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Cardiac Fibrosis: The Fibroblast Awakens
Open accessAbstract
Myocardial fibrosis is a significant global health problem associated with nearly all forms of heart disease. Cardiac fibroblasts comprise an essential cell type in the heart that is responsible for the homeostasis of the extracellular matrix; however, upon injury, these cells transform to a myofibroblast phenotype and contribute to cardiac fibrosis. This remodeling involves pathological changes that include chamber dilation, cardiomyocyte hypertrophy and apoptosis, and ultimately leads to the progression to heart failure. Despite the critical importance of fibrosis in cardiovascular disease, our limited understanding of the cardiac fibroblast impedes the development of potential therapies that effectively target this cell type and its pathological contribution to disease progression. This review summarizes current knowledge regarding the origins and roles of fibroblasts, mediators and signaling pathways known to influence fibroblast function after myocardial injury, as well as novel therapeutic strategies under investigation to attenuate cardiac fibrosis.
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“Nearly all cardiac diseases involve pathological fibrotic remodeling caused by CF proliferation and ECM deposition53.”
From 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels (2021) · cites this paper as [53]
In the citing paper
“Focal cardiac fibrosis that arises post-MI is a major clinical burden that often leads to a cascade of pathological remodeling and may result in heart failure53.”
From 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels (2021) · cites this paper as [53]
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“CFs themselves cannot generate action potentials”
From 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels (2021) · cites this paper as [53]
In the citing paper
“excessive ECM production reduces cardiomyocyte-cardiomyocyte (CM) connectivity, leading to reduced tissue compliance and electrical synchronization53.”
From 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels (2021) · cites this paper as [53]
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1 retracted
D’Souza, K. M., Malhotra, R., Philip, J. L., Staron, M. L., Theccanat, T., Jeevanandam, V., & Akhter, S. A. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.a111.218263 · Cited by 31
RetractedGurtner, G. C., Werner, S., Barrandon, Y., & Longaker, M. T. (2008) · Nature · doi:10.1038/nature07039 · Cited by 6,542
Heart Disease and Stroke Statistics—2015 Update: A Report From the American Heart Association
Mozaffarian, D., Benjamin, E. J., Go, A. S., Arnett, D. K., Blaha, M. J., Cushman, M., de Ferranti, S., Després, J.-P., Fullerton, H. J., Howard, V. J., et al. (2015) · Circulation · doi:10.1161/cir.0000000000000152 · Cited by 5,797
Myofibroblasts and mechano-regulation of connective tissue remodelling
Tomasek, J. J., Gabbiani, G., Hinz, B., Chaponnier, C., & Brown, R. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm809 · Cited by 4,290
A perivascular origin for mesenchymal stem cells in multiple human organs
Crisan, M., Yap, S., Casteilla, L., Chen, C.-W., Corselli, M., Park, T. S., Andriolo, G., Sun, B., Zheng, B., Zhang, L., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.07.003 · Cited by 3,991
Regulation of type I interferon responses
Ivashkiv, L. B., & Donlin, L. T. (2013) · Nature reviews. Immunology · doi:10.1038/nri3581 · Cited by 3,442
A Calcineurin-Dependent Transcriptional Pathway for Cardiac Hypertrophy
