Cadherins: cellular adhesive molecules serving as signalling mediators
Open accessAbstract
The single pass, transmembrane proteins of the cadherin family have been appreciated as important proteins that regulate intercellular adhesion. In addition to this critical function, cadherins contribute to important signalling events that control cellular homeostasis. Many examples exist of classical, desmosomal and atypical cadherins participating in the regulation of signalling events that control homeostatic functions in cells. Much of the work on cadherin mediated signalling focuses on classical cadherins or on specific disease states such as pemphigus vulgaris. Cadherin mediated signalling has been shown to play critical roles during development, in proliferation, apoptosis, disease pathobiology and beyond. It is becoming increasingly clear that cadherins operate through a range of molecular mechanisms. The diversity of pathways and cellular functions regulated by cadherins suggests that we have only scratched the surface in terms of the roles that these versatile proteins play in signalling and cellular function. image
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Cadherins are a family of calcium-dependent transmembrane adhesion proteins that link β- and α-catenin to the actin cytoskeletal network and regulate cellular homeostasis through signaling mediating development, proliferation, apoptosis, and disease pathology.
“Cadherins are a family of calcium-dependent transmembrane adhesion proteins that link β- and α-catenin to the actin cytoskeletal network (Punovuori et al., 2021) and also regulate cellular homeostasis through signaling mediating development, proliferation, apoptosis, and disease pathology (Yulis et al., 2018).”
From APOE3 Christchurch modulates β-catenin/Wnt signaling in iPS cell-derived cerebral organoids from Alzheimer’s cases (2024) · cites this paper as Yulis et al., 2018
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Wnt/β-catenin signaling and disease
Clevers, H., & Nusse, R. (2012) · Cell · doi:10.1016/j.cell.2012.05.012 · Cited by 5,554 · see citing works
Loss of E-Cadherin Promotes Metastasis via Multiple Downstream Transcriptional Pathways
Önder, T. T., Gupta, P. B., Mani, S. A., Yang, J., Lander, E. S., & Weinberg, R. A. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-2938 · Cited by 1,527 · see citing works
Cell adhesion and signalling by cadherins and Ig-CAMs in cancer
Cavallaro, U., & Christofori, G. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1276 · Cited by 1,314 · see citing works
Adherens junctions: from molecules to morphogenesis
Harris, T., & Tepass, U. (2010) · Nature reviews. Molecular cell biology · doi:10.1038/nrm2927 · Cited by 983 · see citing works
Cadherins and cancer: how does cadherin dysfunction promote tumor progression?
Jeanes, A., Gottardi, C. J., & Yap, A. S. (2008) · Oncogene · doi:10.1038/onc.2008.343 · Cited by 764 · see citing works
Labernadie, A., Kato, T., Brugués, A., Serra‐Picamal, X., Derzsi, S., Arwert, E. N., Weston, A., González-Tarragó, V., Elósegui-Artola, A., Albertazzi, L., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3478 · Cited by 747 · see citing works
E-cadherin mediates contact inhibition of proliferation through Hippo signaling-pathway components
Kim, N.-G., Koh, E., Chen, X., & Gumbiner, B. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103345108 · Cited by 698 · see citing works
Marambaud, P., Shioi, J., Serban, G., Georgakopoulos, A., Sarner, S., Nagy, V., Baki, L., Wen, P., Efthimiopoulos, S., Shao, Z., et al. (2002) · The EMBO Journal · doi:10.1093/emboj/21.8.1948 · Cited by 686 · see citing works
Interplay of Cadherin-Mediated Cell Adhesion and Canonical Wnt SignalingPreprint
Heuberger, J., & Birchmeier, W. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a002915 · Cited by 616 · see citing works
The cadherin-catenin adhesion system in signaling and cancer
