The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
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 601–700 of 1,000
Shang, Z., Li, X., Sun, H. Q., Xiao, G.-N., Wang, C., & Gong, Q. (2014) · International Journal of Oral Science · doi:10.1038/ijos.2014.2 · Cited by 26
Kook, S., Heo, J. S., & Lee, J. (2015) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-015-2329-y · Cited by 25
Fan, H.-L., Ji, F., Lin, Y., Zhang, M.-L., QIN, W., Zhou, Q., & WU, Q. (2016) · Molecular Medicine Reports · doi:10.3892/mmr.2016.4849 · Cited by 26
A single gene connects stiffness in glaucoma and the vascular system
Borrás, T. (2016) · Experimental Eye Research · doi:10.1016/j.exer.2016.08.022 · Cited by 26
TIMP Loss Activates Metalloproteinase-TNFα-DKK1 Axis To Compromise Wnt Signaling and Bone Mass
Chen, Y., Aiken, A., Saw, S., Weiss, A., Fang, H., & Khokha, R. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3585 · Cited by 27
Functional Effects of WNT10A Rare Variants Associated with Tooth Agenesis
Zeng, Y. F., Baugh, E. H., Akyalçın, S., & Letra, A. (2020) · Journal of Dental Research · doi:10.1177/0022034520962728 · Cited by 26
Cheng, B., Feng, X., Gao, Y., Jian, S.-Q., Liu, S.-R., Wang, M., Xie, Y.-F., Wang, L., Feng, Z., & Yang, H. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.657953 · Cited by 26
Park, K.-R., Park, J. E., Kim, B., Kwon, I. K., Hong, J. T., & Yun, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111362 · Cited by 27
Piezo protein determines stem cell fate by transmitting mechanical signals
Qiu, X., Deng, Z., Wang, M., Feng, Y., Bi, L., & Li, L. (2022) · Human Cell · doi:10.1007/s13577-022-00853-8 · Cited by 26
Xu, Y., Wu, C., Wu, Y. R., Tong, P., Jin, H., Yu, N., & Xiao, L. (2012) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-012-1294-2 · Cited by 26
Stable Genetic Alterations of β-Catenin and ROR2 Regulate the Wnt Pathway, Affect the Fate of MSCs
Cai, S., Liu, A., He, H., Chen, Q., Yang, Y., Guo, F., Huang, Y., Liu, L., & Qiu, H. (2013) · Journal of Cellular Physiology · doi:10.1002/jcp.24500 · Cited by 26
Pustylnik, S., Fiorino, C., Nabavi, N., Zappitelli, T., da Silva, R., Aubin, J. E., & Harrison, R. E. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.481515 · Cited by 25
Cao, Z., Fu, Y., Sun, X., Zhang, Q., Xu, F., & Li, Y. (2016) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2015.11.023 · Cited by 26
Määttä, J. A., Bendre, A., Laanti, M., Büki, K. G., Rantakari, P., Tervola, P., Saarimäki, J., POUTANEN, M. H., Härkönen, P. L., & Väänänen, K. (2016) · BoneKEy Reports · doi:10.1038/bonekey.2016.14 · Cited by 26
Carr, F. E., Tai, P. W. L., Barnum, M. S., Gillis, N. E., Evans, K. G., Taber, T. H., White, J. H., Tomczak, J. A., Jaworski, D. M., Zaidi, S. K., et al. (2016) · Endocrinology · doi:10.1210/en.2015-2046 · Cited by 26
Self-citationClough, B. H., Ylöstalo, J., Browder, E., McNeill, E. P., Bartosh, T. J., Rawls, H. R., Nakamoto, T., & Gregory, C. A. (2016) · Calcified Tissue International · doi:10.1007/s00223-016-0215-6 · Cited by 26
Liang, G., Liu, N., He, M., Yang, J., Liang, Z., Gao, X., Rahhal, A. H., He, Q., Zhang, H., & Zha, Z. (2017) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26260 · Cited by 26