Molkentin, J. D., Lu, J., Antos, C. L., Markham, B. E., Richardson, J. A., Robbins, J. M., Grant, S. R., & Olson, E. N. (1998) · Cell · doi:10.1016/s0092-8674(00)81573-1 · Cited by 2,566
Self-citationDirect reprogramming of fibroblasts into functional cardiomyocytes by defined factors
Ieda, M., Fu, J.-D., Delgado-Olguin, P., Vedantham, V., Hayashi, Y., Bruneau, B. G., & Srivastava, D. (2010) · Cell · doi:10.1016/j.cell.2010.07.002 · Cited by 2,454
TGF-β signaling and the fibrotic response
Leask, A., & Abraham, D. J. (2004) · The FASEB Journal · doi:10.1096/fj.03-1273rev · Cited by 2,319
Endothelial-to-mesenchymal transition contributes to cardiac fibrosis
Zeisberg, E. M., Tarnavski, O., Zeisberg, M., Dorfman, A. L., McMullen, J. R., Gustafsson, E., Chandraker, A. K., Yuan, X., Pu, W. T., Roberts, A. B., et al. (2007) · Nature Medicine · doi:10.1038/nm1613 · Cited by 2,251
Cited by
Sorted by citations
Items 101–200 of 999
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Felisbino, M. B., & McKinsey, T. A. (2018) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2018.05.003 · Cited by 124
AMPK: a therapeutic target of heart failure—not only metabolism regulation
Li, X., Liu, J., Lü, Q., Ren, D., Sun, X., Rousselle, T. V., Tan, Y., & Li, J. (2018) · Bioscience Reports · doi:10.1042/bsr20181767 · Cited by 122
Mori, Y., Novruzov, E., Schmitt, D. R., Cardinale, J., Watabe, T., Choyke, P. L., Alavi, A. A., Haberkorn, U., & Giesel, F. L. (2024) · npj Imaging · doi:10.1038/s44303-024-00053-z · Cited by 129
The Effect of Resveratrol on the Cardiovascular System from Molecular Mechanisms to Clinical Results
Gál, R., Deres, L., Tóth, K., Halmosi, R., & Habon, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810152 · Cited by 126
Wu, J., Subbaiah, K. C. V., Xie, L. H., Jiang, F., Khor, E.-S., Mickelsen, D. M., Myers, J. R., Tang, W. H. W., & Yao, P. (2020) · Circulation Research · doi:10.1161/circresaha.119.315999 · Cited by 115
Crosstalk between TGF-β and WNT signalling pathways during cardiac fibrogenesis
Działo, E., Tkacz, K., & Błyszczuk, P. (2018) · Acta Biochimica Polonica · doi:10.18388/abp.2018_2635 · Cited by 115
NIKOLOV, A. G., & Popovski, N. K. (2022) · Metabolites · doi:10.3390/metabo12040297 · Cited by 122
Mineralocorticoid Receptor Signaling as a Therapeutic Target for Renal and Cardiac Fibrosis
Tesch, G. H., & Young, M. J. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00313 · Cited by 112
Qishen granule attenuates cardiac fibrosis by regulating TGF-β /Smad3 and GSK-3β pathway
Zeng, Z., Wang, Q., Yang, X., Ren, Y., Jiao, S., Zhu, Q., Guo, D., Xia, K., Wang, Y., Li, C., et al. (2019) · Phytomedicine · doi:10.1016/j.phymed.2019.152949 · Cited by 109
Cardiac Fibrosis in the Multi-Omics Era: Implications for Heart Failure
Ghazal, R., Wang, M., Liu, D., Tschumperlin, D. J., & Pereira, N. L. (2025) · Circulation Research · doi:10.1161/circresaha.124.325402 · Cited by 128
Developmental and regenerative paradigms of cilia regulated hedgehog signaling
Kopinke, D., Norris, A. M., & Mukhopadhyay, S. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.05.029 · Cited by 106
Cardiac Fibrosis: Cellular Effectors, Molecular Pathways, and Exosomal Roles
Jiang, W., Xiong, Y., Li, X., & Yang, Y. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.715258 · Cited by 111
Li, S., Zhu, Z., Xue, M., Yi, X., Liang, J., Niu, C. S., Chen, G., Shen, Y., Zhang, H., Jiayong, Z., et al. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2019.01.019 · Cited by 107
Role of the Epigenome in Heart Failure
Papait, R., Serio, S., & Condorelli, G. (2020) · Physiological Reviews · doi:10.1152/physrev.00037.2019 · Cited by 107
