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Canonical WNT Signaling Promotes Osteogenesis by Directly Stimulating Runx2 Gene Expression
Open accessAbstract
Both activating and null mutations of proteins required for canonical WNT signaling have revealed the importance of this pathway for normal skeletal development. However, tissue-specific transcriptional mechanisms through which WNT signaling promotes the differentiation of bone-forming cells have yet to be identified. Here, we address the hypothesis that canonical WNT signaling and the bone-related transcription factor RUNX2/CBFA1/AML3 are functionally linked components of a pathway required for the onset of osteoblast differentiation. Our findings show that, in bone of the SFRP1 (secreted frizzled-related protein-1)-null mouse, which exhibits activated WNT signaling and a high bone mass phenotype, there is a significant increase in expression of T-cell factor (TCF)-1, Runx2, and the RUNX2 target gene osteocalcin. We demonstrate by mutational analysis that a functional TCF regulatory element responsive to canonical WNT signaling resides in the promoter of the Runx2 gene (-97 to -93). By chromatin immunoprecipitation, recruitment of beta-catenin and TCF1 to the endogenous Runx2 gene is shown. Coexpression of TCF1 with canonical WNT proteins resulted in a 2-5-fold activation of Runx2 promoter activity and a 7-8-fold induction of endogenous mRNA in mouse pluripotent mesenchymal and osteoprogenitor cells. This enhancement was abrogated by SFRP1. Taken together, our results provide evidence for direct regulation of Runx2 by canonical WNT signaling and suggest that Runx2 is a target of beta-catenin/TCF1 for the stimulation of bone formation. We propose that WNT/TCF1 signaling, like bone morphogenetic protein/transforming growth factor-beta signaling, activates Runx2 gene expression in mesenchymal cells for the control of osteoblast differentiation and skeletal development.
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“Many studies have demonstrated that β-catenin is required for bone formation and is activated during multiple stages of osteoblast differentiation to regulate both osteoblast and osteoclast.40–43”
From Bone remodeling: an operational process ensuring survival and bone mechanical competence (2022) · cites this paper as [43]
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The Wnt Signaling Pathway in Development and Disease
Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325
Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation
Ducy, P., Zhang, R., Geoffroy, V., Ridall, A. L., & Karsenty, G. (1997) · Cell · doi:10.1016/s0092-8674(00)80257-3 · Cited by 4,246
Komori, T., Yagi, H., Nomura, S., Yamaguchi, A., Sasaki, K., Deguchi, K., Shimizu, Y., Bronson, R. T., Gao, Y.-H., Inada, M., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80258-5 · Cited by 4,244
Otto, F., Thornell, A., Crompton, T., Denzel, A., Gilmour, K. C., Rosewell, I. R., Stamp, G., Beddington, R. S. P., Mundlos, S., Olsen, B. R., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80259-7 · Cited by 2,813
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development
Gong, Y., Slee, R. B., Fukai, N., Rawadi, G., Roman-Roman, S., Reginato, A. M., Wang, H., Cundy, T., Glorieux, F. H., Lev, D., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00571-2 · Cited by 2,235
Day, T. F., Guo, X., Garrett-Beal, L., & Yang, Y. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.03.016 · Cited by 1,616
High Bone Density Due to a Mutation in LDL-Receptor–Related Protein 5
Boyden, L. M., Mao, J., Belsky, J., Mitzner, L., Farhi, A., Mitnick, M. A., Wu, D., Insogna, K., & Lifton, R. P. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa013444 · Cited by 1,591
Secreted antagonists of the Wnt signalling pathway
Kawano, Y., & Kypta, R. (2003) · Journal of Cell Science · doi:10.1242/jcs.00623 · Cited by 1,584
Canonical wnt signaling in differentiated osteoblasts controls osteoclast differentiation.
