PARP-1 Inhibition Prevents Oxidative and Nitrosative Stress–Induced Endothelial Cell Death via Transactivation of the VEGF Receptor 2
Abstract
Objective— PARP-1, a DNA base repair enzyme, is activated by DNA breaks induced by oxidative (ROS) and nitrosative (RNS) stress. By consuming NAD + , PARP-1 activation can lead to ATP depletion and cell death. Studies suggest that inhibiting PARP-1 activity can attenuate pathologies associated with vascular smooth muscle and endothelial dysfunction. PARP-1 inhibition can also activate the prosurvival serine/threonine kinase, Akt. Vascular endothelial growth factor (VEGF) regulates endothelial cell survival via Akt activation downstream of VEGF receptor 2 (VEGFR2) activation. Here we investigated the hypothesis that PARP-1 inhibition protects human umbilical vein endothelial cells (HUVECs) from ROS- and RNS-induced cell death by limiting NAD + depletion and by activating a prosurvival signaling pathway via VEGFR2 phosphorylation. Methods and Results— We activated PARP-1 in HUVECs by treatment with hydrogen peroxide (H 2 O 2 ) and peroxynitrite (ONOO − ). Both depleted HUVECs of NAD + and ATP, processes that were limited by the PARP-1 inhibitor, PJ34. ONOO − and H 2 O 2 -induced cell death and apoptosis were attenuated in cells treated with PJ34 or PARP-1 siRNA. PARP-1 inhibition increased Akt, BAD, and VEGFR2 phosphorylation in HUVECs and in PJ34-treated rabbit aortas. The VEGFR2-specific tyrosine kinase inhibitor SU1498 decreased PARP-1 inhibition-mediated phosphorylation of VEGFR2 and Akt, and also reversed survival effects of PJ34. Finally, PARP-1 inhibition protected cells from death induced by serum starvation, evidence for a role in cell survival independent of energy protection. Conclusions— PARP-1 inhibition prevents ROS- and RNS-induced HUVEC death by maintaining cellular energy in the form of NAD + and ATP, and also by activating a survival pathway via VEGFR2, Akt, and BAD phosphorylation.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
PARP1 inhibitors have limited clinical use because of toxicity.
“They sensitize tumours to DNA damage, but they have limited use due to toxicity223–225.”
From NAD+ metabolism and its roles in cellular processes during ageing (2021) · cites this paper as [225]
Cites
Biochemistry and molecular cell biology of diabetic complications
Brownlee, M. (2001) · Nature · doi:10.1038/414813a · Cited by 9,107 · see citing works
Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
Datta, S. R., Dudek, H., Tao, X., Masters, S., Fu, H., Gotoh, Y., & Greenberg, M. E. (1997) · Cell · doi:10.1016/s0092-8674(00)80405-5 · Cited by 5,689 · see citing works
Role of Oxidative Modifications in Atherosclerosis
Stocker, R., & Keaney, J. F. (2004) · Physiological Reviews · doi:10.1152/physrev.00047.2003 · Cited by 2,611 · see citing works
Asahara, T., Takahashi, T., Masuda, H., Kalka, C., Chen, D., Iwaguro, H., Inai, Y., Silver, M., & Isner, J. M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.14.3964 · Cited by 1,856 · see citing works
14-3-3 Proteins and Survival Kinases Cooperate to Inactivate BAD by BH3 Domain Phosphorylation
Datta, S. R., Katsov, A., Hu, L. S., Petros, A. M., Fesik, S. W., Yaffe, M. B., & Greenberg, M. E. (2000) · Molecular Cell · doi:10.1016/s1097-2765(05)00012-2 · Cited by 663 · see citing works
Nor, J. E., Christensen, J. B., Mooney, D. J., & Polverini, P. J. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65284-4 · Cited by 641 · see citing works
Diabetic endothelial dysfunction: the role of poly(ADP-ribose) polymerase activation
Soriano, F. G., Virág, L., Jagtap, P. G., Szabó, É., Mabley, J. G., Liaudet, L., Marton, A., Hoyt, D. G., Murthy, K. G. K., Salzman, A. L., et al. (2001) · Nature Medicine · doi:10.1038/83241 · Cited by 602 · see citing works
Poly(ADP-ribose) polymerase-1: what have we learned from the deficient mouse model?
