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Aryl hydrocarbon receptor signaling involved in the invasiveness of LNCaP 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/jcb.20656openalex-snapshot
Aryl hydrocarbon receptor, cell cycle regulation, toxicity, and tumorigenesis
inferredcites →https://doi.org/10.1006/abbi.1996.0190openalex-snapshot
Characterization of the Activated Form of the Aryl Hydrocarbon Receptor in the Nucleus of HeLa Cells in the Absence of Exogenous Ligand
inferredcites →https://doi.org/10.1007/s00204-012-0818-2openalex-snapshot
Biology and function of the aryl hydrocarbon receptor: report of an international and interdisciplinary conference
inferredcites →https://doi.org/10.1016/j.taap.2003.12.025openalex-snapshot
Disruption of cell?cell contact maximally but transiently activates AhR-mediated transcription in 10T1/2 fibroblasts*1
inferredcites →https://doi.org/10.1016/j.taap.2016.04.018openalex-snapshot
2,3,7,8-Tetrachlorodibenzo- p -dioxin has both pro-carcinogenic and anti-carcinogenic effects on neuroendocrine prostate carcinoma formation in TRAMP mice
inferredcites →https://doi.org/10.1021/jm900199uopenalex-snapshot
Modeling of the Aryl Hydrocarbon Receptor (AhR) Ligand Binding Domain and Its Utility in Virtual Ligand Screening to Predict New AhR Ligands
inferredcites →https://doi.org/10.1021/tx5005198openalex-snapshot
Omeprazole Inhibits Pancreatic Cancer Cell Invasion through a Nongenomic Aryl Hydrocarbon Receptor Pathway
inferredcites →https://doi.org/10.1038/nature01606openalex-snapshot
Modulation of oestrogen receptor signalling by association with the activated dioxin receptor
inferredcites →https://doi.org/10.1038/nrc3846openalex-snapshot
Aryl hydrocarbon receptor ligands in cancer: friend and foe
inferredcites →https://doi.org/10.1038/sj.onc.1209553openalex-snapshot
Activation of the dioxin/aryl hydrocarbon receptor (AhR) modulates cell plasticity through a JNK-dependent mechanism
inferredcites →https://doi.org/10.1074/jbc.m112.425009openalex-snapshot
Dioxin Receptor Expression Inhibits Basal and Transforming Growth Factor β-induced Epithelial-to-mesenchymal Transition
inferredcites →https://doi.org/10.1074/jbc.m310492200openalex-snapshot
Cell Density Regulates Intracellular Localization of Aryl Hydrocarbon Receptor
inferredcites →https://doi.org/10.1093/carcin/bgl179openalex-snapshot
The aryl hydrocarbon receptor inhibits prostate carcinogenesis in TRAMP mice
inferredcites →https://doi.org/10.1093/toxsci/kfr249openalex-snapshot
Dietary Ligands of the Aryl Hydrocarbon Receptor Induce Anti-Inflammatory and Immunoregulatory Effects on Murine Dendritic Cells
inferredcites →https://doi.org/10.1124/mol.63.6.1373openalex-snapshot
Aryl Hydrocarbon Receptor Gene Silencing with Small Inhibitory RNA Differentially Modulates Ah-Responsiveness in MCF-7 and HepG2 Cancer Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-05-3132openalex-snapshot
3-Methylcholanthrene and Other Aryl Hydrocarbon Receptor Agonists Directly Activate Estrogen Receptor α
inferredcites →https://doi.org/10.1182/blood-2007-08-109645openalex-snapshot
Activation of the aryl hydrocarbon receptor is essential for mediating the anti-inflammatory effects of a novel low-molecular-weight compound
inferredcites →https://doi.org/10.1186/1471-2121-10-27openalex-snapshot
Aryl hydrocarbon receptor pathway activation enhances gastric cancer cell invasiveness likely through a c-Jun-dependent induction of matrix metalloproteinase-9
inferredcites →https://doi.org/10.1186/1471-2407-14-498openalex-snapshot
The aryl hydrocarbon receptor ligand omeprazole inhibits breast cancer cell invasion and metastasis
inferredcites →https://doi.org/10.1371/journal.pone.0095058openalex-snapshot
The Aryl Hydrocarbon Receptor Is Constitutively Active in Advanced Prostate Cancer Cells