Wu, Y., Chang, T., Chen, W., Wang, X., Li, J., Chen, Y., You, Y., Shen, Z., Yu, Q., & Zhang, Y. (2020) · Bioactive Materials · doi:10.1016/j.bioactmat.2020.08.031 · Cited by 106
Yang, E. Y., Ghosn, M. G., Khan, M. A., Gramze, N. L., Brunner, G., Nabi, F., Nambi, V., Nagueh, S. F., Nguyen, D. T., Graviss, E. A., et al. (2019) · Circulation Cardiovascular Imaging · doi:10.1161/circimaging.119.009535 · Cited by 107
Wu, N., Xu, J., Du, W. W., Li, X., Awan, F. M., Li, F., Mısır, S., Eshaghi, E., Lyu, J., Zhou, L., et al. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.12.004 · Cited by 102
Mapping the cardiac vascular niche in heart failure
Peisker, F., Halder, M., Nagai, J. S., Ziegler, S. M., Kaesler, N., Hoeft, K., Li, R., Bindels, E. M., Kuppe, C., Moellmann, J., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30682-0 · Cited by 103
Cardiac Fibroblast p38 MAPK: A Critical Regulator of Myocardial Remodeling
Turner, N. A., & Blythe, N. M. (2019) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd6030027 · Cited by 101
Warbrick, I., & Rabkin, S. W. (2019) · Obesity Reviews · doi:10.1111/obr.12828 · Cited by 100
Min, S., Kim, S., Sim, W., Choi, Y. S., Joo, H., Park, J.-H., Lee, S.-J., Kim, H., Lee, M. J., Jeong, I., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46928-y · Cited by 107
Zhang, Y., Lin, X., Chu, Y., Chen, X., Du, H., Zhang, H., Xu, C., Xie, H. B., Ruan, Q., Lin, J., et al. (2021) · Cardiovascular Diabetology · doi:10.1186/s12933-021-01312-8 · Cited by 99
Zhang, L., He, J., Wang, J., Liu, J., Chen, Z., Deng, B., Wei, L., Wu, H., Liang, B., Li, H., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03750-4 · Cited by 100
Cardiac Fibrosis in the Pressure Overloaded Left and Right Ventricle as a Therapeutic Target
Schimmel, K., Ichimura, K., Reddy, S., Haddad, F., & Spiekerkoetter, E. F. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.886553 · Cited by 106
Guo, S., Meng, X., Yang, X., Liu, X., Ouyang, C., & Liu, C. (2017) · Acta Pharmacologica Sinica · doi:10.1038/aps.2017.92 · Cited by 97
The impacts of age and frailty on heart rate and sinoatrial node function
Moghtadaei, M., Jansen, H. J., Mackasey, M., Rafferty, S. A., Bogachev, O., Sapp, J. L., Howlett, S. E., & Rose, R. A. (2016) · The Journal of Physiology · doi:10.1113/jp272979 · Cited by 95
Liu, X., Yin, K., Chen, L., Chen, W., Li, W., Zhang, T., Sun, Y., Yuan, M., Wang, H., Song, Y., et al. (2023) · Cell Discovery · doi:10.1038/s41421-022-00490-3 · Cited by 100
Pathophysiology of Aortic Stenosis and Future Perspectives for Medical Therapy
Zheng, K. H., Tzolos, E., & Dweck, M. R. (2019) · Cardiology Clinics · doi:10.1016/j.ccl.2019.09.010 · Cited by 106
Mitochondrial CaMKII causes adverse metabolic reprogramming and dilated cardiomyopathy
Luczak, E. D., Wu, Y., Granger, J. M., Joiner, M.-L. A., Wilson, N. R., Gupta, A. K., Umapathi, P., Murphy, K. R., Gaido, O. E. R., Sabet, A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18165-6 · Cited by 96
Signaling cascades in the failing heart and emerging therapeutic strategies
He, X., Du, T., Long, T., Liao, X., Dong, Y., & Huang, Z. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00972-6 · Cited by 108
Shao, D., Liu, X., Wu, J., Zhang, A., Bai, Y., Zhao, P., & Li, J. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154177 · Cited by 93
Lombardi, R., Chen, S. N., Ruggiero, A., Gurha, P., Czernuszewicz, G. Z., Willerson, J. T., & Marian, A. J. (2016) · Circulation Research · doi:10.1161/circresaha.115.308136 · Cited by 97
miR-146a Suppresses SUMO1 Expression and Induces Cardiac Dysfunction in Maladaptive Hypertrophy
Oh, J. G., Watanabe, S., Lee, A., Gorski, P. A., Lee, P., Jeong, D., Liang, L., Liang, Y., Baccarini, A., Sahoo, S., et al. (2018) · Circulation Research · doi:10.1161/circresaha.118.312751 · Cited by 93
