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Published in: Cardiovascular Toxicology 5/2024

31-03-2024 | Review

Addressing Cardiovascular Toxicity Risk of Electronic Nicotine Delivery Systems in the Twenty-First Century: “What Are the Tools Needed for the Job?” and “Do We Have Them?”

Authors: Mark Chandy, Thomas Hill III, Nerea Jimenez-Tellez, Joseph C. Wu, S. Emma Sarles, Edward Hensel, Qixin Wang, Irfan Rahman, Daniel J. Conklin

Published in: Cardiovascular Toxicology | Issue 5/2024

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Abstract

Cigarette smoking is positively and robustly associated with cardiovascular disease (CVD), including hypertension, atherosclerosis, cardiac arrhythmias, stroke, thromboembolism, myocardial infarctions, and heart failure. However, after more than a decade of ENDS presence in the U.S. marketplace, uncertainty persists regarding the long-term health consequences of ENDS use for CVD. New approach methods (NAMs) in the field of toxicology are being developed to enhance rapid prediction of human health hazards. Recent technical advances can now consider impact of biological factors such as sex and race/ethnicity, permitting application of NAMs findings to health equity and environmental justice issues. This has been the case for hazard assessments of drugs and environmental chemicals in areas such as cardiovascular, respiratory, and developmental toxicity. Despite these advances, a shortage of widely accepted methodologies to predict the impact of ENDS use on human health slows the application of regulatory oversight and the protection of public health. Minimizing the time between the emergence of risk (e.g., ENDS use) and the administration of well-founded regulatory policy requires thoughtful consideration of the currently available sources of data, their applicability to the prediction of health outcomes, and whether these available data streams are enough to support an actionable decision. This challenge forms the basis of this white paper on how best to reveal potential toxicities of ENDS use in the human cardiovascular system—a primary target of conventional tobacco smoking. We identify current approaches used to evaluate the impacts of tobacco on cardiovascular health, in particular emerging techniques that replace, reduce, and refine slower and more costly animal models with NAMs platforms that can be applied to tobacco regulatory science. The limitations of these emerging platforms are addressed, and systems biology approaches to close the knowledge gap between traditional models and NAMs are proposed. It is hoped that these suggestions and their adoption within the greater scientific community will result in fresh data streams that will support and enhance the scientific evaluation and subsequent decision-making of tobacco regulatory agencies worldwide.

Graphical Abstract

Models for Cardiovascular Toxicity Testing E-cigarettes and nicotine delivery systems can be examined using multiple model systems. In silico models might predict adverse cardiovascular effects that can be screened for using 2-D and 3-D models using induced pluripotent stem cell (iPSC) derived cardiac tissue and “omics” profiling such as single-cell RNA sequencing (scRNA-seq) or high-throughput functional analysis with a multiple electrode array (MEA). Biologic plausibility of detected effects can be corroborated using ex vivo or in vivo models, which may also lead to the discovery of new biomarkers or treatments for CVD.
Literature
3.
go back to reference Services Usdohah. (2010). A report of the surgeon general. How tobacco smoke causes disease: What it means to you. US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, Office on Smoking And Health. Services Usdohah. (2010). A report of the surgeon general. How tobacco smoke causes disease: What it means to you. US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, Office on Smoking And Health.
4.
go back to reference National Heart L, and Blood Institute. What Is An Arrythmia? National Heart L, and Blood Institute. What Is An Arrythmia?
8.
go back to reference Medicine USNLO. (2021). Coronary heart disease. Medicine USNLO. (2021). Coronary heart disease.
