Benjamin Zanghellini , Nicole Zechmann , Dieter Baurecht , Tilman A. Grünewald , Manfred Burghammer , Bernadette Liegl-Atzwanger , Andreas Leithner , Anton Davydok , Helga Lichtenegger
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引用次数: 0
摘要
骨肉瘤(Osteosarcoma,OS)是人类最常见的恶性原发性骨肿瘤,有多种亚型。肿瘤是通过产生未成熟骨的恶性成骨细胞形成的。本文基于小角 X 射线散射(SAXS)、广角 X 射线衍射(WAXS)、背散射电子成像(BEI)和拉曼光谱等多模态方法,研究了两种不同亚型的骨肉瘤,分别来自一名患有大面积硬化的传统骨肉瘤患者和一名骨旁骨肉瘤患者。研究发现,两种肿瘤的患病部位的矿物质颗粒尺寸和胶原矿物质复合体的定向程度都有所降低,同时结晶度也有所下降。两个人的肿瘤材料在矿化程度上存在明显差异。碳酸盐与磷酸盐的比率也存在进一步的差异,该比率与骨矿物质中碳酸盐的替代程度有关,也表明了骨矿物质的周转率。骨矿物晶体 c 轴的收缩被证明是另一个非常敏感的参数,有可能指示恶性肿瘤。
Multimodal analysis and comparison of stoichiometric and structural characteristics of parosteal and conventional osteosarcoma with massive sclerosis in human bone
Osteosarcoma (OS) is the most common malignant primary bone tumor in humans and occurs in various subtypes. Tumor formation happens through malignant osteoblasts producing immature bone. In the present paper we studied two different subtypes of osteosarcoma, from one individual with conventional OS with massive sclerosis and one individual with parosteal OS, based on a multimodal approach including small angle x-ray scattering (SAXS), wide angle x-ray diffraction (WAXS), backscattered electron imaging (BEI) and Raman spectroscopy. It was found that both tumors showed reduced mineral particle sizes and degree of orientation of the collagen-mineral composite in the affected areas, alongside with a decreased crystallinity. Distinct differences between the tumor material from the two individuals were found in the degree of mineralization. Further differences were observed in the carbonate to phosphate ratio, which is related to the degree of carbonate substitution in bone mineral and indicative of the turnover rate. The contraction of the c-axis of the bone mineral crystals proved to be a further, very sensitive parameter, potentially indicative of malignancy.
期刊介绍:
Journal of Structural Biology (JSB) has an open access mirror journal, the Journal of Structural Biology: X (JSBX), sharing the same aims and scope, editorial team, submission system and rigorous peer review. Since both journals share the same editorial system, you may submit your manuscript via either journal homepage. You will be prompted during submission (and revision) to choose in which to publish your article. The editors and reviewers are not aware of the choice you made until the article has been published online. JSB and JSBX publish papers dealing with the structural analysis of living material at every level of organization by all methods that lead to an understanding of biological function in terms of molecular and supermolecular structure.
Techniques covered include:
• Light microscopy including confocal microscopy
• All types of electron microscopy
• X-ray diffraction
• Nuclear magnetic resonance
• Scanning force microscopy, scanning probe microscopy, and tunneling microscopy
• Digital image processing
• Computational insights into structure