Glass, D. A., Bialek, P., Ahn, J. D., Starbuck, M., Patel, M. S., Clevers, H., Taketo, M. M., Long, F., McMahon, A. P., Lang, R. A., et al. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.02.017 · Cited by 1,558
Antiretroviral-Drug Resistance among Patients Recently Infected with HIV
Little, S. J., Holte, S., Routy, J., Daar, E. S., Markowitz, M., Collier, A. C., Koup, R. A., Mellors, J. W., Connick, E., Conway, B., et al. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa013552 · Cited by 1,138
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Research works printed but not linked: 2
- Church, 2002, Int. J. Dev. Biol., 46, 927
- Hovanes, 2001, Nat. Genet., 28, 53
Cited by
Sorted by citations
Items 501–600 of 1,000
Gordon, A. C., Southam, L., Loughlin, J. A., Wilson, A. G., Stockley, I., Hamer, A. J., Eastell, R., & Wilkinson, J. M. (2007) · Journal of Orthopaedic Research® · doi:10.1002/jor.20446 · Cited by 36
Regulation of Breast Cancer-induced Bone Lesions by β-Catenin Protein Signaling
Chen, Y., Shi, H. Y., Stock, S. R., Stern, P. H., & Zhang, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.294595 · Cited by 35
Celecoxib inhibits osteoblast maturation by suppressing the expression of Wnt target genes
Nagano, A., Arioka, M., Takahashi‐Yanaga, F., Matsuzaki, E., & Sasaguri, T. (2016) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2016.11.003 · Cited by 35
The effect of parathyroid hormone on osteogenesis is mediated partly by osteolectin
Zhang, J., Cohen, A., Shen, B., Du, L., Tasdogan, A., Zhao, Z., Shane, E. J., & Morrison, S. J. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2026176118 · Cited by 35
The microRNA expression profiles of mouse mesenchymal stem cell during chondrogenic differentiation
Yang, B., Guo, H., Zhang, Y., Dong, S.-W., & Ying, D. (2011) · BMB Reports · doi:10.5483/bmbrep.2011.44.1.28 · Cited by 35
Sclerostin: From Molecule to Clinical Biomarker
Omran, A. S., Atanasova, D., Landgren, F., & Magnusson, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094751 · Cited by 44
The Contribution of Wnt Signaling to Vascular Complications in Type 2 Diabetes Mellitus
la Torre, R. S.-D., García‐Fontana, C., González-Salvatierra, S., Andújar-Vera, F., Martínez-Heredia, L., García-Fontana, B., & Muñoz‐Torres, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23136995 · Cited by 34
Gordeladze, J. O., Djouad, F., Brondello, J., Noël, D., Duroux-Richard, I., Apparailly, F., & Jørgensen, C. (2009) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.143 · Cited by 36
Tai, P. W. L., Wu, H., Gordon, J. A. R., Whitfield, T. W., Barutcu, A. R., van Wijnen, A. J., Lian, J. B., Stein, G. S., & Stein, J. L. (2014) · Gene · doi:10.1016/j.gene.2014.05.044 · Cited by 34
Self-citationBhattacharyya, S., Pal, S., & Chattopadhyay, N. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.02.028 · Cited by 34
Jiang, T., Zhou, B., Huang, L., Wu, H., Huang, J., Liang, T., Liu, H., Zheng, L. X., & Zhao, J. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000430196 · Cited by 34
Chu, T., Teng, J., Jiang, L., Zhong, H., & Han, B. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.12.076 · Cited by 34
Tsai, H.-L., Deng, W.-P., Lai, W. T., Chiu, W., Yang, C.-B., Tsai, Y., Hwang, S., & Renshaw, P. F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104937 · Cited by 33
