The DOI matches its Crossref record; 187 of the 189 references it cites were found in a registry or an index, and 2 are not checked yet.
Hyaluronan: from extracellular glue to pericellular cue
Overview
Integrity signals
Registry
Cites
Statistics
Verification
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?
In the citing paper
“Another major component of the ECM is HA, a glycosaminoglycan (GAG) that regulates lubrication through the binding of water, and is responsible for various cellular processes related to movement and maturation.”
From Unraveling and Harnessing the Immune Response at the Cell–Biomaterial Interface for Tissue Engineering Purposes (2024) · cites this paper as [259]
In the citing paper
“Furthermore, because HASs retain the growing hyaluronan polymer while synthesizing and extruding it from the cell surface (Toole, 2004), they might act as anchor molecules for the PNN.”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Toole, 2004
Citations
Cites
Hanahan, D., & Weinberg, R. A. (2000) · Cell · doi:10.1016/s0092-8674(00)81683-9 · Cited by 29,219
Prospective identification of tumorigenic breast cancer cells
Al‐Hajj, M., Wicha, M. S., Benito‐Hernández, A., Morrison, S. J., & Clarke, M. F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0530291100 · Cited by 10,579
Epithelial–mesenchymal transitions in tumour progression
Thiery, J. P. (2002) · Nature reviews. Cancer · doi:10.1038/nrc822 · Cited by 6,767
New functions for the matrix metalloproteinases in cancer progression
Egeblad, M., & Werb, Z. (2002) · Nature Reviews Cancer · doi:10.1038/nrc745 · Cited by 6,108
Multidrug resistance in cancer: role of ATP–dependent transporters
Gottesman, M. M., Fojo, T., & Bates, S. E. (2002) · Nature Reviews Cancer · doi:10.1038/nrc706 · Cited by 5,536
Dissemination and growth of cancer cells in metastatic sites
Chambers, A. F., Groom, A. C., & MacDonald, I. C. (2002) · Nature reviews. Cancer · doi:10.1038/nrc865 · Cited by 4,018
Convergence of Wnt, ß-Catenin, and Cadherin Pathways
Nelson, W. J., & Nusse, R. (2004) · Science · doi:10.1126/science.1094291 · Cited by 2,537
CD44: From adhesion molecules to signalling regulators
Ponta, H., Sherman, L. S., & Herrlich, P. A. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1004 · Cited by 2,458
CD44 is the principal cell surface receptor for hyaluronate
Aruffo, A. A., Stamenkovic, I., Melnick, M., Underhill, C. B., & Seed, B. (1990) · Cell · doi:10.1016/0092-8674(90)90694-a · Cited by 2,439
Bissell, M. J., & Radisky, D. (2001) · Nature Reviews Cancer · doi:10.1038/35094059 · Cited by 2,180
Cited by
Sorted by citations
Items 201–300 of 1,001
Roles of Proteoglycans and Glycosaminoglycans in Cancer Development and Progression
Wei, J., Hu, M., Huang, K., Lin, S., & Du, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21175983 · Cited by 169
Choi, K. Y., Jeon, E. J., Yoon, H. Y., Lee, B. S., Na, J. H., Min, K. H., Kim, S. Y., Myung, S., Lee, S., Chen, X. S., et al. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.05.029 · Cited by 168
Immunological functions of hyaluronan and its receptors in the lymphatics
Jackson, D. G. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00803.x · Cited by 169
3D Printing‐Based Hydrogel Dressings for Wound Healing
Zhou, X., Yu, X., You, T., Zhao, B., Dong, L., Huang, C., Zhou, X., Xing, M. M. Q., Qian, W., & Luo, G. (2024) · Advanced Science · doi:10.1002/advs.202404580 · Cited by 168
Rugg, M. S., Willis, A. C., Mukhopadhyay, D., Hascall, V., Fries, E., Fülöp, C., Milner, C. M., & Day, A. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501332200 · Cited by 167
Alberti, S., Soler‐Illia, G. J. A. A., & Azzaroni, O. (2015) · Chemical Communications · doi:10.1039/c4cc10414e · Cited by 166
Tam, R. Y., Smith, L. J., & Shoichet, M. S. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6b00543 · Cited by 166
Regulation of vascular permeability by sphingosine 1-phosphate
Wang, L., & Dudek, S. M. (2008) · Microvascular Research · doi:10.1016/j.mvr.2008.09.005 · Cited by 166
