The DOI matches its Crossref record; 171 of the 171 references it cites were found in a registry or an index.
Disorders of Bone Remodeling
Open accessAbstract
The skeleton provides mechanical support for stature and locomotion, protects vital organs, and controls mineral homeostasis. A healthy skeleton must be maintained by constant bone modeling to carry out these crucial functions throughout life. Bone remodeling involves the removal of old or damaged bone by osteoclasts (bone resorption) and the subsequent replacement of new bone formed by osteoblasts (bone formation). Normal bone remodeling requires a tight coupling of bone resorption to bone formation to guarantee no alteration in bone mass or quality after each remodeling cycle. However, this important physiological process can be derailed by a variety of factors, including menopause-associated hormonal changes, age-related factors, changes in physical activity, drugs, and secondary diseases, which lead to the development of various bone disorders in both women and men. We review the major diseases of bone remodeling, emphasizing our current understanding of the underlying pathophysiological mechanisms.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“OPG, a soluble receptor also produced by osteoblasts that acts as a decoy receptor and neutralizes RANKL, prevents RANKL from interacting with RANK and consequently inhibits osteoclast proliferation, activity, and survival [73, 74].”
From The Effect of Tobacco Smoking on Bone Mass: An Overview of Pathophysiologic Mechanisms (2018) · cites this paper as [73]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Once RANKL binds to its natural receptor, expressed by osteoclast precursor cells, it stimulates osteoclast precursor differentiation to active mature osteoclasts and accelerates bone resorption [73].”
From The Effect of Tobacco Smoking on Bone Mass: An Overview of Pathophysiologic Mechanisms (2018) · cites this paper as [73]
In the citing paper
“Abnormal increase in osteoclast formation and activity leads to some bone diseases such as osteoporosis, where resorption exceeds formation causing decreased bone density and increased bone fractures [105].”
From Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (2015) · cites this paper as [105]
In the citing paper
“In patients with chronic liver disease, the balance between osteoclasts and osteoblasts is affected by liver disease, resulting in BRU imbalance [46,50].”
From Bone diseases in patients with chronic liver disease (2019) · cites this paper as [46]
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
Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413
Osteoclast differentiation and activation
Boyle, W. J., Simonet, W. S., & Lacey, D. L. (2003) · Nature · doi:10.1038/nature01658 · Cited by 6,670
Osteoporosis Prevention, Diagnosis, and Therapy
NIH Consensus Development Panel on Osteoporosis Prevention, D. (2001) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.285.6.785 · Cited by 5,529
Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation.
Lacey, D. L., Timms, E., Tan, H.-L., Kelley, M. J., Dunstan, C. R., Burgess, T., Elliott, R., Colombero, A., Elliott, G., Scully, S., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81569-x · Cited by 5,439
Osteoprotegerin: a novel secreted protein involved in the regulation of bone density.
Simonet, W. S., Lacey, D. L., Dunstan, C. R., Kelley, M., Chang, M.-S., Lüthy, R., Nguyen, H. Q., Wooden, S., Bennett, L., Boone, T., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80209-3 · Cited by 5,130
Mitochondria, Oxidants, and Aging
Balaban, R. S., Nemoto, S., & Finkel, T. (2005) · Cell · doi:10.1016/j.cell.2005.02.001 · Cited by 4,388
Yasuda, H., Shima, N., Nakagawa, N., Yamaguchi, K., Kinosaki, M., Mochizuki, S.-I., Tomoyasu, A., Yano, K., Goto, M., Murakami, A., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.3597 · Cited by 4,224
Bone Resorption by Osteoclasts
Teitelbaum, S. L. (2000) · Science · doi:10.1126/science.289.5484.1504 · Cited by 3,962
OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph node organogenesis.
Kong, Y.-Y., Yoshida, H., Sarosi, I., Tan, H.-L., Timms, E., Capparelli, C., Morony, S., Oliveira-dos-Santos, A. J., Van, G., Itie, A., et al. (1999) · Nature · doi:10.1038/16852 · Cited by 3,351
Manolagas, S. C. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.2.0395 · Cited by 2,639
Research works printed but not linked: 11
- McGowen JA, 2004, Bone Health and Osteoporosis: A Report of the Surgeon General, 69
- Raisz LG., 1988, Ciba Found. Symp., 136, 226
- Mundy GR., 1991, Ciba Found. Symp., 157, 137
- Andersen TL, 2009, Br. J. Haematol., 48, 551
- Heaney RP, 1978, J. Lab. Clin. Med., 92, 964
- 10.1210/en.142.6.2205 · DOI · Paper page
- 10.1172/JCI200317215 · DOI · Paper page
- 10.1210/jc.83.12.4257 · DOI
- Peretz A, 1989, J. Rheumatol., 16, 363
- Takata S, 2001, J. Med. Investig., 48, 147
- Block GA, 2006, Clinical Guide to the Basics of Bone and Mineral Metabolism in CKD, 77
Cited by
Sorted by citations
Items 401–500 of 1,000
Giordani, C., Matacchione, G., Giuliani, A., Valli, D., Scarpa, E. S., Antonelli, A., Sabbatinelli, J., Giacchetti, G., Sabatelli, S., Olivieri, F., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24108820 · Cited by 26
Carvacrol Inhibits Osteoclastogenesis and Negatively Regulates the Survival of Mature Osteoclasts
Deepak, V., Kasonga, A. E., Kruger, M. C., & Coetzee, M. (2016) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b16-00117 · Cited by 26
Role and mechanism of action of leucine-rich repeat kinase 1 in bone
Xing, W., Goodluck, H., Zeng, C., & Mohan, S. (2017) · Bone Research · doi:10.1038/boneres.2017.3 · Cited by 24
F2r negatively regulates osteoclastogenesis through inhibiting the Akt and NFκB signaling pathways
Zhang, Y., Wang, H., Zhu, G., Qian, A., & Chen, W. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.41867 · Cited by 25
“Thus, targeting negative regulators of osteoclasts may serve as an effective approach to treat pathological bone diseases related to osteoclast over-activation [6].”
