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1. Full Text Missing-in-metastasis protein downregulates CXCR4 by promoting ubiquitylation and interaction with small Rab GTPases
by Li, Lushen and Baxter, Shaneen S and Gu, Ning and Ji, Min and Zhan, Xi
Journal of cell science, ISSN 0021-9533, 04/2017, Volume 130, Issue 8, pp. 1475 - 1485
MIM | CXCR4 | AIP4 | Rab7 | Ubiquitylation | MVBs | Life Sciences & Biomedicine | Science & Technology | Cell Biology | rab GTP-Binding Proteins - metabolism | Down-Regulation | Humans | Neoplasm Proteins - immunology | Neoplasm Proteins - metabolism | Endosomes - metabolism | Mice, Knockout | Protein Transport | Receptors, CXCR4 - metabolism | Ubiquitination | Animals | Chemokine CXCL12 - metabolism | Transport Vesicles - metabolism | Microfilament Proteins - immunology | Protein Binding | Endocytosis - genetics | Mice | Microfilament Proteins - metabolism | HeLa Cells | Neoplasm Proteins - genetics | Microfilament Proteins - genetics | Coils | Ubiquitin | GTP-binding protein | Membranes | CXCL12 protein | Guanosine triphosphatases | Metastasis | SDF-1 protein | CXCR4 protein | Metastases | Proteins | Clonal deletion | Rab5 protein | Internalization | Protein transport | Curvature | Ubiquitin-protein ligase | Cytoplasm | Index Medicus
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2. Full Text Targeting AU-rich element-mediated mRNA decay with a truncated active form of the zinc-finger protein TIS11b/BRF1 impairs major hallmarks of mammary tumorigenesis
by Rataj, Felicitas and Planel, Séverine and Denis, Josiane and Roelants, Caroline and Filhol, Odile and Guyon, Laurent and Feige, Jean-Jacques and Cherradi, Nadia
Oncogene, ISSN 0950-9232, 06/2019, Volume 38, Issue 26, pp. 5174 - 5190
Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Human Umbilical Vein Endothelial Cells | Chlorocebus aethiops | Recombinant Fusion Proteins - pharmacology | Humans | Carcinogenesis - genetics | Cells, Cultured | Gene Expression Regulation, Neoplastic | TATA-Binding Protein Associated Factors - genetics | Carcinogenesis - metabolism | RNA Stability - genetics | Protein Isoforms - physiology | AU Rich Elements - genetics | Animals | Breast Neoplasms - genetics | TATA-Binding Protein Associated Factors - physiology | Breast Neoplasms - pathology | Gain of Function Mutation - physiology | Recombinant Fusion Proteins - genetics | Female | Zinc Fingers - genetics | Mice | Mice, Inbred BALB C | COS Cells | Protein Isoforms - genetics | Care and treatment | Messenger RNA | Breast cancer | Genetic aspects | Research | Binding proteins | Vascular endothelial growth factor | Vimentin | CXCL12 protein | Mesenchyme | Medical innovations | Serine | Cell fusion | Drug resistance | Proteins | N-Cadherin | Clonal deletion | Fractalkine | Tumorigenesis | Fusion protein | Pentraxins | mRNA turnover | Tumor cell lines | SDF-1 protein | Cadherin | Endothelial cells | RNA-binding protein | Hypoxia | Monocyte chemoattractant protein 1 | Chemokines | Index Medicus | Life Sciences
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3. Full Text The Lim1 oncogene as a new therapeutic target for metastatic human renal cell carcinoma
by Hamaidi, Imène and Coquard, Catherine and Danilin, Sabrina and Dormoy, Valérian and Béraud, Claire and Rothhut, Sylvie and Barthelmebs, Mariette and Benkirane-Jessel, Nadia and Lindner, Véronique and Lang, Hervé and Massfelder, Thierry
Oncogene, ISSN 0950-9232, 01/2019, Volume 38, Issue 1, pp. 60 - 72
Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | RNA, Small Interfering - genetics | Kidney Neoplasms - genetics | Humans | Neoplasm Proteins - physiology | Gene Expression Regulation, Neoplastic | Carcinoma, Renal Cell - genetics | Neoplasm Proteins - antagonists & inhibitors | LIM-Homeodomain Proteins - antagonists & inhibitors | Molecular Targeted Therapy | Gene Knockdown Techniques | Lung Neoplasms - secondary | RNA Interference | Epithelial-Mesenchymal Transition | Neoplasm Proteins - genetics | Kidney Neoplasms - therapy | Oncogenes | Transcription Factors - physiology | Signal Transduction | Neoplasm Invasiveness | Von Hippel-Lindau Tumor Suppressor