Moussian, B., Tång, E., Tonning, A., Helms, S., Schwarz, H., Nüsslein‐Volhard, C., & Uv, A. (2005) · Development · doi:10.1242/dev.02177 · Cited by 165
Injectable Acellular Hydrogels for Cardiac Repair
Tous, E., Purcell, B. P., Ifkovits, J. L., & Burdick, J. A. (2011) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-011-9291-1 · Cited by 164
Target Specific Intracellular Delivery of siRNA/PEI−HA Complex by Receptor Mediated Endocytosis
Jiang, G., Park, K., Kim, J., Kim, K. S., & Hahn, S. K. (2009) · Molecular Pharmaceutics · doi:10.1021/mp800176t · Cited by 164
Hyaluronan metabolism: a major paradox in cancer biology
Stern, R. (2005) · Pathologie Biologie · doi:10.1016/j.patbio.2004.12.021 · Cited by 164
Inflammation-induced Uptake and Degradation of the Lymphatic Endothelial Hyaluronan Receptor LYVE-1
Johnson, L. A., Prevo, R., Clasper, S., & Jackson, D. G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702889200 · Cited by 164
Silva, C. R., Babo, P. S., Gulino, M., Costa, L., Oliveira, J. M., Silva‐Correia, J., Domingues, R. M. A., Reis, R. L., & Gomes, M. E. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.07.035 · Cited by 169
γδ T cell–induced hyaluronan production by epithelial cells regulates inflammation
Jameson, J., Cauvi, G., Sharp, L. L., Witherden, D. A., & Havran, W. L. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20042057 · Cited by 162
Becker, L. C., Bergfeld, W. F., Belsito, D. V., Klaassen, C. D., Marks, J. G., Shank, R. C., Slaga, T. J., Snyder, P. W., Panel, W. C. I. R. E., & Andersen, F. A. (2009) · International Journal of Toxicology · doi:10.1177/1091581809337738 · Cited by 161
Evaluation of the 3p21.3 tumour-suppressor gene cluster
Hesson, L. B., Cooper, W. N., & Latif, F. (2007) · Oncogene · doi:10.1038/sj.onc.1210547 · Cited by 161
Diabetic foot ulcer: Challenges and future
Li, Y., Rong, G.-C., & Wu, Q. (2022) · World Journal of Diabetes · doi:10.4239/wjd.v13.i12.1014 · Cited by 168
Neural stem cell niches: Roles for the hyaluronan-based extracellular matrix
Preston, M. (2011) · Frontiers in Bioscience-Scholar · doi:10.2741/218 · Cited by 160
Plasma YKL-40: A Potential New Cancer Biomarker?
Johansen, J. S., Schultz, N. A., & Jensen, B. V. (2009) · Future Oncology · doi:10.2217/fon.09.66 · Cited by 160
Liang, C., Shi, S., Meng, Q., Liang, D., Ji, S., Zhang, B., Qin, Y., Xu, J., Ni, Q., & Yu, X. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.255 · Cited by 166
Jackson, D. G. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.02.001 · Cited by 168
Physical biology of the cancer cell glycocalyx
Kuo, J. C., Gandhi, J. G., Zia, R. N., & Paszek, M. J. (2018) · Nature Physics · doi:10.1038/s41567-018-0186-9 · Cited by 165
Current trends in biologics delivery to restore intervertebral disc anabolism
Fontana, G., See, E. Y.-S., & Pandit, A. S. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.08.008 · Cited by 159
Grass, G. D., & Toole, B. P. (2015) · Bioscience Reports · doi:10.1042/bsr20150256 · Cited by 159
Self-citationCarulli, D., Rhodes, K. E., & Fawcett, J. W. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21231 · Cited by 158
Dissecting the Dual Nature of Hyaluronan in the Tumor Microenvironment
Liu, M., Tölg, C., & Turley, E. A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00947 · Cited by 161
Hyaluronan and versican in the control of human T-lymphocyte adhesion and migration
Evanko, S. P., Potter‐Perigo, S., Bollyky, P. L., Nepom, G. T., & Wight, T. N. (2011) · Matrix Biology · doi:10.1016/j.matbio.2011.10.004 · Cited by 157
Benitez, A., Yates, T. J., López, L. E., Cerwinka, W. H., Bakkar, A., & Lokeshwar, V. B. (2011) · Cancer Research · doi:10.1158/0008-5472.can-10-4610 · Cited by 157
CD44, Hyaluronan, the Hematopoietic Stem Cell, and Leukemia-Initiating Cells
Zöller, M. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00235 · Cited by 162
DeAngelis, P. L., Liu, J., & Linhardt, R. J. (2013) · Glycobiology · doi:10.1093/glycob/cwt016 · Cited by 159
