The DOI matches its Crossref record; 44 of the 46 references it cites were found in a registry or an index.
Novel Nox inhibitor VAS2870 attenuates PDGF-dependent smooth muscle cell chemotaxis, but not proliferation☆
Abstract
OBJECTIVE: Reactive oxygen species (ROS) produced by NAD(P)H oxidases (Nox) play a significant role in the pathophysiology of cardiovascular diseases. Expression and activity of NAD(P)H oxidases are regulated by growth factors such as angiotensin II and platelet-derived growth factor (PDGF). We characterized the effects of the novel Nox inhibitor VAS2870 on PDGF-dependent ROS liberation and cellular events in vascular smooth muscle cells (VSMC). METHODS AND RESULTS: PDGF-BB increased NAD(P)H oxidase activity (lucigenin-enhanced chemiluminescence) and intracellular ROS levels (detected by confocal laserscanning microscopy using 2,7-DCF) to 229+/-9% and 362+/-54% at 1 and 2 h, respectively. Preincubation with VAS2870 (10 and 20 microM) completely abolished PDGF-mediated NAD(P)H oxidase activation and ROS production. Since ROS are involved in various growth factor-induced cellular functions, the influence of VAS2870 on PDGF-induced DNA synthesis and chemotaxis was determined. PDGF promoted a 4.2+/-0.2-fold increase of VSMC migration (modified Boyden chamber, p<0.01) and increased DNA synthesis by maximally 3.2+/-0.4-fold (BrdU incorporation, p<0.01) in a concentration-dependent manner. Preincubation with VAS2870 (0.1-20 microM) did not affect PDGF-induced cell cycle progression. However, it abolished PDGF-dependent chemotaxis of VSMC in a concentration-dependent manner (100% inhibition at 10 microM). These findings were related to PDGF-dependent signaling events. Western blot analyses using phospho-specific antibodies revealed that the downstream signaling molecules Akt, Erk, and Src were activated by PDGF. However, VAS2870 blocked PDGF-dependent activation of Src, but not of Akt and Erk, in a concentration-dependent manner. CONCLUSIONS: VAS2870 effectively suppresses growth factor-mediated ROS liberation in VSMC. Furthermore, it completely inhibits PDGF-dependent VSMC migration, whereas it does not affect DNA synthesis. These divergent effects reflect the critical role of Src activity, which-in contrast to Akt and Erk-appears to be redox-sensitive and is absolutely required for PDGF-induced chemotaxis, but not cell cycle progression.
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
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
“This scheme has been found to apply to virtually all the heme protein–mediated nitrite reduction reactions studied to date, including Hb (248, 447), Mb (247, 862), neuroglobin (Ngb) (932, 945), Cygb (182, 571, 780), cystathionine β-synthase (CBS) (149, 350), globin X (184), plant and cyanobacterial Hb (phytohemoglobins) (905, 946), flavohemoglobin (340), heme-albumin (43), cytochrome c (41), prot”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [932]
In the citing paper
“It was recently demonstrated that, as observed with other globins, deoxygenated Ngb can also reduce nitrite to NO (932, 945).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [932]
In the citing paper
“However, although initial experiments suggested VAS2870 to be Nox2-specific, it is definitely not [341,393,403,404].”