Protein - physiology | Transcription Factors - antagonists & inhibitors | Lung Neoplasms - therapy | Transcription Factors - genetics | LIM-Homeodomain Proteins - genetics | Lung Neoplasms - prevention & control | RNA, Small Interfering - therapeutic use | Carcinoma, Renal Cell - secondary | Carcinoma, Renal Cell - therapy | Cell Line, Tumor | LIM-Homeodomain Proteins - physiology | Cell Movement | Complications and side effects | Care and treatment | Transcription factors | Genetic aspects | Carcinoma, Renal cell | Metastasis | Gene expression | Health aspects | Risk factors | Cell proliferation | Intravenous administration | Mesenchyme | Fibronectin | Lymph nodes | Metastases | Cell adhesion & migration | Angiogenesis | Signal transduction | Cell adhesion | Gene transfer | Therapeutic applications | siRNA | SDF-1 protein | CXCR4 protein | Immune checkpoint | Hedgehog protein | Kidney cancer | Tumor suppressor genes | VHL protein | Neoplasia | Paxillin | Cell migration | Clear cell-type renal cell carcinoma | Apoptosis | Index Medicus | Life Sciences | Human health and pathology | Urology and Nephrology | Biochemistry, Molecular Biology | Genomics | Cancer
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4. Full Text Structural Basis of the Interaction between Chemokine Stromal Cell-derived Factor-1/CXCL12 and Its G-protein-coupled Receptor CXCR4
by Yutaka Kofuku and Chie Yoshiura and Takumi Ueda and Hiroaki Terasawa and Takahiro Hirai and Sae Tominaga and Masako Hirose and Yoshitake Maeda and Hideo Takahashi and Yuya Terashima and Kouji Matsushima and Ichio Shimada
The Journal of biological chemistry, ISSN 0021-9258, 12/2009, Volume 284, Issue 50, pp. 35240 - 35250
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Protein Structure, Tertiary | Chemokine CXCL12 - chemistry | Chemokine CXCL12 - genetics | Chemokine CXCL12 - metabolism | Humans | Models, Molecular | Nuclear Magnetic Resonance, Biomolecular | Receptors, CXCR4 - genetics | Structure-Activity Relationship | Receptors, CXCR4 - chemistry | Receptors, CXCR4 - metabolism | CXCL12 protein | G protein-coupled receptors | Purification | Crystallization | Data processing | Guanine nucleotide-binding protein | SDF-1 protein | CXCR4 protein | Metastases | Infection | N.M.R | Signal transduction | Chemokines | Cancer | Index Medicus | Protein Structure and Folding
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5. Full Text Targeting the CXCR4/CXCL12 axis in treating epithelial ovarian cancer
by Mao, T.L and Fan, K.F and Liu, C.L
Gene therapy, ISSN 0969-7128, 10/2017, Volume 24, Issue 10, pp. 621 - 629
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Genetics & Heredity | Biotechnology & Applied Microbiology | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Receptors, CXCR4 - antagonists & inhibitors | Humans | Heterocyclic Compounds - pharmacology | rhoA GTP-Binding Protein - metabolism | Mice, SCID | RNAi Therapeutics - methods | Receptors, CXCR4 - metabolism | Ovarian Neoplasms - genetics | Animals | Chemokine CXCL12 - genetics | Chemokine CXCL12 - metabolism | Cell Line, Tumor | Ovarian Neoplasms - therapy | Carcinoma - genetics | Carcinoma - therapy | Female | Mice, Inbred NOD | Receptors, CXCR4 - genetics | Mice | rac1 GTP-Binding Protein - metabolism | Care and treatment | RNA | Analysis | Development and progression | Metastasis | Health aspects | Ovarian cancer | Cancer | Cdc42 protein | Cell proliferation | Flow cytometry | CXCL12 protein | Ovarian carcinoma | Leukocyte migration | Toxicity | Cytotoxicity | RhoA protein | Rac1 protein | mRNA | Tumor cell lines | SDF-1 protein | CXCR4 protein | Metastases | Cytometry | Xenografts | Biocompatibility | Chemokines | Cell migration | Tumors | Index Medicus
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6. Full Text The impact of stromal Hic-5 on the tumorigenesis of colorectal cancer through lysyl oxidase induction and stromal remodeling
by Omoto, Tomokatsu and Kim-Kaneyama, Joo-Ri and Lei, Xiao-Feng and Orimo, Akira and Ohnishi, Koji and Yoshihara, Kosuke and Miyauchi, Aya and Li, Shuo and Gao, Lin and Umemoto, Takahiro and Tanaka, Junichi and Nakahara, Kenta and Takeya, Motohiro and Ishida, Fumio and Kudo, Shin-Ei and Haraguchi, Shogo and Miyazaki, Takuro and Miyazaki, Akira
