factor 2 - metabolism | Female | MicroRNAs - genetics | Plasminogen Activator Inhibitor 1 - genetics | Thrombospondin 1 - metabolism
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3. Full Text Human 'brite/beige' adipocytes develop from capillary networks, and their implantation improves metabolic homeostasis in mice
by Min, So Yun and Kady, Jamie and Nam, Minwoo and Rojas-Rodriguez, Raziel and Berkenwald, Aaron and Kim, Jong Hun and Noh, Hye-Lim and Kim, Jason K and Cooper, Marcus P and Fitzgibbons, Timothy and Brehm, Michael A and Corvera, Silvia
Nature Medicine, ISSN 1078-8956, 03/2016, Volume 22, Issue 3, pp. 312 - 318
Uncoupling protein 1 (UCP1) is highly expressed in brown adipose tissue, where it generates heat by uncoupling electron transport from ATP production. UCP1 is... 
MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | WHITE | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ADULT HUMANS | BROWN ADIPOSE-TISSUE | IDENTIFICATION | CELL BIOLOGY | OBESITY | GENE | INFLAMMATION | EXPRESSION | Enkephalins - metabolism | Humans | Middle Aged | Ion Channels - genetics | Male | RNA, Messenger - metabolism | Enkephalins - genetics | Mitochondrial Proteins - metabolism | Diet, High-Fat | Iodide Peroxidase - metabolism | Adipocytes, Brown - transplantation | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Oxygen Consumption | Apoptosis Regulatory Proteins - metabolism | Protein Precursors - metabolism | Mice | Iodide Peroxidase - genetics | Blood Glucose - metabolism | Integrin beta1 - genetics | Adipocytes, White - metabolism | Glucose Intolerance - metabolism | Proprotein Convertase 1 - genetics | Adipocytes, Brown - metabolism | Homeostasis | Mitochondrial Proteins - genetics | DNA-Binding Proteins - metabolism | Polymerase Chain Reaction | Apoptosis Regulatory Proteins - genetics | Adult | Female | Capillaries | Glucose Tolerance Test | Protein Precursors - genetics | Proprotein Convertase 1 - metabolism | Cell Transplantation | Adipocytes, White - transplantation | DNA-Binding Proteins - genetics | Obesity - metabolism | Integrin beta1 - metabolism | Interleukin-33 - genetics | Animals | Ion Channels - metabolism | Receptor, Platelet-Derived Growth Factor alpha - genetics | Adipocytes - metabolism | Fluorescent Antibody Technique | Interleukin-33 - metabolism | Adipocytes - transplantation | Aged | Glucose Clamp Technique | Uncoupling Protein 1 | Neovascularization, Physiologic | Adipose tissues | Physiological aspects | Genetic aspects | Research | cytokine | human adipocyte | glucose | progenitors | adipokine | capillary | adrenergic | thermogenic adipose tissue | implant
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4. Full Text Endothelial destabilization by angiopoietin-2 via integrin β1 activation
by Hakanpaa, Laura and Sipila, Tuomas and Leppanen, Veli-Matti and Gautam, Prson and Nurmi, Harri and Jacquemet, Guillaume and Eklund, Lauri and Ivaska, Johanna and Alitalo, Kari and Saharinen, Pipsa
Nature Communications, ISSN 2041-1723, 01/2015, Volume 6, Issue 1, p. 5962
Angiopoietins regulate vascular homeostasis via the endothelial Tie receptor tyrosine kinases. Angiopoietin-1 (Ang1) supports endothelial stabilization via... 