Shall, S., & de MURCIA, G. (2000) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(00)00016-1 · Cited by 534 · see citing works
Jin, Z., Ueba, H., Tanimoto, T., Lungu, A. O., Frame, M. D. S., & Berk, B. C. (2003) · Circulation Research · doi:10.1161/01.res.0000089257.94002.96 · Cited by 388 · see citing works
Self-citationHassa, P. O., Haenni, S. S., Buerki, C., Meier, N. I., Lane, W. S., Owen, H., Gersbach, M., Imhof, R., & Hottiger, M. O. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507553200 · Cited by 306 · see citing works
Poly(ADP-ribose) polymerase: killer or conspirator? The ‘suicide hypothesis’ revisited
Chiarugi, A. (2002) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(00)01902-7 · Cited by 298 · see citing works
The Enzymatic and DNA Binding Activity of PARP-1 Are Not Required for NF-κB Coactivator Function
Hassa, P. O., Covic, M., Hasan, S., Imhof, R., & Hottiger, M. O. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m106528200 · Cited by 296 · see citing works
Bürkle, A. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04864.x · Cited by 294 · see citing works
Soriano, F. G., Pacher, P., Mabley, J. G., Liaudet, L., & Szabó, C. (2001) · Circulation Research · doi:10.1161/hh2001.097797 · Cited by 190 · see citing works
Zou, M., Hou, X., Shi, C., Nagata, D., Walsh, K., & Cohen, R. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204512200 · Cited by 189 · see citing works
Yamawaki, H., Lehoux, S., & Berk, B. C. (2003) · Circulation · doi:10.1161/01.cir.0000089373.49941.c4 · Cited by 173 · see citing works
Self-citationTapodi, A., Debreceni, B., Hanto, K., Bognar, Z., Wittmann, I., Gallyas, F., Varbiro, G., & Sumegi, B. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507075200 · Cited by 166 · see citing works
Endothelial cell response to lactate: Implication of PAR modification of VEGF
Kumar, V. B. S., Viji, R. I., Kiran, M. S., & Sudhakaran, P. R. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20955 · Cited by 143 · see citing works
Oumouna‐Benachour, K., Hans, C. P., Suzuki, Y., Naura, A. S., Datta, R., Belmadani, S., Fallon, K. B., Woods, C., & Boulares, A. H. (2007) · Circulation · doi:10.1161/circulationaha.106.668756 · Cited by 109 · see citing works
Jin, Z., Wong, C. N., Wu, J., & Berk, B. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m500294200 · Cited by 107 · see citing works
Self-citationNoncleavable poly(ADP-ribose) polymerase-1 regulates the inflammation response in mice
Pétrilli, V., Herceg, Z., Hassa, P. O., Patel, N. S. A., Paola, R. D., Cortes, U., Dugo, L., Mota‐Filipe, H., Thiemermann, C., Hottiger, M. O., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200421854 · Cited by 105 · see citing works
Reactive Oxygen Species and Death
Bennett, M. R. (2001) · Circulation Research · doi:10.1161/hh0701.089955 · Cited by 103 · see citing works
Drel, V. R., Pacher, P., Stevens, M. J., & Obrosova, I. G. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.12.034 · Cited by 96 · see citing works
The effect of PARP inhibitor on ischaemic cell death, its related inflammation and survival signals
Koh, S., Park, Y., Song, C. W., Kim, J. G., Kim, K., Kim, J., Kim, M., Lee, S. R., Kim, D. W., Yu, H., et al. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03632.x · Cited by 93 · see citing works
Noncleavable poly(ADP-ribose) polymerase-1 regulates the inflammation response in mice
Pétrilli, V., Herceg, Z., Hassa, P. O., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21854 · Cited by 93 · see citing works
Muthumani, K., Choo, A. Y., Zong, W., Madesh, M., Hwang, D. S., Arumugam, P., Thieu, K. P., Emmanuel, J., Kumar, S., Thompson, C. B., et al. (2006) · Nature Cell Biology · doi:10.1038/ncb1352 · Cited by 78 · see citing works
Poly(ADP-ribose)polymerase inhibition decreases angiogenesis
Rajesh, M., Mukhopadhyay, P., Godlewski, G., Bátkai, S., Haskó, G., Liaudet, L., & Pacher, P. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.09.160 · Cited by 77 · see citing works