Conacci‐Sorrell, M., Zhurinsky, J., & Ben‐Ze'ev, A. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15429 · Cited by 532 · see citing works
The cadherin-catenin adhesion system in signaling and cancer
Conacci‐Sorrell, M., Zhurinsky, J., & Ben‐Ze'ev, A. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215429 · Cited by 464 · see citing works
Structure and Biochemistry of Cadherins and CateninsPreprint
Shapiro, L. S., & Weis, W. I. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003053 · Cited by 460 · see citing works
Three neural tubes in mouse embryos with mutations in the T-box gene Tbx6
Chapman, D. L., & Papaioannou, V. E. (1998) · Nature · doi:10.1038/35624 · Cited by 420 · see citing works
Lampugnani, M. G., Zanetti, A., Corada, M., Takahashi, T., Balconi, G., Breviario, F., Orsenigo, F., Cattelino, A., Kemler, R., Daniel, T. O., et al. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200209019 · Cited by 410 · see citing works
Desmosomes: New Perspectives on a Classic
Green, K. J., & Simpson, C. L. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5701015 · Cited by 401 · see citing works
A non-canonical Notch complex regulates adherens junctions and vascular barrier function
Polacheck, W. J., Kutys, M. L., Yang, J., Eyckmans, J., Wu, Y., Vasavada, H. H., Hirschi, K. K., & Chen, C. S. (2017) · Nature · doi:10.1038/nature24998 · Cited by 339 · see citing works
Sherrill, J. D., KC, K., Wu, D. X.-Y., Djukic, Z., Caldwell, J. M., Stucke, E. M., Kemme, K. A., Costello, M. S., Mingler, M. K., Blanchard, C., et al. (2013) · Mucosal Immunology · doi:10.1038/mi.2013.90 · Cited by 314 · see citing works
Yoshikawa, Y., Fujimori, T., McMahon, A., & Takada, S. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8502 · Cited by 308 · see citing works
Direct cadherin-activated cell signaling
Yap, A. S., & Kovács, É. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200208156 · Cited by 296 · see citing works
Cadherin-mediated cellular signaling
Wheelock, M. J., & Johnson, K. R. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(03)00101-7 · Cited by 280 · see citing works
A central role for cadherin signaling in cancer
Kourtidis, A., Lu, R., Pence, L. J., & Anastasiadis, P. Z. (2017) · Experimental Cell Research · doi:10.1016/j.yexcr.2017.04.006 · Cited by 251 · see citing works
Linking E-cadherin mechanotransduction to cell metabolism through force-mediated activation of AMPK
Bays, J., Campbell, H., Heidema, C., Sebbagh, M., & DeMali, K. A. (2017) · Nature Cell Biology · doi:10.1038/ncb3537 · Cited by 225 · see citing works
Perrais, M., Chen, X., Perez-Moreno, M., & Gumbiner, B. M. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-04-0348 · Cited by 219 · see citing works
Shoval, I., Ludwig, A., & Kalcheim, C. (2006) · Development · doi:10.1242/dev.02742 · Cited by 213 · see citing works
Getsios, S., Simpson, C. L., Kojima, S.-I., et al. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200809044 · Cited by 210 · see citing works
Twist1-induced dissemination preserves epithelial identity and requires E-cadherin
Shamir, E. R., Pappalardo, E., Jorgens, D. M., Coutinho, K., Tsai, W.-T., Aziz, K., Auer, M., Tran, P. T., Bader, J. S., & Ewald, A. J. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201306088 · Cited by 204 · see citing works
The Ectodomain Shedding of E-cadherin by ADAM15 Supports ErbB Receptor Activation
Najy, A. J., Day, K. C., & Day, M. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801329200 · Cited by 195 · see citing works
Pemphigus vulgaris identifies plakoglobin as key suppressor of c‐Myc in the skin
Williamson, L., Raess, N. A., Caldelari, R., Zakher, A., de Bruin, A., Posthaus, H., Bolli, R., Hunziker, T., Suter, M. M., & Müller, E. J. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601224 · Cited by 180 · see citing works
Desmosome assembly and dynamics
Nekrasova, O. E., & Green, K. J. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.06.004 · Cited by 177 · see citing works
