Department of Orthopedics & Traumatology, Taipei Veterans General Hospital, Taipei, Taiwan.
Department of orthopedics, Therapeutical and Musculoskeletal Tumor Research Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Sci Rep. 2020 Feb 7;10(1):2105. doi: 10.1038/s41598-019-56024-7.
Biological reconstruction of allografts and recycled autografts have been widely implemented in high-grade osteogenic sarcoma. For treating tumor-bearing autografts, extracorporeal irradiation (ECIR) and liquid nitrogen (LN) freezing techniques are being used worldwide as a gold standard treatment procedure. Both the methods aim to eradicate the tumor cells from the local recurrence and restore the limb function. Therefore, it is essential and crucial to find, and compare the alterations at molecular and physiological levels of the treated and untreated OGS recycled autografts to obtain valuable clinical information for better clinical practice. Thus, we aimed to investigate the significantly expressed altered proteins from ECIR-and cryotherapy/freezing- treated OGS (n = 12) were compared to untreated OGS (n = 12) samples using LC-ESI-MS/MS analysis, and the selected proteins from this protein panel were verified using immunoblot analysis. From our comparative proteomic analysis identified a total of 131 differentially expressed proteins (DEPs) from OGS. Among these, 91 proteins were up-regulated (2.5 to 3.5-folds), and 40 proteins were down-regulated (0.2 to 0.5 folds) (p < 0.01 and 0.05). The functional enrichment analysis revealed that the identified DEPs have belonged to more than 10 different protein categories include cytoskeletal, extracellular matrix, immune, enzyme modulators, and cell signaling molecules. Among these, we have confirmed two potential candidates' expressions levels such as Fibronectin and Protein S100 A4 using western blot analysis. Our proteomic study revealed that LN-freezing and ECIR treatments are effectively eradicating tumor cells, and reducing the higher expressions of DEPs at molecular levels which may help in restoring the limb functions of OGS autografts effectively. To the best of our knowledge, this is the first proteomic study that compared proteomic profiles among freezing, ECIR treated with untreated OGS in recycled autografts. Moreover, the verified proteins could be used as prognostic or diagnostic markers that reveal valuable scientific information which may open various therapeutic avenues in clinical practice to improve patient outcomes.
同种异体移植物和再循环自体移植物的生物重建已广泛应用于高级成骨肉瘤。为了治疗肿瘤-bearing 自体移植物,体外照射(ECIR)和液氮(LN)冷冻技术作为金标准治疗方法正在全球范围内使用。这两种方法的目的都是从局部复发中消灭肿瘤细胞,并恢复肢体功能。因此,有必要和关键是要找到并比较治疗和未治疗的 OGS 再循环自体移植物在分子和生理水平上的变化,以获得有价值的临床信息,从而改善临床实践。因此,我们旨在使用 LC-ESI-MS/MS 分析比较 ECIR 和冷冻/冻结治疗的 OGS(n = 12)与未治疗的 OGS(n = 12)样本中明显表达的改变蛋白,并使用免疫印迹分析验证该蛋白组中的选定蛋白。通过比较蛋白质组学分析,从 OGS 中鉴定出总共 131 种差异表达蛋白(DEPs)。其中,91 种蛋白上调(2.5 到 3.5 倍),40 种蛋白下调(0.2 到 0.5 倍)(p < 0.01 和 0.05)。功能富集分析表明,鉴定出的 DEPs 属于 10 种以上不同的蛋白质类别,包括细胞骨架、细胞外基质、免疫、酶调节剂和细胞信号分子。在这些蛋白中,我们使用 Western blot 分析验证了两个潜在候选蛋白的表达水平,如纤连蛋白和 S100A4 蛋白。我们的蛋白质组学研究表明,LN 冷冻和 ECIR 治疗有效地消灭了肿瘤细胞,并降低了分子水平上更高的 DEPs 表达,这可能有助于有效地恢复 OGS 自体移植物的肢体功能。据我们所知,这是首次比较冷冻、ECIR 治疗与未治疗 OGS 再循环自体移植物之间蛋白质组学图谱的研究。此外,验证的蛋白可以用作预后或诊断标志物,揭示有价值的科学信息,这可能为临床实践中改善患者预后开辟各种治疗途径。