Ali, D., Hamam, R., Al-Fayez, M., Kassem, M. S., Aldahmash, A. M., & Alajez, N. M. (2016) · Stem Cells Translational Medicine · doi:10.5966/sctm.2015-0331 · Cited by 34
Li, J., Zeng, Z., Zhao, Y., Jing, D., Tang, C., Ding, Y., & Feng, X. (2017) · Scientific Reports · doi:10.1038/s41598-017-11090-7 · Cited by 34
Wang, Y., Pan, J., Zhang, Y., Li, X., Zhang, Z., Wang, P., Qin, Z., & Li, J. (2018) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbm.b.34105 · Cited by 34
Comparative ontogeny and phylogeny of the upper jaw skeleton in amniotes
Richman, J. M., Buchtová, M., & Boughner, J. C. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20716 · Cited by 34
Protein Kinase Cα (PKCα) Regulates Bone Architecture and Osteoblast Activity
Galea, G. L., Meakin, L. B., Williams, C. M., Hulin-Curtis, S. L., Lanyon, L. E., Poole, A. W., & Price, J. S. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.580365 · Cited by 32
Context Clues: The Importance of Stem Cell–Material Interactions
Khalil, A. S., Xie, A. W., & Murphy, W. L. (2013) · ACS Chemical Biology · doi:10.1021/cb400801m · Cited by 33
Nantavisai, S., Pisitkun, T., Osathanon, T., Pavasant, P., Kalpravidh, C., Dhitavat, S., Makjaroen, J., & Sawangmake, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-77656-0 · Cited by 33
Wnt5a attenuates Wnt3a-induced alkaline phosphatase expression in dental follicle cells
Sakisaka, Y., Tsuchiya, M., Nakamura, T., Tamura, M., Shimauchi, H., & Nemoto, E. (2015) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.06.013 · Cited by 34
Integrative physiology of the aging bone: insights from animal and cellular models
Syed, F. A., & Hoey, K. A. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05813.x · Cited by 33
Brun, J., Fromigué, O., Dieudonné, F., Marty, C., Chen, J., Dahan, J., Yu, W., & Marie, P. J. (2012) · Bone · doi:10.1016/j.bone.2012.11.020 · Cited by 34
Pakvasa, M., Alverdy, A., Mostafa, S., Wang, E., Fu, L., Li, A., Oliveira, L., Athiviraham, A., Lee, M. J., Wolf, J. M., et al. (2017) · Genes & Diseases · doi:10.1016/j.gendis.2017.07.006 · Cited by 33
Boning up on glypicans—opportunities for new insights into bone biology
Dwivedi, P. P., Lam, N. N., & Powell, B. C. (2013) · Cell Biochemistry and Function · doi:10.1002/cbf.2939 · Cited by 34
Gao, W., Zhang, H., Chang, G., Xie, Z.-Q., Wang, H., Ma, L., Han, Z., Li, Q., & Pang, T. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356661 · Cited by 32
Zhou, Y., Li, J., Zhou, K., Liao, X., Zhou, X., & Shen, K. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28638 · Cited by 33
Potential Biomarkers to Improve the Prediction of Osteoporotic Fractures
Kim, B., Lee, S. H., & Koh, J. (2020) · Endocrinology and Metabolism · doi:10.3803/enm.2020.35.1.55 · Cited by 34
Loss of chemerin triggers bone remodeling in vivo and in vitro
Han, L., Zhang, Y., Wan, S., Wei, Q., Shang, W.-B., Huang, G., Fang, P., & Min, W. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101322 · Cited by 33
Hwang, J., Cha, P.-H., Han, G., Bách, T. T., Min, D. S., & Choi, K. (2015) · Experimental & Molecular Medicine · doi:10.1038/emm.2014.115 · Cited by 32
Viale-Bouroncle, S., Klingelhöffer, C., Ettl, T., Reichert, T. E., & Morsczeck, C. O. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.12.008 · Cited by 32
Prostaglandin E2 modulates components of the Wnt signaling system in bone and prostate cancer cells
Liu, X., Kirschenbaum, A. M., Weinstein, B. M., Zaidi, M., Shen, Y., & Levine, A. C. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.03.057 · Cited by 32
