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Sulforaphane down-regulates COX-2 expression by activating p38 and inhibiting NF-κB-DNA-binding activity in human bladder T24 cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1097-0142(20010701)92:1<188::aid-cncr1308>3.0.co;2-wopenalex-snapshot
Relation between cyclooxygenase-2 expression and tumor invasiveness and patient survival in transitional cell carcinoma of the urinary bladder
inferredcites →https://doi.org/10.1002/cncr.11425openalex-snapshot
Involvement of the p38 mitogen‐activated protein kinase cascade in hepatocellular carcinoma
inferredcites →https://doi.org/10.1002/mc.20224openalex-snapshot
Dietary agents as histone deacetylase inhibitors
inferredcites →https://doi.org/10.1016/j.bcp.2005.03.015openalex-snapshot
Role of PI3K/Akt and MEK/ERK signaling pathways in sulforaphane- and erucin-induced phase II enzymes and MRP2 transcription, G2/M arrest and cell death in Caco-2 cells
inferredcites →https://doi.org/10.1016/j.biocel.2006.03.021openalex-snapshot
Signalling networks regulating cyclooxygenase-2
inferredcites →https://doi.org/10.1016/j.ccr.2004.07.012openalex-snapshot
Binding at and transactivation of the COX-2 promoter by nuclear tyrosine kinase receptor ErbB-2
inferredcites →https://doi.org/10.1016/j.mrfmmm.2004.04.017openalex-snapshot
Cancer-preventive isothiocyanates: measurement of human exposure and mechanism of action
inferredcites →https://doi.org/10.1016/j.plefa.2004.11.001openalex-snapshot
Control of cyclooxygenase-2 transcriptional activation by pro-inflammatory mediators
inferredcites →https://doi.org/10.1016/j.toxlet.2008.05.014openalex-snapshot
p38 MAPK activation and mitochondrial depolarization mediate the cytotoxicity of Taiwan cobra phospholipase A2 on human neuroblastoma SK-N-SH cells
inferredcites →https://doi.org/10.1016/s0070-2137(01)80001-7openalex-snapshot
Cellular thiols and redox-regulated signal transduction
inferredcites →https://doi.org/10.1016/s0090-4295(02)01909-xopenalex-snapshot
Association of cyclooxygenase-2 expression with prognosis of stage T1 grade 3 bladder cancer
inferredcites →https://doi.org/10.1021/tx990189wopenalex-snapshot
Inhibition of Human Cytochrome P450 Enzymes by 1,2-Dithiole-3-thione, Oltipraz and Its Derivatives, and Sulforaphane
inferredcites →https://doi.org/10.1038/sj.onc.1209936openalex-snapshot
Mutual cross-talk between reactive oxygen species and nuclear factor-kappa B: molecular basis and biological significance
inferredcites →https://doi.org/10.1093/carcin/23.8.1399openalex-snapshot
Sulforaphane and its glutathione conjugate but not sulforaphane nitrile induce UDP-glucuronosyl transferase (UGT1A1) and glutathione transferase (GSTA1) in cultured cells
inferredcites →https://doi.org/10.1097/01.ju.0000043638.89552.edopenalex-snapshot
Cyclooxygenase-2 is Highly Expressed in Carcinoma in Situ and T1 Transitional Cell Carcinoma of the Bladder
inferredcites →https://doi.org/10.1111/j.1753-4887.2008.00065.xopenalex-snapshot
Dietary agents as histone deacetylase inhibitors: sulforaphane and structurally related isothiocyanates
inferredcites →https://doi.org/10.1158/0008-5472.can-04-3567openalex-snapshot
Transitional Cell Hyperplasia and Carcinomas in Urinary Bladders of Transgenic Mice with Keratin 5 Promoter-Driven Cyclooxygenase-2 Overexpression
inferredcites →https://doi.org/10.1158/0008-5472.can-07-6171openalex-snapshot
Serotonin Receptors, Novel Targets of Sulforaphane Identified by Proteomic Analysis in Caco-2 Cells
inferredcites →https://doi.org/10.1158/1535-7163.mct-05-0041openalex-snapshot
Mitochondria are the primary target in isothiocyanate-induced apoptosis in human bladder cancer cells
inferredcites →https://doi.org/10.1207/s15327914nc382_5openalex-snapshot
Disposition of Glucosinolates and Sulforaphane in Humans After Ingestion of Steamed and Fresh Broccoli
inferredcites →https://doi.org/10.2174/1389200043489027openalex-snapshot
Isothiocyanates in the Chemoprevention of Bladder Cancer
inferredcites →https://doi.org/10.3181/00379727-207-2320227openalex-snapshot
Sulforaphane retards the growth of human PC-3 xenografts and inhibits HDAC activity in human subjects.