From Functions of ROS in Macrophages and Antimicrobial Immunity (2021) · cites this paper as [404]
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
Endothelial dysfunction in cardiovascular diseases: the role of oxidant stress
Cai, H., & Harrison, D. G. (2000) · Circulation Research · doi:10.1161/01.res.87.10.840 · Cited by 3,839
Requirement for Generation of H 2 O 2 for Platelet-Derived Growth Factor Signal Transduction
Sundaresan, M., Yu, Z.-X., Ferrans, V. J., Irani, K., & Finkel, T. (1995) · Science · doi:10.1126/science.270.5234.296 · Cited by 2,520
The smooth muscle cell in culture
Chamley-Campbell, J. H., CAMPBELL, G. R., & Ross, R. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.1.1 · Cited by 1,560
Cell transformation by the superoxide-generating oxidase Mox1
Suh, Y.-A., Arnold, R. S., Lassegue, B., Shi, J., Xu, X., Sorescu, D., Chung, A. B., Griendling, K. K., & Lambeth, J. D. (1999) · Nature · doi:10.1038/43459 · Cited by 1,480
Vascular NAD(P)H oxidases: specific features, expression, and regulation
Lassegue, B. P., & Clempus, R. E. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00758.2002 · Cited by 1,026
Superoxide Production and Expression of Nox Family Proteins in Human Atherosclerosis
Sorescu, D., Weiss, D., Lassègue, B., Clempus, R. E., Szöcs, K., Sorescu, G. P., Valppu, L., Quinn, M. T., Lambeth, J. D., Vega, J. D., et al. (2002) · Circulation · doi:10.1161/01.cir.0000012917.74432.66 · Cited by 847
Identification of Renox, an NAD(P)H oxidase in kidney
Geiszt, M., Kopp, J. B., Várnai, P., & Leto, T. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.130135897 · Cited by 840
Lassègue, B., Sorescu, D., Szöcs, K., Yin, Q., Akers, M., Zhang, Y., Grant, S. L., Lambeth, J. D., & Griendling, K. K. (2001) · Circulation Research · doi:10.1161/hh0901.090299 · Cited by 839
Homologs of gp91 phox : cloning and tissue expression of Nox3, Nox4, and Nox5
Cheng, G., Cao, Z., Xu, X., Meir, E. G. V., & Lambeth, J. D. (2001) · Gene · doi:10.1016/s0378-1119(01)00449-8 · Cited by 820
The superoxide-generating NADPH oxidase: structural aspects and activation mechanism
Vignais, P. V. (2002) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-002-8520-9 · Cited by 799
Research works printed but not linked: 1
- Sundaresan M, Yu ZX, Ferrans VJ, Irani K, Finkel T. Requirement for generation of H2O2 for platelet-derived growth factor signal trans- duction. Science 1995;270:296 -9.
Cited by
Sorted by citations
Items 201–263 of 263
Is Nox4 a key regulator of the activated state of fibroblasts in systemic sclerosis?
Böhm, M., Dosoki, H., & Kerkhoff, C. (2014) · Experimental Dermatology · doi:10.1111/exd.12497 · Cited by 12
Optimization and Characterization of an Inhibitor for NADPH Oxidase 1 (NOX-1)
Gianni, D., Nicolas, N., Zhang, H., Mardirossian, C. D., Kister, J., Martínez, L. E., Ferguson, J., Roush, W. R., Brown, S., Bokoch, G., et al. (2011) · Europe PMC (PubMed Central) · Cited by 12
Valdés, Á. O., Treuer, A. V., Barrios, G., Ponce, N., Fuentealba, R., Dulce, R. A., & González, D. R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19082404 · Cited by 12
Shah, A. M., & SAUER, H. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.05.018 · Cited by 12
Self-citationDeletion of Rap1 disrupts redox balance and impairs endothelium-dependent relaxations