Singh, R., Kaundal, R. K., Zhao, B., Bouchareb, R., & Lebeche, D. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2020.105414 · Cited by 94
Liu, J., Zhuang, T., Pi, J., Chen, X., Zhang, Q., Li, Y., Wang, H., Shen, Y., Tomlinson, B., Chan, P., et al. (2019) · Circulation · doi:10.1161/circulationaha.119.039767 · Cited by 92
CMR–Derived Extracellular Volume Fraction as a Marker for Myocardial Fibrosis
Lurz, J. A., Luecke, C. F., Lang, D. J., Besler, C., Rommel, K., Klingel, K., Kandolf, R., Adams, V., Schoene, K., Hindricks, G., et al. (2017) · JACC. Cardiovascular imaging · doi:10.1016/j.jcmg.2017.01.025 · Cited by 92
Hao, K., Lei, W., Wu, H., Wu, J., Yang, Z., Yan, S., Lu, X., Li, J., Xia, X., Han, X., et al. (2019) · Theranostics · doi:10.7150/thno.33920 · Cited by 93
Soroudi, S., Jaafari, M. R., & Arabi, L. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.06.023 · Cited by 96
Rodriguez, P. Q., Sassi, Y., Troncone, L., Bénard, L., Ishikawa, K., Gordon, R. E., Lamas, S., Laborda, J., Hajjar, R. J., & Lebeche, D. (2018) · European Heart Journal · doi:10.1093/eurheartj/ehy188 · Cited by 90
CAR-Macrophage Therapy Alleviates Myocardial Ischemia-Reperfusion Injury
Wang, J., Du, H., Xie, W., Bi, J., Zhang, H., Liu, X., Wang, Y., Zhang, S., Lei, A., He, C., et al. (2024) · Circulation Research · doi:10.1161/circresaha.124.325212 · Cited by 91
Mechanically dynamic PDMS substrates to investigate changing cell environments
Yeh, Y., Corbin, E. A., Caliari, S. R., Ouyang, L., Vega, S. L., Truitt, R., Han, L., Margulies, K. B., & Burdick, J. A. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.08.033 · Cited by 92
Feng, Y., Zhang, Y., & Xiao, H. (2017) · Science China Life Sciences · doi:10.1007/s11427-017-9197-5 · Cited by 92
Pirfenidone for idiopathic pulmonary fibrosis and beyond
Aimo, A., Spitaleri, G., Nieri, D., Tavanti, L. M., Meschi, C., Panichella, G., Lupón, J., Pistelli, F., Carrozzi, L., Bayes-Genis, A., et al. (2022) · Cardiac Failure Review · doi:10.15420/cfr.2021.30 · Cited by 88
The Role of Cyclic AMP Signaling in Cardiac Fibrosis
Delaunay, M., Osman, H., Kaiser, S., & Diviani, D. (2019) · Cells · doi:10.3390/cells9010069 · Cited by 91
Rizvi, Z. A., Dalal, R., Sadhu, S., Binayke, A., Dandotiya, J., Kumar, Y., Shrivastava, T., Gupta, S. K., Aggarwal, S., Tripathy, M. R., et al. (2022) · eLife · doi:10.7554/elife.73522 · Cited by 89
Multiscale drug screening for cardiac fibrosis identifies MD2 as a therapeutic target
Zhang, H., Thai, P. N., Shivnaraine, R. V., Ren, L., Wu, X., Siepe, D. H., Liu, Y., Tu, C., Shin, H. S., Caudal, A., et al. (2024) · Cell · doi:10.1016/j.cell.2024.09.034 · Cited by 96
Feng, H., Cao, J., Zhang, G., & Wang, Y. (2017) · Planta Medica · doi:10.1055/s-0043-103415 · Cited by 86
Genetic Regulation of Fibroblast Activation and Proliferation in Cardiac Fibrosis
Park, S., Ranjbarvaziri, S., Lay, F. D., Zhao, P., Miller, M. J., Dhaliwal, J. S., Huertas-Vazquez, A., Wu, X., Qiao, R., Soffer, J. M., et al. (2018) · Circulation · doi:10.1161/circulationaha.118.035420 · Cited by 85
Verma, S. K., Garikipati, V. N. S., Krishnamurthy, P., Schumacher, S. M., Grisanti, L. A., Cimini, M., Cheng, Z. A., Khan, M., Yue, Y., Benedict, C., et al. (2017) · Circulation · doi:10.1161/circulationaha.117.027889 · Cited by 84
Growth Differentiation Factor 15 in Adverse Cardiac Remodelling: From Biomarker to Causal Player
Wesseling, M., de Poel, J. H. C., & de Jager, S. C. A. (2020) · ESC Heart Failure · doi:10.1002/ehf2.12728 · Cited by 85
Wang, B., Wang, H., Zhang, M., Ji, R., Wei, J., Xin, Y., & Jiang, X. M. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15479 · Cited by 91