Pálfi, A., Tóth, A., Hantó, K., Deres, P., Szabados, E., Szereday, Z., Kulcsár, G., Kálai, T., Hideg, K., Gallyas, F., et al. (2006) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2006.03.427 · Cited by 66 · see citing works
Yeh, T.-Y. J., Meyer, T. N., Schwesinger, C., Tsun, Z.-Y., Lee, R. M., & Chi, N. (2006) · Biochemical Journal · doi:10.1042/bj20060713 · Cited by 45 · see citing works
Benkő, R., Pacher, P., Vaslin, A., Kollai, M., & Szabó, C. (2004) · Life Sciences · doi:10.1016/j.lfs.2004.04.007 · Cited by 42 · see citing works
Mabley, J. G., & Soriano, F. G. (2005) · Current Vascular Pharmacology · doi:10.2174/1570161054368571 · Cited by 41 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
NAD+ metabolism and its roles in cellular processes during ageing
Covarrubias, A. J., Perrone, R., Grozio, A., & Verdin, E. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00313-x · Cited by 1,617 · see citing works
Incalza, M. A., D’Oria, R., Natalicchio, A., Perrini, S., Laviola, L., & Giorgino, F. (2017) · Vascular Pharmacology · doi:10.1016/j.vph.2017.05.005 · Cited by 1,375 · see citing works
Therapeutic Potential of NAD-Boosting Molecules: The In Vivo Evidence
Rajman, L., Chwalek, K., & Sinclair, D. A. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.02.011 · Cited by 865 · see citing works
Parthanatos: mitochondrial‐linked mechanisms and therapeutic opportunities
Fatokun, A. A., Dawson, V. L., & Dawson, T. M. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12416 · Cited by 594 · see citing works
ROS-triggered endothelial cell death mechanisms: Focus on pyroptosis, parthanatos, and ferroptosis
Zheng, D., Liu, J., Piao, H., Zhu, Z., Wei, R., & Liu, K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1039241 · Cited by 574 · see citing works
The inflammatory response in sepsis
Bosmann, M., & Ward, P. A. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.09.004 · Cited by 559 · see citing works
Molecular Biology of Atherosclerosis
Hopkins, P. N. (2013) · Physiological Reviews · doi:10.1152/physrev.00004.2012 · Cited by 456 · see citing works
Thomas, S. R., Witting, P. K., & Drummond, G. R. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2027 · Cited by 383 · see citing works
Banerjee, S. N., & Kaye, S. B. (2013) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-12-2243 · Cited by 355 · see citing works
Nakamura, Y., Kawazoe, A., Lordick, F., Janjigian, Y. Y., & Shitara, K. (2021) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-021-00492-2 · Cited by 302 · see citing works
Targeting protein modifications in metabolic diseases: molecular mechanisms and targeted therapies
Wu, X., Xu, M., Geng, M., Chen, S., Little, P. J., Xu, S., & Weng, J. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01439-y · Cited by 290 · see citing works
Qiao, X., Yin, J., Zheng, Z., Li, L., & Feng, X. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01620-y · Cited by 203 · see citing works
Lu, M., Hu, L., Hu, G., & Bian, J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.09.014 · Cited by 187 · see citing works
Nicotinamide Phosphoribosyltransferase in Malignancy: A Review
Shackelford, R. E., Mayhall, K., Maxwell, N. M., Kandil, E. H., & Coppola, D. (2013) · Genes & Cancer · doi:10.1177/1947601913507576 · Cited by 127 · see citing works
Nitrosative Stress and Its Association with Cardiometabolic Disorders
Pérez-Torres, I., Manzano-Pech, L., Rubio-Ruiz, M. E., Soto, M. E., & Guarner‐Lans, V. (2020) · Molecules · doi:10.3390/molecules25112555 · Cited by 124 · see citing works
Wang, T., Wang, L., Moreno‐Vinasco, L., Lang, G. D., Siegler, J. H., Mathew, B., Usatyuk, P. V., Samet, J. M., Geyh, A. S., Breysse, P. N., et al. (2012) · Particle and Fibre Toxicology · doi:10.1186/1743-8977-9-35 · Cited by 117 · see citing works
Making the best of PARP inhibitors in ovarian cancer
