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      Bortezomib Is Cytotoxic to the Human Growth Plate and Permanently Impairs Bone Growth in Young Mice

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          Abstract

          Bortezomib, a novel proteasome inhibitor approved for the treatment of cancer in adults, has recently been introduced in pediatric clinical trials. Any tissue-specific side effects on bone development have to our knowledge not yet been explored. To address this, we experimentally studied the effects of bortezomib in vivo in young mice and in vitro in organ cultures of rat metatarsal bones and human growth plate cartilage, as well as in a rat chondrocytic cell line. We found that bortezomib while efficiently blocking the ubiquitin/proteasome system (UPS) caused significant growth impairment in mice, by increasing resting/stem-like chondrocyte apoptosis. Our data support a local action of bortezomib, directly targeting growth plate chondrocytes leading to decreased bone growth since no suppression of serum levels of insulin-like growth factor-I (IGF-I) was observed. A local effect of bortezomib was confirmed in cultured rat metatarsal bones where bortezomib efficiently caused growth retardation in a dose dependent and irreversible manner, an effect linked to increased chondrocyte apoptosis, mainly of resting/stem-like chondrocytes. The cytotoxicity of bortezomib was also evaluated in a unique model of cultured human growth plate cartilage, which was found to be highly sensitive to bortezomib. Mechanistic studies of apoptotic pathways indicated that bortezomib induced activation of p53 and Bax, as well as cleavage of caspases and poly-ADP-ribose polymerase (PARP) in exposed chondrocytes. Our observations, confirmed in vivo and in vitro, suggest that bone growth could potentially be suppressed in children treated with bortezomib. We therefore propose that longitudinal bone growth should be closely monitored in ongoing clinical pediatric trials of this promising anti-cancer drug.

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          Most cited references47

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          Proteasome inhibitors: from research tools to drug candidates.

          The 26S proteasome is a 2.4 MDa multifunctional ATP-dependent proteolytic complex, which degrades the majority of cellular polypeptides by an unusual enzyme mechanism. Several groups of proteasome inhibitors have been developed and are now widely used as research tools to study the role of the ubiquitin-proteasome pathway in various cellular processes, and two inhibitors are now in clinical trials for treatment of multiple cancers and stroke.
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              Apoptosis in cancer.

              In the last decade, basic cancer research has produced remarkable advances in our understanding of cancer biology and cancer genetics. Among the most important of these advances is the realization that apoptosis and the genes that control it have a profound effect on the malignant phenotype. For example, it is now clear that some oncogenic mutations disrupt apoptosis, leading to tumor initiation, progression or metastasis. Conversely, compelling evidence indicates that other oncogenic changes promote apoptosis, thereby producing selective pressure to override apoptosis during multistage carcinogenesis. Finally, it is now well documented that most cytotoxic anticancer agents induce apoptosis, raising the intriguing possibility that defects in apoptotic programs contribute to treatment failure. Because the same mutations that suppress apoptosis during tumor development also reduce treatment sensitivity, apoptosis provides a conceptual framework to link cancer genetics with cancer therapy. An intense research effort is uncovering the underlying mechanisms of apoptosis such that, in the next decade, one envisions that this information will produce new strategies to exploit apoptosis for therapeutic benefit.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                30 November 2012
                : 7
                : 11
                : e50523
                Affiliations
                [1 ]Pediatric Endocrinology Unit, Department of Women’s and Childreńs Health, Karolinska Institutet, Stockholm, Sweden
                [2 ]Pediatric Endocrinology Unit, Department of Pediatrics, University of Patras, Rio, Greece
                [3 ]Pediatric Orthopedic Clinic, Department of Women’s and Children's Health, Karolinska Institutet, Stockholm, Sweden
                [4 ]Department of Anatomy, Institute of Biomedicine, University of Turku, Turku, Finland
                Ohio State University, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: EE FZ DC HW LS. Performed the experiments: EE FZ HW TJH. Analyzed the data: EE FZ TJH. Contributed reagents/materials/analysis tools: LS. Wrote the paper: EE FZ DC TJH LS.

                Article
                PONE-D-12-23025
                10.1371/journal.pone.0050523
                3511518
                23226303
                51275253-1aca-433a-a020-373989af7f17
                Copyright @ 2012

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 2 August 2012
                : 22 October 2012
                Page count
                Pages: 14
                Funding
                This work was supported by the Swedish Research Council, the Swedish Childhood Cancer Foundation, Stiftelsen Frimurare Barnhuset Stockholm, and Sällskapet Barnavård. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Anatomy and Physiology
                Musculoskeletal System
                Biomechanics
                Cell Mechanics
                Bone
                Cartilage
                Physiological Processes
                Homeostasis
                Model Organisms
                Animal Models
                Molecular Cell Biology
                Signal Transduction
                Signaling in Cellular Processes
                Apoptotic Signaling
                Cell Death
                Toxicology
                Toxic Agents
                Medicine
                Endocrinology
                Pediatric Endocrinology
                Oncology
                Oncology Agents
                Pediatric Oncology
                Pediatrics
                Growth Retardation

                Uncategorized
                Uncategorized

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