Voriconazole-induced periostitis: a new rheumatic disorder
Adwan, M. H. (2016) · Clinical Rheumatology · doi:10.1007/s10067-016-3341-7 · Cited by 26
Ma, X., Bian, Y., Yuan, H., Chen, N., Pan, Y., Zhou, W., Gao, S., Du, X. Z., Hao, S., Yan, Z., et al. (2020) · Aging · doi:10.18632/aging.103277 · Cited by 25
A mechano-chemo-biological model for bone remodeling with a new mechano-chemo-transduction approach
Ashrafi, M., Gubaua, J. E., Pereira, J. T., Gahlichi, F., & Doblaré, M. (2020) · Biomechanics and Modeling in Mechanobiology · doi:10.1007/s10237-020-01353-0 · Cited by 25
Melnik, S., Gabler, J., Dreher, S. I., Hecht, N., Hofmann, N., Grossner, T. L., & Richter, W. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-02026-6 · Cited by 26
Qin, Z., Li, Y., Li, J., Jiang, L., Zhang, Z., Chang, K., Yang, Q., Chen, S., Liao, R., & Su, B. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5195 · Cited by 25
Xu, K., Zhang, L., Yu, N., Ren, Z., Wang, T., Zhang, Y., Zhao, X., & Yu, T. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03324-5 · Cited by 25
Higher-intensity ultrasound accelerates fracture healing via mechanosensitive ion channel Piezo1
Inoue, S., Li, C., Hatakeyama, J., Jiang, H., Kuroki, H., & Moriyama, H. (2023) · Bone · doi:10.1016/j.bone.2023.116916 · Cited by 25
Fleischhacker, V., Milosic, F., Bricelj, M., Kührer, K., Wahl‐Figlash, K., Heimel, P., Diendorfer, A. B., Nardini, E., Fischer, I., Stangl, H., et al. (2024) · Aging Cell · doi:10.1111/acel.14139 · Cited by 23
The Effects of Myocilin Expression on Functionally Relevant Trabecular Meshwork Genes: A Mini-Review
Borrás, T. (2014) · Journal of Ocular Pharmacology and Therapeutics · doi:10.1089/jop.2013.0218 · Cited by 25
Cecchinato, F., Karlsson, J. E., Ferroni, L., Gardin, C., Galli, S., Wennerberg, A., Zavan, B., Andersson, M., & Jimbo, R. (2015) · Materials Science and Engineering C · doi:10.1016/j.msec.2015.03.026 · Cited by 25
Tsai, P., Chien, Y., Chuang, J.-H., Chou, S., Chien, C.-H., Lai, Y.-H., Li, H.-Y., Ko, Y.-L., Chang, Y.-L., Wang, C.-Y., et al. (2015) · Stem Cells and Development · doi:10.1089/scd.2015.0066 · Cited by 25
Kerkhofs, J., Leijten, J., Bolander, J., Luyten, F. P., Post, J. N., & Geris, L. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162052 · Cited by 24
The Proteasome and Myeloma-Associated Bone Disease
Accardi, F., Toscani, D., Costa, F., Aversa, F., & Giuliani, N. (2017) · Calcified Tissue International · doi:10.1007/s00223-017-0349-1 · Cited by 25
Lin, S., Ueng, S. W., Niu, C., Yuan, L., Yang, C.-Y., Chen, W., Lee, M. S.-S., & Chen, J. (2013) · Stem Cell Research · doi:10.1016/j.scr.2013.10.007 · Cited by 25
Effects of Eclipta prostrata on gut microbiota of SAMP6 mice with osteoporosis
Zhao, X., Ai, J.-Q., Mao, H., & Gao, X. (2019) · Journal of Medical Microbiology · doi:10.1099/jmm.0.000936 · Cited by 26
Effects of Nel-like molecule-1 and bone morphogenetic protein 2 combination on rat pulp repair
Wu, J., Wang, Q., Han, Q., Zhu, H., Li, M., Fang, Y., & Wang, X. (2019) · Journal of Molecular Histology · doi:10.1007/s10735-019-09822-2 · Cited by 24