Banerjee, S. N., Kaye, S. B., & Ashworth, A. (2010) · Nature Reviews Clinical Oncology · doi:10.1038/nrclinonc.2010.116 · Cited by 105 · see citing works
Byun, J., Kim, M., Eum, D., Yoon, C., Seo, W. D., Park, K. H., Hyun, J. W., Lee, Y., Lee, J., Yoon, M., et al. (2009) · Molecular Pharmacology · doi:10.1124/mol.109.056259 · Cited by 86 · see citing works
Roy, B. (2025) · Medical Sciences · doi:10.3390/medsci13030087 · Cited by 89 · see citing works
The Role of Oxidative Stress in Acute Ischemic Stroke‐Related Thrombosis
Li, Z., Bi, R., Sun, S., Chen, S., Chen, J., Hu, B., & Jin, H. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/8418820 · Cited by 76 · see citing works
Subcellular Localization of Oxidants and Redox Modulation of Endothelial Nitric Oxide Synthase
Maron, B. A., & Michel, T. M. (2012) · Circulation Journal · doi:10.1253/circj.cj-12-1207 · Cited by 75 · see citing works
Kwok, H., Ng, W. Y., Yang, M. S. M., Mak, N. K., Wong, R. N., & Yue, P. Y. K. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.11.013 · Cited by 74 · see citing works
Naked mole rat cells display more efficient excision repair than mouse cells
Evdokimov, A. N., Kutuzov, M. M., Petruseva, I. O., Lukjanchikova, N., Kashina, E. V., Kolova, E., Zemerova, T., Romanenko, S. A., Perelman, P. L., Prokopov, D., et al. (2018) · Aging · doi:10.18632/aging.101482 · Cited by 73 · see citing works
AMPKα2 exerts its anti-inflammatory effects through PARP-1 and Bcl-6
Gongol, B., Marin, T., Peng, I.-C., Woo, B., Martin, M., King, S., Sun, W., Johnson, D. A., Chien, S., & Shyy, J. Y.-J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1222051110 · Cited by 61 · see citing works
Saad, M. I., Abdelkhalek, T. M., Saleh, M. M., Kamel, M. A. E.-N., Youssef, M., Tawfik, S. H., & Domínguez, H. (2015) · Endocrine · doi:10.1007/s12020-015-0709-4 · Cited by 59 · see citing works
Alonso, V., Gortázar, A. R., Ardura, J. A., Andrade‐Zapata, I., Alvarez-Arroyo, M. V., & Esbrit, P. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21547 · Cited by 59 · see citing works
Li, F., Abuarab, N., & Sivaprasadarao, A. (2016) · Journal of Cell Science · doi:10.1242/jcs.179796 · Cited by 58 · see citing works
Effect of Diabetes Mellitus on the Pharmacokinetics and Pharmacodynamics of Tuberculosis Treatment
Alfarisi, O., Mave, V., Gaikwad, S., Sahasrabudhe, T. R., Ramachandran, G., Kumar, H., Gupte, N., Kulkarni, V., Deshmukh, S., Atre, S. R., et al. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01383-18 · Cited by 60 · see citing works
Signaling pathways in brain ischemia: Mechanisms and therapeutic implications
Lin, W., Zhao, X., Cheng, J., Li, L., Jiang, Q., Zhang, Y., & Han, F. (2023) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108541 · Cited by 60 · see citing works
Hemorrhagic Transformation After Tissue Plasminogen Activator Treatment in Acute Ischemic Stroke
Liu, C., Xie, J., Sun, S., Li, H., Li, T., Jiang, C. Q., Chen, X., Wang, J., Le, A., Wang, J., et al. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00985-1 · Cited by 58 · see citing works
The role of Cediranib in ovarian cancer
Orbegoso, C., Marquina, G., George, A. J., & Banerjee, S. N. (2017) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2017.1383384 · Cited by 52 · see citing works
Peroxynitrite Induces Gene Expression in Intervertebral Disc Cells
Poveda, L., Hottiger, M. O., Boos, N., & Wuertz‐Kozak, K. (2009) · Spine · doi:10.1097/brs.0b013e31819f2330 · Cited by 47 · see citing works
Rom, S., Zuluaga‐Ramirez, V., Reichenbach, N. L., Dykstra, H., Gajghate, S., Pacher, P., & Persidsky, Y. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0729-x · Cited by 47 · see citing works
Targeted Therapy in Ovarian Cancer
Lim, H. J., & Ledger, W. J. (2016) · Women s Health · doi:10.2217/whe.16.4 · Cited by 46 · see citing works
PARP and PARG Inhibitors—New Therapeutic Targets in Cancer Treatment
Fauzee, N. J. S., Pan, J., & Wang, Y. (2010) · Pathology & Oncology Research · doi:10.1007/s12253-010-9266-6 · Cited by 46 · see citing works