Cell Line | Endothelial Cells - metabolism | Angiopoietin-2 - genetics | Humans | Male | Mice, Transgenic | Angiopoietin-1 - metabolism | Angiopoietin-2 - metabolism | Receptor, TIE-2 - genetics | Integrin beta1 - metabolism | Pregnancy | Angiopoietin-1 - genetics | Animals | Female | Receptor, TIE-2 - metabolism | Mice | Integrin beta1 - genetics | Real-Time Polymerase Chain Reaction
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5. Full Text Gene expression profiling combined with functional analysis identify integrin beta1 (ITGB1) as a potential prognosis biomarker in triple negative breast cancer
by Klahan, Sukhontip and Huang, Chi-Cheng and Huang, Wan-Chen and Chang, Che-Mai and Chang, Wei-Chiao and Wong, Henry Sung-Ching and Wu, Mei-Shin and Lin, Yu-Chiao and Lu, Hsing-Fang and Hou, Ming-Feng
Pharmacological Research, ISSN 1043-6618, 02/2016, Volume 104, pp. 31 - 37
Triple negative breast cancer (TNBC) accounts for approximately 15–20% of all types of breast cancer, and treatment is still limited. This type of breast... 
ITGB1 | Store-operated calcium channel | Triple negative breast cancer | Cell migration | RNA, Small Interfering - genetics | Cell Proliferation | Prognosis | Calcium - metabolism | Humans | Asian Continental Ancestry Group - genetics | Gene Expression Regulation, Neoplastic | Gene Silencing | Gene Expression Profiling | RNA, Messenger - metabolism | Integrin beta1 - metabolism | Triple Negative Breast Neoplasms - genetics | Cell Cycle | Taiwan | Cell Line, Tumor | Female | Biomarkers, Tumor - genetics | Integrin beta1 - genetics | Cell Movement | Medical colleges | Pharmacogenetics | Natural language interfaces | Drugstores | Breast cancer | Gene expression | Language processing | Analysis | Pharmacy | Genetic research | Computational linguistics | Integrins
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6. Full Text Identification of genes that regulate epithelial cell migration using an siRNA screening approach
by Selfors, Laura M and Brugge, Joan S and Simpson, Kaylene J and Reynolds, Angela and Leake, Devin and Khvorova, Anastasia and Bui, James
Nature Cell Biology, ISSN 1465-7392, 09/2008, Volume 10, Issue 9, pp. 1027 - 1038
To provide a systematic analysis of genes that regulate epithelial cell migration, we performed a high throughput wound healing screen with MCF-10A breast... 
RNA INTERFERENCE | TARGET | ADHESION | ONCOGENESIS | GTPASES | SUPPRESSORS | ROLES | MOVEMENT | CARCINOMA | POLARIZATION | CELL BIOLOGY | RNA, Small Interfering - genetics | Cell Adhesion Molecules - genetics | Reproducibility of Results | Cell Proliferation | Epithelial Cells - metabolism | Genetic Testing | Signal Transduction | Humans | Actins - metabolism | Wound Healing | Gene Regulatory Networks | Cell Adhesion Molecules - metabolism | beta Catenin - metabolism | Cell Movement - genetics | beta Catenin - genetics | Actins - genetics | Integrin beta1 - metabolism | Phenotype | Transfection | Time Factors | Cell Line, Tumor | Epithelial Cells - cytology | Integrin beta1 - genetics | Physiological aspects | Control | Genetic aspects | Metastasis | Research | Cell migration
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7. Full Text Integrin beta1 over‐expression associates with resistance to tyrosine kinase inhibitor gefitinib in non‐small cell lung cancer
by Ju, Lixia and Zhou, Caicun and Li, Wei and Yan, Linghua
Journal of Cellular Biochemistry, ISSN 0730-2312, 12/2010, Volume 111, Issue 6, pp. 1565 - 1574
The epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) such as gefitinib and erlotinib have been widely used in treating patients with... 