A Positive Role of Cadherin in Wnt/β-Catenin Signalling during Epithelial-Mesenchymal Transition
Howard, S. M., Deroo, T., Fujita, Y., & Itasaki, N. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023899 · Cited by 163 · see citing works
A Role for the Cleaved Cytoplasmic Domain of E-cadherin in the Nucleus
Ferber, E. C., Kajita, M., Wadlow, A., Tobiansky, L., Niessen, C. M., Ariga, H., Daniel, J. M., & Fujita, Y. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m708887200 · Cited by 162 · see citing works
Inhibition of Rho A activity causes pemphigus skin blistering
Waschke, J., Spindler, V., Bruggeman, P., et al. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200605125 · Cited by 162 · see citing works
VE‐cadherin is a critical endothelial regulator of TGF‐β signalling
Rudini, N., Felici, A., Giampietro, C., Lampugnani, M. G., Corada, M., Swirsding, K., Garrè, M., Liebner, S., Letarte, M., ten Dijke, P., et al. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.46 · Cited by 157 · see citing works
Bae, G.-Y., Choi, S., Lee, J., Jo, J., Lee, J., Kim, J., & Cha, H. (2013) · Oncotarget · doi:10.18632/oncotarget.1463 · Cited by 144 · see citing works
Desmoglein Versus Non-desmoglein Signaling in Pemphigus Acantholysis
Chernyavsky, A. I., Arredondo, J., Kitajima, Y., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611365200 · Cited by 140 · see citing works
Kashef, J., Köhler, A., Kuriyama, S., Alfandari, D., Mayor, R., & Wedlich, D. (2009) · Genes & Development · doi:10.1101/gad.519409 · Cited by 136 · see citing works
Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation
Harmon, R. M., Simpson, C. L., Johnson, J. L., Koetsier, J. L., Dubash, A. D., Najor, N. A., Sarig, O., Sprecher, E., & Green, K. J. (2013) · Journal of Clinical Investigation · doi:10.1172/jci65220 · Cited by 134 · see citing works
E-cadherin controls β-catenin and NF-κB transcriptional activity in mesenchymal gene expression
Solanas, G., Porta-de-la-Riva, M., Agustí, C., Casagolda, D., Sánchez-Aguilera, F., Larriba, M. J., Pons, F., Peiró, S., Escrivà, M., Múñoz, A., et al. (2008) · Journal of Cell Science · doi:10.1242/jcs.021667 · Cited by 133 · see citing works
Maher, M. T., Flozak, A. S., Stocker, A. M., Chenn, A., & Gottardi, C. J. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200811108 · Cited by 123 · see citing works
Actomyosin contractility and collective migration: may the force be with you
Pandya, P., Orgaz, J. L., & Sanz‐Moreno, V. (2017) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2017.06.006 · Cited by 115 · see citing works
Brennan, D., Hu, Y., Joubeh, S., Choi, Y. W., Whitaker‐Menezes, D., O'Brien, T., Uitto, J., Rodeck, U., & Mahoney, M. G. (2007) · Journal of Cell Science · doi:10.1242/jcs.03392 · Cited by 113 · see citing works
Kamekura, R., Kolegraff, K. N., Nava, P., et al. (2013) · Oncogene · doi:10.1038/onc.2013.442 · Cited by 107 · see citing works
Zhang, J., Shemezis, J. R., McQuinn, E. R., Wang, J., Sverdlov, M., & Chenn, A. (2013) · Neural Development · doi:10.1186/1749-8104-8-7 · Cited by 107 · see citing works
p38MAPK Signaling and Desmoglein-3 Internalization Are Linked Events in Pemphigus Acantholysis
Jolly, P. S., Berkowitz, P., Bektas, M., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.087999 · Cited by 107 · see citing works
Dusek, R. L., Getsios, S., Chen, F., Park, J. K., Amargo, E. V., Cryns, V. L., & Green, K. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508258200 · Cited by 106 · see citing works
Kourtidis, A., Ngok, S. P., Pulimeno, P., Feathers, R. W., Shull, L. C., Baker, T. R., Carr, J. M., Yan, I. K., Borgés, S., Perez, E. A., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3227 · Cited by 105 · see citing works
E-Cadherin Couples Death Receptors to the Cytoskeleton to Regulate Apoptosis
Lu, M., Marsters, S. A., Ye, X., Luis, E., Gonzalez, L. C., & Ashkenazi, A. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.04.029 · Cited by 102 · see citing works