The Cardiovascular Therapeutic Potential of Propolis—A Comprehensive Review
Silva, H., Francisco, R. C., Saraiva, A., Francisco, S., Carrascosa, C., & Raposo, A. (2021) · Biology · doi:10.3390/biology10010027 · Cited by 71 · see citing works
Shang, F., Zhang, J., Li, Z., Zhang, J., Yin, Y., Wang, Y., Marin, T., Gongol, B., Xiao, H., Zhang, Y., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151845 · Cited by 44 · see citing works
Role of Sirtuins in Tumor Angiogenesis
Edatt, L., Poyyakkara, A., Raji, G. R., Ramachandran, V., Shankar, S. S., & Kumar, V. B. S. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2019.01516 · Cited by 43 · see citing works
MicroRNAs Modulate Oxidative Stress in Hypertension through PARP‐1 Regulation
Dluzen, D. F., Kim, Y., Bastian, P., Zhang, Y., Lehrmann, E., Becker, K. G., Hooten, N. N., & Evans, M. K. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3984280 · Cited by 39 · see citing works
Zarkasi, K. A., Murad, N. A. A., Ahmad, N., Jamal, R., & Abdullah, N. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19020647 · Cited by 38 · see citing works
TDP1 and PARP1 Deficiency Are Cytotoxic to Rhabdomyosarcoma Cells
Fam, H. K., Walton, C., Mitra, S. A., Chowdhury, M. K., Osborne, N., Choi, K., Sun, G., Wong, P. C. W., O’Sullivan, M. J., Turashvili, G., et al. (2013) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-12-0575 · Cited by 39 · see citing works
Bosseboeuf, E., & Raimondi, C. (2020) · Cells · doi:10.3390/cells9092055 · Cited by 38 · see citing works
Exploring the role of parthanatos in CNS injury: Molecular insights and therapeutic approaches
Zhang, J., Hu, X., Geng, Y., Xiang, L., Wu, Y., Li, Y., Yang, L., & Zhou, K. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.04.031 · Cited by 37 · see citing works
Wu, X., Deng, G., Li, M., Li, Y., Ma, C., Wang, Y., & Liu, X. (2015) · BMC Immunology · doi:10.1186/s12865-015-0080-5 · Cited by 37 · see citing works
Hao, T., & Rockwell, P. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.05.036 · Cited by 37 · see citing works
Wang, C., Zhang, F., Wang, L., Zhang, Y., Li, X., Huang, K., Du, M., Liu, F., Huang, S., Guan, Y., et al. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00160-13 · Cited by 37 · see citing works
The Molecular Basis of COVID-19 Pathogenesis, Conventional and Nanomedicine Therapy
Kouhpayeh, S., Shariati, L., Boshtam, M., Rahimmanesh, I., Mirian, M., Esmaeili, Y., Najaflu, M., Khanahmad, N., Zeinalian, M., Trovato, M., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115438 · Cited by 34 · see citing works
Thioredoxin-Interacting Protein Mediates Nuclear–to–Plasma Membrane Communication
Spindel, O. N., Chen, Y., & Berk, B. C. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.244681 · Cited by 35 · see citing works
Self-citationMitochondrial mechanisms in amyloid beta peptide-induced cerebrovascular degeneration
Hsu, M., Sheu, J., Lin, C., Shen, M., & Hsu, C. Y. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.08.003 · Cited by 34 · see citing works
Shin, S.-J., Moon, K. C., Park, K. U., & Ha, E. (2012) · Biochimie · doi:10.1016/j.biochi.2012.03.023 · Cited by 34 · see citing works
Vaschetto, R., Kuiper, J. W., Musters, R. J. P., Eringa, E. C., Corte, F. D., Murthy, K. G. K., Groeneveld, A. B. J., & Plötz, F. B. (2010) · Critical Care · doi:10.1186/cc8932 · Cited by 33 · see citing works
Oxidative Stress Genes, Antioxidants and Coronary Artery Disease in Type 2 Diabetes Mellitus
Tibaut, M., & Petrovi, D. (2016) · Cardiovascular & Hematological Agents in Medicinal Chemistry · doi:10.2174/1871525714666160407143416 · Cited by 33 · see citing works
NAMPT and NAMPT-controlled NAD Metabolism in Vascular Repair
Wang, P., Li, W., Liu, J., & Miao, C. (2015) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000000332 · Cited by 32 · see citing works
Critical role of bad phosphorylation by Akt in cytostatic resistance of human bladder cancer cells.