inferredcites →https://doi.org/10.1615/critreveukargeneexpr.v18.i3.20openalex-snapshot
The Aryl Hydrocarbon Receptor Complex and the Control of Gene Expression
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4670506openalex-extracted
Agent Orange Exposure Enhances the Increased Risk of Cardiovascular Disease in Veterans with Myeloproliferative Neoplasms
inferred← citeshttps://doi.org/10.1002/ajh.27438openalex-snapshot
Risk of myeloproliferative neoplasms among U.S. Veterans from Korean, Vietnam, and Persian Gulf War eras
inferred← citeshttps://doi.org/10.1016/j.envres.2019.108902openalex-snapshot
Phthalate exposure and prostate cancer in a population-based nested case-control study
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108303openalex-snapshot
Aryl hydrocarbon receptor is a tumor promoter in MYCN-amplified neuroblastoma cells through suppression of differentiation
inferred← citeshttps://doi.org/10.1016/j.virusres.2021.198399openalex-snapshot
LMP2A suppresses the role of AHR pathway through ERK signal pathway in EBV-associated gastric cancer
inferred← citeshttps://doi.org/10.1080/21541264.2024.2334106openalex-snapshot
Aryl hydrocarbon receptor as a drug target in advanced prostate cancer therapy – obstacles and perspectives
inferred← citeshttps://doi.org/10.1089/dna.2017.3783openalex-snapshot
Aryl Hydrocarbon Receptor Suppresses the Prostate Cancer LNCaP Cell Growth and Invasion by Promoting DNA Damage Response Under Oxidative Stress
inferred← citeshttps://doi.org/10.1134/s1990519x19010048openalex-snapshot
Additional Prognostic Markers of Human Colon Adenocarcinoma
inferred← citeshttps://doi.org/10.1134/s1990750819010116openalex-snapshot
Aryl-Hydrocarbon Receptor as a Potential Target for Anticancer Therapy
inferred← citeshttps://doi.org/10.1134/s2079057021010379openalex-snapshot
Aryl Hydrocarbon Receptor-Interacting Protein (AIP) in the Human Dermis with Aging
inferred← citeshttps://doi.org/10.1134/s2079057021020053openalex-snapshot
Aryl Hydrocarbon Receptor in Human Dermal Fibroblasts in the Aging Process
inferred← citeshttps://doi.org/10.1172/jci70712openalex-snapshot
Inhibition of the aryl hydrocarbon receptor/polyamine biosynthesis axis suppresses multiple myeloma
inferred← citeshttps://doi.org/10.1186/s12964-023-01058-8openalex-snapshot
When AHR signaling pathways meet viral infections
inferred← citeshttps://doi.org/10.14789/jmj.2019.65.5-plopenalex-snapshot
Publications from Juntendo University Graduate School of Medicine, 2017 [3/6]
inferred← citeshttps://doi.org/10.18097/pbmc20186405397openalex-snapshot
Aryl-hydrocarbon receptor as a potential target for anticancer therapy
inferred← citeshttps://doi.org/10.2174/1389450120666181109092225openalex-snapshot
Aryl Hydrocarbon Receptor: Its Regulation and Roles in Transformation and Tumorigenesis
inferred← citeshttps://doi.org/10.22088/ijmcm.bums.12.3.275openalex-snapshot
CD44 rs13347C>T Variants in 3'UTR and Prostate Neoplasms: A Case-control Study and Bioinformatics Approach.
inferred← citeshttps://doi.org/10.3390/cancers14112793openalex-snapshot
The Kynurenine Pathway and Cancer: Why Keep It Simple When You Can Make It Complicated
inferred← citeshttps://doi.org/10.3390/ijms22010387openalex-snapshot
How the AHR Became Important in Cancer: The Role of Chronically Active AHR in Cancer Aggression
inferred← citeshttps://doi.org/10.4067/s0717-95022023000501348openalex-snapshot
Differential Effect of ITE on the Aryl Hydrocarbon Receptor Signaling in Breast Cancer Tissue: A Histopathological Study
inferred← citeshttps://doi.org/10.7868/s0041377118100028openalex-snapshot
АНАЛИЗ ДОПОЛНИТЕЛЬНЫХ ПРОГНОСТИЧЕСКИХ МАРКЕРОВ АДЕНОКАРЦИНОМЫ ТОЛСТОЙ КИШКИ ЧЕЛОВЕКА, "Цитология"
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