Oncogene, ISSN 0950-9232, 03/2018, Volume 37, Issue 9, pp. 1205 - 1219
Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Cell Proliferation | Prognosis | Cancer-Associated Fibroblasts - metabolism | Stromal Cells - pathology | Coculture Techniques | Humans | Male | Intracellular Signaling Peptides and Proteins - metabolism | LIM Domain Proteins - metabolism | Azoxymethane - toxicity | Biomarkers, Tumor | Carcinogenesis - metabolism | Cytoskeletal Proteins - physiology | Tumor Cells, Cultured | Intracellular Signaling Peptides and Proteins - genetics | Colorectal Neoplasms - metabolism | Fibroblasts - metabolism | DNA-Binding Proteins - physiology | Signal Transduction | Mice, Inbred C57BL | Stromal Cells - metabolism | Fibroblasts - pathology | Colorectal Neoplasms - chemically induced | Protein-Lysine 6-Oxidase | Mice, Knockout | Carcinogenesis - pathology | Cancer-Associated Fibroblasts - pathology | Animals | LIM Domain Proteins - genetics | LIM Domain Proteins - physiology | Mice | Colorectal Neoplasms - pathology | Apoptosis | Extracellular matrix | Genetic aspects | Research | Carcinogenesis | Colorectal cancer | Cell culture | CXCL12 protein | Collagen (type I) | Hydrogen peroxide | Transcription | Colorectal carcinoma | Metastasis | SDF-1 protein | Lysyl oxidase | IL-1β | Metastases | Colon cancer | Azoxymethane | Rodents | Fibroblasts | Tumorigenesis | Index Medicus
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7. Full Text Upregulation of CXCR4 is functionally crucial for maintenance of stemness in drug-resistant non-small cell lung cancer cells
by Jung, M.-J and Rho, J.-K and Kim, Y.-M and Jung, J.E and Jin, Y.B and Ko, Y.-G and Lee, J.-S and Lee, S.-J and Lee, J.C and Park, M.-J
Oncogene, ISSN 0950-9232, 01/2013, Volume 32, Issue 2, pp. 209 - 221
non-small cell lung cancer | CXCR4 | STAT3 signaling | tumorigenicity | cancer stem cell | PI3K/PTEN/Akt/mTOR signaling | Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Lung Neoplasms - drug therapy | Up-Regulation | Phosphorylation | TOR Serine-Threonine Kinases - metabolism | Neoplastic Stem Cells - drug effects | Phosphatidylinositol 3-Kinase - antagonists & inhibitors | Humans | Lung Neoplasms - metabolism | Heterocyclic Compounds - pharmacology | Drug Resistance, Neoplasm | Lung Neoplasms - pathology | Chemokine CXCL12 - secretion | RNA Interference | Female | Receptors, CXCR4 - genetics | Proto-Oncogene Proteins c-akt - metabolism | Phosphatidylinositol 3-Kinase - metabolism | Neoplastic Stem Cells - physiology | STAT3 Transcription Factor - genetics | STAT3 Transcription Factor - metabolism | Carcinoma, Non-Small-Cell Lung - pathology | PTEN Phosphohydrolase - genetics | Signal Transduction | Receptors, CXCR4 - antagonists & inhibitors | Carcinoma, Non-Small-Cell Lung - metabolism | PTEN Phosphohydrolase - metabolism | Tyrphostins - pharmacology | Mice, SCID | Receptors, CXCR4 - metabolism | Animals | Mice, Nude | Cell Line, Tumor | Mice | Pyridines - pharmacology | RNA, Small Interfering | Carcinoma, Non-Small-Cell Lung - drug therapy | STAT3 Transcription Factor - antagonists & inhibitors | Care and treatment | Stem cells | Cancer cells | Development and progression | Research | Lung cancer, Non-small cell | Cancer | Signal transduction | Drug resistance | Lung cancer | TOR protein | Secretion | Stat3 protein | Non-small cell lung carcinoma | AKT protein | Data processing | Tumorigenicity | siRNA | Tumor cell lines | SDF-1 protein | CXCR4 protein | 1-Phosphatidylinositol 3-kinase | Transfection | PTEN protein | Index Medicus
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8. Full Text Fatty‐acid‐binding protein 4 as a novel contributor to mononuclear cell activation and endothelial cell dysfunction in atherosclerosis
by Wu, Yen-Wen and Chang, Ting-Ting and Chang, Chia-Chi and Chen, Jaw-Wen
International journal of molecular sciences, ISSN 1661-6596, 12/2020, Volume 21, Issue 23, pp. 1 - 16