Hou, W., Fu, H. E., Liu, X., Duan, K., Lu, X., Lu, M., Sun, T., Guo, T., & Weng, J. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.9b01237 · Cited by 24
GATA4 regulates mesenchymal stem cells via direct transcriptional regulation of the WNT signalosome
Khalid, A. B., Pence, J. C., Suthon, S., Lin, J., Miranda‐Carboni, G. A., & Krum, S. A. (2020) · Bone · doi:10.1016/j.bone.2020.115819 · Cited by 24
At the nuclear envelope of bone mechanobiology
Birks, S., & Uzer, G. (2021) · Bone · doi:10.1016/j.bone.2021.116023 · Cited by 22
Choi, B. B. R., Choi, J., Kang, T.-H., Lee, S.-J., & Kim, G. (2021) · Biomedicines · doi:10.3390/biomedicines9111542 · Cited by 24
Cho, Y., Bae, H., Lee, D., Yoon, W., Woo, K. M., Baek, J., Lee, G., Park, J., Ku, Y., & Ryoo, H. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25183 · Cited by 24
Mahl, C., Egea, V., Megens, R. T. A., Pitsch, T., Santovito, D., Weber, C., & Ries, C. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2054-4 · Cited by 24
Kazantseva, J., Kivil, A., Tints, K., Kazantseva, A., Neuman, T., & Palm, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074799 · Cited by 24
Isolation and characterization of multipotent mesenchymal stem cells in nasal polyps
Cho, J.-S., Park, J., Kang, J.-H., Kim, S. E., Park, I., & Lee, H.-M. (2014) · Experimental Biology and Medicine · doi:10.1177/1535370214553898 · Cited by 24
Wnt/β-catenin signaling is required for distraction osteogenesis in rats
Wang, X., Luo, E., Bi, R., Ye, B., Hu, J., & Zou, S. (2017) · Connective Tissue Research · doi:10.1080/03008207.2017.1300154 · Cited by 24
Kato, T., Khánh, V. C., Sato, K., Kimura, K., Yamashita, T., Sugaya, H., Yoshioka, T., Mishima, H., & Ohneda, O. (2017) · Stem Cells and Development · doi:10.1089/scd.2017.0199 · Cited by 24
Diao, Y., Chen, B., Wei, L., & Wang, Z. (2018) · Scientific Reports · doi:10.1038/s41598-018-30992-8 · Cited by 24
The Rho GTPase RAC1 in Osteoblasts Controls Their Function
Huck, K., Sens, C., Würfel, C., Zoeller, C., & Nakchbandi, I. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020385 · Cited by 24
Gao, Q., Hou, Y., Li, Z., Hu, J., Huo, D., Zheng, H., Zhang, J., Yao, X., Gao, R., Wu, X., et al. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16672 · Cited by 24
Cruzat, F., Henríquez, B., Villagra, A., Hepp, M. I., Lian, J. B., van Wijnen, A. J., Stein, J. L., Imbalzano, A. N., Stein, G. S., & Montecino, M. A. (2009) · Biochemistry · doi:10.1021/bi9004792 · Cited by 24
Self-citationAminova, L. R., & Wilson, B. A. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.00975.x · Cited by 23
Wang, Y., Wu, M.-H., Cheung, M. P. L., Sham, M. H., Akiyama, H., Chan, D., Cheah, K. S. E., & Cheung, M. C. H. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.04.018 · Cited by 24
The Roles of Long Non-Protein-Coding RNAs in Osteo-Adipogenic Lineage Commitment
Yoshioka, H., & Yoshiko, Y. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061236 · Cited by 23
Park, K.-R., Leem, H. H., Cho, M., Kang, S. W., & Yun, H. (2020) · Phytomedicine · doi:10.1016/j.phymed.2020.153347 · Cited by 22
Nanoparticle-mediated selective Sfrp-1 silencing enhances bone density in osteoporotic mice