Wong, K. K. H., Cai, Y., Fan, Y., Chen, X., Vanhoutte, P. M., & Tang, E. H. C. (2017) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2017.12.009 · Cited by 11
Kalinovic, S., Stamm, P., Oelze, M. W., Steven, S., Kröller‐Schön, S., Kvandová, M., Zielonka, J., Münzel, T. F., & Daiber, A. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.03.041 · Cited by 11
Xu, Y., Wei, Y., Wang, Y., Yin, L.-M., Park, G., Liu, Y., & Yang, Y. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.02.098 · Cited by 11
Ishizawa, K., Izawa‐Ishizawa, Y., Dorjsuren, N., Miki, E., Kihira, Y., Ikeda, Y., Hamano, S., Kawazoe, K., Minakuchi, K., Tomita, S., et al. (2009) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfp520 · Cited by 11
NADPH oxidase activity: Spectrophotometric determination of superoxide using pyrogallol red
Cortés‐Ríos, J., Torres, M. J., Campos-Bustamante, M. P., Romero‐Parra, J., Letelier, M. E., Pessoa-Mahana, C. D., Chung, H., & Faúndez, M. (2017) · Analytical Biochemistry · doi:10.1016/j.ab.2017.08.013 · Cited by 11
Association of Nox1 and Vinculin With Colon Cancer Progression
Sun, Z., & Liu, F. (2013) · Cancer Investigation · doi:10.3109/07357907.2013.789897 · Cited by 10
VAS3947 Induces UPR-Mediated Apoptosis through Cysteine Thiol Alkylation in AML Cell Lines
Dor, M. E., Dakik, H., Polomski, M., Haudebourg, E., Brachet‐Botineau, M., Gouilleux, F., Prié, G., Zibara, K., & Mazurier, F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155470 · Cited by 10
Allen, C., & Bayraktutan, U. (2008) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2008.05.021 · Cited by 10
Redmond, E. M., & Cahill, P. A. (2012) · Cardiovascular Research · doi:10.1093/cvr/cvs020 · Cited by 10
Readers' choice: Hot papers downloaded in 2006
Martinson, B., Piper, H. M., David Garcia-dorado, A., & Elizabeth, A. M. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.01.013 · Cited by 10
An RbohC and RbohE-mediated ROS oscillatory circuit regulates root cap turnover in Arabidopsis
Shin, Y.-S., Jeon, W.-T., Jung, H., Do, T. H. T., & Lee, Y. (2025) · iScience · doi:10.1016/j.isci.2025.114056 · Cited by 7
Liu, Y., Liang, S., Shi, D., Zhang, Y., Bai, C., & Ye, R. D. (2023) · PLoS ONE · doi:10.1371/journal.pone.0285206 · Cited by 9
Wang, W.-L., Yeh, Y.-T., Chen, L.-J., & Chiu, J. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.01.049 · Cited by 9
Howitt, L., Matthaei, K. I., Drummond, G. R., & Hill, C. E. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1548-5 · Cited by 8
Kim, J., Lee, K. P., Kim, B. S., Lee, S. J., Moon, B. S., & Baek, S. (2020) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2020.24.3.241 · Cited by 8
Development of a caffeic acid–phthalimide hybrid compound for NADPH oxidase inhibition
dos Santos, W. H., Yoguim, M. I., Daré, R. G., da Silva‐Filho, L. C., Silva, S. D. O., & Ximenes, V. F. (2021) · RSC Advances · doi:10.1039/d1ra01066b · Cited by 8
Redox Regulation of the Microcirculation
Kadlec, A. O., & Gutterman, D. D. (2019) · Comprehensive physiology · doi:10.1002/cphy.c180039 · Cited by 10
Kumar, G., Saini, M., & Kundu, S. (2021) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2020-0732 · Cited by 6
Isoform-Selective Nox Inhibitors: Advances and Future Perspectives
Dustin, C. M., Cifuentes-Pagano, E., & Pagano, P. J. (2023) · Springer eBooks · doi:10.1007/978-3-031-23752-2_21 · Cited by 5