E-cadherin engagement stimulates proliferation via Rac1
Liu, W. F., Nelson, C. M., Pirone, D. M., & Chen, C. S. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200510087 · Cited by 102 · see citing works
Overlapping and divergent signaling pathways of N-cadherin and VE-cadherin in endothelial cells
Giampietro, C., Taddei, A., Corada, M., et al. (2012) · Blood · doi:10.1182/blood-2011-09-381012 · Cited by 97 · see citing works
McCusker, C., Cousin, H., Neuner, R., & Alfandari, D. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-05-0535 · Cited by 96 · see citing works
Kolegraff, K. N., Nava, P., Helms, M. N., Parkos, C. A., & Nusrat, A. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-10-0845 · Cited by 93 · see citing works
Self-citationp38 MAPK Activation Is Downstream of the Loss of Intercellular Adhesion in Pemphigus Vulgaris
Mao, X., Sano, Y., Park, J. M., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.172874 · Cited by 85 · see citing works
Beyond steric hindrance: The role of adhesion signaling pathways in the pathogenesis of pemphigus
Sharma, P. M., Mao, X., & Payne, A. S. (2007) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2007.05.005 · Cited by 83 · see citing works
Hawkins, K., Mohamet, L., Ritson, S., Merry, C., & Ward, C. M. (2012) · Stem Cells · doi:10.1002/stem.1148 · Cited by 79 · see citing works
Lee, H. E., Berkowitz, P., Jolly, P. S., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m808204200 · Cited by 74 · see citing works
Pretel, M., España, A., Marquina, M., Pelacho, B., López-Picazo, J. M., & López-Zabalza, M. J. (2009) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.00893.x · Cited by 70 · see citing works
A Pathophysiologic Role for Epidermal Growth Factor Receptor in Pemphigus Acantholysis
Bektas, M., Jolly, P. S., Berkowitz, P., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.438010 · Cited by 68 · see citing works
Cadherin Engagement Improves Insulin Secretion of Single Human β-Cells
Parnaud, G., Lavallard, V., Bédat, B., Matthey-Doret, D., Morel, P., Berney, T., & Bosco, D. (2014) · Diabetes · doi:10.2337/db14-0257 · Cited by 64 · see citing works
Schmidt, E., & Waschke, J. (2009) · Autoimmunity Reviews · doi:10.1016/j.autrev.2009.01.011 · Cited by 62 · see citing works
Cui, T., Chen, Y., Yang, L., et al. (2012) · Carcinogenesis · doi:10.1093/carcin/bgs273 · Cited by 60 · see citing works
Tsang, S. M., Brown, L., Lin, K., Liu, L., Piper, K., O’Toole, E. A., Grose, R. P., Hart, I. R., Garrod, D. R., Fortune, F., et al. (2012) · The Journal of Pathology · doi:10.1002/path.3982 · Cited by 59 · see citing works
An Adult Passive Transfer Mouse Model to Study Desmoglein 3 Signaling in Pemphigus Vulgaris
Schulze, K., Galichet, A., Sayar, B. S., Scothern, A., Howald, D., Zymann, H., Siffert, M., Zenhäusern, D., Bolli, R., Koch, P. J., et al. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.299 · Cited by 57 · see citing works
Inflammation-induced desmoglein-2 ectodomain shedding compromises the mucosal barrier
Kamekura, R., Nava, P., Feng, M., et al. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-03-0147 · Cited by 57 · see citing works
Bedzhov, I., Liszewska, E., Kanzler, B., & Stemmler, M. P. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002609 · Cited by 55 · see citing works
Arulanandam, R., Vultur, A., Cao, J., et al. (2009) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-08-0469 · Cited by 54 · see citing works
Desmosomal Cadherins and Signaling: Lessons from Autoimmune Disease
Spindler, V., & Waschke, J. (2014) · Cell Communication & Adhesion · doi:10.3109/15419061.2013.877000 · Cited by 54 · see citing works
E-cadherin impairment increases cell survival through Notch-dependent upregulation of Bcl-2
Ferreira, A. C., Suriano, G., Mendes, N. M., et al. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr469 · Cited by 48 · see citing works
