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Effects of emodin on the gene expression profiling of human breast carcinoma 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/mc.20231openalex-snapshot
p53 and its downstream proteins as molecular targets of cancer
inferredcites →https://doi.org/10.1002/ptr.1987openalex-snapshot
Evaluation of oriental medicinal herbs for estrogenic and antiproliferative activities
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/s12272-001-1221-6openalex-snapshot
Emodin-induced apoptosis in human breast cancer BCap-37 cells through the mitochondrial signaling pathway
inferredcites →https://doi.org/10.1016/0092-8674(93)90500-popenalex-snapshot
WAF1, a potential mediator of p53 tumor suppression
inferredcites →https://doi.org/10.1016/j.bcp.2005.04.026openalex-snapshot
Emodin induces apoptosis in human lung adenocarcinoma cells through a reactive oxygen species-dependent mitochondrial signaling pathway
inferredcites →https://doi.org/10.1016/j.biocel.2004.08.007openalex-snapshot
Effect of all-trans-retinoic acid on mRNA binding protein p62 in human gastric cancer cells
inferredcites →https://doi.org/10.1016/j.canlet.2003.10.018openalex-snapshot
Autocrine inhibition of chemotherapy response in human liver tumor cells by insulin-like growth factor-II
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.02.016openalex-snapshot
Alteration of subcellular redox equilibrium and the consequent oxidative modification of nuclear factor κB are critical for anticancer cytotoxicity by emodin, a reactive oxygen species-producing agent
inferredcites →https://doi.org/10.1016/j.lfs.2006.08.008openalex-snapshot
Emodin inhibits TNF α-induced MMP-1 expression through suppression of activator protein-1 (AP-1)
inferredcites →https://doi.org/10.1016/s0006-2952(02)01386-2openalex-snapshot
Emodin induces apoptosis in human promyeloleukemic HL-60 cells accompanied by activation of caspase 3 cascade but independent of reactive oxygen species production
inferredcites →https://doi.org/10.1016/s0024-3205(02)01900-8openalex-snapshot
The antiproliferative activity of aloe-emodin is through p53-dependent and p21-dependent apoptotic pathway in human hepatoma cell lines
inferredcites →https://doi.org/10.1016/s0304-3835(98)00212-2openalex-snapshot
Apoptosis is induced in aging SV40 T antigen-transformed human fibroblasts through p53- and p21CIP1/WAF1-independent pathways
inferredcites →https://doi.org/10.1016/s0304-419x(99)00004-9openalex-snapshot
DNA microarray technology: the anticipated impact on the study of human disease
inferredcites →https://doi.org/10.1016/s1357-2725(98)00048-xopenalex-snapshot
Molecules in focus Insulin-like growth factor II (IGF-II)
inferredcites →https://doi.org/10.1038/369414a0openalex-snapshot
A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis
inferredcites →https://doi.org/10.1038/sj.cdd.4400421openalex-snapshot
Trophic support promotes survival of bcl-x-deficient telencephalic cells in vitro
inferredcites →https://doi.org/10.1038/sj.onc.1201998openalex-snapshot
Emodin (3-methyl-1,6,8-trihydroxyanthraquinone) inhibits TNF-induced NF-κB activation, IκB degradation, and expression of cell surface adhesion proteins in human vascular endothelial cells
inferredcites →https://doi.org/10.1074/jbc.274.50.35297openalex-snapshot
COP9 Signalosome-directed c-Jun Activation/Stabilization Is Independent of JNK
inferredcites →https://doi.org/10.1074/jbc.275.10.7337openalex-snapshot
p53 Induces Apoptosis by Caspase Activation through Mitochondrial Cytochrome c Release
inferredcites →https://doi.org/10.1093/emboj/20.7.1630openalex-snapshot
COP9 signalosome‐specific phosphorylation targets p53 to degradation by the ubiquitin system
inferredcites →https://doi.org/10.1096/fasebj.12.6.469openalex-snapshot
A novel protein complex involved in signal transduction possessing similarities to 26S proteasome subunits
inferredcites →https://doi.org/10.1126/science.270.5235.467openalex-snapshot
Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray
inferredcites →https://doi.org/10.1158/0008-5472.can-2820-2openalex-snapshot
Emodin Enhances Arsenic Trioxide-Induced Apoptosis via Generation of Reactive Oxygen Species and Inhibition of Survival Signaling
inferredcites →https://doi.org/10.1167/iovs.07-0393openalex-snapshot
Emodin Suppression of Ocular Surface Inflammatory Reaction
inferredcites →https://doi.org/10.1186/1471-2407-5-97openalex-snapshot
Novel curcumin- and emodin-related compounds identified by in silico 2D/3D conformer screening induce apoptosis in tumor cells
inferredcites →https://doi.org/10.1242/jcs.115.3.467openalex-snapshot
The COP9 signalosome: at the interface between signal transduction and ubiquitin-dependent proteolysis
inferredcites →https://doi.org/10.1248/yakushi.122.403openalex-snapshot
Rhubarb Use in Patients Treated with Kampo Medicines-A Risk for Gastric Cancer?