12.
go back to reference Arastoo, S., Haptonstall, K. P., Choroomi, Y., Moheimani, R., Nguyen, K., Tran, E., et al. (2020). Acute and chronic sympathomimetic effects of E-cigarette and tobacco cigarette smoking: Role of nicotine and non-nicotine constituents. American Journal of Physiology-Heart and Circulatory Physiology, 319(2), 262–70. https://doi.org/10.1152/Ajpheart.00192.2020CrossRef Arastoo, S., Haptonstall, K. P., Choroomi, Y., Moheimani, R., Nguyen, K., Tran, E., et al. (2020). Acute and chronic sympathomimetic effects of E-cigarette and tobacco cigarette smoking: Role of nicotine and non-nicotine constituents. American Journal of Physiology-Heart and Circulatory Physiology, 319(2), 262–70. https://​doi.​org/​10.​1152/​Ajpheart.​00192.​2020CrossRef
17.
go back to reference Conklin, D. J., Schick, S., Blaha, M. J., Carll, A., Defilippis, A., Ganz, P., et al. (2019). Cardiovascular injury induced by tobacco products: Assessment of risk factors and biomarkers of harm. A tobacco centers of regulatory science compilation. American Journal of Physiology - Heart and Circulatory Physiology, 316(4), 801–27. https://doi.org/10.1152/Ajpheart.00591.2018CrossRef Conklin, D. J., Schick, S., Blaha, M. J., Carll, A., Defilippis, A., Ganz, P., et al. (2019). Cardiovascular injury induced by tobacco products: Assessment of risk factors and biomarkers of harm. A tobacco centers of regulatory science compilation. American Journal of Physiology - Heart and Circulatory Physiology, 316(4), 801–27. https://​doi.​org/​10.​1152/​Ajpheart.​00591.​2018CrossRef
18.
go back to reference Rao, P., Han, D. D., Tan, K., Mohammadi, L., Derakhshandeh, R., Navabzadeh, M., et al. (2022). Comparable impairment of vascular endothelial function by a wide range of electronic nicotine delivery devices. Nicotine & Tobacco Research, 24(7), 1055–62. https://doi.org/10.1093/Ntr/Ntac019CrossRef Rao, P., Han, D. D., Tan, K., Mohammadi, L., Derakhshandeh, R., Navabzadeh, M., et al. (2022). Comparable impairment of vascular endothelial function by a wide range of electronic nicotine delivery devices. Nicotine & Tobacco Research, 24(7), 1055–62. https://​doi.​org/​10.​1093/​Ntr/​Ntac019CrossRef
19.
go back to reference Rao, P., Liu, J., & Springer, M. L. (2020). Juul and combusted cigarettes comparably impair endothelial function. Tobacco Regulatory Science, 6(1), 30–7.CrossRefPubMedPubMedCentral Rao, P., Liu, J., & Springer, M. L. (2020). Juul and combusted cigarettes comparably impair endothelial function. Tobacco Regulatory Science, 6(1), 30–7.CrossRefPubMedPubMedCentral
26.
go back to reference Mp, Lutolf, Jl, Lauer-Fields., Hg, Schmoekel, At, Metters, Fe, Weber, Gb, Fields, et al. (2003). Synthetic Matrix Metalloproteinase-Sensitive Hydrogels For The Conduction Of Tissue Regeneration: Engineering Cell-Invasion Characteristics. Proceedings Of The National Academy Of Sciences., 100(9), 5413. https://doi.org/10.1073/Pnas.0737381100CrossRef Mp, Lutolf, Jl, Lauer-Fields., Hg, Schmoekel, At, Metters, Fe, Weber, Gb, Fields, et al. (2003). Synthetic Matrix Metalloproteinase-Sensitive Hydrogels For The Conduction Of Tissue Regeneration: Engineering Cell-Invasion Characteristics. Proceedings Of The National Academy Of Sciences., 100(9), 5413. https://​doi.​org/​10.​1073/​Pnas.​0737381100CrossRef
28.
go back to reference Frankel, A., Buckman, R., & Kerbel, R. S. (1997). Abrogation of taxol-induced G2-M arrest and apoptosis in human ovarian cancer cells grown as multicellular tumor spheroids. Cancer Research, 57(12), 2388.PubMed Frankel, A., Buckman, R., & Kerbel, R. S. (1997). Abrogation of taxol-induced G2-M arrest and apoptosis in human ovarian cancer cells grown as multicellular tumor spheroids. Cancer Research, 57(12), 2388.PubMed
29.