BackgroundKanniyappan, H., Venkatesan, M., Panji, J., Ramasamy, M., & Muthuvijayan, V. (2020) · Microporous and Mesoporous Materials · doi:10.1016/j.micromeso.2020.110687 · Cited by 25
Impact of Chronic Inflammation in Psoriasis on Bone Metabolism
Saalbach, A., & Kunz, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.925503 · Cited by 25
“In addition, vitamin D or calcium deficiency, reduction of physical activity, or therapeutic interventions like long-term glucocorticoid treatment are related to secondary osteoporosis (4).”
BackgroundWang, R., Wang, Y., Niu, Y., He, D., Jin, S., Li, Z., Zhu, L., Chen, L., Wu, X., Ding, C., et al. (2023) · ACS Central Science · doi:10.1021/acscentsci.3c00794 · Cited by 25
Byun, H., Jang, G. N., Jeong, H., Lee, J., Huh, S. J., Lee, S., Kim, E., & Shin, H. (2023) · Biomaterials Research · doi:10.1186/s40824-023-00473-9 · Cited by 25
“…in a critical-sized defect reportedly delays bone healing by generating reactive oxygen species (ROS), and the accumulation of oxidative stress upregulates the expression of inflammatory cytokines which are detrimental to cell viability and inhibit osteogenic differentiation of stem cells [16, 17].”
BackgroundThe impact of thyroid autoimmunity (TPOAb) on bone density and fracture risk in postmenopausal women
Polovina, S. P., Miljić, D., Zivojinović, S., Milic, N. M., Micić, D., & Popović-Brkić, V. (2017) · HORMONES · doi:10.14310/horm.2002.1719 · Cited by 25
Wang, T., Liu, Q., Zhou, L., Yuan, J., Lin, X., Zeng, R., Liang, X., Zhao, J., & Xu, J. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161126039 · Cited by 25
“Excessive osteoclast formation and activity cause bone disorders, such as osteoporosis, metastatic bone disease, and inflammatory arthritis, where bone resorption exceeds bone formation [30].”
BackgroundRole of Regulators of G Protein Signaling Proteins in Bone Physiology and Pathophysiology
Jules, J., Yang, S., Chen, W., & Li, Y. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2015.02.002 · Cited by 27
“Enhanced osteoclast formation and/or activity are responsible for many disorders of skeletal deficiency.(10) Osteoclastogenesis requires”
BackgroundBone complications of cancer treatment
Zhu, N., Ni, H., Guo, S., Shen, Y., & Chen, Q. (2024) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2024.102828 · Cited by 24
Zhao, L., Liu, C., Chen, X., He, Z., Zhang, S., Zhang, A.-A., Tang, S., Wu, Z., Liu, C., & Yuan, Y. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.09.032 · Cited by 24
“…not only enhances the adipogenic differentiation capacity of mesenchymal stem cells but also accelerates the breakdown metabolism of newly formed bone calluses, thereby hindering the generation of bone bridging at defective sites and significantly impairing bone regenerative capabilities [12].”
BackgroundAbiramasundari, G., Gowda, C. M. M., Pampapathi, G., Praveen, S., Shivamurugan, S., Vijay–Kumar, M., Devi, A., & SREEPRIYA, M. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.12.094 · Cited by 24
Staphylococcus aureus Protein A induces osteoclastogenesis via the NF-κB signaling pathway
Ren, L., Wang, H., He, X., Song, M., Chen, X.-Q., & Xu, Y. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7316 · Cited by 24
“While RANKL is a key osteoclastogenic cytokine, the binding of RANKL to its receptor RANK recruits tumor necrosis factor receptor-associated factor 6, resulting in the activation of NF-κ B, phosphatidylinositol 3-kinase (PI-3K)/Akt, p38, c-Jun N-terminal kinase (JNK) and extracellular…”
Role of nitric oxide in type 1 diabetes-induced osteoporosis
Jeddi, S., Yousefzadeh, N., Kashfi, K., & Ghasemi, A. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114888 · Cited by 26
Yao, C., Yang, B.-Y., & Li, Y. E. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.832808 · Cited by 24
“Therefore, tissue engineering techniques provide the strategies to accelerate bone remodeling by using versatile chemical and physical treatments and has been of interest as new strategies for bone regeneration (Feng and McDonald, 2011).”