Choi, J. Y., Lai, J. K., Xiong, Z., Ren, M., Moorer, M. C., Stains, J. P., & Cao, K. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3549 · Cited by 34
Sun, T., Liu, M., Yao, S., Ji, Y., Xiong, Z., Tang, K., Chen, K., Yang, H., & Guo, X. (2018) · Tissue Engineering Part A · doi:10.1089/ten.tea.2017.0398 · Cited by 31
The Role of Wnt/β-Catenin Pathway Mediators in Aortic Valve Stenosis
Khan, K., Yu, B., Kiwan, C. M., Shalal, Y., Filimon, S., Cipro, M., Shum‐Tim, D., Cecere, R., & Schwertani, A. G. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00862 · Cited by 31
Kwak, J., Zara, J. N., Chiang, M., Ngo, R., Shen, J., James, A. W., Le, K. M., Moon, C., Zhang, X., Gou, Z., et al. (2012) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0042 · Cited by 31
Curculigoside Improves Osteogenesis of Human Amniotic Fluid-Derived Stem Cells
Liu, M., Li, Y., & Yang, S. (2013) · Stem Cells and Development · doi:10.1089/scd.2013.0261 · Cited by 31
Dentin Dysplasia in Notum Knockout Mice
Vogel, P., Read, R. W., Hansen, G. M., Powell, D. R., Kantaputra, P. N., Zambrowicz, B., & Brommage, R. (2016) · Veterinary Pathology · doi:10.1177/0300985815626778 · Cited by 31
Rutledge, K., & Cheng, Q. (2016) · Journal of Nanomedicine & Nanotechnology · doi:10.4172/2157-7439.1000350 · Cited by 31
A Reciprocal Interaction between β-Catenin and Osterix in Cementogenesis
Choi, H., Kim, T.-H., Yang, S., Lee, J., You, H., & Cho, E. (2017) · Scientific Reports · doi:10.1038/s41598-017-08607-5 · Cited by 31
Zhao, X., Chen, J.-J., Zhang, G., Wang, Y.-C., Si, S.-Y., Chen, L., & Wang, Z. (2017) · Scientific Reports · doi:10.1038/s41598-017-10929-3 · Cited by 32
Differentiation of osteoblasts: the links between essential transcription factors
Khotib, J., Marhaeny, H. D., Miatmoko, A., Budiatin, A. S., Ardianto, C., Rahmadi, M., Pratama, Y. A., & Tahir, M. (2022) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2022.2148749 · Cited by 30
β-Catenin: A Key Molecule in Osteoblast Differentiation
Wróbel, E., Wojdasiewicz, P., Mikulska, A., & Szukiewicz, D. (2025) · Biomolecules · doi:10.3390/biom15071043 · Cited by 33
Chiu, R., Smith, K. E., Gene, K. A., Ma, T., Smith, R. L., & Goodman, S. B. (2009) · Journal of Orthopaedic Research® · doi:10.1002/jor.21035 · Cited by 30
Stemistry: The Control of Stem Cells in Situ Using Chemistry
Davies, S. G., Kennewell, P. D., Russell, A. J., Seden, P. T., Westwood, R., & Wynne, G. M. (2015) · Journal of Medicinal Chemistry · doi:10.1021/jm500838d · Cited by 32
Low-dose PTH increases osteoblast activity via decreased Mef2c/Sost in senescent osteopenic mice
Saidak, Z., Hénaff, C. L., Azzi, S., Marty, C., & Marie, P. J. (2014) · Journal of Endocrinology · doi:10.1530/joe-14-0249 · Cited by 30
Parathyroid Hormone-Related Protein Analogs as Osteoporosis Therapies
Esbrit, P., Herrera, S., Portal‐Núñez, S., Nogués, X., & Díez‐Pérez, A. (2015) · Calcified Tissue International · doi:10.1007/s00223-015-0050-1 · Cited by 30
Liou, S., Hsu, J., Chu, H., Lin, H., Chen, I., & Yeh, J. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24904 · Cited by 30
Zhang, X., Chen, Q., Liu, J., Fan, C., Wei, Q., Chen, Z., & Mao, X. (2017) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2017.0023 · Cited by 30
MicroRNA-146a knockdown suppresses the progression of ankylosing spondylitis by targeting dickkopf 1
