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Anticancer Potential of Resveratrol, β-Lapachone and Their Analogues

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1 of the 155 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.3892/mmr.2017.7680 (notice 2024-06-10).

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inferredcites →https://doi.org/10.1002/advs.201801807openalex-snapshot
A pH/ROS Cascade‐Responsive Charge‐Reversal Nanosystem with Self‐Amplified Drug Release for Synergistic Oxidation‐Chemotherapy
inferredcites →https://doi.org/10.1002/ijc.11344openalex-snapshot
Resveratrol analog (Z)‐3,5,4′‐trimethoxystilbene is a potent anti‐mitotic drug inhibiting tubulin polymerization
inferredcites →https://doi.org/10.1002/mnfr.200700252openalex-snapshot
The grape and wine constituent piceatannol inhibits proliferation of human bladder cancer cells via blocking cell cycle progression and inducing Fas/membrane bound Fas ligand‐mediated apoptotic pathway
inferredcites →https://doi.org/10.1002/mnfr.200800123openalex-snapshot
Resveratrol analog‐3,5,4′‐trimethoxy‐trans‐stilbene inhibits invasion of human lung adenocarcinoma cells by suppressing the MAPK pathway and decreasing matrix metalloproteinase‐2 expression
inferredcites →https://doi.org/10.1006/excr.1999.4790openalex-snapshot
Activation of a Cysteine Protease in MCF-7 and T47D Breast Cancer Cells during β-Lapachone-Mediated Apoptosis
inferredcites →https://doi.org/10.1006/taap.2002.9438openalex-snapshot
Inhibition of Poly(ADP-ribose) Polymerase Activation Attenuates β-Lapachone-Induced Necrotic Cell Death in Human Osteosarcoma Cells
inferredcites →https://doi.org/10.1007/bf03402095openalex-snapshot
β-Lapachone Induces Cell Cycle Arrest and Apoptosis in Human Colon Cancer Cells
inferredcites →https://doi.org/10.1007/s00280-010-1525-4openalex-snapshot
Pharmacokinetics, oral bioavailability, and metabolic profile of resveratrol and its dimethylether analog, pterostilbene, in rats
inferredcites →https://doi.org/10.1007/s00394-004-0471-5openalex-snapshot
The grape and wine polyphenol piceatannol is a potent inducer of apoptosis in human SK-Mel-28 melanoma cells
inferredcites →https://doi.org/10.1007/s00432-014-1771-7openalex-snapshot
Synergic effects of artemisinin and resveratrol in cancer cells
inferredcites →https://doi.org/10.1007/s10637-009-9231-yopenalex-snapshot
Comparison of the cytotoxic effect of lapachol, α-lapachone and pentacyclic 1,4-naphthoquinones on human leukemic cells
inferredcites →https://doi.org/10.1007/s11101-009-9158-0openalex-snapshot
Metabolic constituents of grapevine and grape-derived products
inferredcites →https://doi.org/10.1007/s11101-011-9209-1openalex-snapshot
The chemical and biological activities of quinones: overview and implications in analytical detection
inferredcites →https://doi.org/10.1007/s12013-013-9703-8openalex-snapshot
Resveratrol Induces Pro-oxidant Effects and Time-Dependent Resistance to Cytotoxicity in Activated Hepatic Stellate Cells
inferredcites →https://doi.org/10.1007/s13318-015-0310-5openalex-snapshot
Intestinal Permeability of β-Lapachone and Its Cyclodextrin Complexes and Physical Mixtures
inferredcites →https://doi.org/10.1016/0006-2952(91)90284-copenalex-snapshot
High levels of expression of the NAD(P)H:Quinone oxidoreductase (NQO1) gene in tumor cells compared to normal cells of the same origin
inferredcites →https://doi.org/10.1016/0277-5379(90)90127-fopenalex-snapshot
Effect of topoisomerase modulators on cisplatin cytotoxicity in human ovarian carcinoma cells
inferredcites →https://doi.org/10.1016/0306-4492(78)90063-1openalex-snapshot