BackgroundTanshinone Ameliorates Glucocorticoid-Induced Bone Loss via Activation of AKT1 Signaling Pathway
Wang, Y., Liu, L., Qu, Z., Wang, D., Huang, W., Kong, L., & Yan, L. W. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.878433 · Cited by 24
“In osteoporosis patients, bone mass and strength decreases significantly whereas fracture risk can potentially increase (Feng and McDonald, 2011).”
BackgroundPositive and Negative Regulators of Sclerostin Expression
Iwamoto, R., Koide, M., Udagawa, N., & Kobayashi, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094895 · Cited by 27
Functional engineering strategies of 3D printed implants for hard tissue replacement
Chen, C., Huang, B., Liu, Y., Liu, F., & Lee, I.-S. (2022) · Regenerative Biomaterials · doi:10.1093/rb/rbac094 · Cited by 24
“hydroxyapatite (HA) interacting with type I collagen and other non-collagenous proteins [3, 4].”
BackgroundAnwar, A., Sapra, L., Gupta, N., Ojha, R. P., Verma, B., & Srivastava, R. K. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.31036 · Cited by 26
“Bone is comprised of four types of cells: osteoblasts, osteoclasts, osteocytes, and bone lining cells (Feng & McDonald, 2011; Parfitt, 1994).”
BackgroundIn silico assessment of the bone regeneration potential of complex porous scaffolds
Asbai-Ghoudan, R., Nasello, G., Pérez, M. Á., Verbruggen, S. W., de Galarreta, S. R., & Rodríguez-Flórez, N. (2023) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2023.107381 · Cited by 24
“In those cases, the reduction in mechanical properties is accompanied by a change in the normal metabolic balance and affect the bone formation rate [71,72].”
BackgroundFerulic acid impairs osteoclast fusion and exacerbates survival of mature osteoclasts
Sagar, T., Rantlha, M., Kruger, M. C., Coetzee, M., & Deepak, V. (2016) · Cytotechnology · doi:10.1007/s10616-016-0009-8 · Cited by 24
A new role for HERPUD1 and ERAD activation in osteoblast differentiation and mineralization
Américo-Da-Silva, L., Diaz, J., Bustamante, M., Mancilla, G., Oyarzún, I., Verdejo, H., & Quiroga, C. (2018) · The FASEB Journal · doi:10.1096/fj.201701229rr · Cited by 25
“The physiopathology of low BMD is related to gender and age, but also to such variables as systemic inflammatory diseases, medication use, nutritional deficiencies, endocrine disorders, and other conditions that may promote decreases in osteoblast-dependent matrix secretion or increases in osteoclastic resorption (3,…”
BackgroundPatel, D., & Saxena, B. (2024) · Journal of Orthopaedic Reports · doi:10.1016/j.jorep.2024.100472 · Cited by 29
kaleshtari, A. H., Farjaminejad, S., Hasani, M., Farjaminejad, R., Foroozandeh, A., Abdouss, M., & Hasanzadeh, M. (2025) · Carbohydrate Polymer Technologies and Applications · doi:10.1016/j.carpta.2025.100692 · Cited by 28
Ahn, S. H., Lee, S., Kim, H., Lee, S. H., Kim, B., & Koh, J. (2016) · Endocrine Research · doi:10.3109/07435800.2016.1155600 · Cited by 23
“In particular, substantial evidence indicates that estrogen deficiency during the bone loss stage, including the menopausal transition and menopause, can cause relative increases in osteoclastic bone resorption by directly affecting bone cells (29) and indirectly involving diverse mechanisms, such as reactive oxygen s…”
BackgroundMusson, D. S., Gao, R., Watson, M., Lin, J., Park, Y. E., Tuari, D., Callon, K. E., Zhu, M. F., Dalbeth, N., Naot, D., et al. (2019) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-019-1089-x · Cited by 23
Na, W., Lee, E., Kang, M., Kim, Y., Kim, D. Y., Oh, H., Kim, S., Oh, S. Y., & Kang, Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228581 · Cited by 24
“can be deranged by various factors such as menopause-associated hormonal changes, age-related factors, changes in physical activity, drugs, and secondary diseases [2].”