70.
go back to reference Feyen, D. A., Mckeithan, W. L., Bruyneel, A. A. N., Spiering, S., Hörmann, L., Ulmer, B., Zhang, H., Briganti, F., Schweizer, M., Hegyi, B., Liao, Z., Pölönen, R.-P., Ginsburg, K. S., Lam, C. K., Serrano, R., Wahlquist, C., Kreymerman, A., Vu, M., Amatya, P. L., … Mercola, M. (2020). Metabolic maturation media improves physiological function of human IPSC-derived cardiomyocytes. Cell Reports, 32, 107925.CrossRefPubMed Feyen, D. A., Mckeithan, W. L., Bruyneel, A. A. N., Spiering, S., Hörmann, L., Ulmer, B., Zhang, H., Briganti, F., Schweizer, M., Hegyi, B., Liao, Z., Pölönen, R.-P., Ginsburg, K. S., Lam, C. K., Serrano, R., Wahlquist, C., Kreymerman, A., Vu, M., Amatya, P. L., … Mercola, M. (2020). Metabolic maturation media improves physiological function of human IPSC-derived cardiomyocytes. Cell Reports, 32, 107925.CrossRefPubMed
73.
go back to reference Ribeiro, A. J., Ang, Y. S., Fu, J. D., Rivas, R. N., Mohamed, T. M., Higgs, G. C., et al. (2015). Contractility of single cardiomyocytes differentiated from pluripotent stem cells depends on physiological shape and substrate stiffness. Proceedings of the National Academy of Sciences USA, 112(41), 12705–10. https://doi.org/10.1073/Pnas.1508073112CrossRef Ribeiro, A. J., Ang, Y. S., Fu, J. D., Rivas, R. N., Mohamed, T. M., Higgs, G. C., et al. (2015). Contractility of single cardiomyocytes differentiated from pluripotent stem cells depends on physiological shape and substrate stiffness. Proceedings of the National Academy of Sciences USA, 112(41), 12705–10. https://​doi.​org/​10.​1073/​Pnas.​1508073112CrossRef
78.
go back to reference Bertino, J. S., Jr., Owens, R. C., Jr., Carnes, T. D., & Iannini, P. B. (2002). Gatifloxacin-associated corrected Qt interval prolongation, torsades de pointes, and ventricular fibrillation in patients with known risk factors. Clinical Infectious Diseases, 34(6), 861–3. https://doi.org/10.1086/339075CrossRefPubMed Bertino, J. S., Jr., Owens, R. C., Jr., Carnes, T. D., & Iannini, P. B. (2002). Gatifloxacin-associated corrected Qt interval prolongation, torsades de pointes, and ventricular fibrillation in patients with known risk factors. Clinical Infectious Diseases, 34(6), 861–3. https://​doi.​org/​10.​1086/​339075CrossRefPubMed
79.
go back to reference Nystoriak, M. A., Kilfoil, P. J., Lorkiewicz, P. K., Ramesh, B., Kuehl, P. J., Mcdonald, J., et al. (2019). Comparative effects of parent and heated cinnamaldehyde on the function of human IPSC-derived cardiac myocytes. Toxicology In Vitro: An International Journal Published in Association with Bibra, 61, 104648. https://doi.org/10.1016/J.Tiv.2019.104648CrossRefPubMed Nystoriak, M. A., Kilfoil, P. J., Lorkiewicz, P. K., Ramesh, B., Kuehl, P. J., Mcdonald, J., et al. (2019). Comparative effects of parent and heated cinnamaldehyde on the function of human IPSC-derived cardiac myocytes. Toxicology In Vitro: An International Journal Published in Association with Bibra, 61, 104648. https://​doi.​org/​10.​1016/​J.​Tiv.​2019.​104648CrossRefPubMed
82.