Brown, D. V., Filiz, G., Daniel, P. M., Hollande, F., Dworkin, S., Amiridis, S., Kountouri, N., Ng, W., Morokoff, A. P., & Mantamadiotis, T. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172791 · Cited by 166
Engineering an Artificial T‐Cell Stimulating Matrix for Immunotherapy
Hickey, J. W., Dong, Y. W., Chung, J. W., Salathe, S. F., Pruitt, H. C., Li, X., Chang, C. K. W., Fraser, A. K., Bessell, C. A., Ewald, A. J., et al. (2019) · Advanced Materials · doi:10.1002/adma.201807359 · Cited by 156
Mechanochemical Signaling of the Extracellular Matrix in Epithelial-Mesenchymal Transition
Scott, L. E., Weinberg, S. H., & Lemmon, C. A. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00135 · Cited by 165
Alginate–hyaluronan composite hydrogels accelerate wound healing process
Catanzano, O., D’Esposito, V., Acierno, S., Ambrosio, M. R., Caro, C. D., Avagliano, C., Russo, P., Russo, R., Miro, A., Ungaro, F., et al. (2015) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2015.05.081 · Cited by 160
Li, Y., Li, L., Brown, T. J., & Heldin, P. (2007) · International Journal of Cancer · doi:10.1002/ijc.22550 · Cited by 155
Applications of Biocompatible Scaffold Materials in Stem Cell-Based Cartilage Tissue Engineering
Zhao, X., Hu, D. A., Wu, D., He, F., Wang, H., Huang, L., Shi, D., Liu, Q., Ni, N., Pakvasa, M., et al. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.603444 · Cited by 154
Arranz, A. M., Perkins, K. L., Irie, F., Lewis, D. P., Hrabe, J., Xiao, F., Itano, N., Kimata, K., Hrabetova, S., & Yamaguchi, Y. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3458-13.2014 · Cited by 154
Burnside, E. R., & Bradbury, E. J. (2013) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12114 · Cited by 161
Glioblastoma Behaviors in Three-Dimensional Collagen-Hyaluronan Composite Hydrogels
Rao, S. S., DeJesus, J., Short, A. R., Otero, J. J., Sarkar, A., & Winter, J. O. (2013) · ACS Applied Materials & Interfaces · doi:10.1021/am402097j · Cited by 167
Impact of the hyaluronan‐rich tumor microenvironment on cancer initiation and progression
Itano, N., Zhuo, L., & Kimata, K. (2008) · Cancer Science · doi:10.1111/j.1349-7006.2008.00885.x · Cited by 155
Wan, J. (2012) · Polymers · doi:10.3390/polym4021084 · Cited by 152
Inhibition of Hyaluronan Synthesis Accelerates Murine Atherosclerosis
Nagy, N., Freudenberger, T., Melchior‐Becker, A., Roeck, K., ter Braak, M., Jastrow, H., Kinzig, M., Lucke, S., Suvorava, T., Kojda, G., et al. (2010) · Circulation · doi:10.1161/circulationaha.110.972653 · Cited by 152
Downregulation of Spry2 by miR-21 triggers malignancy in human gliomas
Kwak, H.-J., Kim, Y.-J., Chun, K.-R., Woo, Y. M., Park, S.-J., Jeong, J.-A., Jo, S. H., Kim, T. H., Min, H. S., Chae, J. S., et al. (2011) · Oncogene · doi:10.1038/onc.2010.620 · Cited by 151
Hu, Q., Zhu, Y., Mei, J., Liu, Y. L., & Zhou, G. (2025) · Journal of Hematology & Oncology · doi:10.1186/s13045-025-01717-y · Cited by 157
Blends and composites of exopolysaccharides; properties and applications: A review
Hussain, A., Zia, K. M., Tabasum, S., Noreen, A., Ali, M., Iqbal, R., & Zuber, M. (2016) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2016.09.104 · Cited by 154
Pályi‐Krekk, Z., Barok, M., Isola, J. J., Tammi, M., ̋si, J. S., & Nagy, P. (2007) · European Journal of Cancer · doi:10.1016/j.ejca.2007.08.018 · Cited by 149
Kesharwani, P., Banerjee, S., Padhyé, S., Sarkar, F. H., & Iyer, A. K. (2015) · Biomacromolecules · doi:10.1021/acs.biomac.5b00941 · Cited by 148
Zhao, Q., Geng, H., Wang, Y., Gao, Y., Huang, J., Wang, Y., Zhang, J., & Wang, S. (2014) · ACS Applied Materials & Interfaces · doi:10.1021/am505824d · Cited by 147
The Complex Interplay Between Extracellular Matrix and Cells in Tissues
Manou, D., Caon, I., Bouris, P., Triantaphyllidou, I., Giaroni, C., Passi, A. G., Karamanos, N. K., Vigetti, D., & Theocharis, A. D. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9133-4_1 · Cited by 147