González, A., López, B., Ravassa, S., José, G. S., & Dı́ez, J. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.06.001 · Cited by 88
Gallic acid improves cardiac dysfunction and fibrosis in pressure overload-induced heart failure
Jin, L., Sun, S., Ryu, Y., Piao, Z. H., Liu, B., Choi, S. Y., Kim, G. R., Kim, H.-S., Kee, H. J., & Jeong, M. H. (2018) · Scientific Reports · doi:10.1038/s41598-018-27599-4 · Cited by 88
Chen, R.-R., Fan, X., Chen, G., Zeng, G., Xue, Y., Liu, X., & Wang, C. (2019) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2019.01.031 · Cited by 84
Osteopontin: A Promising Therapeutic Target in Cardiac Fibrosis
Mohamed, I. A., Gadeau, A., Hasan, A., Abdulrahman, N., & Mraiche, F. (2019) · Cells · doi:10.3390/cells8121558 · Cited by 84
Li, W., Lou, X., Zha, Y., Qin, Y., Zha, J., Hong, L., Xie, Z., Yang, S.-D., Wang, C., An, J., et al. (2023) · eLife · doi:10.7554/elife.80479 · Cited by 87
Genetic tools for identifying and manipulating fibroblasts in the mouse
Swonger, J. M., Liu, J. S., Ivey, M. J., & Tallquist, M. D. (2016) · Differentiation · doi:10.1016/j.diff.2016.05.009 · Cited by 85
Non-ischemic dilated cardiomyopathy and cardiac fibrosis
Cojan-Minzat, B. O., Zlibut, A., & Agoşton-Coldea, L. (2020) · Heart Failure Reviews · doi:10.1007/s10741-020-09940-0 · Cited by 87
Armutçu, F. (2019) · Inflammation Research · doi:10.1007/s00011-019-01271-7 · Cited by 80
Zheng, D., Zhang, Y., Hu, Y., Guan, J. Z., Xu, L., Xiao, W., Zhong, Q., Ren, C., Lü, J., Liang, J., et al. (2019) · FEBS Journal · doi:10.1111/febs.14780 · Cited by 82
Endothelial ERG alleviates cardiac fibrosis via blocking endothelin-1-dependent paracrine mechanism
Zhang, X., Hu, C., Yuan, Y., Song, P. K., Kong, C., Wu, H., Xu, S., Ma, Z., & Tang, Q. (2021) · Cell Biology and Toxicology · doi:10.1007/s10565-021-09581-5 · Cited by 81
The Synergistic Cooperation between TGF-β and Hypoxia in Cancer and Fibrosis
Mallikarjuna, P., Zhou, Y., & Landström, M. (2022) · Biomolecules · doi:10.3390/biom12050635 · Cited by 84
Mechanisms linking adipose tissue inflammation to cardiac hypertrophy and fibrosis
Anthony, S., Guarnieri, A., Gozdiff, A., Helsley, R. N., Owens, A. P., & Tranter, M. (2019) · Clinical Science · doi:10.1042/cs20190578 · Cited by 82
Targeting Fibrosis: From Molecular Mechanisms to Advanced Therapies
Di, X., Li, Y., Wei, J., Li, T., & Liao, B. (2024) · Advanced Science · doi:10.1002/advs.202410416 · Cited by 92
Roy, B. (2025) · Medical Sciences · doi:10.3390/medsci13030087 · Cited by 103
Vascularized cardiac spheroids as novel 3D in vitro models to study cardiac fibrosis
Figtree, G. A., Bubb, K. J., Tang, O., Kizana, E., & Gentile, C. (2017) · Cells Tissues Organs · doi:10.1159/000477436 · Cited by 79
WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling
Chen, H., Moreno‐Moral, A., Pesce, F., Devapragash, N., Mancini, M., Heng, E. L., Rotival, M., Srivastava, P. K., Harmston, N., Shkura, K., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11551-9 · Cited by 76
Dual Role of Triptolide in Interrupting the NLRP3 Inflammasome Pathway to Attenuate Cardiac Fibrosis
Pan, X., Liu, Y., Cen, Y., Xiong, Y., Li, J., Ding, Y., Tong, Y.-F., Liu, T., Chen, X., & Zhang, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20020360 · Cited by 79
González, A., Richards, M., de Boer, R. A., Thum, T., Arfsten, H., Hülsmann, M., Falcão‐Pires, I., Dı́ez, J., Foo, R., Chan, M. Y., et al. (2022) · European Journal of Heart Failure · doi:10.1002/ejhf.2493 · Cited by 82
Yao, H., He, Q., Huang, C., Wei, S., Gong, Y., Li, X., Liu, W., Xu, Z., Wu, H., Zheng, C., et al. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.08.016 · Cited by 78