83.
84.
go back to reference Talih, S., Balhas, Z., Eissenberg, T., Salman, R., Karaoghlanian, N., El Hellani, A., et al. (2015). Effects of user puff topography, device voltage, and liquid nicotine concentration on electronic cigarette nicotine yield: measurements and model predictions. Nicotine & Tobacco Research, 17(2), 150–7. https://doi.org/10.1093/Ntr/Ntu174uCrossRef Talih, S., Balhas, Z., Eissenberg, T., Salman, R., Karaoghlanian, N., El Hellani, A., et al. (2015). Effects of user puff topography, device voltage, and liquid nicotine concentration on electronic cigarette nicotine yield: measurements and model predictions. Nicotine & Tobacco Research, 17(2), 150–7. https://​doi.​org/​10.​1093/​Ntr/​Ntu174uCrossRef
89.
go back to reference Cirillo, S., Vivarelli, F., Turrini, E., Fimognari, C., Burattini, S., Falcieri, E., et al. (2019). The customizable E-cigarette resistance influences toxicological outcomes: Lung degeneration, inflammation, and oxidative stress-induced in a rat model. Toxicological Sciences, 172(1), 132–45. https://doi.org/10.1093/Toxsci/Kfz176CrossRefPubMed Cirillo, S., Vivarelli, F., Turrini, E., Fimognari, C., Burattini, S., Falcieri, E., et al. (2019). The customizable E-cigarette resistance influences toxicological outcomes: Lung degeneration, inflammation, and oxidative stress-induced in a rat model. Toxicological Sciences, 172(1), 132–45. https://​doi.​org/​10.​1093/​Toxsci/​Kfz176CrossRefPubMed
94.
go back to reference Ozturk-Oncel, M. O., Heras-Bautista, C. O., Uzun, L., Hur, D., Hescheler, J., Pfannkuche, K., et al. (2021). Impact of poly(dimethylsiloxane) surface modification with conventional and amino acid-conjugated self-assembled monolayers on the differentiation of induced pluripotent stem cells into cardiomyocytes. ACS Biomaterials Science & Engineering, 7(4), 1539–51. https://doi.org/10.1021/Acsbiomaterials.0c01434CrossRef Ozturk-Oncel, M. O., Heras-Bautista, C. O., Uzun, L., Hur, D., Hescheler, J., Pfannkuche, K., et al. (2021). Impact of poly(dimethylsiloxane) surface modification with conventional and amino acid-conjugated self-assembled monolayers on the differentiation of induced pluripotent stem cells into cardiomyocytes. ACS Biomaterials Science & Engineering, 7(4), 1539–51. https://​doi.​org/​10.​1021/​Acsbiomaterials.​0c01434CrossRef
113.
go back to reference Winniford, M. D. (1990). Smoking and cardiovascular function. Jhypertenssuppl., 8(5), S17–S23. Winniford, M. D. (1990). Smoking and cardiovascular function. Jhypertenssuppl., 8(5), S17–S23.
115.
go back to reference Epa Us. (2020). User’s Guide For T.E.S.T. (Version 5.1) (Toxicity estimation software tool): A program to estimate toxicity from molecular structure. Epa Us. (2020). User’s Guide For T.E.S.T. (Version 5.1) (Toxicity estimation software tool): A program to estimate toxicity from molecular structure.
120.
go back to reference Celermajer, D. S., Adams, M. R., Clarkson, P., Robinson, J., Mccredie, R., Donald, A., et al. (1996). Passive smoking and impaired endothelium-dependent arterial dilatation in healthy young adults. New England Journal of Medicine, 334(3), 150–4.CrossRefPubMed Celermajer, D. S., Adams, M. R., Clarkson, P., Robinson, J., Mccredie, R., Donald, A., et al. (1996). Passive smoking and impaired endothelium-dependent arterial dilatation in healthy young adults. New England Journal of Medicine, 334(3), 150–4.CrossRefPubMed
121.