integrin β1 | gefitinib | resistance | non‐small cell lung cancer | non-small cell lung cancer | GENE-MUTATIONS | GEFITINIB | ACTIVATION | INTEGRIN B1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | NON-SMALL CELL LUNG CANCER | ACQUIRED-RESISTANCE | SENSITIVITY | PHASE-II | EGFR | CELL BIOLOGY | GROWTH-FACTOR RECEPTOR | AMPLIFICATION | LINE | RESISTANCE | ERLOTINIB | Cell Cycle - genetics | Cell Adhesion - genetics | Apoptosis - drug effects | Humans | Carcinoma, Non-Small-Cell Lung - metabolism | Apoptosis - genetics | Antineoplastic Agents - therapeutic use | Cell Adhesion - drug effects | Reverse Transcriptase Polymerase Chain Reaction | Sequence Analysis, DNA | Cell Movement - genetics | Integrin beta1 - metabolism | Cell Movement - drug effects | Drug Resistance, Neoplasm - genetics | Protein Kinase Inhibitors - therapeutic use | Quinazolines - therapeutic use | Cell Line, Tumor | Cell Proliferation - drug effects | Carcinoma, Non-Small-Cell Lung - drug therapy | Cell Cycle - drug effects | Integrin beta1 - genetics
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8. Full Text Neutrophil extracellular traps sequester circulating tumor cells via β1‐integrin mediated interactions
by Najmeh, Sara and Cools‐Lartigue, Jonathan and Rayes, Roni F and Gowing, Stephen and Vourtzoumis, Phil and Bourdeau, France and Giannias, Betty and Berube, Julie and Rousseau, Simon and Ferri, Lorenzo E and Spicer, Jonathan D
International Journal of Cancer, ISSN 0020-7136, 05/2017, Volume 140, Issue 10, pp. 2321 - 2330
Despite advances in cancer treatment, metastasis remains today the main cause of cancer death. Local control through complete surgical resection of the primary... 
Inflammation - pathology | RNA, Small Interfering - genetics | Cell Proliferation | Neoplastic Cells, Circulating - pathology | Extracellular Traps - metabolism | Humans | Lung Neoplasms - metabolism | Neoplastic Cells, Circulating - metabolism | Lung Neoplasms - pathology | Male | Neutrophil Infiltration | Integrin beta1 - chemistry | Inflammation - metabolism | Flow Cytometry | Tumor Cells, Cultured | Disease Models, Animal | Neutrophils - pathology | Mice, Inbred C57BL | Cell Adhesion | Blotting, Western | Integrin beta1 - metabolism | Animals | Fluorescent Antibody Technique | Mice | Integrin beta1 - genetics
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9. Full Text Role of a disintegrin and metalloprotease 10 in Staphylococcus aureus α-hemolysin–mediated cellular injury
by Georgia A. Wilke and Juliane Bubeck Wardenburg and Richard P. Novick
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2010, Volume 107, Issue 30, pp. 13473 - 13478
Staphylococcus aureus α-hemolysin (Hla), a potent cytotoxin, plays an important role in the pathogenesis of staphylococcal diseases, including those caused by... 