Evaluating the Efficiency of Hyaluronic Acid for Tumor Targeting via CD44
Spadea, A., Rosa, J. M. R. D. L., Tirella, A., Ashford, M. B., Williams, K. J., Stratford, I. J., Tirelli, N., & Mehibel, M. (2019) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.9b00083 · Cited by 147
Baranova, N. S., Nilebäck, E., Haller, F. M., Briggs, D. C., Svedhem, S., Day, A. J., & Richter, R. P. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.247395 · Cited by 150
Current and Emerging Therapies in Metastatic Pancreatic Cancer
Manji, G. A., Olive, K. P., Saenger, Y. M., & Oberstein, P. (2017) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-16-2319 · Cited by 145
Therapeutic Angiogenesis: Controlled Delivery of Angiogenic Factors
Chu, H., & Wang, Y. (2012) · Therapeutic Delivery · doi:10.4155/tde.12.50 · Cited by 151
Chondroitin sulfates and their binding molecules in the central nervous system
Djerbal, L., Lortat-Jacob, H., & Kwok, J. (2017) · Glycoconjugate Journal · doi:10.1007/s10719-017-9761-z · Cited by 144
Hodde, J. P., Janis, A. D., Ernst, D. M. J., Zopf, D. A., Sherman, D. M., & Johnson, C. (2007) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-007-2300-x · Cited by 144
Neutrophils promote motility of cancer cells via a hyaluronan‐mediated TLR4/PI3K activation loop
Wu, Y., Zhao, Q., Peng, C., Sun, L., Li, X., & Kuang, D. (2011) · The Journal of Pathology · doi:10.1002/path.2947 · Cited by 146
DuFort, C. C., DelGiorno, K. E., & Hingorani, S. R. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.03.040 · Cited by 144
Stromal dynamic reciprocity in cancer: intricacies of fibroblastic-ECM interactions
Alexander, J. I., & Cukierman, E. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.05.002 · Cited by 149
Efficient TGFβ-induced epithelial–mesenchymal transition depends on hyaluronan synthase HAS2
Porsch, H., Bernert, B., Mehić, M., Theocharis, A. D., Heldin, C., & Heldin, P. (2012) · Oncogene · doi:10.1038/onc.2012.475 · Cited by 142
Hyaluronan: Towards novel anti-cancer therapeutics
Karbownik, M. S., & Nowak, J. Z. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)71465-8 · Cited by 142
Park, H., Jin, Y., Shin, J., Yang, K., Lee, C., Yang, H. S., & Cho, S. (2016) · Biomacromolecules · doi:10.1021/acs.biomac.5b01670 · Cited by 142
The state of CD44 activation in cancer progression and therapeutic targeting
Guo, Q., Yang, C., & Gao, F. (2021) · FEBS Journal · doi:10.1111/febs.16179 · Cited by 144
Tumor Cells Enhance Their Own CD44 Cleavage and Motility by Generating Hyaluronan Fragments
Sugahara, K. N., Hirata, T., Hayasaka, H., Stern, R., Murai, T., & Miyasaka, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m506740200 · Cited by 142
Identification of uPAR-positive Chemoresistant Cells in Small Cell Lung Cancer
Gutova, M., Najbauer, J., Gevorgyan, A., Metz, M. Z., Weng, Y., Shih, C.-C., & Aboody, K. S. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000243 · Cited by 141
Ma, G., Liu, Y., Peng, C., Fang, D., He, B., & Nie, J. (2011) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2011.04.082 · Cited by 141
Role of hyaluronan in pancreatic cancer biology and therapy: Once again in the spotlight
Sato, N., Kohi, S., Hirata, K., & Goggins, M. (2016) · Cancer Science · doi:10.1111/cas.12913 · Cited by 142
Spontaneous Metastasis of Prostate Cancer Is Promoted by Excess Hyaluronan Synthesis and Processing
Bharadwaj, A. G., Kovar, J. L., Loughman, E., Elowsky, C. G., Oakley, G. G., & Simpson, M. A. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080501 · Cited by 141
Zhang, Y., Wu, D., Zhao, X., Pakvasa, M., Tucker, A. B., Luo, H., Qin, K. H., Hu, D. A., Wang, E. J., Li, A. J., et al. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.598607 · Cited by 140
Mandal, C. C., Ghosh-Choudhury, N., Yoneda, T., Choudhury, G. G., & Ghosh-Choudhury, N. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.193714 · Cited by 138
How does chondroitinase promote functional recovery in the damaged CNS?