NAD(P)H oxidase isoforms as therapeutic targets for diabetic complications
Gray, S. P., Jha, J. C., Marco, E. D., & Jandeleit-Dahm, K. A. M. (2014) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.2014.887984 · Cited by 5
Isoform-selective NADPH oxidase inhibitor panel for pharmacological target validationPreprint
Dao, V. T.-V., Elbatreek, M. H., Altenhöfer, S., Casas, A. I., Pachado, M. P., Neullens, C. T., Knaus, U., & Schmidt, H. H. H. W. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/382226 · Cited by 5
Hagiwara, S., Jha, J. C., & Cooper, M. E. (2013) · Diabetology International · doi:10.1007/s13340-013-0148-5 · Cited by 4
NADPH oxidase inhibitor VAS2870 prevents staurosporine-induced cell death in rat astrocytes
Šimenc, J., Jurič, D. M., & Lipnik‐Štangelj, M. (2019) · Radiology and Oncology · doi:10.2478/raon-2019-0002 · Cited by 5
Oxidative Stress and Novel Antioxidant Approaches to Reduce Diabetic Complications
Min, S., Sharma, A., & de H, J. B. (2012) · InTech eBooks · doi:10.5772/35020 · Cited by 4
Taye, A., & Wind, S. (2010) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 4
Role of NADPH Oxidase in Beta Cell Dysfunction
Weaver, J. R., & Taylor, D. (2014) · Springer eBooks · doi:10.1007/978-94-007-6884-0_46-3 · Cited by 4
NADPH Oxidase in Pancreatic β-Cell Function
de Jesus, D. S. (2024) · Current Molecular Biology Reports · doi:10.1007/s40610-024-00159-8 · Cited by 4
Manogue, M. R., Bennett, J. R., Holland, D. S., Choi, C., Drake, D. A., Taylor, M. S., & Weber, D. S. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/305686 · Cited by 4
Chauhan, A. K., Lee, K. H., & Magoski, N. S. (2021) · The Journal of Physiology · doi:10.1113/jp282302 · Cited by 3
NADPH oxidase controls EGF-induced proliferation via an ERK1/2-independent mechanism
Tyurin‐Kuzmin, P. A., Agaronyan, K., Morozov, Y. I., Mishina, N. M., Belousov, V. V., & Vorotnikov, A. V. (2010) · BIOPHYSICS · doi:10.1134/s0006350910060126 · Cited by 3
Sharma, A., & de Haan, J. B. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_155 · Cited by 3
Valdés, Á. O., Barrios, G., Ponce, N., Dulce, R. A., & González, D. R. (2018) · Preprints.org · doi:10.20944/preprints201804.0190.v1 · Cited by 3
Gu, Z., Luo, S., Wu, C., Shu, D., Li, C., Yang, S., Liu, G., & Yang, R. (2025) · Analytical Chemistry · doi:10.1021/acs.analchem.5c03773 · Cited by 2
Role of NADPH Oxidase in β Cell Dysfunction
Weaver, J. R., & Taylor, D. (2014) · Springer eBooks · doi:10.1007/978-94-007-6686-0_46 · Cited by 2
de Haan, J. B., Jandeleit-Dahm, K. A. M., & Allen, T. J. (2011) · Humana Press eBooks · doi:10.1007/978-1-60761-956-7_1 · Cited by 2
Oxidative Stress and Nitric Oxide in Cerebral Ischemic Reperfusion Injury
Ma, J., Liu, Z., & Shi, Z. (2018) · Springer series in translational stroke research · doi:10.1007/978-3-319-90194-7_7 · Cited by 2
Ishii, S., Ashino, T., Fujimori, H., & Numazawa, S. (2021) · Free Radical Research · doi:10.1080/10715762.2021.1887485 · Cited by 2
Advanced therapeutics for renal inflammation
Singh, M. P., Makkar, R., Behl, T., & Pathak, K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99988-5.00008-5 · Cited by 1
Role of NADPH Oxidase in b Cell Dysfunction 34
Weaver, J. R., & Taylor, D. (2015)
Bokoch, G. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1160970.621894
Gerling, I., & Kakoola, D. N. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1160970.621860