inferredcites →https://doi.org/10.1677/joe.1.06039openalex-snapshot
Dexamethasone-induced intrauterine growth restriction impacts the placental prolactin family, insulin-like growth factor-II and the Akt signaling pathway
inferredcites →https://doi.org/10.2174/1573406053402497openalex-snapshot
Apoptosis Signaling Pathways in Lung Diseases
inferredcites →https://doi.org/10.3736/jcim20050309openalex-snapshot
Effects of perioperative administration of rhubarb on acute inflammatory response in patients with gastric cancer
inferredcites →https://doi.org/10.3748/wjg.v11.i33.5218openalex-snapshot
Antitumor and synergistic effect of Chinese medicine "bushen huayu jiedu recipe" and chemotherapy on transplanted animal hepatocarcinoma.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112854zenodo-depositor-declared
Emodin - A natural anthraquinone derivative with diverse pharmacological activities
inferred← citeshttps://doi.org/10.1002/jat.2838openalex-snapshot
Exploration of effects of emodin in selected cancer cell lines: enhanced growth inhibition by ascorbic acid and regulation of LRP1 and AR under hypoxia‐like conditions
inferred← citeshttps://doi.org/10.1007/978-981-13-6920-9_2openalex-snapshot
Synthetic Analogs of Phytochemicals
inferred← citeshttps://doi.org/10.1007/978-981-32-9147-8_3openalex-snapshot
Role of Ayurveda in Cancer Treatment
inferred← citeshttps://doi.org/10.1007/s00253-009-2054-0openalex-snapshot
Effect of emodin on Candida albicans growth investigated by microcalorimetry combined with chemometric analysis
inferred← citeshttps://doi.org/10.1007/s12195-011-0163-1openalex-snapshot
Probing the Chemo-Mechanical Effects of an Anti-Cancer Drug Emodin on Breast Cancer Cells
inferred← citeshttps://doi.org/10.1016/j.biomed.2012.03.003openalex-snapshot
Anticancer potential of emodin
inferred← citeshttps://doi.org/10.1016/j.ejphar.2009.10.035openalex-snapshot
Anti-tumor activity of emodin against human chronic myelocytic leukemia K562 cell lines in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.ejphar.2010.03.034openalex-snapshot
A study on inhibition mechanism of breast cancer cells by bis-type triaziquone
inferred← citeshttps://doi.org/10.1016/j.ejphar.2013.02.021openalex-snapshot
Emodin ameliorates lipopolysaccharide-induced mastitis in mice by inhibiting activation of NF-κB and MAPKs signal pathways
inferred← citeshttps://doi.org/10.1016/j.intimp.2014.05.019openalex-snapshot
Emodin inhibits LPS-induced inflammatory response by activating PPAR-γ in mouse mammary epithelial cells
inferred← citeshttps://doi.org/10.1016/j.jddst.2015.10.019openalex-snapshot
Pharmacokinetics and tissue distribution of emodin loaded nanoemulsion in rats
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120314openalex-snapshot
Inclusion complexation of emodin with various β-cyclodextrin derivatives: Preparation, characterization, molecular docking, and anticancer activity
inferred← citeshttps://doi.org/10.1111/j.1476-5381.2010.00993.xopenalex-snapshot
Emodin suppresses lipopolysaccharide‐induced pro‐inflammatory responses and NF‐κB activation by disrupting lipid rafts in CD14‐negative endothelial cells
inferred← citeshttps://doi.org/10.1142/s0192415x23500787openalex-snapshot