Di, G., Kong, L., Zhao, Q., & Ding, T. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.11.067 · Cited by 30
The Interplay of WNT and PPARγ Signaling in Vascular Calcification
Reinhold, S., Blankesteijn, W. M., & Foulquier, S. (2020) · Cells · doi:10.3390/cells9122658 · Cited by 30
Salehi, A. R., Mobarhan, M. A., Mohammadi, J., Shahsavarani, H., Shokrgozar, M. A., & Alipour, A. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.30239 · Cited by 31
Bone formation and bone repair: The roles and crosstalk of osteoinductive signaling pathways
Jing, Z., Liang, Z., Yang, L., Du, W., Yu, T., Tang, H., Li, C., & Wei, W. (2022) · Process Biochemistry · doi:10.1016/j.procbio.2022.04.033 · Cited by 30
Biglycan mediates suture expansion osteogenesis via potentiation of Wnt/β-catenin signaling
Wang, H., Sun, W. S., Ma, J., Pan, Y., Wang, L., & Zhang, W. (2014) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2014.12.032 · Cited by 30
Staines, K. A., Prideaux, M., Allen, S., Buttle, D. J., Pitsillides, A. A., & Farquharson, C. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25282 · Cited by 30
Tanshinol Rescues the Impaired Bone Formation Elicited by Glucocorticoid Involved in KLF15 Pathway
Yang, Y., Su, Y., Wang, D., Chen, Y., Liu, Y., Luo, S., Wu, T., & Liao, C. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/1092746 · Cited by 30
Role of osteoblast suppression in multiple myeloma
Stewart, P., & Shaughnessy, J. D. (2006) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20774 · Cited by 31
Sato, M., Saitoh, I., Kiyokawa, Y., Iwase, Y., Kubota, N., Ibano, N., Noguchi, H., Yamasaki, Y., & Inada, E. (2021) · Cells · doi:10.3390/cells10123338 · Cited by 29
Sonomechanobiology: Vibrational stimulation of cells and its therapeutic implications
Ambattu, L. A., & Yeo, L. Y. (2023) · Biophysics Reviews · doi:10.1063/5.0127122 · Cited by 31
Xu, X., Shan, M., Chu, C., Bie, S., Wang, H., & Cai, S. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.131440 · Cited by 29
INO80 is Required for Osteogenic Differentiation of Human Mesenchymal Stem Cells
Zhou, C., Zou, J., Zou, S., & Li, X. (2016) · Scientific Reports · doi:10.1038/srep35924 · Cited by 29
Oh, Y., Ahn, C., & Je, J. (2020) · Marine Drugs · doi:10.3390/md18100510 · Cited by 29
Wnt7a promotes the osteogenic differentiation of human mesenchymal stem cells
Yang, L., Li, Q., Zhang, J., Li, P., An, P., Wang, C., Hu, P., Zou, X., Dou, X., & Zhu, L. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.4927 · Cited by 29
Saraswati, S., Deskins, D. L., Holt, G. E., & Young, P. P. (2012) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2012.00767.x · Cited by 29
Pulsed electromagnetic fields inhibit bone loss in streptozotocin-induced diabetic rats
Zhou, J. M., Li, X., Liao, Y., Feng, W., Fu, C., & Guo, X. (2014) · Endocrine · doi:10.1007/s12020-014-0439-z · Cited by 29
Galindo, M. A., Kahler, R. A., Teplyuk, N. M., Stein, J. L., Lian, J. B., Stein, G. S., Westendorf, J. J., & van Wijnen, A. J. (2007) · Journal of Molecular Histology · doi:10.1007/s10735-007-9143-0 · Cited by 29
Self-citationEffects of hyperbaric oxygen on the osteogenic differentiation of mesenchymal stem cells
Lin, S., Ueng, S. W., Niu, C., Yuan, L., Yang, C.-Y., Chen, W., Lee, M. S.-S., & Chen, J. (2014) · BMC Musculoskeletal Disorders · doi:10.1186/1471-2474-15-56 · Cited by 29
Cross-talk between NR4A orphan nuclear receptors and β-catenin signaling pathway in osteoblasts