Superoxide anion production and trypanocidal action of naphthoquinones on Trypanosoma cruzi
inferredcites →https://doi.org/10.1016/0921-8777(91)90049-uopenalex-snapshot
Effect of specific enzyme inhibitors on replication, total genome DNA repair and on gene-specific DNA repair after UV irradiation in CHO cells
inferredcites →https://doi.org/10.1016/b978-0-12-689650-3.50005-0openalex-snapshot
Distribution and Biogenesis
inferredcites →https://doi.org/10.1016/j.addr.2012.09.037openalex-snapshot
Liposomal drug delivery systems: From concept to clinical applications
inferredcites →https://doi.org/10.1016/j.bcp.2009.06.109openalex-snapshot
2,3′,4,4′,5′-Pentamethoxy-trans-stilbene, a resveratrol derivative, is a potent inducer of apoptosis in colon cancer cells via targeting microtubules
inferredcites →https://doi.org/10.1016/j.bcp.2011.12.017openalex-snapshot
NAD(P)H:quinone oxidoreductase 1 (NQO1) in the sensitivity and resistance to antitumor quinones
inferredcites →https://doi.org/10.1016/j.biocel.2009.08.005openalex-snapshot
The resveratrol analogue 4,4′-dihydroxy-trans-stilbene inhibits cell proliferation with higher efficiency but different mechanism from resveratrol
inferredcites →https://doi.org/10.1016/j.biocel.2010.05.007openalex-snapshot
Piceatannol induces Fas and FasL up-regulation in human leukemia U937 cells via Ca2+/p38α MAPK-mediated activation of c-Jun and ATF-2 pathways
inferredcites →https://doi.org/10.1016/j.biomaterials.2018.12.032openalex-snapshot
Integrated block copolymer prodrug nanoparticles for combination of tumor oxidative stress amplification and ROS-responsive drug release
inferredcites →https://doi.org/10.1016/j.biopha.2014.02.001openalex-snapshot
DMU-212 inhibits tumor growth in xenograft model of human ovarian cancer
inferredcites →https://doi.org/10.1016/j.biopha.2018.08.085openalex-snapshot
Resveratrol analogue, trans-4,4′-dihydroxystilbene (DHS), inhibits melanoma tumor growth and suppresses its metastatic colonization in lungs
inferredcites →https://doi.org/10.1016/j.biopha.2018.09.159openalex-snapshot
NQO1 induction mediated by photodynamic therapy synergizes with β-Lapachone-halogenated derivative against melanoma
inferredcites →https://doi.org/10.1016/j.bmc.2007.10.038openalex-snapshot
Trypanosoma cruzi: Activities of lapachol and α- and β-lapachone derivatives against epimastigote and trypomastigote forms
inferredcites →https://doi.org/10.1016/j.bmc.2009.02.014openalex-snapshot
4,4′-Dihydroxy-trans-stilbene, a resveratrol analogue, exhibited enhanced antioxidant activity and cytotoxicity
inferredcites →https://doi.org/10.1016/j.bmc.2012.10.047openalex-snapshot
Synthesis and anti-inflammatory evaluations of β-lapachone derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2016.01.024openalex-snapshot
Novel naphtho[2,1-d]oxazole-4,5-diones as NQO1 substrates with improved aqueous solubility: Design, synthesis, and in vivo antitumor evaluation
inferredcites →https://doi.org/10.1016/j.bmcl.2011.12.095openalex-snapshot
A resveratrol analog, phoyunbene B, induces G2/M cell cycle arrest and apoptosis in HepG2 liver cancer cells
inferredcites →https://doi.org/10.1016/j.canlet.2008.03.057openalex-snapshot
Cancer chemopreventive and therapeutic potential of resveratrol: Mechanistic perspectives
inferredcites →https://doi.org/10.1016/j.cbi.2013.12.009openalex-snapshot
Effects of hydroxylated resveratrol analogs on oxidative stress and cancer cells death in human acute T cell leukemia cell line
inferredcites →https://doi.org/10.1016/j.ejmech.2014.07.079openalex-snapshot