BackgroundNiu, Q., He, J., Wu, M.-K., Liu, J., Lu, X., Zhang, L., & Jin, Z. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119480 · Cited by 23
Integration of mechanics and biology in computer simulation of bone remodeling
Pant, A., Paul, E., Niebur, G. L., & Vahdati, A. (2021) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2021.05.001 · Cited by 24
Evaluation of Dexamethasone-Induced Osteoporosis In Vivo Using Zebrafish Scales
Chaichit, S., Sato, T., Yu, H., Tanaka, Y., Ogra, Y., Mizoguchi, T., & Itoh, M. (2021) · Pharmaceuticals · doi:10.3390/ph14060536 · Cited by 23
“Aging and hormonal changes lead to an imbalance between bone resorption by osteoclasts and bone formation by osteoblasts [2,3].”
BackgroundLü, J., Zhang, Y., Liang, J., Diao, J., Liu, P., & Zhao, H. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6301433 · Cited by 23
“Patients with OP show increased osteoclast differentiation and decreased osteoblast differentiation [3].”
BackgroundEffect of Regulator of G Protein Signaling Proteins on Bone
Yuan, G., & Yang, S. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.842421 · Cited by 22
“Bone homeostasis is dynamically maintained by the processes of bone formation and resorption, which initiates with the osteoclasts-derived resorption of the calcified bone matrix and is followed by the osteoblast-regulated bone formation (1, 2).”
BackgroundDietary Acid Load and Bone Health: A Systematic Review and Meta-Analysis of Observational Studies
Gholami, F., Naghshi, S., Samadi, M., Rasaei, N., & Mirzaei, K. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.869132 · Cited by 23
The circadian clock has roles in mesenchymal stem cell fate decision
Gao, W., Li, R., Ye, M., Zhang, L., Zheng, J., Yang, Y., Wei, X., & Zhao, Q. S. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02878-0 · Cited by 22
“The dynamic balance of bone formation and resorption under strict time control ensures bone mass integrity and bone structure and function [27].”
BackgroundSheng, S., Wu, Y., Dai, Z.-H., Jin, C., He, G.-L., Jin, S., Zhao, B.-Y., Zhou, X., Xie, C., Zheng, G., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154739 · Cited by 23
Rashid, S. S., Wilson, S. G., Zhu, K., Walsh, J. P., Xu, J., & Mullin, B. H. (2023) · Genes · doi:10.3390/genes14040916 · Cited by 23
“The disease is characterised by an imbalance between resorption and formation that affects the homeostasis of the bone, that is, there is more resorption than formation, leading to structural weakness [11,12].”
Specific RANK Cytoplasmic Motifs Drive Osteoclastogenesis
Li, Y., Shi, Z., Jules, J., Chen, S., Kesterson, R. A., Zhao, D., Zhang, P., & Feng, X. (2019) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3810 · Cited by 23
“The impaired bone formation and mineralization in the KI mice likely result from the coupling of bone formation to bone resorption during bone remodeling.((3)) However, our KI mice do not have abnormalities such as the retarded growth, shortened long bones, and defective tooth eruption found in RANK KO mice.”
BackgroundSelf-citationBone-implantable devices for drug delivery applications
Ray, P., Hasnain, M. S., Koley, A., & Nayak, A. K. (2019) · Elsevier eBooks · doi:10.1016/b978-0-08-102420-1.00021-2 · Cited by 23
Schistosome infection promotes osteoclast-mediated bone loss
Li, W., Wei, C., Xu, L., Yu, B., Chen, Y., Lu, D., Zhang, L., Song, X., Dong, L., Zhou, S., et al. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009462 · Cited by 22
“Bone homeostasis is maintained by the dynamic balance between osteoclastic bone resorption and osteoblastic bone formation [33].”
BackgroundLee, K. I.-R., Chen, J.-H., & Chen, K.-H. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020641 · Cited by 26
“In parallel, estrogen deficiency functionally suppresses Wnt/ β -catenin signaling, leading to impaired osteoblast differentiation and reduced bone formation, a process further compounded by increased oxidative stress and osteoblast dysfunction [48,55,58].”
Jules, J., Wang, S., Shi, Z., Liu, J., Shi, W., & Feng, X. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.667535 · Cited by 23
“Furthermore, osteoclasts are implicated in the pathogenesis of various bone diseases, including postmenopausal osteoporosis (2) and bone loss in inflammatory bone conditions such as rheumatoid arthritis and periodontitis (3).”
BackgroundSelf-citationGong, R., Xiao, H., Zhang, Y., Zhao, Q., Su, K., Xu, L., Mo, C., Zhang, Q., Du, Y., Lyu, F.-Y., et al. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab146 · Cited by 22
Zhao, Y., Shao, G., Liu, X., & Li, Z. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.866625 · Cited by 23
“This cycle broadly has four stages: 1) activation, when osteoclasts are activated and resorb bone to form a resorption pit; 2) reversal, after the completion of resorption when osteoblast precursors are recruited to the resorption pit; 3) formation, when osteoblasts deposit bone mineral and matrix to fill the pit; and…”
BackgroundZhang, L., Zhu, K., Xu, J.-Z., Chen, X., Sheng, C., Zhang, D., Yang, Y., Sun, L., Zhao, H., Wang, X., et al. (2023) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4925 · Cited by 23
“(50) Therefore, impaired differentiation of osteoblasts and osteoclasts induced by CBP/p300 inhibition could have undesirable consequences for skeletal integrity.”