García‐García, P., Reyes, R., García‐Sánchez, D., Pérez-Campo, F. M., Rodríguez-Rey, J. C., Évora, C., Díaz‐Rodríguez, P., & Delgado, A. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01674-5 · Cited by 23
Sukarawan, W., Rattanawarawipa, P., Yaemkleebbua, K., Nowwarote, N., Pavasant, P., Limjeerajarus, C. N., & Osathanon, T. (2023) · International Endodontic Journal · doi:10.1111/iej.13888 · Cited by 23
Medina, M. A., Ugarte, G. D., Vargas, M. F., Ávila, M. E., Ñecuñir, D., Elorza, Á. A., Gutierrez, S. E., & Ferrari, G. V. D. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25258 · Cited by 23
Wang, Z., Chen, H., Yu, Y., Zhang, J., Cheuk, K. Y., Ng, B. K. W., Qiu, Y., Guo, X., Cheng, J. C. Y., & Lee, W. (2017) · Scientific Reports · doi:10.1038/srep40265 · Cited by 23
Liu, W., Saelens, W., Rainer, P. Y., Biočanin, M., Gardeux, V., Gralak, A. J., van Mierlo, G., Gebhart, A., Russeil, J., Liu, T., et al. (2025) · Nature Genetics · doi:10.1038/s41588-025-02343-7 · Cited by 26
Bone Anabolic Agents for the Treatment of Multiple Myeloma
Vallet, S., & Raje, N. S. (2011) · Cancer Microenvironment · doi:10.1007/s12307-011-0090-7 · Cited by 22
Man, X., Yang, L., Liu, S., Yang, L., Li, M., & Fu, Q. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10125 · Cited by 24
Isopsoralen ameliorates H2O2‑induced damage in osteoblasts via activating the Wnt/β‑catenin pathway
Li, Y., Wu, B., Liang, J., & Li, F. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.7741 · Cited by 23
Arroyo, R., López, S., Romo, E., Montoya, G. A., Hoz, L., Pedraza, C., Garfias, Y., & Arzate, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041307 · Cited by 23
TRPM8 Channel Promotes the Osteogenic Differentiation in Human Bone Marrow Mesenchymal Stem Cells
Henao, J. C., Grismaldo, A., Barreto, A., Rodríguez-Pardo, V. M., Mejía-Cruz, C. C., Leal-García, E., Pérez-Núñez, R., Rojas, P., Latorre, R., Carvacho, I., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.592946 · Cited by 22
KPT-330 Prevents Aortic Valve Calcification via a Novel C/EBPβ Signaling Pathway
Dutta, P., Kodigepalli, K. M., LaHaye, S., Thompson, J. W., Rains, S., Nagel, C., Thatcher, K., Hinton, R. B., & Lincoln, J. (2021) · Circulation Research · doi:10.1161/circresaha.120.318503 · Cited by 24
p85α Regulates Osteoblast Differentiation by Cross-talking with the MAPK Pathway
Wu, X., Shi, C., Orlando, S. A., Yuan, J., Kim, E. T., Munugalavadla, V., Mali, R. S., Kapur, R., & Yang, F. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.187351 · Cited by 22
Transcription Factors in Craniofacial Development
Gou, Y., Zhang, T., & Xu, J. (2015) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2015.07.009 · Cited by 24
Dong, P., Zhu, D., Deng, X., Zhang, Y., Ma, J., Sun, X., & Liu, Y. (2018) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36541 · Cited by 22
Hosseini, F. S., Soleimanifar, F., Khojasteh, A., & Ardeshirylajimi, A. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27921 · Cited by 22
Sweeney, K., Cameron, E. R., & Blyth, K. (2020) · PubMed · doi:10.14348/molcells.2019.0310 · Cited by 25
Park, K., Lee, H., Cho, M., & Yun, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103700 · Cited by 22