Rajalin, A.-M., & Aarnisalo, P. (2011) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2011.02.018 · Cited by 30
Yokose, S., & Naka, T. (2010) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-010-0185-0 · Cited by 29
Kim, D., Kim, J.-W., Hyun, H., Kim, K., & Roh, S. (2014) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2014.04.014 · Cited by 29
Puerarin promotes osteogenesis and inhibits adipogenesis in vitro
Wang, N., Wang, X., Cheng, W., Cao, H., Zhang, P., & Qin, L. (2013) · Chinese Medicine · doi:10.1186/1749-8546-8-17 · Cited by 29
Aslani, S., Abhari, A., Sakhinia, E., Sanajou, D., Rajabi, H., & Rahimzadeh, S. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27582 · Cited by 29
Pérez‐García, S., Carrión, M., Villanueva‐Romero, R., Hermida‐Gómez, T., Fernández-Moreno, M., Mellado, M., Blanco, F. J., Juarranz, Y., & Gomariz, R. P. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14283 · Cited by 29
Matsubayashi, S., Nakashima, M., Kumagai, K., Egashira, M., Naruke, Y., Kondo, H., Hayashi, T., & Shindo, H. (2009) · Pathology - Research and Practice · doi:10.1016/j.prp.2009.02.011 · Cited by 29
Prashar, P., Yadav, P. S., Samarjeet, F., & Bandyopadhyay, A. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.02.015 · Cited by 28
Liu, H., Peng, F., Liu, Z., Jiang, F., Li, L., Gao, S., Wang, G., Song, J., Ruan, E., Shao, Z., et al. (2016) · International Journal of Oncology · doi:10.3892/ijo.2016.3815 · Cited by 28
Hosaka, C., Kunisada, M., Koyanagi‐Aoi, M., Masaki, T., Takemori, C., Taniguchi‐Ikeda, M., Aoi, T., & Nishigori, C. (2019) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12779 · Cited by 28
Tsou, P., Palisoc, P. J., Ali, M. M., Khanna, D., & Sawalha, A. H. (2021) · Arthritis & Rheumatology · doi:10.1002/art.41694 · Cited by 27
Park, K.-R., Kim, S., Cho, M., & Yun, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052483 · Cited by 29
Poleboina, S., Sheth, V. G., Sharma, N., Sihota, P., Kumar, N., & Tikoo, K. (2022) · Nanomedicine · doi:10.2217/nnm-2021-0401 · Cited by 28
Fu, T., Liu, Y., Huang, X., Guo, Y., Shen, J., & Shen, H. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02979-w · Cited by 28
AlMuraikhi, N. A., Binhamdan, S., Alaskar, H., Alotaibi, A., Tareen, S., Manikandan, M., & Alfayez, M. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087164 · Cited by 32
MicroRNA-24 Regulates Osteogenic Differentiation via Targeting T-Cell Factor-1
Zhao, W., Wu, C., Dong, Y., Ma, Y., Jin, Y., & Ji, Y. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160511699 · Cited by 30
Михайлович, Г. П., Gershovich, J. G., Zhambalova, A. P., Romanov, Y. A., & Buravkova, L. B. (2011) · Acta Astronautica · doi:10.1016/j.actaastro.2011.07.028 · Cited by 28
Yun, S., Yoon, H., & Chung, Y. (2009) · APOPTOSIS · doi:10.1007/s10495-009-0348-4 · Cited by 28
Liu, N., Gu, B., Liu, N., Nie, X., Zhang, B., Zhou, X., & Deng, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093364 · Cited by 28
Gao, H., Zhai, M., Wang, P., Zhang, X., Cai, J., Chen, X., Shen, G., Luo, E., & Jing, D. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.6608 · Cited by 28
Jing, D., Yan, Z., Cai, J., Tong, S., Li, X., Guo, Z., & Luo, E. (2017) · Bone · doi:10.1016/j.bone.2017.10.001 · Cited by 28
Simão, M., Camacho, A., Ostertag, A., Cohen-Solal, M., Pinto, I. J., Porto, G., Hang-Korng, E., & Cancela, M. L. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207441 · Cited by 32