Involvement of the Apoptotic Mechanism in Pemphigus Foliaceus Autoimmune Injury of the Skin
Li, N., Zhao, M., Wang, J., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.1.711 · Cited by 48 · see citing works
Lin, Z., Zhang, C., Zhang, M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085296 · Cited by 46 · see citing works
Politi, E., Angelakopoulou, A., Grapsa, D., et al. (2016) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000001419 · Cited by 46 · see citing works
The GEF Bcr activates RhoA/MAL signaling to promote keratinocyte differentiation via desmoglein-1
Dubash, A. D., Koetsier, J. L., Amargo, E. V., et al. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201304133 · Cited by 45 · see citing works
Tsang, S. M., Brown, L., Gadmor, H., et al. (2012) · Experimental Cell Research · doi:10.1016/j.yexcr.2012.07.002 · Cited by 44 · see citing works
Dellon, E. S., Higgins, L. L., Beitia, R., et al. (2016) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.13672 · Cited by 41 · see citing works
Johnson, J. L., Koetsier, J. L., Sirico, A., Agidi, A. T., Antonini, D., Missero, C., & Green, K. J. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.124 · Cited by 39 · see citing works
Park, S.-Y., Shin, J., & Kee, S. (2017) · Cancer Science · doi:10.1111/cas.13321 · Cited by 37 · see citing works
Inhibition of FAK prevents blister formation in the neonatal mouse model of pemphigus vulgaris
Gil, P., Mòdol, T., España, A., et al. (2012) · Experimental Dermatology · doi:10.1111/j.1600-0625.2012.01441.x · Cited by 36 · see citing works
Yulis, M., Quirós, M., Hilgarth, R., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0380-9 · Cited by 30 · see citing works
Self-citationConant, K. E., Daniele, S. G., Bozzelli, P. L., Abdi, T., Edwards, A. A., Szklarczyk, A., Olchefske, I., Ottenheimer, D. J., & Maguire‐Zeiss, K. A. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-0827-4 · Cited by 29 · see citing works
E ‐Cadherin enhances neuregulin signaling and promotes S chwann cell myelination
Basak, S., Desai, D., Rho, E. H., et al. (2015) · Glia · doi:10.1002/glia.22822 · Cited by 23 · see citing works
Segal, J. M., & Ward, C. M. (2017) · Scientific Reports · doi:10.1038/srep41827 · Cited by 10 · see citing works
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Cadherins in early neural development
Punovuori, K., Malaguti, M., & Lowell, S. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03815-9 · Cited by 39 · see citing works
Perez-Corredor, P., Vanderleest, T. E., Vacano, G. N., Sanchez, J. S., Villalba-Moreno, N. D., Marino, C., Krasemann, S., Mendivil-Perez, M. A., Aguillón, D., Jiménez-Del-Río, M., et al. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1373568 · Cited by 28 · see citing works
- Authors
- Yulis, M., Kusters, D. H. M., & Nusrat, A.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Nusrat, Asma
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2018-08-08
- Volume
- 596
- Issue
- 17
- Pages
- 3883-3898
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- PMC
- PMC6117591
- OpenAlex
- W2890788959
- Cited by
- 60
- References
- 80
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 8 · 2023: 13 · 2022: 9 · 2021: 6 · 2020: 3 · 2019: 8 · 2018: 2
- FWCI
- 0.69
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Deep Blue (University of Michigan) (submittedVersion)
- Funders
- Queen Mary, University of London (608765)
- National Institutes of Health (DK055679)
- Topics
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Connexins and lens biology
- Keywords
- cadherins, classical cadherins, desmosomal cadherins, atypical cadherin, cell adhesion, signal transduction, pemphigus vulgaris, desmosomes, apoptosis, cell proliferation, development (biology), disease pathobiology
- MeSH terms
- Animals, Cell Adhesion, Cell Differentiation, Humans, Neoplasms, Signal Transduction, Cadherins, Apoptosis
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