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地诺单抗对骨巨细胞瘤影响的体外研究:与唑来膦酸的比较

In Vitro Study of the Effects of Denosumab on Giant Cell Tumor of Bone: Comparison with Zoledronic Acid.

作者信息

Shibuya Isao, Takami Masamichi, Miyamoto Arei, Karakawa Akiko, Dezawa Akira, Nakamura Shigeru, Kamijo Ryutaro

机构信息

Department of Biochemistry, Showa University School of Dentistry, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan.

Department of Orthopaedic Surgery, Teikyo University Mizonokuchi Hospital, 3-8-3 Mizonokuchi, Takatsu-ku, Kawasaki, Kanagawa, 213-8507, Japan.

出版信息

Pathol Oncol Res. 2019 Jan;25(1):409-419. doi: 10.1007/s12253-017-0362-8. Epub 2017 Nov 20.

Abstract

Giant cell tumor of bone (GCTB) is a locally aggressive primary bone tumor that contains numerous osteoclasts formed from marrow-derived precursors through receptor activator of nuclear factor κ-B ligand (RANKL), an osteoclast differentiation factor expressed in neoplastic cells of GCTB. Denosumab, a fully human monoclonal antibody targeting RANKL, has recently been used for the treatment of GCTB, and superior treatment effects have been reported. The aim of this work was to elucidate the mechanism of action of denosumab, and the differences between denosumab and zoledronic acid at the level of GCTB cells. We isolated GCTB cells from 3 patients and separated them into osteoclasts, osteoclast precursors and proliferating spindle-shaped stromal cells (the true neoplastic component), and examined the action of denosumab on differentiation, survival and bone resorption activity of osteoclasts. Denosumab and zoledronic acid inhibited osteoclast differentiation from mononuclear cells containing osteoclast precursors. Zoledronic acid inhibited osteoclast survival, whereas an inhibitory effect of denosumab on osteoclast survival was not observed. The inhibitory effect on bone resorption by both agents was confirmed in culture on dentin slices. Furthermore, zoledronic acid showed dose-dependent inhibition of cell growth of neoplastic cells whereas denosumab had no inhibitory effect on these cells. Denosumab has an inhibitory effect on osteoclast differentiation, but no inhibitory effects on survival of osteoclasts or growth of neoplastic cells in GCTBs.

摘要

骨巨细胞瘤(GCTB)是一种具有局部侵袭性的原发性骨肿瘤,其中含有大量由骨髓来源的前体细胞通过核因子κ-B受体激活剂配体(RANKL)形成的破骨细胞,RANKL是一种在GCTB肿瘤细胞中表达的破骨细胞分化因子。地诺单抗是一种靶向RANKL的全人单克隆抗体,最近已被用于治疗GCTB,并且已报道了其卓越的治疗效果。这项工作的目的是阐明地诺单抗的作用机制,以及在GCTB细胞水平上地诺单抗与唑来膦酸之间的差异。我们从3例患者中分离出GCTB细胞,并将其分为破骨细胞、破骨细胞前体细胞和增殖的梭形基质细胞(真正的肿瘤成分),并研究了地诺单抗对破骨细胞分化、存活和骨吸收活性的作用。地诺单抗和唑来膦酸均抑制含有破骨细胞前体细胞的单核细胞向破骨细胞的分化。唑来膦酸抑制破骨细胞存活,而未观察到地诺单抗对破骨细胞存活的抑制作用。两种药物对牙本质切片培养中的骨吸收的抑制作用均得到证实。此外,唑来膦酸显示出对肿瘤细胞生长的剂量依赖性抑制作用,而地诺单抗对这些细胞没有抑制作用。地诺单抗对破骨细胞分化有抑制作用,但对GCTB中破骨细胞的存活或肿瘤细胞的生长没有抑制作用。

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