BackgroundBioceramic materials in bone-implantable drug delivery systems: A review
Nayak, A. K., Maity, M., Barik, H., Behera, S. S., Dhara, A. K., & Hasnain, M. S. (2024) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2024.105524 · Cited by 22
Yang, N., Cui, Y., Tan, J., Fu, X., Han, X., Leng, H., & Song, C. (2013) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-013-0496-z · Cited by 22
“Bisphosphonates function to inhibit bone resorption; however, since bone formation and resorption are coupled, bisphosphonate use may also negatively impact upon bone formation [28].”
DOENÇA ÓSSEA INDUZIDA PELOS GLICOCORTICOIDES: MECANISMOS E IMPORTÂNCIA NA PRÁTICA PEDIÁTRICA
SARINHO, E. S. C., & Melo, V. M. P. P. (2017) · Revista Paulista de Pediatria · doi:10.1590/1984-0462;2017/;35;2;00007 · Cited by 22
Extracellular matrix constitution and function for tissue regeneration and repair
Caldeira, J., Sousa, A., Sousa, D. M., & Barros, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-100803-4.00002-4 · Cited by 24
A meta-analysis of serum osteocalcin level in postmenopausal osteoporotic women compared to controls
Liu, Z., Chen, R., Jiang, Y., Yang, Y., He, L., Luo, C., Dong, J., & Rong, L. (2019) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-019-2863-y · Cited by 22
Friend or Foe? Essential Roles of Osteoclast in Maintaining Skeletal Health
Wang, H., Yang, G., Xiao, Y., Luo, G., Li, G., & Li, Z. (2020) · BioMed Research International · doi:10.1155/2020/4791786 · Cited by 23
“Osteoporosis, the most prevalent disorder of bone remodeling by far, is characterized by the heightened activity of OCs [6, 7].”
BackgroundTissue Engineering Through 3D Bioprinting to Recreate and Study Bone Disease
Pavek, A., Nartker, C., Saleh, M., Kirkham, M., Khajehpour, S., Aghazadeh‐Habashi, A., & Barrott, J. J. (2021) · Biomedicines · doi:10.3390/biomedicines9050551 · Cited by 25
“Bone remolding and turnover is a dynamic process through which, sequential bone-resorption and bone-formation, the new bone tissue replaces the old tissue [1].”
BackgroundThe role of midkine in skeletal remodelling
Liedert, A., Schinke, T., Ignatius, A. A., & Amling, M. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12412 · Cited by 23
“Osteoporosis is the most common metabolic bone disorder worldwide (Pietschmann et al., 2009; Li et al., 2010; Feng and McDonald, 2011).”
BackgroundMethodInfluentialThe Effect of Lycii Radicis Cortex Extract on Bone Formation in Vitro and in Vivo
Park, E., Jin, H., Cho, D., Kim, J., Kim, M.-C., Choi, C. W., Jin, Y., Lee, J., Park, J.-H., Chung, Y., et al. (2014) · Molecules · doi:10.3390/molecules191219594 · Cited by 22
“The two different types of bone cells—osteoblasts that form new bone and osteoclasts that break bone down—both play an important role in the regulation of bone metabolism [10].”
Background3,3′-Diindolylmethane increases bone mass by suppressing osteoclastic bone resorption in mice
Yu, T., Pang, W.-J., & Yang, G.-S. (2014) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2014.11.006 · Cited by 22
The role of myeloid derived suppressor cells in musculoskeletal disorders
Ren, Y., Bäcker, H. C., Müller, M., & Kienzle, A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1139683 · Cited by 23
“The solid bone matrix is constantly being remodeled in response to changes in physical stress (1).”
BackgroundBone microphysiological models for biomedical research
Verdugo-Avello, F., Wychowaniec, J. K., Villacis-Aguirre, C. A., D’Este, M., & Toledo, J. R. (2025) · Lab on a Chip · doi:10.1039/d4lc00762j · Cited by 24
A cellular automata model of bone formation
Scoy, G. K. V., George, E. L., Asantewaa, F. O., Kerns, L. X., Saunders, M. M., & Prieto-Langarica, A. (2017) · Mathematical Biosciences · doi:10.1016/j.mbs.2017.02.001 · Cited by 21
“, extended bed rest and implant introduction) [3, 10, 12, 18, 19].”
BackgroundLambertini, E., Penolazzi, L., Pandolfi, A., Mandatori, D., Sollazzo, V., & Piva, R. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.4890 · Cited by 21
“It is important to underline that identifying molecules capable of simultaneously modulating the activity of osteo‐ blasts and osteoclasts is an important benefit for patients affected by bone loss, as it provides the opportunity to control a complex balance (30,31).”
