Suberoylanilide hydroxamic acid (SAHA; vorinostat) causes bone loss by inhibiting immature osteoblasts

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• 作者：Meghan E. McGee-Lawrence^a ; ^{mcgeelawrence.meghan@mayo.edu} ; Angela L. McCleary-Wheeler^a ; ^{mcclearywheeler.angela@mayo.edu} ; Frank J. Secreto^a ; ^{secreto.frank@mayo.edu} ; David F. Razidlo^a ; ^{razidlo.david@mayo.edu} ; Minzhi Zhang^a ; ^{zhang.minzhi@mayo.edu} ; Bridget A. Stensgard^a ; ^{stensgard.bridget@mayo.edu} ; Xiaodong Li^a ; ^{li.xiaodong@mayo.edu} ; Gary S. Stein^b ; ^{gary.stein@umassmed.edu} ; Jane B. Lian^b ; ^{jane.lian@umassmed.edu} ; Jennifer J. Westendorf^a ; ^{westendorf.jennifer@mayo.edu}
• 关键词：Histone deacetylase inhibitor ; Hdac ; Osteoblasts ; Zolinza ; γ ; H2AX
• 刊名：Bone
• 出版年：2011
• 出版时间：1 May 2011
• 年：2011
• 卷：48
• 期：5
• 页码：1117-1126
• 全文大小：1058 K

文摘

Histone deacetylase (Hdac) inhibitors are used clinically to treat cancer and epilepsy. Although Hdac inhibition accelerates osteoblast maturation and suppresses osteoclast maturation in vitro, the effects of Hdac inhibitors on the skeleton are not understood. The purpose of this study was to determine how the pan-Hdac inhibitor, suberoylanilide hydroxamic acid (SAHA; a.k.a. vorinostat or Zolinza^TM) affects bone mass and remodeling in vivo. Male C57BL/6J mice received daily SAHA (100 mg/kg) or vehicle injections for 3 to 4 weeks. SAHA decreased trabecular bone volume fraction and trabecular number in the distal femur. Cortical bone at the femoral midshaft was not affected. SAHA reduced serum levels of P1NP, a bone formation marker, and also suppressed tibial mRNA levels of type I collagen, osteocalcin and osteopontin, but did not alter Runx2 or osterix transcripts. SAHA decreased histological measures of osteoblast number but interestingly increased indices of osteoblast activity including mineral apposition rate and bone formation rate. Neither serum (TRAcP 5b) nor histological markers of bone resorption were affected by SAHA. P1NP levels returned to baseline in animals which were allowed to recover for 4 weeks after 4 weeks of daily SAHA injections, but bone density remained low. In vitro, SAHA suppressed osteogenic colony formation, decreased osteoblastic gene expression, induced cell cycle arrest, and caused DNA damage in bone marrow-derived adherent cells. Collectively, these data demonstrate that bone loss following treatment with SAHA is primarily due to a reduction in osteoblast number. Moreover, these decreases in osteoblast number can be attributed to the deleterious effects of SAHA on immature osteoblasts, even while mature osteoblasts are resistant to the harmful effects and demonstrate increased activity in vivo, indicating that the response of osteoblasts to SAHA is dependent upon their differentiation state. These studies suggest that clinical use of SAHA and other Hdac inhibitors to treat cancer, epilepsy or other conditions may potentially compromise skeletal structure and function.