go back to reference Celermajer, D. S., Sorensen, K. E., Georgakopoulos, D., Bull, C., Thomas, O., Robinson, J., et al. (1993). Cigarette smoking is associated with dose-related and potentially reversible impairment of endothelium-dependent dilation in healthy young adults. Circulation, 88(5 Pt 1), 2149–55.CrossRefPubMed Celermajer, D. S., Sorensen, K. E., Georgakopoulos, D., Bull, C., Thomas, O., Robinson, J., et al. (1993). Cigarette smoking is associated with dose-related and potentially reversible impairment of endothelium-dependent dilation in healthy young adults. Circulation, 88(5 Pt 1), 2149–55.CrossRefPubMed
122.
go back to reference Puranik, R., & Celermajer, D. S. (2003). Smoking and endothelial function. Progcardiovascdis, 45(6), 443–58. Puranik, R., & Celermajer, D. S. (2003). Smoking and endothelial function. Progcardiovascdis, 45(6), 443–58.
127.
go back to reference Phillips, B., Veljkovic, E., Boue, S., Schlage, W. K., Vuillaume, G., Martin, F., et al. (2016). An 8-month systems toxicology inhalation/cessation study in APOE−/− mice to investigate cardiovascular and respiratory exposure effects of a candidate modified risk tobacco product, Ths 22 compared with conventional cigarettes. Toxicology Science, 149(2), 411–32. https://doi.org/10.1093/Toxsci/Kfv243CrossRef Phillips, B., Veljkovic, E., Boue, S., Schlage, W. K., Vuillaume, G., Martin, F., et al. (2016). An 8-month systems toxicology inhalation/cessation study in APOE/ mice to investigate cardiovascular and respiratory exposure effects of a candidate modified risk tobacco product, Ths 22 compared with conventional cigarettes. Toxicology Science, 149(2), 411–32. https://​doi.​org/​10.​1093/​Toxsci/​Kfv243CrossRef
128.
go back to reference Szostak, J., Wong, E. T., Titz, B., Lee, T., Wong, S. K., Low, T., et al. (2020). A 6-month systems toxicology inhalation study in APOE(−/−) mice demonstrates reduced cardiovascular effects of E-vapor aerosols compared with cigarette smoke. American Journal of Physiology-Heart and Circulatory Physiology, 318(3), H604–H31. https://doi.org/10.1152/Ajpheart.00613.2019CrossRefPubMed Szostak, J., Wong, E. T., Titz, B., Lee, T., Wong, S. K., Low, T., et al. (2020). A 6-month systems toxicology inhalation study in APOE(−/−) mice demonstrates reduced cardiovascular effects of E-vapor aerosols compared with cigarette smoke. American Journal of Physiology-Heart and Circulatory Physiology, 318(3), H604–H31. https://​doi.​org/​10.​1152/​Ajpheart.​00613.​2019CrossRefPubMed
129.
go back to reference Szostak, J., Titz, B., Schlage, W. K., Guedj, E., Sewer, A., Phillips, B., et al. (2020). Structural, functional, and molecular impact on the cardiovascular system in Apoe(−/−) mice exposed to aerosol from candidate modified risk tobacco products, carbon heated tobacco product 1.2 and tobacco heating system 2.2, compared with cigarette smoke. Chemico-Biological Interactions, 315, 108887. https://doi.org/10.1016/J.Cbi.2019.108887CrossRefPubMed Szostak, J., Titz, B., Schlage, W. K., Guedj, E., Sewer, A., Phillips, B., et al. (2020). Structural, functional, and molecular impact on the cardiovascular system in Apoe(−/−) mice exposed to aerosol from candidate modified risk tobacco products, carbon heated tobacco product 1.2 and tobacco heating system 2.2, compared with cigarette smoke. Chemico-Biological Interactions, 315, 108887. https://​doi.​org/​10.​1016/​J.​Cbi.​2019.​108887CrossRefPubMed
132.
136.