Myeloid‐derived suppressor cells in obesity‐associated periodontal disease: A conceptual model
Kwack, K. H., Maglaras, V., Thiyagarajan, R., Zhang, L., & Kirkwood, K. L. (2021) · Periodontology 2000 · doi:10.1111/prd.12384 · Cited by 21
LncRNA KCNQ1OT1 promotes osteogenic differentiation via miR-205-5p/RICTOR axis
Yang, J., Peng, W.-X., & Zhang, M. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2022.113119 · Cited by 21
Liu, T., Jiang, L., Xiang, Z., Li, J., Zhang, Y., Xiang, T., Wang, W., Li, X., Jia, Y., Huang, X., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113140 · Cited by 21
The deubiquitinase UCHL1 negatively controls osteoclastogenesis by regulating TAZ/NFATC1 signalling
Feng, Z., Tao, S., Huang, Z., Zheng, B., Kong, X., Xiang, Y., Zhang, Q., Song, H., Xu, Z., Wei, X., et al. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.82152 · Cited by 21
“Excessive bone resorption contributes to various bone diseases, such as rheumatoid arthritis, bone erosion, and osteoporosis [1-3].”
BackgroundMETTL14 represses osteoclast formation to ameliorate osteoporosis via enhancing GPX4 mRNA stability
Deng, M., Luo, J., Cao, H., Li, Y., Chen, L., & Liu, G. (2023) · Environmental Toxicology · doi:10.1002/tox.23829 · Cited by 21
“Osteoporosis is a common metabolic skeletal disorder with high prevalence in the elderly characterized by loss of bone mass, which leads to an increased risk of fragility fracture.(1,2) Bone mass loss is mainly attributed to decreased bone formation and excessive osteoclast resorption.”
BackgroundM2 macrophages-derived exosomes regulate osteoclast differentiation by the CSF2/TNF-α axis
Zhou, Y., & Hu, G. (2024) · BMC Oral Health · doi:10.1186/s12903-023-03842-x · Cited by 24
“The balance of bone resorption and bone formation ensures normal bone remodeling without changes in bone mass and quality [2].”
BackgroundChin, K., Gengatharan, D., Nasru, F. M., Khairussam, R., Ern, S. L. H., Aminuddin, S., & Ima-Nirwana, S. (2016) · Nutrients · doi:10.3390/nu8120808 · Cited by 21
“Osteoclasts are the bone cells responsible for bone resorption [38].”
BackgroundAdiponectin inhibits osteoclastogenesis by suppressing NF-κB and p38 signaling pathways
Chen, G., Huang, L., Wu, X., Liu, X., Xu, Q., Li, F., Dai, M., & Zhang, B. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.07.162 · Cited by 21
Kim, J. H., Kim, K., Kim, I., Seong, S., Kim, S. W., & Kim, N. (2018) · Bone · doi:10.1016/j.bone.2018.12.010 · Cited by 20
Clinical Application of Bone Turnover Markers in Osteoporosis in Korea
Park, S. Y., Ahn, S. H., Yoo, J., Chung, Y., Jeon, Y. K., Yoon, B., Kim, H. Y., Lee, S. H., Lee, J., & Hong, S. (2019) · Journal of Bone Metabolism · doi:10.11005/jbm.2019.26.1.19 · Cited by 23
Cathepsin Z as a novel potential biomarker for osteoporosis
Dera, A. A., Ranganath, L. R., Barraclough, R., Vinjamuri, S., Hamill, S., & Barraclough, D. L. (2019) · Scientific Reports · doi:10.1038/s41598-019-46068-0 · Cited by 21
Hayhoe, R. P. G., Abdelhamid, A. S., Luben, R., Khaw, K., & Welch, A. A. (2020) · European Journal of Clinical Nutrition · doi:10.1038/s41430-020-0686-4 · Cited by 21
Mohamad, N.-V., Soelaiman, I. N., & Chin, K. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.04.083 · Cited by 21
Mechanical protein polycystin-1 directly regulates osteoclastogenesis and bone resorption
Huang, M., Zhou, J., Li, X., Liu, R., Jiang, Y., Chen, K., Jiao, Y., Yin, X., Liu, L., Sun, Y., et al. (2024) · 中国科学通报:英文版 · doi:10.1016/j.scib.2024.04.044 · Cited by 20
“The skeleton, as a load-bearing tissue, is continuously subjected to mechanical forces [1].”
BackgroundWang, S., Heng, B. C., Qiu, S., Deng, J., Cheung, G. S. P., Jin, L., Zhao, B., & Zhang, C. (2018) · Innate Immunity · doi:10.1177/1753425918812646 · Cited by 20
“Disruption of the balance between osteoblasts and osteoclasts will result in osteopenia/osteoporosis or other metabolic bone diseases.(7) Bone resorptive osteoclasts are multinucleated cells derived from monocyte/macrophage precursors.”