Long-term effects of tripeptide Ile-Pro-Pro on osteoblast differentiation in vitro
Huttunen, M. M., Pekkinen, M., Ahlström, M., & Lamberg-Allardt, C. J. E. (2008) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2007.09.006 · Cited by 22
Liu, F.-L., Chen, C., Lee, C.-C., Wu, C.-C., Hsu, T.-H., Tsai, C., Huang, H., & Chang, D. (2017) · International Journal of Medical Sciences · doi:10.7150/ijms.19268 · Cited by 21
Dawodu, D., Patecki, M., Dumler, I., Haller, H. G., & Kiyan, Y. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04735-5 · Cited by 21
Wang, X., Zou, C., Li, M., Hou, C., Jiang, W., Bian, Z., & Zhu, L. (2022) · Human Cell · doi:10.1007/s13577-022-00825-y · Cited by 22
Tideglusib enhances odontogenic differentiation in human dental pulp stem cellsin vitro
Kornsuthisopon, C., Tompkins, K. A., & Osathanon, T. (2022) · International Endodontic Journal · doi:10.1111/iej.13877 · Cited by 21
Jeong, B., Kim, T. S., Kim, H. S., Lee, S., & Choi, Y. (2015) · Bone · doi:10.1016/j.bone.2015.05.009 · Cited by 21
Bustos-Valenzuela, J. C., Fujita, A., Halcsik, E., Granjeiro, J. M., & Sogayar, M. C. (2011) · BMC Research Notes · doi:10.1186/1756-0500-4-370 · Cited by 21
VIP and CRF reduce ADAMTS expression and function in osteoarthritis synovial fibroblasts
Pérez‐García, S., Carrión, M., Gutiérrez‐Cañas, I., González‐Álvaro, I., Gomariz, R. P., & Juarranz, Y. (2016) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12777 · Cited by 21
Lim, Y., Kim, C. H., Lee, S., Kim, H., Ahn, S. H., Lee, S. H., Koh, J., Rhee, Y., Baek, K. H., Min, Y., et al. (2016) · Calcified Tissue International · doi:10.1007/s00223-016-0160-4 · Cited by 21
Network and pathway-based analyses of genes associated with osteoporosis
Gu, H., Huang, Z., Chen, G., Zhou, K., Zhang, Y., Chen, J., Xu, J., & Yin, X. (2020) · Medicine · doi:10.1097/md.0000000000019120 · Cited by 21
Wu, H., Gao, Y., Xiao, L., Wei, Q., Zhang, N., Su, Z., Ma, C., Ye, T., & Wang, Y. (2021) · Materials & Design · doi:10.1016/j.matdes.2021.109571 · Cited by 21
Liu, J., Zou, L., Wang, J., Schuler, C., Zhao, Z., Li, X., Zhang, J., & Liu, Y. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.087 · Cited by 21
RetractedWilliams, M. J., White, S. C., Joseph, Z., & Hruska, K. A. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1120308 · Cited by 23
Improving oral implant osseointegration in a murine model via W nt signal amplification
Mouraret, S., Hunter, D. J., Bardet, C., Popelut, A., Brunski, J., Chaussain, C., Bouchard, P., & Helms, J. A. (2013) · Journal Of Clinical Periodontology · doi:10.1111/jcpe.12187 · Cited by 20
Aguilar, R., Bustos, F. J., Sáez, M., Rojas, A. P., Allende, M. L., van Wijnen, A. J., van Zundert, B., & Montecino, M. A. (2016) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2016.05.009 · Cited by 20
Zhu, Z., Xie, Q., Huang, Y., Zhang, S., & Chen, Y. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9286 · Cited by 20
LGRs in Skeletal Tissues: An Emerging Role for Wnt‐Associated Adult Stem Cell Markers in Bone
Doherty, L., & Sanjay, A. (2020) · JBMR Plus · doi:10.1002/jbm4.10380 · Cited by 20
Molecular and genetic regulation of osteogenic differentiation of mesenchymal stromal cells