Szántó, Á., Bognár, Z., Szigeti, A., Szabó, A., Farkas, L., & Gallyas, F. (2009) · PubMed · Cited by 32 · see citing works
Oxidative stress: An essential factor in the process of arteriovenous fistula failure
Hu, K., Guo, Y., Li, Y., Lu, C., Cai, C., Zhou, S., Ke, Z., Li, Y., & Wang, W. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.984472 · Cited by 30 · see citing works
Li, W. J., Zhou, J., Li, B., Wang, H., Peng, Y. B., & Wang, Z. (2011) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2010.02176.x · Cited by 30 · see citing works
Lee, J., Trepel, J. B., Choyke, P. L., Cao, L., Sissung, T. M., Houston, N. D., Yu, M., Figg, W. D., Turkbey, I. B., Steinberg, S. M., et al. (2015) · Frontiers in Oncology · doi:10.3389/fonc.2015.00123 · Cited by 26 · see citing works
Protein kinase C: A potential therapeutic target for endothelial dysfunction in diabetes
Xiao, Q., Wang, D., Li, D., Huang, J. H., Ma, F., Zhang, H., Sheng, Y., Zhang, C., & Ha, X. (2023) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2023.108565 · Cited by 25 · see citing works
Methyltransferase Set7/9 as a Multifaceted Regulator of ROS Response
Daks, A. A., Shuvalov, O. Y., Fedorova, O., Parfenyev, S. E., Simon, H., & Barlev, N. A. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.83158 · Cited by 24 · see citing works
Broniowska, K. A., Diers, A. R., Corbett, J. A., & Hogg, N. (2013) · Biochemistry · doi:10.1021/bi400342t · Cited by 24 · see citing works
Cseh, A. M., Fábián, Z., Sümegi, B., & Scorrano, L. (2017) · Oncotarget · doi:10.18632/oncotarget.16859 · Cited by 23 · see citing works
PARP1 inhibition protects mice against Japanese encephalitis virus infection
Desingu, P. A., Mishra, S., Dindi, L., Srinivasan, S., Rajmani, R. S., Ravi, V., Tamta, A. K., Raghu, S., Murugasamy, K., Pandit, A. S., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113103 · Cited by 23 · see citing works
Monte, M. D., Martini, D., Ristori, C., Azara, D., Armani, C., Balbarini, A., & Bagnoli, P. (2011) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-011-0625-y · Cited by 22 · see citing works
Gallorini, M., Maccallini, C., Ammazzalorso, A., Amoia, P., Filippis, B. D., Fantacuzzi, M., Giampietro, L., Cataldi, A., & Amoroso, R. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030495 · Cited by 22 · see citing works
Shiravi, A., Saadatkish, M., Abdollahi, Z., Miar, P., Khanahmad, H., & Zeinalian, M. (2020) · International Journal for Vitamin and Nutrition Research · doi:10.1024/0300-9831/a000676 · Cited by 21 · see citing works
Huang, R., Gao, Y., Duan, Q., Zhang, Q., He, P., Chen, J., Ma, G., Wang, L., Zhang, Y., Nie, K., et al. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03119-4 · Cited by 20 · see citing works
Hatachi, G., Tsuchiya, T., Miyazaki, T., Matsumoto, K., Yamasaki, N., Okita, N., Nanashima, A., Higami, Y., & Nagayasu, T. (2014) · Transplantation · doi:10.1097/tp.0000000000000305 · Cited by 20 · see citing works
Obesity drives depot-specific vascular remodeling in male white adipose tissue
Hasan, S. S., John, D., Rudnicki, M., AlZaim, I., Eberhard, D., Moll, I., Taylor, J., Klein, C., von Heesen, M., Conradi, L., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60910-2 · Cited by 20 · see citing works
Role of PARP and TRPM2 in VEGF Inhibitor‐Induced Vascular Dysfunction