Synthesis and evaluation of the cytotoxic activity of 1,2-furanonaphthoquinones tethered to 1,2,3-1H-triazoles in myeloid and lymphoid leukemia cell lines
inferredcites →https://doi.org/10.1016/j.ejmech.2016.06.019openalex-snapshot
Synthesis and antitumor activity of selenium-containing quinone-based triazoles possessing two redox centres, and their mechanistic insights
inferredcites →https://doi.org/10.1016/j.ejmech.2019.06.056openalex-snapshot
Synthesis of quinones with highlighted biological applications: A critical update on the strategies towards bioactive compounds with emphasis on lapachones
inferredcites →https://doi.org/10.1016/j.ejpb.2012.12.019openalex-snapshot
Administration of the optimized β-Lapachone–poloxamer–cyclodextrin ternary system induces apoptosis, DNA damage and reduces tumor growth in a human breast adenocarcinoma xenograft mouse model
inferredcites →https://doi.org/10.1016/j.ejphar.2008.03.027openalex-snapshot
Trans- and cis-stilbene polyphenols induced rapid perinuclear mitochondrial clustering and p53-independent apoptosis in cancer cells but not normal cells
inferredcites →https://doi.org/10.1016/j.ejphar.2016.07.046openalex-snapshot
Promising therapeutic potential of pterostilbene and its mechanistic insight based on preclinical evidence
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2018.07.022openalex-snapshot
β-Lapachone and its iodine derivatives cause cell cycle arrest at G2/M phase and reactive oxygen species-mediated apoptosis in human oral squamous cell carcinoma cells
inferredcites →https://doi.org/10.1016/j.jconrel.2014.12.027openalex-snapshot
Esterase-activatable β-lapachone prodrug micelles for NQO1-targeted lung cancer therapy
inferredcites →https://doi.org/10.1016/j.jnutbio.2005.01.017openalex-snapshot
Resveratrol as an anticancer nutrient: molecular basis, open questions and promises
inferredcites →https://doi.org/10.1016/j.jss.2011.09.054openalex-snapshot
Pterostilbene and Cancer: Current Review
inferredcites →https://doi.org/10.1016/j.phrs.2019.104265openalex-snapshot
Pterostilbene: Mechanisms of its action as oncostatic agent in cell models and in vivo studies
inferredcites →https://doi.org/10.1016/j.taap.2013.07.019openalex-snapshot
3,5,4′-Trimethoxystilbene, a natural methoxylated analog of resveratrol, inhibits breast cancer cell invasiveness by downregulation of PI3K/Akt and Wnt/β-catenin signaling cascades and reversal of epithelial–mesenchymal transition
inferredcites →https://doi.org/10.1016/j.tibs.2014.04.001openalex-snapshot
Prion-like aggregation of mutant p53 in cancer
inferredcites →https://doi.org/10.1016/j.tiv.2008.03.002openalex-snapshot
Cytotoxic activity of 3,3′,4,4′,5,5′-hexahydroxystilbene against breast cancer cells is mediated by induction of p53 and downregulation of mitochondrial superoxide dismutase
inferredcites →https://doi.org/10.1016/j.tiv.2012.02.003openalex-snapshot
Growth inhibitory effects of 3′-nitro-3-phenylamino nor-beta-lapachone against HL-60: A redox-dependent mechanism
inferredcites →https://doi.org/10.1016/j.tiv.2013.08.002openalex-snapshot
Novel o-naphthoquinones induce apoptosis of EL-4 T lymphoma cells through the increase of reactive oxygen species
inferredcites →https://doi.org/10.1016/j.tiv.2017.06.004openalex-snapshot
The effect of resveratrol, its naturally occurring derivatives and tannic acid on the induction of cell cycle arrest and apoptosis in rat C6 and human T98G glioma cell lines
inferredcites →https://doi.org/10.1016/s0021-9258(18)41552-9openalex-snapshot
beta-Lapachone, a novel DNA topoisomerase I inhibitor with a mode of action different from camptothecin.
inferredcites →https://doi.org/10.1016/s0026-895x(24)12864-7openalex-snapshot
Differential Gene Expression of NAD(P)H:Quinone Oxidoreductase and NRH:Quinone Oxidoreductase in Human Hepatocellular and Biliary Tissue
inferredcites →https://doi.org/10.1016/s0891-5849(00)00310-5openalex-snapshot
Immunodetection of NAD(P)H:quinone oxidoreductase 1 (NQO1) in human tissues
inferredcites →https://doi.org/10.1021/acs.accounts.7b00473openalex-snapshot
Targeting the Prion-like Aggregation of Mutant p53 to Combat Cancer
inferredcites →https://doi.org/10.1021/acs.chemrestox.6b00256openalex-snapshot
Formation and Biological Targets of Quinones: Cytotoxic versus Cytoprotective Effects
inferredcites →https://doi.org/10.1021/acs.jafc.5b00002openalex-snapshot
Targeting Cancer Stem Cells in Breast Cancer: Potential Anticancer Properties of 6-Shogaol and Pterostilbene
inferredcites →https://doi.org/10.1021/ar900179topenalex-snapshot
Ligand Binding and Hydration in Protein Misfolding: Insights from Studies of Prion and p53 Tumor Suppressor Proteins
inferredcites →https://doi.org/10.1021/jf030073copenalex-snapshot
Grape Polyphenol Resveratrol and the Related Molecule 4-Hydroxystilbene Induce Growth Inhibition, Apoptosis, S-Phase Arrest, and Upregulation of Cyclins A, E, and B1 in Human SK-Mel-28 Melanoma Cells
inferredcites →https://doi.org/10.1021/jf071520hopenalex-snapshot
Pterostilbene Induces Apoptosis and Cell Cycle Arrest in Human Gastric Carcinoma Cells
inferredcites →https://doi.org/10.1021/jf101571zopenalex-snapshot
Pterostilbene Inhibits Colorectal Aberrant Crypt Foci (ACF) and Colon Carcinogenesis via Suppression of Multiple Signal Transduction Pathways in Azoxymethane-Treated Mice
inferredcites →https://doi.org/10.1021/jf4004175openalex-snapshot
Long-Term Ethanol Exposure-Induced Hepatocellular Carcinoma Cell Migration and Invasion through Lysyl Oxidase Activation Are Attenuated by Combined Treatment with Pterostilbene and Curcumin Analogues
inferredcites →https://doi.org/10.1021/jf900531mopenalex-snapshot
Mechanisms of Apoptotic Effects Induced by Resveratrol, Dibenzoylmethane, and Their Analogues on Human Lung Carcinoma Cells
inferredcites →https://doi.org/10.1021/jf903067gopenalex-snapshot
3,5,3′,4′,5′-Pentamethoxystilbene (MR-5), a Synthetically Methoxylated Analogue of Resveratrol, Inhibits Growth and Induces G1 Cell Cycle Arrest of Human Breast Carcinoma MCF-7 Cells
inferredcites →https://doi.org/10.1021/mp300140hopenalex-snapshot
The Fraction Dose Absorbed, in Humans, and High Jejunal Human Permeability Relationship
inferredcites →https://doi.org/10.1021/np200906sopenalex-snapshot
Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
inferredcites →https://doi.org/10.1021/np300893nopenalex-snapshot
Cytotoxicity and Modulation of Cancer-Related Signaling by (Z)- and (E)-3,4,3′,5′-Tetramethoxystilbene Isolated from Eugenia rigida
inferredcites →https://doi.org/10.1021/tx9902082openalex-snapshot
Role of Quinones in Toxicology
inferredcites →https://doi.org/10.1038/cddis.2014.202openalex-snapshot
β-Lapachone induces programmed necrosis through the RIP1-PARP-AIF-dependent pathway in human hepatocellular carcinoma SK-Hep1 cells
inferredcites →https://doi.org/10.1038/jid.2009.376openalex-snapshot
3,3′,4,4′,5,5′-Hexahydroxystilbene Impairs Melanoma Progression in a Metastatic Mouse Model
inferredcites →https://doi.org/10.1038/nchembio.546openalex-snapshot
Gain of function of mutant p53 by coaggregation with multiple tumor suppressors
inferredcites →https://doi.org/10.1038/nrd2060openalex-snapshot
Therapeutic potential of resveratrol: the in vivo evidence
inferredcites →https://doi.org/10.1038/nrd4510openalex-snapshot
The re-emergence of natural products for drug discovery in the genomics era
inferredcites →https://doi.org/10.1038/s41388-018-0584-6openalex-snapshot
DHS (trans−4,4′-dihydroxystilbene) suppresses DNA replication and tumor growth by inhibiting RRM2 (ribonucleotide reductase regulatory subunit M2)
inferredcites →https://doi.org/10.1038/s41416-018-0278-4openalex-snapshot
Phase 1 study of ARQ 761, a β-lapachone analogue that promotes NQO1-mediated programmed cancer cell necrosis
inferredcites →https://doi.org/10.1038/s41598-017-02937-0openalex-snapshot
β-lapachone suppresses tumour progression by inhibiting epithelial-to-mesenchymal transition in NQO1-positive breast cancers
inferredcites →https://doi.org/10.1038/s41598-017-12922-2openalex-snapshot
Pterostilbene, a natural phenolic compound, synergizes the antineoplastic effects of megestrol acetate in endometrial cancer
inferredcites →https://doi.org/10.1038/srep32627openalex-snapshot
3′-hydroxy-3,4,5,4′-tetramethoxystilbene, the metabolite of resveratrol analogue DMU-212, inhibits ovarian cancer cell growth in vitro and in a mice xenograft model
inferredcites →https://doi.org/10.1039/c1ob05209hopenalex-snapshot
Synthesis of new 9-hydroxy-α- and 7-hydroxy-β-pyran naphthoquinones and cytotoxicity against cancer cell lines
inferredcites →https://doi.org/10.1042/bst0351156openalex-snapshot
Resveratrol as an antioxidant and pro-oxidant agent: mechanisms and clinical implications
inferredcites →https://doi.org/10.1073/pnas.0538044100openalex-snapshot
Selective killing of cancer cells by β-lapachone: Direct checkpoint activation as a strategy against cancer
inferredcites →https://doi.org/10.1073/pnas.0702176104openalex-snapshot
An NQO1- and PARP-1-mediated cell death pathway induced in non-small-cell lung cancer cells by β-lapachone
inferredcites →https://doi.org/10.1074/jbc.m112.340638openalex-snapshot
Mutant p53 Aggregates into Prion-like Amyloid Oligomers and Fibrils
inferredcites →https://doi.org/10.1074/jbc.m117.813923openalex-snapshot
The NQO1 bioactivatable drug, β-lapachone, alters the redox state of NQO1+ pancreatic cancer cells, causing perturbation in central carbon metabolism
inferredcites →https://doi.org/10.1080/02656730701781895openalex-snapshot
Anti-cancer effect of bio-reductive drug β-lapachon is enhanced by activating NQO1 with heat shock
inferredcites →https://doi.org/10.1080/02656730903049836openalex-snapshot
Heat shock increases expression of NAD(P)H:quinone oxidoreductase (NQO1), mediator of β-lapachone cytotoxicity, by increasing NQO1 gene activity and via Hsp70-mediated stabilisation of NQO1 protein
inferredcites →https://doi.org/10.1080/13543776.2017.1339792openalex-snapshot
Lapachol and lapachone analogs: a journey of two decadesof patent research(1997-2016)
inferredcites →https://doi.org/10.1080/13880200802116610openalex-snapshot
Resveratrol as an Inhibitor of Carcinogenesis
inferredcites →https://doi.org/10.1089/jmf.2006.9.161openalex-snapshot
β -Lapachone, a Quinone Isolated from Tabebuia avellanedae, Induces Apoptosis in HepG2 Hepatoma Cell Line Through Induction of Bax and Activation of Caspase
inferredcites →https://doi.org/10.1093/carcin/bgp121openalex-snapshot
Pterostilbene inhibited tumor invasion via suppressing multiple signal transduction pathways in human hepatocellular carcinoma cells
inferredcites →https://doi.org/10.1093/jn/132.2.298openalex-snapshot
Piceatannol, a Natural Analog of Resveratrol, Inhibits Progression through the S Phase of the Cell Cycle in Colorectal Cancer Cell Lines
inferredcites →https://doi.org/10.1097/pai.0b013e31802e91d0openalex-snapshot
NQO1 Expression in Pancreatic Cancer and Its Potential Use as a Biomarker
inferredcites →https://doi.org/10.1111/j.1476-5381.2010.00785.xopenalex-snapshot
2,3′,4,4′,5′‐Pentamethoxy‐trans‐stilbene, a resveratrol derivative, inhibits colitis‐associated colorectal carcinogenesis in mice
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05842.xopenalex-snapshot
Bioavailability of resveratrol
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05864.xopenalex-snapshot
Chemopreventive effects of resveratrol and resveratrol derivatives
inferredcites →https://doi.org/10.1111/lam.12251openalex-snapshot
Cytotoxicity of lapachol metabolites produced by probiotics
inferredcites →https://doi.org/10.1124/jpet.116.232694openalex-snapshot
β-Lapachone Induces NAD(P)H:Quinone Oxidoreductase-1– and Oxidative Stress–Dependent Heat Shock Protein 90 Cleavage and Inhibits Tumor Growth and Angiogenesis
inferredcites →https://doi.org/10.1124/mol.59.4.784openalex-snapshot
Induction of CDK Inhibitors (p21 WAF1 and p27 Kip1 ) and Bak in the β-Lapachone-Induced Apoptosis of Human Prostate Cancer Cells
inferredcites →https://doi.org/10.1126/science.275.5297.218openalex-snapshot
Cancer Chemopreventive Activity of Resveratrol, a Natural Product Derived from Grapes
inferredcites →https://doi.org/10.1155/2017/3634915openalex-snapshot
Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
inferredcites →https://doi.org/10.1158/0008-5472.can-09-3995openalex-snapshot
β-Lapachone Micellar Nanotherapeutics for Non–Small Cell Lung Cancer Therapy
inferredcites →https://doi.org/10.1158/0008-5472.can-11-3135openalex-snapshot
An NQO1 Substrate with Potent Antitumor Activity That Selectively Kills by PARP1-Induced Programmed Necrosis
inferredcites →https://doi.org/10.1158/1078-0432.ccr-05-0818openalex-snapshot
Heat-Induced Up-Regulation of NAD(P)H:Quinone Oxidoreductase Potentiates Anticancer Effects of β-Lapachone
inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-1528openalex-snapshot
Pterostilbene, an Active Constituent of Blueberries, Suppresses Aberrant Crypt Foci Formation in the Azoxymethane-Induced Colon Carcinogenesis Model in Rats
inferredcites →https://doi.org/10.1158/1078-0432.ccr-10-1983openalex-snapshot
Modulating Endogenous NQO1 Levels Identifies Key Regulatory Mechanisms of Action of β-Lapachone for Pancreatic Cancer Therapy
inferredcites →https://doi.org/10.1158/1078-0432.ccr-18-2560openalex-snapshot
NQO1-dependent, Tumor-selective Radiosensitization of Non–small Cell Lung Cancers
inferredcites →https://doi.org/10.1158/1535-7163.11.3.1openalex-snapshot
Signal transducer and activator of transcription 3 (STAT3) activation in prostate cancer: Direct STAT3 inhibition induces apoptosis in prostate cancer lines
inferredcites →https://doi.org/10.1158/1535-7163.mct-05-0268openalex-snapshot
Resveratrol inhibits Src and Stat3 signaling and induces the apoptosis of malignant cells containing activated Stat3 protein
inferredcites →https://doi.org/10.1158/1535-7163.mct-12-0962openalex-snapshot
Catalase Abrogates β-Lapachone–Induced PARP1 Hyperactivation–Directed Programmed Necrosis in NQO1-Positive Breast Cancers
inferredcites →https://doi.org/10.1158/1535-7163.mct-15-0765openalex-snapshot
NQO1-Mediated Tumor-Selective Lethality and Radiosensitization for Head and Neck Cancer
inferredcites →https://doi.org/10.1159/000358696openalex-snapshot
Resveratrol Reduces the Proinflammatory Effects and Lipopolysaccharide- Induced Expression of HMGB1 and TLR4 in RAW264.7 Cells
inferredcites →https://doi.org/10.1177/0960327113475679openalex-snapshot
Resveratrol inhibits proliferation, angiogenesis and induces apoptosis in colon cancer cells
inferredcites →https://doi.org/10.1186/1471-2407-14-414openalex-snapshot
NQO1 overexpression is associated with poor prognosis in squamous cell carcinoma of the uterine cervix
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/10.1186/1476-4598-3-11openalex-snapshot
Comparison of gene expression in HCT116 treatment derivatives generated by two different 5-fluorouracil exposure protocols.
inferredcites →https://doi.org/10.1186/1756-9966-33-14openalex-snapshot
Clinical implications of high NQO1 expression in breast cancers
inferredcites →https://doi.org/10.1186/s40170-015-0137-1openalex-snapshot
Targeting glutamine metabolism sensitizes pancreatic cancer to PARP-driven metabolic catastrophe induced by ß-lapachone
inferredcites →https://doi.org/10.1371/journal.pone.0048746openalex-snapshot
Transient Transfection of a Wild-Type p53 Gene Triggers Resveratrol-Induced Apoptosis in Cancer Cells
inferredcites →https://doi.org/10.1371/journal.pone.0111814openalex-snapshot
Potent Anti-Cancer Effect of 3′-Hydroxypterostilbene in Human Colon Xenograft Tumors
inferredcites →https://doi.org/10.1371/journal.pone.0176937openalex-snapshot
β-Lapachone suppresses the lung metastasis of melanoma via the MAPK signaling pathway
inferredcites →https://doi.org/10.14670/hh-13.89openalex-snapshot
beta-Lapachone induced cell death in human hepatoma (HepA2) cells.
inferredcites →https://doi.org/10.18632/oncotarget.17879openalex-snapshot
trans-4,4’-Dihydroxystilbene (DHS) inhibits human neuroblastoma tumor growth and induces mitochondrial and lysosomal damages in neuroblastoma cell lines
inferredcites →https://doi.org/10.18632/oncotarget.25631openalex-snapshot
Resveratrol prevents p53 aggregation in vitro and in breast cancer cells
inferredcites →https://doi.org/10.2147/dddt.s186028openalex-snapshot
The synergistic effect of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside combined with Adriamycin on MCF-7 breast cancer cells
inferredcites →https://doi.org/10.2147/ijn.s163929openalex-snapshot
Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
inferredcites →https://doi.org/10.2174/1381612822666160611012532openalex-snapshot
Strategies for Increasing the Solubility and Bioavailability of Anticancer Compounds: β-Lapachone and Other Naphthoquinones
inferredcites →https://doi.org/10.2174/1573406414666180524071409openalex-snapshot
Design, Synthesis and Biological Evaluation of 1H-1,2,3-Triazole-Linked-1H-Dibenzo[b,h]xanthenes as Inductors of ROS-Mediated Apoptosis in the Breast Cancer Cell Line MCF-7
inferredcites →https://doi.org/10.2174/157488406775268246openalex-snapshot
Pharmacometrics of Stilbenes: Seguing Towards the Clinic
inferredcites →https://doi.org/10.3109/02656736.2010.513361openalex-snapshot
Hyperthermia enhances the effect of β-lapachone to cause γH2AX formations and cell death in human osteosarcoma cells
inferredcites →https://doi.org/10.3389/fnut.2016.00008openalex-snapshot
Anticancer Molecular Mechanisms of Resveratrol
inferredcites →https://doi.org/10.3389/fonc.2019.00352openalex-snapshot
Dietary Polyphenols, Resveratrol and Pterostilbene Exhibit Antitumor Activity on an HPV E6-Positive Cervical Cancer Model: An in vitro and in vivo Analysis
inferredcites →https://doi.org/10.3389/fphys.2017.00595openalex-snapshot
Functions of NQO1 in Cellular Protection and CoQ10 Metabolism and its Potential Role as a Redox Sensitive Molecular Switch
inferredcites →https://doi.org/10.3390/ijms141122483openalex-snapshot
Synthetic Resveratrol Analogue, 3,3',4,4',5,5'-Hexahydroxy-trans-Stilbene, Accelerates Senescence in Peritoneal Mesothelium and Promotes Senescence-Dependent Growth of Gastrointestinal Cancers
inferredcites →https://doi.org/10.3390/ijms20061381openalex-snapshot
Progress to Improve Oral Bioavailability and Beneficial Effects of Resveratrol
inferredcites →https://doi.org/10.3390/molecules22061014openalex-snapshot
Cancer Chemoprevention by Resveratrol: The p53 Tumor Suppressor Protein as a Promising Molecular Target
inferredcites →https://doi.org/10.3390/molecules25010228openalex-snapshot
Pterostilbene Suppresses both Cancer Cells and Cancer Stem-Like Cells in Cervical Cancer with Superior Bioavailability to Resveratrol
inferredcites →https://doi.org/10.3390/nu9111188openalex-snapshot
Therapeutic Versatility of Resveratrol Derivatives
inferredcites →https://doi.org/10.3892/ijo.2016.3574openalex-snapshot
2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside suppresses human colorectal cancer cell metastasis through inhibiting NF-κB activation
inferredcites →https://doi.org/10.3892/ijo.2016.3635openalex-snapshot