Ramírez-Corona, A., Reza-Medina, B., Schnabel, D., Lomelı́, H., & Vidal, E. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.13.628279
Methods for Increasing Coenzyme II
Xie, Y., & Sheng, R. (2025) · Springer eBooks · doi:10.1007/978-981-97-9877-3_11
Ultrafine Particles Alter Endothelial Phenotype Through Oxidant Signaling
Snow, S. J. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/3zg6-c529
Activité NADPH oxydase des cellules de leucémie aiguë myéloïde
Leclerc, J. (2013) · theses.fr (ABES) · doi:10.70675/5743e778zd4fdz4faazbccfz81db73478c61
Caractérisation des NADPH oxydases et effet de leur inhibition dans les leucémies aigues myéloïdes
Dakik, H. (2017) · theses.fr (ABES) · doi:10.70675/c50123fez19eaz4414zaf63z4c616441a1d3
Benssouina, F.-Z. (2022) · theses.fr (ABES) · doi:10.70675/276c5067zc483z4f95zb64bz7585a1ebc1e6
Role of NADPH oxidase 2-derived reactive oxygen species in cardiac electrophysiological disorders
Li, B., Dong, Y., Chen, Y., Liu, C., & Li, Y. (2026) · Channels · doi:10.1080/19336950.2026.2696810
Thakur, M., Mutyala, D., Amoliga, A., Ortega, M. C., & Batra, S. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01447-2
Hydrogen Peroxide Regulates Butterfly Wing Eyespot Color Patterns
Nakazato, Y., & Otaki, J. M. (2026) · Insects · doi:10.3390/insects17101032
BindingDB (2020) · UC San Diego · doi:10.7270/q2vd722w
BindingDB Entry 50020295: NADPH Oxidases: From Molecular Mechanisms to Current Inhibitors.
BindingDB (2024) · UC San Diego · doi:10.7270/q2jm2g3p
BindingDB Entry 50032268: Small-molecule inhibitors of NADPH oxidase 4.
BindingDB (2011) · UC San Diego · doi:10.7270/q2f18zz5
BindingDB (2020) · UC San Diego · doi:10.7270/q2j38wjk
Corder, N. L. B. (2014) · eScholarship (California Digital Library)
Metadata
- Authors
- TENFREYHAUS, H., HUNTGEBURTH, M., WINGLER, K., SCHNITKER, J., BAUMER, A., VANTLER, M., BEKHITE, M., WARTENBERG, M., SAUER, H., & ROSENKRANZ, S.
- Affiliations
- University of Cologne (DE)
- Vasopharm (Germany) (DE)
- Justus-Liebig-Universität Gießen (DE)
- Corresponding author
- ROSENKRANZ, S
- Venue
- Cardiovascular Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2006-07-15
- Volume
- 71
- Issue
- 2
- Pages
- 331-341
- ISSN
- 0008-6363 (ISSN-L)
- OpenAlex
- W2136386024
- Cited by
- 259
- References
- 46
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 4 · 2023: 8 · 2022: 7 · 2021: 13 · 2020: 15 · 2019: 15 · 2018: 13 · 2017: 14 · 2016: 9 · 2015: 19 · 2014: 22 · 2013: 24 · 2012: 22
- FWCI
- 7.51
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cardiovascular Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- VAS2870, platelet-derived growth factor, vascular smooth muscle cells, reactive oxygen species, cell proliferation, Src kinase, Akt, ERK, PDGF signaling, cell migration, DNA synthesis, cardiovascular disease, redox signaling, chemiluminescence, BrdU incorporation, immunofluorescence
- MeSH terms
- Becaplermin, Animals, Aorta, Thoracic, Benzoxazoles, Cell Survival, Cells, Cultured, Chemotaxis, DNA, Enzyme Inhibitors, Muscle, Smooth, Vascular, Platelet-Derived Growth Factor, Rats, Inbred WKY, Triazoles, Blotting, Western, Reactive Oxygen Species, src-Family Kinases, NADPH Oxidases, Proto-Oncogene Proteins c-sis, Myocytes, Smooth Muscle, Immunoprecipitation, Cell Proliferation, Rats
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