Neves, K. B., Alves-Lopes, R., Montezano, A. C. I., & Touyz, R. M. (2023) · Journal of the American Heart Association · doi:10.1161/jaha.122.027769 · Cited by 19 · see citing works
Involvement of poly(ADP-ribose) polymerase in paraptotic cell death of D. discoideum
Rajawat, J., Mir, H., Alex, T., Bakshi, S. R., & Begum, R. (2013) · APOPTOSIS · doi:10.1007/s10495-013-0920-9 · Cited by 18 · see citing works
Xanthine Oxidoreductase in the Pathogenesis of Endothelial Dysfunction: An Update
Mudgal, R. K., & Singh, S. (2024) · Current Hypertension Reviews · doi:10.2174/0115734021277772240124075120 · Cited by 14 · see citing works
Li, W. J., Peng, Y., Zhou, J., Li, B., Wang, H., Zhang, J., & Wang, Z. (2012) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2012.02666.x · Cited by 14 · see citing works
Son, J. N., Lho, Y., Shin, S., Kwon, S., Moon, K. C., & Ha, E. (2010) · International Journal of Cardiology · doi:10.1016/j.ijcard.2010.10.098 · Cited by 14 · see citing works
Qin, X., Wang, Y., Li, J., Xiao, Y., & Liu, Z. (2017) · Neoplasma · doi:10.4149/neo_2017_403 · Cited by 14 · see citing works
Sinha, A., Katyal, S., & Kauppinen, T. M. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108502 · Cited by 14 · see citing works
Chen, X., Mu, P., Zhu, L., Mao, X., Chen, S., Zhong, H., & Deng, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22157936 · Cited by 15 · see citing works
Kim, G., Kim, H., Lim, H., & Park, H. (2015) · Cellular Signalling · doi:10.1016/j.cellsig.2015.04.012 · Cited by 14 · see citing works
Chamgordani, M. K., Bardestani, A., Ebrahimpour, S., & Esmaeili, A. (2023) · BMC Pharmacology and Toxicology · doi:10.1186/s40360-023-00725-3 · Cited by 12 · see citing works
Butcko, A. J., Putman, A. K., & Mottillo, E. P. (2024) · Antioxidants · doi:10.3390/antiox13010087 · Cited by 12 · see citing works
Deng, Y., Cai, Y., Liu, L., Lin, X., Pingfan, L., Guo, Y., Han, M. H., & Xu, G. (2018) · The FASEB Journal · doi:10.1096/fj.201800885rr · Cited by 12 · see citing works
Poly (ADP-ribose) Polymerase-1 modulations in the genesis of thrombosis
Safdar, R., Mishra, A., Shah, G. M., & Ashraf, M. Z. (2024) · Journal of Thrombosis and Thrombolysis · doi:10.1007/s11239-024-02974-3 · Cited by 10 · see citing works
The Role of Poly(ADP-Ribose) Polymerase-1 in Cutaneous Wound Healing
Banerjee, J., Lodhi, N., & Nguyen, B.-N. H. (2019) · Advances in Wound Care · doi:10.1089/wound.2018.0821 · Cited by 9 · see citing works
AlAhmad, M., Shitaw, E., & Sivaprasadarao, A. (2025) · Biomolecules · doi:10.3390/biom15081193 · Cited by 8 · see citing works
Castellano, G., Corti, C., Boldrini, L., Gervaso, L., Criscitiello, C., & Curigliano, G. (2023) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2023.102601 · Cited by 8 · see citing works
Xu, W., Wu, Y., Mao, R., Jia, Y., Jiang, H., Zhang, F., Huang, D. Y., He, X., Wang, C., & Huang, K. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01501-5 · Cited by 7 · see citing works
Lechaftois, M., Dréano, E., Palmier, B., Margaill, I., Marchand‐Leroux, C., Bachelot‐Loza, C., & Lerouet, D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110776 · Cited by 7 · see citing works
Trafalis, D. T., Polonifi, A., Dalezis, P., Nikoleousakos, N., Katsamakas, S., & Sarli, V. (2017) · Chemical Biology & Drug Design · doi:10.1111/cbdd.13006 · Cited by 7 · see citing works
Can crosstalk between DOR and PARP reduce oxidative stress mediated neurodegeneration?