inferredcites →https://doi.org/10.3892/ijo.29.4.883openalex-snapshot
Effect of sulforaphane on cell growth, G0/G1 phase cell progression and apoptosis in human bladder cancer T24 cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/pharmacia.73.e187811zenodo-depositor-declared
Anti-inflammatory potential of sulfurous mineral water and sulfur-containing bioactive compounds: a comparative study
inferred← citeshttps://doi.org/10.1007/128_2012_337openalex-snapshot
Chemoprotection Against Cancer by Isothiocyanates: A Focus on the Animal Models and the Protective Mechanisms
inferred← citeshttps://doi.org/10.1007/978-81-322-1533-2_8openalex-snapshot
Mechanisms of Chemopreventive Activity of Sulforaphane
inferred← citeshttps://doi.org/10.1007/s00044-014-0958-4openalex-snapshot
Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer
inferred← citeshttps://doi.org/10.1007/s10555-010-9239-yopenalex-snapshot
Phytochemicals: cancer chemoprevention and suppression of tumor onset and metastasis
inferred← citeshttps://doi.org/10.1007/s11694-017-9589-zopenalex-snapshot
Sulforaphane, polyphenols and related anti-inflammatory and antioxidant activities changes of Egyptian broccoli during growth
inferred← citeshttps://doi.org/10.1007/s11912-019-0782-6openalex-snapshot
Cancer Biomarkers for Integrative Oncology
inferred← citeshttps://doi.org/10.1007/s11912-024-01595-6openalex-snapshot
Traditional Chinese Medicine Herbs for Breast Cancer Prevention and Survival: A Narrative Review of Epidemiological Studies from Taiwan
inferred← citeshttps://doi.org/10.1007/s12012-010-9072-0openalex-snapshot
Protective Effect of Sulforaphane on Human Vascular Endothelial Cells Against Lipopolysaccharide-Induced Inflammatory Damage
inferred← citeshttps://doi.org/10.1007/s12013-012-9360-3openalex-snapshot
Effect of Sulforaphane on Growth Inhibition in Human Brain Malignant Glioma GBM 8401 Cells by Means of Mitochondrial- and MEK/ERK-Mediated Apoptosis Pathway
inferred← citeshttps://doi.org/10.1007/s40495-015-0024-zopenalex-snapshot
Cruciferous Vegetables, Isothiocyanates, and Prevention of Bladder Cancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.12.075openalex-snapshot
Sulforaphane inhibits osteoclast differentiation by suppressing the cell-cell fusion molecules DC-STAMP and OC-STAMP
inferred← citeshttps://doi.org/10.1016/j.bcp.2010.10.005openalex-snapshot
Anti-angiogenic effects of dietary isothiocyanates: Mechanisms of action and implications for human health
inferred← citeshttps://doi.org/10.1016/j.bionut.2012.10.012openalex-snapshot
Sulforaphane (SFN) regulates dedifferentiation and cyclooxygenase-2 (COX-2) expression via MAPkinase pathway in rabbit articular chondrocytes
inferred← citeshttps://doi.org/10.1016/j.canep.2010.09.008openalex-snapshot
Anti-carcinogenic effects of sulforaphane in association with its apoptosis-inducing and anti-inflammatory properties in human cervical cancer cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.10.033openalex-snapshot
Chemoprevention with isothiocyanates – From bench to bedside
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.04.012openalex-snapshot
Role of 4-hydroxynonenal in chemopreventive activities of sulforaphane
inferred← citeshttps://doi.org/10.1016/j.jff.2016.02.034openalex-snapshot
Benzyl isothiocyanate but not benzyl nitrile from Brassicales plants dually blocks the COX and LOX pathway in primary human immune cells
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2012.08.004openalex-snapshot
Epithelial-mesenchymal transition, a novel target of sulforaphane via COX-2/MMP2, 9/Snail, ZEB1 and miR-200c/ZEB1 pathways in human bladder cancer cells
inferred← citeshttps://doi.org/10.1016/j.mrrev.2011.12.001openalex-snapshot
Natural isothiocyanates: Genotoxic potential versus chemoprevention
inferred← citeshttps://doi.org/10.1016/j.nutres.2012.03.014openalex-snapshot
Sulforaphane retards the growth of UM-UC-3 xenographs, induces apoptosis, and reduces survivin in athymic mice
inferred← citeshttps://doi.org/10.1016/j.semcancer.2016.02.001openalex-snapshot
Targeting arachidonic acid pathway by natural products for cancer prevention and therapy
inferred← citeshttps://doi.org/10.1021/jf501944uopenalex-snapshot
Sulforaphane Attenuates Homocysteine-Induced Endoplasmic Reticulum Stress through Nrf-2-Driven Enzymes in Immortalized Human Hepatocytes