Receptors | Epithelial cells | Cell lines | Erythrocytes | Small interfering RNA | Cytotoxicity | Toxins | Cell membranes | Focal adhesions | Staphylococcus aureus | Cellular receptor | Pore-forming cytotoxin | CELLS | INFECTIONS | TYROSINE PHOSPHORYLATION | PROTECTION | pore-forming cytotoxin | TOXIN | MULTIDISCIPLINARY SCIENCES | P130(CAS) | MURINE MODEL | ERYTHROCYTES | PORE | BINDING | cellular receptor | Amyloid Precursor Protein Secretases - genetics | Epithelial Cells - metabolism | Hemolysin Proteins - pharmacology | Staphylococcus aureus - physiology | Hemolysin Proteins - genetics | Humans | Focal Adhesions | Molecular Sequence Data | Immunoblotting | RNA Interference | Membrane Proteins - metabolism | Staphylococcus aureus - metabolism | Staphylococcus aureus - genetics | Amino Acid Sequence | Cell Line | Cell Survival - drug effects | Rabbits | Membrane Proteins - genetics | Electrophoresis, Polyacrylamide Gel | Bacterial Proteins - genetics | ADAM10 Protein | Epithelial Cells - pathology | Host-Pathogen Interactions | Integrin beta1 - metabolism | ADAM Proteins - metabolism | Amyloid Precursor Protein Secretases - metabolism | Bacterial Proteins - pharmacology | Animals | Epithelial Cells - microbiology | Erythrocytes - metabolism | Cell Line, Tumor | Protein Binding | Bacterial Proteins - metabolism | Mutation | ADAM Proteins - genetics | Integrin beta1 - genetics | Hemolysin Proteins - metabolism | Biological Sciences
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10. Full Text Integrin endosomal signalling suppresses anoikis
by Alanko, Jonna and Mai, Anja and Jacquemet, Guillaume and Schauer, Kristine and Kaukonen, Riina and Saari, Markku and Goud, Bruno and Ivaska, Johanna
Nature Cell Biology, ISSN 1465-7392, 11/2015, Volume 17, Issue 11, pp. 1412 - 1421
Integrin-containing focal adhesions transmit extracellular signals across the plasma membrane to modulate cell adhesion, signalling and survival. Although... 
MIGRATION | ADHESOME | RAB21 | TRANSDUCTION | EXTRACELLULAR-MATRIX | CELL-ADHESION | DYNAMIN | FOCAL ADHESION KINASE | CANCER PROGRESSION | ENDOCYTOSIS | CELL BIOLOGY | Focal Adhesion Kinase 1 - genetics | Phosphorylation | Cricetulus | Humans | Extracellular Matrix - metabolism | Endosomes - metabolism | RNA Interference | Anoikis - physiology | Endocytosis - genetics | Focal Adhesion Kinase 1 - metabolism | CHO Cells | rab GTP-Binding Proteins - metabolism | Cell Line | Cricetinae | Anoikis - genetics | Cells, Cultured | Signal Transduction - genetics | Endocytosis - physiology | Mice, Knockout | Integrin beta1 - metabolism | Microscopy, Confocal | Animals | Focal Adhesions - metabolism | Cell Line, Tumor | Protein Binding | Signal Transduction - physiology | Integrin beta1 - genetics
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11. Full Text Integrin expression profiling identifies integrin alpha5 and beta1 as prognostic factors in early stage non-small cell lung cancer
by Dingemans, Anne-Marie C and van den Boogaart, Vivian and Vosse, Bettine A and van Suylen, Robert-Jan and Griffioen, Arjan W and Thijssen, Victor L
Molecular Cancer, ISSN 1476-4598, 06/2010, Volume 9, Issue 1, pp. 152 - 152
Background: Selection of early stage non-small cell lung cancer patients with a high risk of recurrence is warranted in order to select patients who will... 
MIGRATION | INVASION | EPITHELIAL-CELLS | ONCOLOGY | ADENOCARCINOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR-METASTASIS | GENE-EXPRESSION | ADHESION RECEPTORS | Integrin alphaV - biosynthesis | Prognosis | Lung Neoplasms - mortality | Humans | Lung Neoplasms - metabolism | Middle Aged | Male | Gene Expression Profiling | Aged, 80 and over | Adult | Female | Retrospective Studies | Integrin alphaV - genetics | Lung Neoplasms - genetics | Gene Expression | Biomarkers, Tumor - analysis | Carcinoma, Non-Small-Cell Lung - genetics | Carcinoma, Non-Small-Cell Lung - metabolism | Kaplan-Meier Estimate | Reverse Transcriptase Polymerase Chain Reaction | Carcinoma, Non-Small-Cell Lung - mortality | Integrin beta1 - biosynthesis | Disease-Free Survival | Aged | Integrin beta1 - genetics | Polymerase chain reaction | Usage | Physiological aspects | Genetic aspects | Research | Lung cancer, Non-small cell | Integrins
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12. Full Text FZD4 as a mediator of ERG oncogene-induced WNT signaling and epithelial-to-mesenchymal transition in human prostate cancer cells
by Gupta, Santosh and Iljin, Kristiina and Sara, Henri and Mpindi, John Patrick and Mirtti, Tuomas and Vainio, Paula and Rantala, Juha and Alanen, Kalle and Nees, Matthias and Kallioniemi, Olli
Cancer Research, ISSN 0008-5472, 09/2010, Volume 70, Issue 17, pp. 6735 - 6745
TMPRSS2-ERG and other gene fusions involving ETS factors and genes with strong promoter elements are common in prostate cancer. Although ERG activation has... 