Kozhevnikova, M. N., Mikaelyan, A. S., & Starostin, V. I. (2008) · Biology Bulletin · doi:10.1134/s1062359008030011 · Cited by 20
LIU, X., Kirschenbaum, A. M., Yao, S., & Levine, A. C. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1402.017 · Cited by 20
Natural bioactive products in the regulation of bone metabolism and regeneration
Ouyang, X., Ma, Q., Zhou, C., Tang, J., Li, M., Qing, J., Lei, X., Huang, D. A., Liu, H., & Zhang, G. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1683279 · Cited by 26
Targeting Sphingosine-1-Phosphate Signaling to Prevent the Progression of Aortic Valve Disease
Benkhoff, M., Barcik, M., Mourikis, P., Dahlmanns, J., Kahmann, P., Wollnitzke, P., Hering, M., Huckenbeck, T., Hoppe, J., Semleit, N., et al. (2024) · Circulation · doi:10.1161/circulationaha.123.067270 · Cited by 19
Danz, J. C., & Degen, M. (2025) · Frontiers in Oral Health · doi:10.3389/froh.2025.1472711 · Cited by 26
Patil, S. D., & Paul, S. (2014) · Cells Tissues Organs · doi:10.1159/000362226 · Cited by 19
Schoeman, M. A. E., Moester, M. J. C., Oostlander, A. E., Kaijzel, E. L., Valstar, E. R., Nelissen, R. G. H. H., Löwik, C. W. G. M., & de Rooij, K. E. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25241 · Cited by 19
Oh, J. H., Ahn, B., Karadeniz, F., Kim, J., Lee, J. I., Seo, Y., & Kong, C. (2019) · Marine Drugs · doi:10.3390/md17100543 · Cited by 19
Developmental principles informing human pluripotent stem cell differentiation to cartilage and bone
Humphreys, P. A., Mancini, F. E., Ferreira, M. J. S., Woods Jon, S., Ogene, L., & Kimber, S. J. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.11.024 · Cited by 21
Choi, S.-Y., Ryu, H., Oh, E., Choi, J., Cho, J., Kim, C., Kim, Y.-L., & Park, S.-H. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180393 · Cited by 19
Nanomaterials-based Cell Osteogenic Differentiation and Bone Regeneration
Zhang, T., Gao, Y., Cui, W., Li, Y., Xiao, D., & Zhou, R. (2020) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x15666200521083834 · Cited by 18
Altered Bone Status in Rett Syndrome
Pecorelli, A., Cordone, V., Schiavone, M. L., Caffarelli, C., Cervellati, C., Cerbone, G., Gonnelli, S., Hayek, J., & Valacchi, G. (2021) · Life · doi:10.3390/life11060521 · Cited by 18
A Potential Role of Semaphorin 3A during Orthodontic Tooth Movement
Şen, S., Lux, C. J., & Erber, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158297 · Cited by 18
Dysregulation of Wnt signaling in bone of type 2 diabetes mellitus and diabetic Charcot arthropathy
Gassel, L. C., Schneider, S., Banke, I. G. J., Braun, K. F., Volkering, C., Zeeb, L., Burgkart, R., von Eisenhart‐Rothe, R., Biberthaler, P., van Griensven, M., et al. (2022) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-022-05314-9 · Cited by 18
Modulated nanowire scaffold for highly efficient differentiation of mesenchymal stem cells
Perez, J. E., Bajaber, B., Alsharif, N. A., Martínez-Banderas, A. I., Patel, N. S., Sharip, A., Fabrizio, E. M. D., Merzaban, J. S., & Kosel, J. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01488-5 · Cited by 18
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
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