Crespo, D., Asher, R. A., Lin, R., Rhodes, K. E., & Fawcett, J. W. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.05.001 · Cited by 138
Liu, T., Li, N., Yan, Y., Liu, Y., Xiong, K., Liu, Y., Xia, Q., Zhang, H., & Liu, Z. (2019) · Phytotherapy Research · doi:10.1002/ptr.6538 · Cited by 143
Mechanisms and Targets Involved in Dissemination of Ovarian Cancer
Weidle, U. H., Birzele, F., Kollmorgen, G., & Rueger, R. (2016) · Cancer Genomics & Proteomics · doi:10.21873/cgp.20004 · Cited by 137
Hydrogel-exosome system in tissue engineering: A promising therapeutic strategy
Fan, M., Pi, J.-K., Zou, C., Jiang, Y., Li, Q., Zhang, X., Xing, F., Nie, R., Chen, H., & Xie, H. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.04.007 · Cited by 138
Struve, J. N., Maher, P. C., Li, Y., Kinney, S. D., Fehlings, M. G., Kuntz, C., & Sherman, L. S. (2005) · Glia · doi:10.1002/glia.20215 · Cited by 141
Zeilstra, J., Joosten, S. P. J., van Andel, H., Tölg, C., Berns, A. J. M., Snoek, M., van de Wetering, M., Spaargaren, M., Clevers, H. C., & Pals, S. T. (2013) · Oncogene · doi:10.1038/onc.2012.611 · Cited by 137
Role of hyaluronan in glioma invasion
Park, J. B., Kwak, H., & Lee, S. (2008) · Cell Adhesion & Migration · doi:10.4161/cam.2.3.6320 · Cited by 140
Targeting Tumor Microenvironment by Small-Molecule Inhibitors
Zhong, S., Jeong, J.-H., Chen, Z., Chen, Z., & Luo, J. (2019) · Translational Oncology · doi:10.1016/j.tranon.2019.10.001 · Cited by 139
Evaluation of an Internet addiction treatment program for Chinese adolescents in Hong Kong.
Shek, D. T. L., Tang, V. M. Y., & Lo, C.-P. (2009) · PubMed · Cited by 135
HMMR Maintains the Stemness and Tumorigenicity of Glioblastoma Stem-like Cells
Tilghman, J. I., Wu, H., Sang, Y., Shi, X., Guerrero‐Cazares, H., Quiñones‐Hinojosa, A., Eberhart, C. G., Laterra, J., & Ying, M. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-2103 · Cited by 139
Engineering strategies to mimic the glioblastoma microenvironment
Rape, A. D., Ananthanarayanan, B., & Kumar, S. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.08.012 · Cited by 138
Hanjaya‐Putra, D., Wong, K. T., Hirotsu, K. E., Khetan, S., Burdick, J. A., & Gerecht, S. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.05.027 · Cited by 134
The interplay of extracellular matrix and microbiome in urothelial bladder cancer
Alfano, M., Canducci, F., Nebuloni, M., Clementi, M., Montorsi, F., & Salonia, A. (2015) · Nature Reviews Urology · doi:10.1038/nrurol.2015.292 · Cited by 136
Wong, K. M., Horton, K. J., Coveler, A. L., Hingorani, S. R., & Harris, W. P. (2017) · Current Oncology Reports · doi:10.1007/s11912-017-0608-3 · Cited by 137
Liu, H., Korc, M., & Lin, C. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.01.012 · Cited by 134
Rahikkala, A., Pereira, S. A. P., Figueiredo, P., Passos, M. L. C., Araújo, A. R. T. S., Saraiva, M. L. M. F. S., & Santos, H. A. (2018) · Advanced Biosystems · doi:10.1002/adbi.201800020 · Cited by 137
Hyaluronan Accumulates With High-Fat Feeding and Contributes to Insulin Resistance
Kang, L., Lantier, L., Kennedy, A., Bonner, J. S., Mayes, W. H., Bracy, D. P., Bookbinder, L. H., Hasty, A. H., Thompson, C. B., & Wasserman, D. H. (2013) · Diabetes · doi:10.2337/db12-1502 · Cited by 133
Biomaterials for Bioprinting Microvasculature
Barrs, R. W., Jia, J., Silver, S. E., Yost, M. J., & Mei, Y. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00027 · Cited by 134
Role of Versican, Hyaluronan and CD44 in Ovarian Cancer Metastasis