HETEROGENEITY | GENE FUSIONS | TRANSCRIPTS | INVASION | ACTIVATION | ONCOLOGY | TMPRSS2-ERG FUSION | E-CADHERIN | BETA-CATENIN | EXPRESSION | PROGRESSION | Transcriptional Regulator ERG | Prostatic Neoplasms - metabolism | Up-Regulation | Receptors, G-Protein-Coupled - metabolism | Humans | Gene Expression Regulation, Neoplastic | Male | Wnt Proteins - metabolism | Cadherins - biosynthesis | Gene Knockdown Techniques | Prostatic Neoplasms - genetics | Transfection | Trans-Activators - genetics | Trans-Activators - biosynthesis | Cadherins - genetics | Prostatic Neoplasms - pathology | Cell Adhesion - genetics | Gene Silencing | Frizzled Receptors - metabolism | Epithelial Cells - pathology | Signal Transduction - genetics | Integrin beta1 - biosynthesis | Frizzled Receptors - genetics | Cell Line, Tumor | Receptors, G-Protein-Coupled - genetics | Integrin beta1 - genetics | Mesoderm - pathology
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13. Full Text Compact spheroid formation by ovarian cancer cells is associated with contractile behavior and an invasive phenotype
by Sodek, Katharine L and Ringuette, Maurice J and Brown, Theodore J
International Journal of Cancer, ISSN 0020-7136, 05/2009, Volume 124, Issue 9, pp. 2060 - 2070
Ovarian cancer cells are present in malignant ascites both as individual cells and as multicellular spheroid aggregates. Although spheroid formation affords... 
contraction | 3D culture | invasion | myofibroblast | spheroid | Spheroid | Myofibroblast | Contraction | Invasion | SURFACE EPITHELIUM | PERITONEAL | TUMOR-CELLS | E-CADHERIN | PLASMINOGEN-ACTIVATOR RECEPTOR | IN-VITRO | ONCOLOGY | MULTICELLULAR SPHEROIDS | EXTRACELLULAR-MATRIX | GROWTH-FACTOR | spheroids | CARCINOMA | Cell Proliferation | Humans | Transforming Growth Factor beta1 - metabolism | Ovarian Neoplasms - pathology | Spheroids, Cellular - pathology | Extracellular Matrix - metabolism | Transglutaminases - genetics | GTP-Binding Proteins - genetics | Female | Ovarian Neoplasms - metabolism | Tumor Cells, Cultured | Fibroblasts - metabolism | Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase - genetics | Neoplasm Invasiveness | Spheroids, Cellular - metabolism | Transforming Growth Factor beta1 - genetics | Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase - metabolism | Cell Adhesion | Fibronectins - metabolism | Integrin beta1 - metabolism | Receptors, Urokinase Plasminogen Activator - metabolism | Collagen - metabolism | Phenotype | Transglutaminases - metabolism | Connective Tissue Growth Factor - genetics | Fibroblasts - cytology | Receptors, Urokinase Plasminogen Activator - genetics | Integrin beta1 - genetics | Extracellular Matrix - pathology | Connective Tissue Growth Factor - metabolism | Cell Movement | GTP-Binding Proteins - metabolism
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