138.
go back to reference Richardson, A., Krivokhizhina, T., Lorkiewicz, P., D’sousa, S., Bhatnagar, A., Srivastava, S., et al. (2022). Effects of electronic cigarette flavorants on human platelet aggregation ex vivo. Toxicology Reports, 9, 814–20.CrossRefPubMedPubMedCentral Richardson, A., Krivokhizhina, T., Lorkiewicz, P., D’sousa, S., Bhatnagar, A., Srivastava, S., et al. (2022). Effects of electronic cigarette flavorants on human platelet aggregation ex vivo. Toxicology Reports, 9, 814–20.CrossRefPubMedPubMedCentral
139.
go back to reference Conklin, D. J., Cowley, H. R., Wiechmann, R. J., Johnson, G. H., Trent, M. B., & Boor, P. J. (2004). Vasoactive effects of methylamine in isolated human blood vessels: Role of semicarbazide-sensitive amine oxidase, formaldehyde, and hydrogen peroxide. American Journal of Physiology-Heart and Circulatory Physiology, 286(2), H667–H76.CrossRefPubMed Conklin, D. J., Cowley, H. R., Wiechmann, R. J., Johnson, G. H., Trent, M. B., & Boor, P. J. (2004). Vasoactive effects of methylamine in isolated human blood vessels: Role of semicarbazide-sensitive amine oxidase, formaldehyde, and hydrogen peroxide. American Journal of Physiology-Heart and Circulatory Physiology, 286(2), H667–H76.CrossRefPubMed
166.
177.
go back to reference Zhang, Y., Wang, S. J., Han, Z. H., Li, Y. Q., Xue, J. H., Gao, D. F., et al. (2014). PI3K/AKT signaling pathway plays a role in enhancement of ENOS activity by recombinant human angiotensin converting enzyme 2 in human umbilical vein endothelial cells. International Journal of Clinical and Experimental Pathology, 7(11), 8112–7.PubMedPubMedCentral Zhang, Y., Wang, S. J., Han, Z. H., Li, Y. Q., Xue, J. H., Gao, D. F., et al. (2014). PI3K/AKT signaling pathway plays a role in enhancement of ENOS activity by recombinant human angiotensin converting enzyme 2 in human umbilical vein endothelial cells. International Journal of Clinical and Experimental Pathology, 7(11), 8112–7.PubMedPubMedCentral
189.
go back to reference Riss, T. L., Moravec, R. A., Niles, A. L., Duellman, S., Benink, H. A., Worzella, T. J., et al. (2004). Cell viability assays. In S. Markossian, A. Grossman, K. Brimacombe, M. Arkin, D. Auld, C. Austin, et al. (Eds.), Assay guidance manual. Eli Lilly & Company and the National Center for Advancing Translational Sciences. Riss, T. L., Moravec, R. A., Niles, A. L., Duellman, S., Benink, H. A., Worzella, T. J., et al. (2004). Cell viability assays. In S. Markossian, A. Grossman, K. Brimacombe, M. Arkin, D. Auld, C. Austin, et al. (Eds.), Assay guidance manual. Eli Lilly & Company and the National Center for Advancing Translational Sciences.
199.
go back to reference Wang, G. R., Zhu, Y., Halushka, P. V., Lincoln, T. M., & Mendelsohn, M. E. (1998). Mechanism of platelet inhibition by nitric oxide: In vivo phosphorylation of thromboxane receptor by cyclic gmp-dependent protein kinase. Proceedings of the National Academy of Sciences USA, 95(9), 4888–93. https://doi.org/10.1073/Pnas.95.9.4888CrossRef Wang, G. R., Zhu, Y., Halushka, P. V., Lincoln, T. M., & Mendelsohn, M. E. (1998). Mechanism of platelet inhibition by nitric oxide: In vivo phosphorylation of thromboxane receptor by cyclic gmp-dependent protein kinase. Proceedings of the National Academy of Sciences USA, 95(9), 4888–93. https://​doi.​org/​10.​1073/​Pnas.​95.​9.​4888CrossRef
205.