Ween, M. P., Oehler, M. K., & Ricciardelli, C. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms12021009 · Cited by 133
TGFβ and matrix-regulated epithelial to mesenchymal transition
Moustakas, A., & Heldin, P. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.02.004 · Cited by 132
Guo, Y. Q., Yuan, T., Xiao, Z., Tang, P., Xiao, Y., Fan, Y., & Zhang, X. (2012) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-012-4684-5 · Cited by 132
The Extracellular Matrix in Epithelial Ovarian Cancer – A Piece of a Puzzle
Cho, A., Howell, V. M., & Colvin, E. K. (2015) · Frontiers in Oncology · doi:10.3389/fonc.2015.00245 · Cited by 148
Engineered Culture Models for Studies of Tumor-Microenvironment Interactions
Infanger, D. W., Lynch, M. E., & Fischbach, C. (2013) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071811-150028 · Cited by 133
Koch, L., Deiwick, A., Franke, A., Schwanke, K., Haverich, A., Zweigerdt, R., & Chichkov, B. N. (2018) · Biofabrication · doi:10.1088/1758-5090/aab981 · Cited by 132
Hyaluronan Synthesis Induces Microvillus-like Cell Surface Protrusions
Kultti, A. H., Rilla, K. J., Tiihonen, R., Spicer, A. P., Tammi, R., & Tammi, M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512840200 · Cited by 135
Harrell, J. C., Dye, W. W., Allred, D. C., Jedlicka, P., Spoelstra, N. S., Sartorius, C. A., & Horwitz, K. B. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-1769 · Cited by 131
Clark, S. J., Keenan, T. D. L., Fielder, H. L., Collinson, L. J., Holley, R. J., Merry, C. L. R., Kuppevelt, T. H. V., Day, A. J., & Bishop, P. N. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-7909 · Cited by 134
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131
Bell, T. J., Brand, O. J., Morgan, D. J., Salek‐Ardakani, S., Jagger, C. P., Fujimori, T., Cholewa, L., Tilakaratna, V., Östling, J., Thomas, M., et al. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.06.006 · Cited by 134
Structure and Function of Inter-α-Trypsin Inhibitor Heavy Chains
Zhuo, L., & Kimata, K. (2008) · Connective Tissue Research · doi:10.1080/03008200802325458 · Cited by 130
Metadata
- Authors
- Toole, B. P.
- Affiliations
- Medical University of South Carolina (US)
- Corresponding author
- Toole, Bryan P.
- ORCID
- Toole, Bryan P.
- Venue
- Nature Reviews Cancer
- Published
- 2004-07
- Volume
- 4
- Issue
- 7
- Pages
- 528-539
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W2089753996
- Semantic Scholar
- 3488563c03cedbae83c9c1d8423aeb0c6b33a4a3
- Cited by
- 2,125
- References
- 188
- Citations by year
- 2026: 61 · 2025: 78 · 2024: 81 · 2023: 97 · 2022: 93 · 2021: 129 · 2020: 120 · 2019: 120 · 2018: 116 · 2017: 112 · 2016: 150 · 2015: 130 · 2014: 126 · 2013: 103 · 2012: 99
- FWCI
- 3.59
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Physical Sciences › Materials Science › Biomaterials › Hydrogels: synthesis, properties, applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- hyaluronic acid, extracellular matrix, cell microenvironment, tumor microenvironment, embryonic development, wound healing, inflammation, carcinogenesis, cancer therapy
- MeSH terms
- Adult, Animals, Cell Survival, Connective Tissue, Extracellular Matrix, Embryonic and Fetal Development, Forecasting, Humans, Hyaluronic Acid, Hyaluronoglucosaminidase, Inflammation, Joints, Neoplasm Invasiveness, Neoplasm Metastasis, Neoplasms, Neovascularization, Pathologic, Ultrasonography, Wound Healing, Signal Transduction, Drug Resistance, Multiple, Hyaluronan Receptors, Drug Resistance, Neoplasm, Xenograft Model Antitumor Assays
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