期刊文献+

Sclerostin单克隆抗体治疗骨质疏松的研究进展 被引量:3

Research progress on the effect of sclerostin monoclonal antibody in treating osteoporosis
下载PDF
导出
摘要 硬骨素(Sclerostin)是由硬化性骨病(sclerosteosis,SOST)基因编码的蛋白质,可以通过与低密度脂蛋白受体相关蛋白5/6(low density lipoprotein receptor-related protein,LRP5/6)结合达到拮抗Wnt蛋白并抑制成骨的作用,已经作为新的药物靶点用于抗骨质疏松药物研发。目前,围绕Sclerostin单克隆抗体已经进行了许多基础研究和临床研究,结果提示该类药物可以提高骨量、促进骨形成、抑制骨吸收,对于骨质疏松有一定治疗效果。但该类药物应用后的副反应,对骨折的影响等方面的研究数据尚不足,有待完善进一步研究。 Sclerostin,a protein encoded by sclerosteosis( SOST) gene,antagonizes the Wnt protein via the low density lipoprotein receptor-related protein( LRP5/6) receptor and inhibits bone formation. It has been a new target for the treatment of osteoporosis.Both basic and clinical researches have indicated that sclerostin monoclonal antibody can treat osteoporosis by increasing bone mineral density,promoting bone formation and inhibiting bone resorption. However,limited data have evaluated the adverse effects of sclerostin monoclonal antibody and its influence on bone fracture,which deserve further studies.
作者 张阳洋 高艳虹 ZHANG Yangyang GAO Yanhong(Department of Geriatrics, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092, Chin)
出处 《中国骨质疏松杂志》 CAS CSCD 北大核心 2017年第10期1376-1380,共5页 Chinese Journal of Osteoporosis
关键词 骨质疏松 骨硬化蛋白单克隆抗体 Romosozumab Blosozumab Osteoporosis Sclerostin monoclonal antibody Romosozumab Blosozumab
  • 相关文献

参考文献5

二级参考文献149

  • 1许勇,杨桦,乔建瓯,李西华,严兰珍,王龙,徐国江,费俭,傅继粱,王铸钢.骨保护素(Opg)基因敲除小鼠发生高转换型骨质疏松和动脉钙化(英文)[J].生物化学与生物物理进展,2007,34(3):260-266. 被引量:26
  • 2Van Hul W, Balemans W, Van Hul E, Dikkers FG, Obee H, Stokroos RJ, Hildering P, Vanhoenacker F, Van Camp G, Willems PJ. Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21. Am J Hum Genet, 1998, 62(2): 391-399.
  • 3Balemans W, Van Den Ende J, Paes-Alves AF, Dikkers FG, Willems P J, Vanhoenacker F, de Almeida-Melo N, Alves CF, Stratakis CA, Hill SC, Van Hul W. Localization of the gene for sclerosteosis to the van Buchem disease-gene re- gion on chromosome 17q12-q21. Am J Hum Genet, 1999, 64(6): 1661-1669.
  • 4Balemans W, Ebeling M, Patel N, Van Hul E, Olson P, Dioszegi M, Lacza C, Wuyts W, Van Den Ende J, Willems P, Paes-Alves AF, Hill S, Bueno M, Ramos F J, Taeconi P, Dikkers FG, Stratakis C, Lindpainmer K, Vickery B, Fo- ernzler D, Van Hul W. Increased bone density in scleros- teosis is due to the deficiency of a novel secreted protein (SOST). Hum Mol Genet, 2001, 10(5): 537-543.
  • 5Brunkow ME, Gardner JC, Van Ness J, Paeper BW, Kovacevich BR, Proll S, Skonier JE, Zhao L, Sabo P J, Fu YH, Alisch RS, Gillett L, Colbert T, Tacconi P, Galas D, Hamersma H, Beighton P, Mulligan J. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. Am J Hum Genet, 2001, 68(3): 577-589.
  • 6Poole KE, van Bezooijen RL, Loveridge N, Hamersma H, Papapoulos SE, Lbwik CW, Reeve J. Sclerostin is a de- layed secreted product of osteocytes that inhibits bone formation. FASEB J, 2005, 19(13): 1842-1844.
  • 7Mayor C, Brudno M, Schwartz JR, Poliakov A, Rubin EM, Frazer KA, Pachter LS, Dubchak I. VISTA: visualizing global DNA sequence alignments of arbitrary length. Bio- informatics, 2000, 16(1 1): 1046-1047.
  • 8Balemans W, Van Hul W. Human genetics of SOST. J Musculoskelet Neuronal Interact, 2006, 6(4): 355-356.
  • 9Pearce JJ, Penny G, Rossant J. A mouse cerberus/Dan- re- lated gene family. Dev Biol, 1999, 209(1): 98-110.
  • 10Hsu DR, Economides AN, Wang XR, Eimon PM, Harland RM. The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP ac- tivities. Mol Cell, 1998, 1(5): 673-683.

共引文献25

同被引文献25

引证文献3

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部