Chaiyawat Parunya, Pruksakorn Dumnoensun, Pipatwattana Prach, Phanphaisarn Areerak, Teeyakasem Pimpisa, Klangjorhor Jeerawan, Settakorn Jongkolnee
Musculoskeletal Science and Translational Research Center, Department of Orthopedics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Biomedical Engineering Institute, Chiang Mai University, Chiang Mai, Thailand.
J Bone Oncol. 2019 Mar 19;16:100233. doi: 10.1016/j.jbo.2019.100233. eCollection 2019 Jun.
Diverse aberrancy in genetic background, protein profiling, and biological pathways have emerged as important factors hindering discovery of effective treatment of osteosarcoma. In a previous study, we used a proteomic approach to identify some osteosarcoma-related proteins by analysis of protein profiling in individual patients through primary cell culture. Endoplasmic reticulum protein 29 (ERp29) emerged as a protein of interest for further study since accumulating evidence suggests it has broad functions in tumorigenesis of different types of cancer. