The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Reduction-oxidation pathways involved in cancer development: a systematic review of literature reviews
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Figures






Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Several studies have demonstrated the prominent role of ROS as a second messenger in asbestos toxicity mediation26, mainly in the pulmonary mesothelium27.”
From Evaluation of the genotoxic and transformation potential induced by asbestos compared to cleavage fragments (2025) · cites this paper as [27]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
STATs in cancer inflammation and immunity: a leading role for STAT3
Yu, H., Pardoll, D., & Jove, R. (2009) · Nature reviews. Cancer · doi:10.1038/nrc2734 · Cited by 4,383
MAP kinase signalling pathways in cancer
Dhillon, A. S., Hagan, S., Rath, O., & Kolch, W. (2007) · Oncogene · doi:10.1038/sj.onc.1210421 · Cited by 2,995
Wallace, D. C. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3365 · Cited by 2,404
Transcription factors as targets for cancer therapy
Darnell, J. E. (2002) · Nature Reviews Cancer · doi:10.1038/nrc906 · Cited by 1,194
Movafagh, S., Crook, S., & Vo, K. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25074 · Cited by 469
Hypoxia-inducible factor 3 biology: complexities and emerging themes
Duan, C. (2016) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00315.2015 · Cited by 269 · cited 2×
“Knowledge about HIF-3α is limited because of the diversity of HIF-3α variants [54].”
BackgroundThe role of hypoxia-inducible factor-2 in digestive system cancers
Zhao, J., Du, F., Shen, G., Zheng, F., & Xu, B. (2015) · Cell Death & Disease · doi:10.1038/cddis.2014.565 · Cited by 122
The Quest for Selective Nox Inhibitors and Therapeutics: Challenges, Triumphs and Pitfalls
Cifuentes-Pagano, E., Meijles, D. N., & Pagano, P. J. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5620 · Cited by 84 · cited 1×
“However, most of them are not specific to NOX isoforms [91].”
BackgroundNew approaches to selectively target cancer-associated matrix metalloproteinase activity
Tauro, M., McGuire, J., & Lynch, C. C. (2014) · Cancer and Metastasis Reviews · doi:10.1007/s10555-014-9530-4 · Cited by 70
Research works printed but not linked: 91
- Lee, 2015, ROS and energy metabolism in cancer cells: alliance for fast growth, Arch Pharm Res, 38, 338, 10.1007/s12272-015-0550-6 · DOI
- Jones, 2008, Radical-free biology of oxidative stress, Am J Physiol Cell Physiol, 295, C849, 10.1152/ajpcell.00283.2008 · DOI · Paper page
- Telser, 2007, Free radicals and antioxidants in normal physiological functions and human disease, Int J Biochem Cell Biol, 39, 44, 10.1016/j.biocel.2006.07.001 · DOI · Paper page
- Roberts, 2009, Molecular regulation of tumor angiogenesis and perfusion via redox signaling, Chem Rev, 109, 3099, 10.1021/cr8005125 · DOI
- Finkel, 2014, Cellular mechanisms and physiological consequences of redox-dependent signalling, Nat Rev Mol Cell Biol, 15, 411, 10.1038/nrm3801 · DOI · Paper page
- Flohé, 2011, Basic principles and emerging concepts in the redox control of transcription factors, Antioxid Redox Signal, 15, 2335, 10.1089/ars.2010.3534 · DOI
- Spitz, 2006, Redox signaling in cancer biology, Antioxid Redox Signal, 8, 1249, 10.1089/ars.2006.8.1249 · DOI
- LLeonart, 2013, Oxidative stress and cancer: an overview, Ageing Res Rev, 12, 376, 10.1016/j.arr.2012.10.004 · DOI
- Aggarwal, 2010, Oxidative stress, inflammation, and cancer: how are they linked?, Free Radic Biol Med, 49, 1603, 10.1016/j.freeradbiomed.2010.09.006 · DOI · Paper page
- Chiarugi, 2012, Oxidative stress, tumor microenvironment, and metabolic reprogramming: a diabolic liaison, Int J Cell Biol, 2012, 762825
- Spitz, 2014, Reactive oxygen species in normal and tumor stem cells, Adv Cancer Res, 122, 1, 10.1016/B978-0-12-420117-0.00001-3 · DOI
- Wu, 2015, Impact of Oxidative Stress Biomarkers and Carboxymethyllysine (an Advanced Glycation End Product) on Prostate Cancer: A Prospective Study, Clin Genitourin Cancer, 13, e347, 10.1016/j.clgc.2015.04.004 · DOI
- Tjønneland, 2013, Association between 8-oxo-7,8-dihydro-2′-deoxyguanosine excretion and risk of postmenopausal breast cancer: nested case-control study, Cancer Epidemiol Biomarkers Prev, 22, 1289, 10.1158/1055-9965.EPI-13-0229 · DOI · Paper page
- Gius, 2005, Redox-sensitive signaling factors as a novel molecular targets for cancer therapy, Drug Resist Updat, 8, 322, 10.1016/j.drup.2005.09.002 · DOI
- Blasiak, 2014, Role of mitochondria in carcinogenesis, Acta Biochim Pol, 61, 671
- Singh, 2010, Mechanisms associated with mitochondrial-generated reactive oxygen species in cancer, Can J Physiol Pharmacol, 88, 204, 10.1139/Y09-135 · DOI
- Doroshow, 2014, NADPH oxidases: a perspective on reactive oxygen species production in tumor biology, Antioxid Redox Signal, 20, 2873, 10.1089/ars.2013.5603 · DOI
- Cotter, 2014, ROS signalling, NADPH oxidases and cancer, Biochem Soc Trans, 42, 934, 10.1042/BST20140060 · DOI
- Dusting, 2011, NADPH oxidase-mediated redox signaling: roles in cellular stress response, stress tolerance, and tissue repair, Pharmacol Rev, 63, 218, 10.1124/pr.110.002980 · DOI
- Blair, 2011, Cyclooxygenase- and lipoxygenase-mediated DNA damage, Cancer Metastasis Rev, 30, 437, 10.1007/s10555-011-9298-8 · DOI
- Habenicht, 2006, What are cyclooxygenases and lipoxygenases doing in the driver‘s seat of carcinogenesis?, Int J Cancer, 119, 2247, 10.1002/ijc.22153 · DOI
- Chlubek, 2013, The effect of reactive oxygen species on the synthesis of prostanoids from arachidonic acid, J Physiol Pharmacol, 64, 409
- Bentrem, 2014, Involvement of eicosanoids in the pathogenesis of pancreatic cancer: the roles of cyclooxygenase-2 and 5-lipoxygenase, World J Gastroenterol, 20, 10729, 10.3748/wjg.v20.i31.10729 · DOI
- Jain, 2006, The role of nitric oxide in tumour progression, Nat Rev Cancer, 6, 521, 10.1038/nrc1910 · DOI
- Nath, 2015, The dual role of iNOS in cancer, Redox Biol, 6, 334, 10.1016/j.redox.2015.08.009 · DOI
- Bogdan, 2015, Nitric oxide synthase in innate and adaptive immunity: an update, Trends Immunol, 36, 161, 10.1016/j.it.2015.01.003 · DOI · Paper page
- Phang, 2012, Proline dehydrogenase (oxidase) in cancer, Biofactors, 38, 398, 10.1002/biof.1036 · DOI
- Franklin, 2006, Reactive oxygen species-induced activation of the MAP kinase signaling pathways, Antioxid Redox Signal, 8, 1775, 10.1089/ars.2006.8.1775 · DOI
- Choi, 2015, Compromised MAPK signaling in human diseases: an update, Arch Toxicol, 89, 867, 10.1007/s00204-015-1472-2 · DOI
- Klotz, 2005, Phosphoinositide 3-kinase signaling in the cellular response to oxidative stress, Biol Chem, 386, 207
- Lee, 2011, Targeting the BMK1 MAP kinase pathway in cancer therapy, Clin Cancer Res, 17, 3527, 10.1158/1078-0432.CCR-10-2504 · DOI
- Nebreda, 2009, Signal integration by JNK and p38 MAPK pathways in cancer development, Nat Rev Cancer, 9, 537, 10.1038/nrc2694 · DOI
- Ahmadi, 2014, Akt and p53R2, partners that dictate the progression and invasiveness of cancer, DNA Repair (Amst), 22, 24, 10.1016/j.dnarep.2014.07.001 · DOI
- Hirsch, 2014, PI3K/AKT signaling pathway and cancer: an updated review, Ann Med, 46, 372, 10.3109/07853890.2014.912836 · DOI
- Kaushal, 2014, Oxidative Stress Mechanisms and their Modulation
- Regad, 2015, Targeting RTK Signaling Pathways in Cancer, Cancers (Basel), 7, 1758, 10.3390/cancers7030860 · DOI
- Studzinski, 2014, Non-receptor protein tyrosine kinases signaling pathways in normal and cancer cells, Crit Rev Clin Lab Sci, 51, 125, 10.3109/10408363.2013.874403 · DOI
- Chiarugi, 2005, PTPs versus PTKs: the redox side of the coin, Free Radic Res, 39, 353, 10.1080/10715760400027987 · DOI
- Tonks, 2006, Protein tyrosine phosphatases: from genes, to function, to disease, Nat Rev Mol Cell Biol, 7, 833, 10.1038/nrm2039 · DOI
- Böhmer, 2006, Protein-tyrosine phosphatases and cancer, Nat Rev Cancer, 6, 307, 10.1038/nrc1837 · DOI
- Kazanietz, 2014, Protein kinase C and cancer: what we know and what we do not, Oncogene, 33, 5225, 10.1038/onc.2013.524 · DOI · Paper page
- Pinton, 2010, Redox control of protein kinase C: cell- and disease-specific aspects, Antioxid Redox Signal, 13, 1051, 10.1089/ars.2009.2825 · DOI
- Chen, 2013, Mst1 and Mst2 kinases: regulations and diseases, Cell Biosci, 3, 31, 10.1186/2045-3701-3-31 · DOI
- Levonen, 2014, Role of the Keap1-Nrf2 pathway in cancer, Adv Cancer Res, 122, 281, 10.1016/B978-0-12-420117-0.00008-6 · DOI
- Jaiswal, 2013, The transcription factor NF-E2-related factor 2 (Nrf2): a protooncogene?, FASEB J, 27, 414, 10.1096/fj.12-217257 · DOI
- Surh, 2014, Oncogenic potential of Nrf2 and its principal target protein heme oxygenase-1, Free Radic Biol Med, 67, 353, 10.1016/j.freeradbiomed.2013.10.819 · DOI
- Wang, 2014, Nrf2: bane or blessing in cancer?, J Cancer Res Clin Oncol, 140, 1251, 10.1007/s00432-014-1627-1 · DOI
- Chiarugi, 2013, Redox molecular machines involved in tumor progression, Antioxid Redox Signal, 19, 1828, 10.1089/ars.2012.5040 · DOI
- Ghosh, 2009, The NF-kappaB family of transcription factors and its regulation, Cold Spring Harb Perspect Biol, 1, a000034
- Ichikawa, 2006, Nuclear factor-kappa B: A holy grail in cancer prevention and therapy, Curr Signal Transduct Ther, 1, 25, 10.2174/157436206775269235 · DOI
- Kong, 2008, NF-kappaB signaling pathway and its therapeutic implications in human diseases, Int Rev Immunol, 27, 293, 10.1080/08830180802276179 · DOI
- Sandaltzopoulos, 2008, Reactive oxygen species and HIF-1 signalling in cancer, Cancer Lett, 266, 12, 10.1016/j.canlet.2008.02.028 · DOI
- Monte, 2011, Interaction of p53 with tumor suppressive and oncogenic signaling pathways to control cellular reactive oxygen species production, Antioxid Redox Signal, 15, 1749, 10.1089/ars.2010.3652 · DOI
- Pervaiz, 2012, Redox regulation of p53, redox effectors regulated by p53: a subtle balance, Antioxid Redox Signal, 16, 1285, 10.1089/ars.2011.4434 · DOI
- Galeotti, Role of MnSOD and p66shc in mitochondrial response to p53, Antioxid Redox Signal.2011;, 15, 1715
- Gorgoulis, 2012, PIG3: a novel link between oxidative stress and DNA damage response in cancer, Cancer Lett, 327, 97, 10.1016/j.canlet.2011.12.009 · DOI
- Basaga, 2012, Tumor suppressor genes and ROS: complex networks of interactions, Free Radic Biol Med, 52, 7, 10.1016/j.freeradbiomed.2011.09.035 · DOI
- Kuphal, 2014, AP-1/c-Jun transcription factors: regulation and function in malignant melanoma, Eur J Cell Biol, 93, 76, 10.1016/j.ejcb.2013.10.003 · DOI
- Papavassiliou, 2007, The activator protein-1 transcription factor in respiratory epithelium carcinogenesis, Mol Cancer Res, 5, 109, 10.1158/1541-7786.MCR-06-0311 · DOI
- Wagner, 2003, AP-1: a double-edged sword in tumorigenesis, Nat Rev Cancer, 3, 859, 10.1038/nrc1209 · DOI
- Maśliński, 2012, Current overview of functions of FoxO proteins, with special regards to cellular homeostasis, cell response to stress, as well as inflammation and aging, Adv Med Sci, 57, 183, 10.2478/v10039-012-0039-1 · DOI
- Lam, 2011, Sense and sensitivity: FOXO and ROS in cancer development and treatment, Antioxid Redox Signal, 14, 675, 10.1089/ars.2010.3383 · DOI
- Storz, 2011, Forkhead homeobox type O transcription factors in the responses to oxidative stress, Antioxid Redox Signal, 14, 593, 10.1089/ars.2010.3405 · DOI
- Gouilleux, 2013, Oxidative metabolism in cancer: A STAT affair?, JAK-STAT, 2, e25764, 10.4161/jkst.25764 · DOI
- He, 2009, Wnt/beta-catenin signaling: components, mechanisms, and diseases, Dev Cell, 17, 9, 10.1016/j.devcel.2009.06.016 · DOI · Paper page
- Lee, 2013, The way Wnt works: components and mechanism, Growth Factors, 31, 1, 10.3109/08977194.2012.752737 · DOI
- Monga, 2011, Role of Wnt/β-catenin signaling in liver metabolism and cancer, Int J Biochem Cell Biol, 43, 1021, 10.1016/j.biocel.2009.09.001 · DOI
- Kelley, 2009, The many functions of APE1/Ref-1: not only a DNA repair enzyme, Antioxid Redox Signal, 11, 601, 10.1089/ars.2008.2194 · DOI
- Mantha, 2014, APE1/Ref-1 as an emerging therapeutic target for various human diseases: phytochemical modulation of its functions, Exp Mol Med, 46, e106, 10.1038/emm.2014.42 · DOI
- Datta, 2012, Alterations in the Smad pathway in human cancers, Front Biosci (Landmark Ed), 17, 1281, 10.2741/3986 · DOI
- Matsuda, 2014, Link between PI3K/AKT/PTEN Pathway and NOX Proteinin Diseases, Aging Dis, 5, 203, 10.14336/AD.2014.0500203 · DOI
- Gregg, 2013, Lung cancer biomarkers for the assessment of modified risk tobacco products: an oxidative stress perspective, Biomarkers, 18, 183, 10.3109/1354750X.2013.777116 · DOI
- Gotteland, 2012, Differential protective effects of quercetin, resveratrol, rutin and epigallocatechin gallate against mitochondrial dysfunction induced by indomethacin in Caco-2 cells, Chem Biol Interact, 195, 199, 10.1016/j.cbi.2011.12.007 · DOI
- Ohigashi, 2007, Targeting NOX, INOS and COX-2 in inflammatory cells: chemoprevention using food phytochemicals, Int J Cancer, 121, 2357, 10.1002/ijc.23161 · DOI · Paper page
- Aggarwal, 2013, Therapeutic roles of curcumin: lessons learned from clinical trials, AAPS J, 15, 195, 10.1208/s12248-012-9432-8 · DOI
- Dennis, 2009, The chemopreventive agent myoinositol inhibits Akt and extracellular signal-regulated kinase in bronchial lesions from heavy smokers, Cancer Prev Res (Phila), 2, 370, 10.1158/1940-6207.CAPR-08-0209 · DOI
- Cao, 2015, The role of targeting kinase activity by natural products in cancer chemoprevention and chemotherapy (Review), Oncol Rep, 34, 547, 10.3892/or.2015.4029 · DOI
- Dong, 2008, Raf and MEK protein kinases are direct molecular targets for the chemopreventive effect of quercetin, a major flavonol in red wine, Cancer Res, 68, 946, 10.1158/0008-5472.CAN-07-3140 · DOI
- Hu, 2015, Discovery of direct inhibitors of Keap1-Nrf2 protein-protein interaction as potential therapeutic and preventive agents, Acta Pharm Sin B, 5, 285, 10.1016/j.apsb.2015.05.008 · DOI
- Srivastava, 2011, Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications, Biochem Pharmacol, 82, 1807, 10.1016/j.bcp.2011.07.093 · DOI
- Arbiser, 2012, Targeting NADPH oxidases for the treatment of cancer and inflammation, Cell Mol Life Sci, 69, 2435, 10.1007/s00018-012-1017-2 · DOI
- Selemidis, 2014, Understanding the biology of reactive oxygen species and their link to cancer: NADPH oxidases as novel pharmacological targets, Clin Exp Pharmacol Physiol, 41, 533, 10.1111/1440-1681.12238 · DOI
- Procopio, 2010, Lipoxygenase inhibitors for cancer prevention: promises and risks, Curr Pharm Des, 16, 725, 10.2174/138161210790883822 · DOI
- Reddanna, 2012, Structure and ligand based drug design strategies in the development of novel 5- LOX inhibitors, Curr Med Chem, 19, 3763, 10.2174/092986712801661112 · DOI
- Tan, 2015, Cyclooxygenase-2 inhibitors in lung cancer treatment: bench to bed, Eur J Pharmacol, 769, 127, 10.1016/j.ejphar.2015.11.007 · DOI
- Munkarah, 2006, The effects of the inhibition of inducible nitric oxide synthase on angiogenesis of epithelial ovarian cancer, Am J Obstet Gynecol, 194, 1110, 10.1016/j.ajog.2005.12.019 · DOI
- El-Naggar, 2012, Targeting the MAPK-RAS-RAF signaling pathway in cancer therapy, Expert Opin Ther Targets, 16, 103, 10.1517/14728222.2011.645805 · DOI
- Tabernero, 2013, Development of PI3K inhibitors: lessons learned from early clinical trials, Nat Rev Clin Oncol, 10, 143, 10.1038/nrclinonc.2013.10 · DOI
- Young, 2013, Transcriptional regulation and its misregulation in disease, Cell, 152, 1237, 10.1016/j.cell.2013.02.014 · DOI
- Turkson, 2013, Therapeutic modulators of STAT signalling for human diseases, Nat Rev Drug Discov, 12, 611, 10.1038/nrd4088 · DOI
- Vakoc, 2015, Targeting Transcription Factors in Cancer, Trends Cancer, 1, 53, 10.1016/j.trecan.2015.07.001 · DOI · Paper page
Cited by
Sorted by citations
Stagni, V., Cirotti, C., & Barilà, D. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00073 · Cited by 52
La Maestra, S., Militello, G. M., Alberti, S., Benvenuti, M., & Gaggero, L. (2025) · Scientific Reports · doi:10.1038/s41598-025-86325-z · Cited by 10
Schiavello, M., Gazzano, E., Bergandi, L., Silvagno, F., Libener, R., Riganti, C., & Aldieri, E. (2021) · Cancers · doi:10.3390/cancers13051138 · Cited by 8
Retracted
Metadata
- Authors
- Gào, X., & Schöttker, B.
- Venue
- Oncotarget
- Publisher
- Impact Journals, LLC
- Published
- 2017-04-16
- Volume
- 8
- Issue
- 31
- Pages
- 51888-51906
- ISSN
- 1949-2553
- PMC
- PMC5584299
- Cited by
- 147
- References
- 9
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review