Research Progress and New Perspectives of Anticancer Effects of Emodin
inferred← citeshttps://doi.org/10.1155/2013/131306openalex-snapshot
Antiangiogenic Activity and Pharmacogenomics of Medicinal Plants from Traditional Korean Medicine
inferred← citeshttps://doi.org/10.1177/1535370214530247openalex-snapshot
Emodin attenuates systemic and liver inflammation in hyperlipidemic mice administrated with lipopolysaccharides
inferred← citeshttps://doi.org/10.13005/ojc/380320openalex-snapshot
A Comprehensive Review on Medicinal Plants against Lung Cancer
inferred← citeshttps://doi.org/10.1371/journal.pone.0144781openalex-snapshot
Antitumor Effects and Mechanism of Novel Emodin Rhamnoside Derivatives against Human Cancer Cells In Vitro
inferred← citeshttps://doi.org/10.2174/1573394714666180321151315openalex-snapshot
Cancer Chemotherapy by Novel Bio-active Natural Products: Looking Towards the Future
inferred← citeshttps://doi.org/10.30799/jnpr.058.18040103openalex-snapshot
Potentilla fulgens: A Systematic Review on Traditional Uses, Pharmacology and Phytochemical Study with Reference to Anticancer Activity
inferred← citeshttps://doi.org/10.3390/cancers13112733openalex-snapshot
Is Emodin with Anticancer Effects Completely Innocent? Two Sides of the Coin
inferred← citeshttps://doi.org/10.3390/ijms242115789openalex-snapshot
Therapeutic Potential of 1,8-Dihydroanthraquinone Derivatives for Breast Cancer
inferred← citeshttps://doi.org/10.3892/etm.2012.516openalex-snapshot
Downregulation of phosphatase of regenerating liver-3 is involved in the inhibition of proliferation and apoptosis induced by emodin in the SGC-7901 human gastric carcinoma cell line
inferred← citeshttps://doi.org/10.3892/ijmm.2018.3638openalex-snapshot
Emodin inhibits epithelial‑mesenchymal transition and metastasis of triple negative breast cancer via antagonism of CC‑chemokine ligand�5 secreted from adipocytes
inferred← citeshttps://doi.org/10.3892/mmr.2017.6254openalex-snapshot
Inhibitory effect of emodin on fatty acid synthase, colon cancer proliferation and apoptosis
inferred← citeshttps://doi.org/10.3892/or.2013.2741openalex-snapshot
The distinct mechanisms of the antitumor activity of emodin in different types of cancer (Review)
inferred← citeshttps://doi.org/10.3892/or.2014.3585openalex-snapshot
Inhibitory effect of emodin on migration, invasion and metastasis of human breast cancer MDA-MB-231 cells in vitro and in vivo
inferred← citeshttps://doi.org/10.4236/cmb.2017.71001openalex-snapshot
Molecular Docking and ADMET Study of Emodin Derivatives as Anticancer Inhibitors of NAT2, COX2 and TOP1 Enzymes
inferred← citeshttps://doi.org/10.5530/pj.2016.3.5openalex-snapshot
Updates on Traditional Medicinal Plants for Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.62400/jbs.v5i3.7057openalex-snapshot
Anti-proliferative effects of Rhamnus frangula miller leaf and bark extracts on HEK293 and MCF-7 cell lines and evaluation of Bax and Bcl-2 genes expression level in MCF-7 cells
inferred← citeshttps://doi.org/10.7150/ijbs.70447openalex-snapshot
The versatile emodin: A natural easily acquired anthraquinone possesses promising anticancer properties against a variety of cancers
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