inferred← citeshttps://doi.org/10.1080/01635581.2020.1856895openalex-snapshot
Targeting Major Signaling Pathways of Bladder Cancer with Phytochemicals: A Review
inferred← citeshttps://doi.org/10.1080/10590501.2011.551317openalex-snapshot
Dietary Flavonoids as Cancer Prevention Agents
inferred← citeshttps://doi.org/10.1111/j.1742-7843.2010.00613.xopenalex-snapshot
Fisetin, a Dietary Flavonoid, Induces Cell Cycle Arrest and Apoptosis through Activation of p53 and Inhibition of NF‐Kappa B Pathways in Bladder Cancer Cells
inferred← citeshttps://doi.org/10.1111/nure.12060openalex-snapshot
Sulforaphane: translational research from laboratory bench to clinic
inferred← citeshttps://doi.org/10.1136/jitc-2023-007983openalex-snapshot
Sulforaphane activates CD8+ T cells antitumor response through IL-12RB2/MMP3/FasL-induced MDSCs apoptosis’
inferred← citeshttps://doi.org/10.1155/2012/415231openalex-snapshot
Apoptosis Induction in Primary Human Colorectal Cancer Cell Lines and Retarded Tumor Growth in SCID Mice by Sulforaphane
inferred← citeshttps://doi.org/10.1159/000490394openalex-snapshot
Sulforaphane, a Chemopreventive Compound, Inhibits Cyclooxygenase-2 and Microsomal Prostaglandin E Synthase-1 Expression in Human HT-29 Colon Cancer Cells
inferred← citeshttps://doi.org/10.1164/rccm.201011-1780ocopenalex-snapshot
Transforming Growth Factor-β and Nuclear Factor E2–related Factor 2 Regulate Antioxidant Responses in Airway Smooth Muscle Cells: Role in Asthma
inferred← citeshttps://doi.org/10.1177/1934578x19858221openalex-snapshot
Natural Sulforaphane From Broccoli Seeds Against Influenza A Virus Replication in MDCK Cells
inferred← citeshttps://doi.org/10.1201/9781315371443-4openalex-snapshot
A Review on Food-Associated Carcinogenesis
inferred← citeshttps://doi.org/10.1515/bc.2010.134openalex-snapshot
Breakdown products of neoglucobrassicin inhibit activation of Nrf2 target genes mediated by myrosinase-derived glucoraphanin hydrolysis products
inferred← citeshttps://doi.org/10.18632/oncotarget.16015openalex-snapshot
Sulforaphane for the chemoprevention of bladder cancer: molecular mechanism targeted approach
inferred← citeshttps://doi.org/10.3109/13880209.2012.749923openalex-snapshot
The role of cyclooxygenase-derived oxidative stress in surgically induced lymphedema in a mouse tail model
inferred← citeshttps://doi.org/10.3171/2016.8.jns161197openalex-snapshot
Sulforaphane suppresses the growth of glioblastoma cells, glioblastoma stem cell–like spheroids, and tumor xenografts through multiple cell signaling pathways
inferred← citeshttps://doi.org/10.3389/fnut.2020.00064openalex-snapshot
Organosulfur Compounds: A Review of Their Anti-inflammatory Effects in Human Health
inferred← citeshttps://doi.org/10.3389/fphar.2023.1254236openalex-snapshot
Sulforaphane and bladder cancer: a potential novel antitumor compound
inferred← citeshttps://doi.org/10.3390/cancers13194796openalex-snapshot
Sulforaphane: A Broccoli Bioactive Phytocompound with Cancer Preventive Potential
inferred← citeshttps://doi.org/10.3390/ijms22115938openalex-snapshot
Sulforaphane Impact on Reactive Oxygen Species (ROS) in Bladder Carcinoma
inferred← citeshttps://doi.org/10.3390/molecules23112983openalex-snapshot
Anti-Carcinogenic Glucosinolates in Cruciferous Vegetables and Their Antagonistic Effects on Prevention of Cancers
inferred← citeshttps://doi.org/10.3390/molecules25030575openalex-snapshot
Molecular Mechanisms of the Anti-Cancer Effects of Isothiocyanates from Cruciferous Vegetables in Bladder Cancer
inferred← citeshttps://doi.org/10.3390/molecules26164919openalex-snapshot
The Inhibitory Effect of Sulforaphane on Bladder Cancer Cell Depends on GSH Depletion-Induced by Nrf2 Translocation
inferred← citeshttps://doi.org/10.3892/ijmm.2015.2396openalex-snapshot
Sulforaphane exerts anti-inflammatory effects against lipopolysaccharide-induced acute lung injury in mice through the Nrf2/ARE pathway
inferred← citeshttps://doi.org/10.3892/or.2017.5565openalex-snapshot
Differential effects of sulforaphane in regulation of angiogenesis in a co-culture model of endothelial cells and pericytes
inferred← citeshttps://doi.org/10.5282/edoc.16905openalex-snapshot
Non-neuronale Expression und Funktion des sensorischen Kationenkanals TRPA1 in Tumorzellen
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