The resveratrol analogue, 3,4,5,4′-trans-tetramethoxystilbene, inhibits the growth of A375 melanoma cells through multiple anticancer modes of action
inferredcites →https://doi.org/10.3892/mmr.2014.2716openalex-snapshot
Resveratrol inhibits the proliferation of human melanoma cells by inducing G1/S cell cycle arrest and apoptosis
inferredcites →https://doi.org/10.3892/mmr.2017.7680openalex-snapshot
2,3,5,4-tetrahydroxy diphenylethylene-2-O-glucoside inhibits the adhesion and invasion of A549 human lung cancer cells
inferredcites →https://doi.org/10.3892/or.19.6.1621openalex-snapshot
Novel resveratrol analogs induce apoptosis and cause cell cycle arrest in HT29 human colon cancer cells: Inhibition of ribonucleotide reductase activity
inferredcites →https://doi.org/10.4062/biomolther.2014.026openalex-snapshot
β-lapachone-Induced Apoptosis of Human Gastric Carcinoma AGS Cells Is Caspase-Dependent and Regulated by the PI3K/Akt Pathway
inferredcites →https://doi.org/10.4062/biomolther.2014.112openalex-snapshot
Role of Annexin A5 on Mitochondria-Dependent Apoptosis Induced by Tetramethoxystilbene in Human Breast Cancer Cells
inferredcites →https://doi.org/10.4062/biomolther.2015.029openalex-snapshot
Preclinical Pharmacokinetic Evaluation of β-Lapachone: Characteristics of Oral Bioavailability and First-Pass Metabolism in Rats
inferredcites →https://doi.org/10.4103/0973-1482.158035openalex-snapshot
(Z)-3,4,3',5'-tetramethoxystilbene, a natural product, induces apoptosis and reduces viability of paclitaxel-and cisplatin-resistant osteosarcoma cells
inferredcites →https://doi.org/10.4103/1735-5362.251853openalex-snapshot
Pterostilbene increases Fas expression in T-lymphoblastic leukemia cell lines
inferredcites →https://doi.org/10.4161/cbt.2.2.237openalex-snapshot
μ-Calpain Activation in β-Lapachone-Mediated Apoptosis
inferredcites →https://doi.org/10.4161/cbt.4.1.1382openalex-snapshot
Efficacy of beta-lapachone in pancreatic cancer treatment: Exploiting the novel, therapeutic target NQO1
inferredcites →https://doi.org/10.4196/kjpp.2013.17.1.9openalex-snapshot
Impact of Micellar Vehicles on in situ Intestinal Absorption Properties of Beta-Lapachone in Rats
inferredcites →https://doi.org/10.5344/ajev.1992.43.1.49openalex-snapshot
Concentration of the Phytoalexin Resveratrol in Wine
inferredcites →https://doi.org/10.5483/bmbrep.2003.36.2.223openalex-snapshot
Suppression of Human Prostate Cancer Cell Growth by β-Lapachone via Down-regulation of pRB Phosphorylation and Induction of Cdk Inhibitor p21WAF1/CIP1
inferredcites →https://doi.org/10.7314/apjcp.2012.13.1.131openalex-snapshot
ABO Blood Group and Risk of Pancreatic Cancer in a Turkish Population in Western Blacksea Region

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1016/j.nexres.2025.100651openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/00268976.2022.2129107openalex-snapshot
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inferred← citeshttps://doi.org/10.1515/psr-2021-0043openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-2007998/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-5327911/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.2174/0113895575436825260115100522openalex-snapshot
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inferred← citeshttps://doi.org/10.2754/avb202392010079openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnut.2023.1258516openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphar.2023.1287505openalex-snapshot
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inferred← citeshttps://doi.org/10.4103/1735-5362.251853openalex-snapshot
Pterostilbene increases Fas expression in T-lymphoblastic leukemia cell lines
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Lapachol and (α/β)-lapachone as inhibitors of SARS-CoV-2 main protease (Mpro) and hACE-2: ADME properties, docking and dynamic simulation approaches
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Anticancer, Apoptotic, Cell Migration and Invasion Inhibition and in silico Molecular Docking Studies of Naringetol in A-549 Human Lung Cancer Cells
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