Pulik, Ł., Mierzejewski, B., Ciemerych, M. A., Brzóska, E., & Łęgosz, P. (2020) · Cells · doi:10.3390/cells9061324 · Cited by 28
Babo, P. S., Santo, V. E., Gomes, M. E., & Reis, R. L. (2016) · Macromolecular Bioscience · doi:10.1002/mabi.201600141 · Cited by 27
Kim, G.-J., Kim, D. J., Lee, K.-J., Kim, D., Chung, K., Choi, J., & An, J. H. (2020) · Nanomaterials · doi:10.3390/nano10020230 · Cited by 28
MACF1 promotes osteoblast differentiation by sequestering repressors in cytoplasm
Hu, L., Yin, C., Chen, D., Wu, Z., Liang, S., Zhang, Y., Huang, Z., Liu, S., Xu, X., Chen, Z., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-021-00744-9 · Cited by 28
de Castro, L. F., Sworder, B. J., Mui, B. W. H., Futrega, K., Berendsen, A. D., Phillips, M. D., Burbach, N. J., Cherman, N., Kuznetsov, S. A., Gabet, Y., et al. (2021) · Bone Research · doi:10.1038/s41413-021-00169-7 · Cited by 27
Dargoush, S. A., Hanaee‐Ahvaz, H., Irani, S., Soleimani, M., Khatami, S. M., & Sohi, A. N. (2022) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.3297 · Cited by 27
Wincent, E., Stegeman, J. J., & Jönsson, M. E. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.02.014 · Cited by 26
Xin, H., Xin, F., Zhou, S., & Guan, S. (2013) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2013.1242 · Cited by 27
McCarthy, T. L. (2011) · Steroids · doi:10.1016/j.steroids.2011.10.016 · Cited by 28
Shen, J., Chen, X., Jia, H., Meyers, C. A., Shrestha, S., Asatrian, G., Ding, C., Tsuei, R., Zhang, X., Péault, B., et al. (2017) · Tissue Engineering Part A · doi:10.1089/ten.tea.2016.0387 · Cited by 29
Tao, W., Ayala-Haedo, J., Field, M. G., Pelaez, D., & Wester, S. T. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-22237 · Cited by 27
Metadata
- Authors
- Gaur, T., Lengner, C. J., Hovhannisyan, H., Bhat, R. A., Bodine, P. V. N., Komm, B. S., Javed, A., van Wijnen, A. J., Stein, J. L., Stein, G. S., & Lian, J. B.
- Affiliations
- University of Massachusetts Chan Medical School (US)
- Wyeth (US)
- Corresponding author
- Lian, Jane B.
- ORCID
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2005-09
- Volume
- 280
- Issue
- 39
- Pages
- 33132-33140
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2153720415
- Cited by
- 1,170
- References
- 70
- Citations by year
- 2026: 32 · 2025: 40 · 2024: 43 · 2023: 46 · 2022: 64 · 2021: 80 · 2020: 96 · 2019: 68 · 2018: 56 · 2017: 73 · 2016: 65 · 2015: 74 · 2014: 57 · 2013: 67 · 2012: 55
- FWCI
- 13.80
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK032520, P30-DK32520)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR049069, P01 AR 48818, P01AR048818, AR 39588, R01AR039588)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- Wnt/β-catenin signaling, Runx2, bone formation, osteogenic differentiation, SFRP1, TCF1, β-catenin, osteocalcin, skeletal development, mesenchymal cells, osteoprogenitor cells
- MeSH terms
- Secreted Frizzled-Related Proteins, Animals, Cell Differentiation, Cells, Cultured, Fibroblasts, Membrane Proteins, Mice, Transgenic, Models, Biological, Osteoblasts, Osteogenesis, Promoter Regions, Genetic, RNA, Messenger, Signal Transduction, Gene Expression Regulation, Developmental, Intercellular Signaling Peptides and Proteins, Chromatin Immunoprecipitation, Core Binding Factor Alpha 1 Subunit, Mice, Hepatocyte Nuclear Factor 1-alpha, Mesenchymal Stem Cells
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