Endothelial dysfunction | Adhesion molecules | Coronary artery disease | Fatty acid‐binding protein 4 | Atherosclerosis | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Cell culture | Phosphorylation | Vascular cell adhesion molecule 1 | Antibodies | Cardiovascular disease | Leukocytes (mononuclear) | Adipocytes | Kinases | Proteins | Body mass index | Signal transduction | Cell activation | Tumor necrosis factor-TNF | Stat1 protein | Diabetes mellitus (non-insulin dependent) | Vascular endothelial growth factor | Heart diseases | Hypertension | Creatinine | Intercellular adhesion molecule 1 | Coronary artery | Extracellular signal-regulated kinase | Metabolism | SDF-1 protein | Insulin | Endothelial cells | Monocytes | Arteriosclerosis | Coronary vessels | Body size | Diabetes | P-selectin | Index Medicus | atherosclerosis | coronary artery disease | fatty acid-binding protein 4 | endothelial dysfunction
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9. Full Text Elevating CXCR7 Improves Angiogenic Function of EPCs via Akt/GSK-3β/Fyn-Mediated Nrf2 Activation in Diabetic Limb Ischemia
by Dai, Xiaozhen and Yan, Xiaoqing and Zeng, Jun and Chen, Jing and Wang, Yuehui and Chen, Jun and Li, Yan and Barati, Michelle T and Wintergerst, Kupper A and Pan, Kejian and Nystoriak, Matthew A and Conklin, Daniel J and Rokosh, Gregg and Epstein, Paul N and Li, Xiaokun and Tan, Yi
Circulation research, ISSN 0009-7330, 01/2017, Volume 120, Issue 5, pp. e7 - e23
chemokine CXCL12 | angiogenesis | endothelial progenitor cells | hindlimb ischemia | CXC chemokine receptor type 7 | Cardiac & Cardiovascular Systems | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Diabetes Mellitus - pathology | Humans | Oxidative Stress - physiology | Cells, Cultured | Diabetes Mellitus - metabolism | Ischemia - metabolism | Male | Mice, Transgenic | Glycogen Synthase Kinase 3 beta - metabolism | Gene Knockdown Techniques | Neovascularization, Physiologic - physiology | Endothelial Progenitor Cells - physiology | Animals | Proto-Oncogene Proteins c-fyn - metabolism | Hindlimb - blood supply | NF-E2-Related Factor 2 - metabolism | HEK293 Cells | Hindlimb - pathology | Receptors, CXCR - biosynthesis | Mice | Proto-Oncogene Proteins c-akt - metabolism | Hindlimb - metabolism | Ischemia - pathology | Oxidative stress | Phosphorylation | Glucose kinase | AKT protein | Glucose | Kinases | Proteins | Angiogenesis | Ischemia | Catalase | Rodents | Heme | Localization | Fyn protein | Glycogen | Quinone | Diabetes mellitus | Glycogen synthase kinase 3 | Heme oxygenase (decyclizing) | SDF-1 protein | Progenitor cells | Chemokine receptors | CXCR4 protein | Nuclear transport | 1-Phosphatidylinositol 3-kinase | NAD | Oxygenase | Lipoproteins | NAD(P)H dehydrogenase | Stem cells | Diabetes | Apoptosis | Index Medicus | Mechanisms | Signal Transduction | Endothelial progenitor celsl | Cell Signaling | Cell Therapy | chemokine receptor CXCR7 | hind limb ischemia | chemoreceptor | Basic Science Research
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10. Full Text Resveratrol pretreatment enhanced homing of SDF‐1α‐preconditioned bone marrow‐derived mesenchymal stem cells in a rat model of liver cirrhosis
by Hajinejad, Mehrdad and Pasbakhsh, Parichehr and Omidi, Ameneh and Mortezaee, Keywan and Nekoonam, Saied and Mahmoudi, Reza and Kashani, Iraj Ragerdi
Journal of cellular biochemistry, ISSN 0730-2312, 03/2018, Volume 119, Issue 3, pp. 2939 - 2950
stromal cell‐derived factor‐1 (SDF‐1) | homing | precondition | liver | resveratrol | bone marrow‐derived mesenchymal stem cells (BMSCs) | bone marrow-derived mesenchymal stem cells (BMSCs) | stromal cell-derived factor-1 (SDF-1) | Flow cytometry | CXCL12 protein | Mesenchyme | Liver | p53 Protein | Stem cell transplantation | Transplantation | Matrix metalloproteinase | Homing | Rodents | Resveratrol | Bone marrow | Metalloproteinase | Pretreatment | Spleen | Injection | SDF-1 protein | SIRT1 protein | CXCR4 protein | Bile duct | Cirrhosis | Cytometry | Animals | Hepatocytes | Lungs | Stem cells | Strategy | Protein expression | Immunofluorescence | Preconditioning | Liver cirrhosis | Cell migration | Liver transplantation | Bile | Index Medicus
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