Raina, R., & Sen, D. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.07.011 · Cited by 7 · see citing works
Capoluongo, E. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110536 · Cited by 7 · see citing works
Shafiq, M., Lone, Z. R., Abdulkareem, A. O., Kaur, G., Navya, S., Singh, H., Jagavelu, K., & Hanif, K. (2023) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2023.102200 · Cited by 6 · see citing works
Nikoleousakos, N., Dalezis, P., Polonifi, A., Geromichalou, E. G., Sagredou, S., Alifieris, C. E., Deligiorgi, M. V., Sarli, V., & Trafalis, D. T. (2021) · Biomedicines · doi:10.3390/biomedicines9081028 · Cited by 5 · see citing works
Molecular Mechanisms of Plant Extracts in Protecting Aging Blood Vessels
Luo, Y., Zhang, Z., Zheng, W., Zeng, Z., Fan, L., Zhao, Y., Huang, Y., Cao, S., Yu, S., & Shen, L. (2024) · Nutrients · doi:10.3390/nu16142357 · Cited by 4 · see citing works
Current Knowledge of Obesity‐Related Vascular Injury
Liu, J., & Yang, D. (2025) · Obesity Reviews · doi:10.1111/obr.70080 · Cited by 3 · see citing works
Inferring Molecular Processes Heterogeneity from Transcriptional Data
Gogolewski, K., Wronowska, W., Lech, A., Lesyng, B., & Gambin, A. (2017) · BioMed Research International · doi:10.1155/2017/6961786 · Cited by 3 · see citing works
Combining targeted therapies in ovarian cancer
Scambia, G., Salutari, V., & Ferrandina, G. (2014) · The Lancet Oncology · doi:10.1016/s1470-2045(14)70421-8 · Cited by 3 · see citing works
Halldórsson, H., Thors, B., & Þorgeirsson, G. (2015) · Nucleosides Nucleotides & Nucleic Acids · doi:10.1080/15257770.2014.984072 · Cited by 3 · see citing works
The Sound of Silence: RNAi in Poly (ADP-Ribose) Research
Blenn, C., Wyrsch, P., & Althaus, F. (2012) · Genes · doi:10.3390/genes3040779 · Cited by 3 · see citing works
Behjati, M., Hashemi, M. M., Kazemi, M., Salehi, M., & Javanmard, S. H. (2017) · Advanced Biomedical Research · doi:10.4103/2277-9175.204591 · Cited by 3 · see citing works
Chen, X., Mu, P., Zhu, L., Mao, X., Chen, S., Zhong, H., & Deng, Y. (2021) · Research Square · doi:10.21203/rs.3.rs-506960/v1 · Cited by 3 · see citing works
Kuang, L., Chen, Q., Liu, Z., Wu, L., & Wu, S.-G. (2025) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000001728 · Cited by 2 · see citing works
- Authors
- Mathews, M. T., & Berk, B. C.
- Affiliations
- University of Rochester Medicine (US)
- ORCID
- Berk, Bradford C.
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2008-04
- Volume
- 28
- Issue
- 4
- Pages
- 711-717
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2080180491
- Cited by
- 120
- References
- 30
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 7 · 2023: 10 · 2022: 5 · 2021: 8 · 2020: 9 · 2019: 3 · 2018: 4 · 2017: 10 · 2016: 6 · 2015: 6 · 2014: 4 · 2013: 13 · 2012: 7
- FWCI
- 3.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Oncology › PARP inhibition in cancer therapy
- Keywords
- PARP1 inhibition, oxidative stress, nitrosative stress, endothelial cell death, VEGF receptor 2, Akt signaling, Bad phosphorylation, NAD+ depletion, ATP depletion, hydrogen peroxide, peroxynitrite, PJ34, endothelial cell survival, apoptosis, human umbilical vein endothelial cells
- MeSH terms
- Poly(ADP-ribose) Polymerase Inhibitors, Poly (ADP-Ribose) Polymerase-1, Adenosine Triphosphate, Cells, Cultured, Cinnamates, Enzyme Inhibitors, Humans, NAD, Oxidation-Reduction, Phenanthrenes, Poly(ADP-ribose) Polymerases, Transcriptional Activation, Nitrosation, Cell Death, Apoptosis, Oxidative Stress, Reactive Nitrogen Species, RNA, Small Interfering, Vascular Endothelial Growth Factor Receptor-2, Endothelial Cells
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