go back to reference Cao, Y., Gong, Y., Liu, L., Zhou, Y., Fang, X., Zhang, C., et al. (2017). The use of human umbilical vein endothelial cells (Huvecs) as an in vitro model to assess the toxicity of nanoparticles to endothelium: A review. Journal of Applied Toxicology, 37(12), 1359–69. https://doi.org/10.1002/Jat.3470CrossRefPubMed Cao, Y., Gong, Y., Liu, L., Zhou, Y., Fang, X., Zhang, C., et al. (2017). The use of human umbilical vein endothelial cells (Huvecs) as an in vitro model to assess the toxicity of nanoparticles to endothelium: A review. Journal of Applied Toxicology, 37(12), 1359–69. https://​doi.​org/​10.​1002/​Jat.​3470CrossRefPubMed
206.
go back to reference Yu, S. Y., Song, Y. M., Li, A. M., Yu, X. J., Zhao, G., Song, M. B., et al. (2009). Isolation and characterization of human coronary artery-derived endothelial cells in vivo from patients undergoing percutaneous coronary interventions. Journal of Vascular Research, 46(5), 487–94. https://doi.org/10.1159/000200964CrossRefPubMed Yu, S. Y., Song, Y. M., Li, A. M., Yu, X. J., Zhao, G., Song, M. B., et al. (2009). Isolation and characterization of human coronary artery-derived endothelial cells in vivo from patients undergoing percutaneous coronary interventions. Journal of Vascular Research, 46(5), 487–94. https://​doi.​org/​10.​1159/​000200964CrossRefPubMed
208.
go back to reference Frenkel, N., Poghosyan, S., Alarcon, C. R., Garcia, S. B., Queiroz, K., Van Den Bent, L., et al. (2021). Long-lived human lymphatic endothelial cells to study lymphatic biology and lymphatic vessel/tumor coculture in a 3D microfluidic model. ACS Biomaterials Science & Engineering, 7(7), 3030–42. https://doi.org/10.1021/Acsbiomaterials.0c01378CrossRef Frenkel, N., Poghosyan, S., Alarcon, C. R., Garcia, S. B., Queiroz, K., Van Den Bent, L., et al. (2021). Long-lived human lymphatic endothelial cells to study lymphatic biology and lymphatic vessel/tumor coculture in a 3D microfluidic model. ACS Biomaterials Science & Engineering, 7(7), 3030–42. https://​doi.​org/​10.​1021/​Acsbiomaterials.​0c01378CrossRef
212.
213.
go back to reference Catalioto, R. M., Cucchi, P., Renzetti, A. R., Criscuoli, M., & Subissi, A. (1996). Human umbilical vein smooth muscle cells as a model to study thrombin generation and function: effect of thrombin inhibitors. Thrombosis and Haemostasis, 76(4), 603–9.CrossRefPubMed Catalioto, R. M., Cucchi, P., Renzetti, A. R., Criscuoli, M., & Subissi, A. (1996). Human umbilical vein smooth muscle cells as a model to study thrombin generation and function: effect of thrombin inhibitors. Thrombosis and Haemostasis, 76(4), 603–9.CrossRefPubMed
Metadata
Title
Addressing Cardiovascular Toxicity Risk of Electronic Nicotine Delivery Systems in the Twenty-First Century: “What Are the Tools Needed for the Job?” and “Do We Have Them?”
Authors
Mark Chandy
Thomas Hill III
Nerea Jimenez-Tellez
Joseph C. Wu
S. Emma Sarles
Edward Hensel
Qixin Wang
Irfan Rahman
Daniel J. Conklin
Publication date
31-03-2024
Publisher
Springer US
Published in
Cardiovascular Toxicology / Issue 5/2024
Print ISSN: 1530-7905
Electronic ISSN: 1559-0259
DOI
https://doi.org/10.1007/s12012-024-09850-9

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