BackgroundSato, C., Yamazaki, D., Sato, M., Takeshima, H., Memtily, N., Hatano, Y., Tsukuba, T., & Sakai, E. (2019) · Scientific Reports · doi:10.1038/s41598-019-43608-6 · Cited by 20
Expression and Role of Ubiquitin-Specific Peptidases in Osteoblasts
Hariri, H., & St‐Arnaud, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147746 · Cited by 21
“Maintaining the integrity of the coupling process between osteoblasts and osteoclasts is crucial, in order to avoid skeletal pathologies such as osteoporosis and osteopetrosis [42].”
BackgroundPGC-1: a key regulator in bone homeostasis
Chen, H., Fan, W., He, H., & Huang, F. P. (2021) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-021-01263-w · Cited by 20
“Bone remodeling requires a tight coupling of bone resorption to bone formation, during which osteoclasts remove old or damaged bone and osteoblasts subsequently form new bone [5].”
BackgroundSemeghini, M. S., Scalize, P. H., Coelho, M. C., Fernandes, R. R., Pitol, D. L., Tavares, M. S., de Sousa, L. G., Ribeiro, A. A. C. M., Siéssere, S., & Bombonato‐Prado, K. F. (2022) · Journal of Anatomy · doi:10.1111/joa.13672 · Cited by 20
Liu, X., Jiang, C., Fan, R., Liu, T., Li, Y., Zhong, D., Zhou, L., Liu, T., Li, J., & Jin, R. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.935326 · Cited by 22
Mahalingam, C. D., Sampathi, B. R., Sharma, S., Datta, T., Das, V., Abou‐Samra, A., & Datta, N. S. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0372 · Cited by 20
CCAAT/Enhancer-binding Protein α (C/EBPα) Is Important for Osteoclast Differentiation and Activity
Jules, J., Chen, W., Feng, X., & Li, Y. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.674598 · Cited by 20
“Moreover, OCs are implicated in the pathogenesis and morbidity of numerous bone diseases, including periodontitis, rheumatoid arthritis, and post-menopausal osteoporosis (12, 13).”
Self-citationLiang, W., Li, L., Cui, X., Tang, Z., Wei, X., Pan, H., & Li, B. (2016) · Journal of Applied Biomaterials & Functional Materials · doi:10.5301/jabfm.5000295 · Cited by 20
“Bone mass is regulated by new bone formation and replacement of damaged bone, processes which are referred to as bone remodeling (5).”
BackgroundChan, W. C. W., Tsang, K. Y., Cheng, Y., Ng, V. C. W., Chik, H., Tan, Z., Boot-Handford, R., BOYDE, A., Cheung, K., Cheah, K. S. E., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx339 · Cited by 20
Regulation of bone blood flow in humans: The role of nitric oxide, prostaglandins, and adenosine
HEINONEN, I. H. A., Boushel, R., Hellsten, Y., & Kalliokoski, K. K. (2018) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/sms.13064 · Cited by 20
Ahn, S. H., Chen, Z., Lee, J., Lee, S., Min, S. H., Kim, N. D., & Lee, T. (2018) · Molecules · doi:10.3390/molecules23123139 · Cited by 20
“Bones are constantly formed and reabsorbed by osteoblasts and osteoclast destruction, respectively [20].”
BackgroundRat sinus mucosa‐ and periosteum‐derived exosomes accelerate osteogenesis
Sun, R., Xu, S., & Zuo-lin, W. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28758 · Cited by 21
“Osteoblasts are derived from MSCs that reside in the bone marrow and circulation (Feng & McDonald, 2011; Modder & Khosla, 2008).”
BackgroundKim, S.-I., Kim, Y., Kang, B. G., Kang, M., Lee, E., Kim, D. Y., Oh, H., Oh, S. Y., Na, W., Lim, S. S., et al. (2020) · Phytomedicine · doi:10.1016/j.phymed.2020.153351 · Cited by 20
Ficus deltoidea promotes bone formation in streptozotocin-induced diabetic rats
Samsulrizal, N., Goh, Y. M., Ahmad, H., Dom, S. M., Azmi, N. S., Zin, N. S. N. M., & Ebrahimi, M. M. (2021) · Pharmaceutical Biology · doi:10.1080/13880209.2020.1865411 · Cited by 20
“A failure in the delicate balance between these two processes leads to osteoarthritis and osteoporosis (Logar et al. 2007; Feng and McDonald 2011).”
BackgroundInhibition of RANKL-Induced Osteoclastogenesis by Novel Mutant RANKL
Jang, Y., Sohn, H. M., Ko, Y. J., Hyun, H., & Lim, W. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22010434 · Cited by 20
“However, excessive osteoclast activity leads to an imbalance between bone resorption and formation, which is often observed in patients with osteoporosis [3,4].”
BackgroundThe phytochemical plumbagin reciprocally modulates osteoblasts and osteoclasts
Yadav, A. M., Bagade, M. M., Ghumnani, S., Raman, S., Saha, B., Kubatzky, K. F., & Ashma, R. (2021) · Biological Chemistry · doi:10.1515/hsz-2021-0290 · Cited by 20
“Abnormal activation of osteoclasts is found in pathological conditions like bone metastasis and inflammatory arthritis in which periarticular erosion and painful osteolytic lesions occur (Feng and McDonald 2011; Seeman and Delmas 2006; Takayanagi 2007).”
BackgroundPark, E., Kim, J., Yeo, S., Lim, E., Choi, C. W., Choi, S., Li, W. Y., Lee, J., Park, J.-H., Huh, D., et al. (2019) · Nutrients · doi:10.3390/nu11112716 · Cited by 21
“Imbalanced processes between bone resorption a d bone formation cause abnormal bone metabolic dise ses such as osteoporosis [1].”
BackgroundFoxk1 promotes bone formation through inducing aerobic glycolysis
Peng, S., Liu, C., Feng, N., Wang, Z., Zheng, K., Xie, Y., Long, H., 李志忠, & Long, H. (2024) · Cell Death and Differentiation · doi:10.1038/s41418-024-01371-w · Cited by 20
“Osteoblast dysfunction caused by aging leads the imbalance of bone formation and bone resorbing, resulting in occurrence of osteoporosis [5, 6].”
Shi, R., Zhan, H., Jiang, S., Lin, K., & Yuan, C. (2025) · Advanced Science · doi:10.1002/advs.202511099 · Cited by 19
Xue, S., Shao, Q., Zhu, L., Jiang, Y., Wang, C., Xue, B., Lu, H., Sang, W., & Ma, J. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.105826 · Cited by 19
NRF2 Is an Upstream Regulator of MYC-Mediated Osteoclastogenesis and Pathological Bone Erosion
Park, P. S. U., Mun, S. H., Zeng, S. L., Kim, H., Bae, S., & Park‐Min, K. (2020) · Cells · doi:10.3390/cells9092133 · Cited by 19
“When these multinucleated osteoclasts resorb bone at a higher intensity than bone-forming osteoblasts, pathological bone loss occurs [11,12].”
BackgroundTsukazaki, H., Kikuta, J., Ao, T., Morimoto, A., Fukuda, C., Tsuda, E., Minoshima, M., Kikuchi, K., Kaito, T., & Ishii, M. (2021) · Bone · doi:10.1016/j.bone.2021.116095 · Cited by 19
Rudiansyah, M., El‐Sehrawy, A. A. M. A., Ahmad, I. S., Terefe, E. M., Abdelbasset, W. K., Bokov, D. O., Salazar, A., Rizaev, J. A., Muthanna, F. M. S., & Shalaby, M. N. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120717 · Cited by 19
Liu, L., Zhang, Z., Aimaijiang, M., Liu, M., Huang, L., Pan, Z., Liu, S., Qi, S., Zhang, X., Wang, H., et al. (2022) · Nano Letters · doi:10.1021/acs.nanolett.2c04078 · Cited by 19
WHIM Syndrome-linked CXCR4 mutations drive osteoporosis
Anginot, A., Nguyen, J., Nader, Z. A., Rondeau, V., Bonaud, A., Kalogeraki, M., Boutin, A., Lemos, J. P., Bisio, V., Koenen, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37791-4 · Cited by 20
Metadata
- Authors
- Feng, X., & McDonald, J. M.
- Affiliations
- University of Alabama at Birmingham (US)
- ORCID
- Feng, Xu
- Venue
- Annual Review of Pathology: Mechanisms of Disease
- Publisher
- Annual Reviews
- Published
- 2011-02-28
- Volume
- 6
- Issue
- 1
- Pages
- 121-145
- ISSN
- 1553-4006 (ISSN-L)
- 1553-4014
- PMC
- PMC3571087
- OpenAlex
- W2166266977
- Cited by
- 1,272
- References
- 171
- Citations by year
- 2026: 59 · 2025: 109 · 2024: 102 · 2023: 124 · 2022: 135 · 2021: 142 · 2020: 107 · 2019: 117 · 2018: 86 · 2017: 68 · 2016: 59 · 2015: 47 · 2014: 36 · 2013: 37 · 2012: 29
- FWCI
- 3.28
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Annual Review of Pathology Mechanisms of Disease (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (R01CA109119)
- National Institute of Neurological Disorders and Stroke (R21NS061677, NS061677)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (5P30 AR0406031, R01AR047830, AR 47830, R01AR050235)
- Topics
- 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
- Health Sciences › Medicine › Oncology › Bone health and treatments
- Keywords
- bone remodeling, bone resorption, bone formation, osteoclasts, osteoblasts, bone disease, menopause, hormonal changes, age-related bone loss, physical activity, drug-induced bone loss, mineral homeostasis, pathophysiology
- MeSH terms
- Animals, Bone Diseases, Humans, Bone Remodeling
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