Huang, S., Chen, B., Su, Y., Alex, L., Humeres, C. D., Shinde, A. V., Conway, S. J., & Frangogiannis, N. G. (2019) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2019.05.006 · Cited by 78
Lavall, D., Jacobs, N., Mahfoud, F., Kolkhof, P., Böhm, M., & Laufs, U. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.07.001 · Cited by 78
Fibroblast activation and heterogeneity in fibrotic disease
Zhang, X., Zhang, Y., & Liu, Y. (2025) · Nature Reviews Nephrology · doi:10.1038/s41581-025-00969-8 · Cited by 86
Rawal, S., Munasinghe, P. E., Nagesh, P. T., Lew, K. S., Jones, G. T., Williams, M. J. A., Davis, P. J., Bunton, D., Galvin, I. F., Manning, P. J., et al. (2017) · Clinical Science · doi:10.1042/cs20160916 · Cited by 77
Ginsenoside Rh2 Improves Cardiac Fibrosis via PPARδ–STAT3 Signaling in Type 1-Like Diabetic Rats
Lo, S., Hsu, C., Niu, H., Niu, C., Cheng, J., & Chen, Z. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071364 · Cited by 78
Hypoxia-induced H19/YB-1 cascade modulates cardiac remodeling after infarction
Choong, O. K., Chen, C.-Y., Zhang, J., Lin, J.-H., Lin, P.-J., Ruan, S., Kamp, T. J., & Hsieh, P. C. H. (2019) · Theranostics · doi:10.7150/thno.35218 · Cited by 79
Iqubal, A., Sharma, S., Ansari, M. A., Najmi, A. K., Syed, M. A., Ali, J., Alam, M. M., Ahmad, S., & Haque, S. E. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.172666 · Cited by 78
Ca2+ Signaling in Cardiac Fibroblasts and Fibrosis-Associated Heart Diseases
Feng, J., Armillei, M. K., Yu, A. S., Liang, B. T., Runnels, L. W., & Yue, L. (2019) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd6040034 · Cited by 75
Cardiac Fibrosis: Key Role of Integrins in Cardiac Homeostasis and Remodeling
Meagher, P., Lee, X., Lee, J., Visram, A., Friedberg, M. K., & Connelly, K. A. (2021) · Cells · doi:10.3390/cells10040770 · Cited by 79
McKinsey, T. A., Foo, R., Anene-Nzelu, C. G., Travers, J. G., Vagnozzi, R. J., Weber, N., & Thum, T. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac142 · Cited by 84
Self-citationChen, G., Chelu, M. G., Dobrev, D., & Li, N. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01115 · Cited by 78
ST2/IL-33 signaling in cardiac fibrosis
Vianello, E., Dozio, E., Tacchini, L., Frati, L., & Romanelli, M. M. C. (2019) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2019.105619 · Cited by 75
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Metadata
- Authors
- Travers, J. G., Kamal, F. A., Robbins, J., Yutzey, K. E., & Blaxall, B. C.
- Affiliations
- Cincinnati Children's Hospital Medical Center (US)
- Venue
- Circulation Research
- Published
- 2016-03-18
- Volume
- 118
- Issue
- 6
- Pages
- 1021-1040
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- PMC
- PMC4800485
- OpenAlex
- W2299099463
- Cited by
- 1,596
- References
- 261
- Citations by year
- 2026: 156 · 2025: 175 · 2024: 184 · 2023: 182 · 2022: 156 · 2021: 211 · 2020: 163 · 2019: 143 · 2018: 98 · 2017: 95 · 2016: 30
- FWCI
- 21.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (P01HL069779, R01HL129772, R01HL091475, R01HL134312, R01HL132551, R01HL133695, U54HL119810)
- National Institute of General Medical Sciences (R01GM097347)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Keywords
- myocardial fibrosis, cardiac fibroblasts, myofibroblast differentiation, extracellular matrix homeostasis, myocardial injury, cardiac remodeling, cardiomyocyte hypertrophy, cardiomyocyte apoptosis, heart failure, signaling pathways, treatment options
- MeSH terms
- Animals, Fibroblasts, Fibrosis, Heart Failure, Humans, Cardiomyopathies, Inflammation Mediators, Myofibroblasts
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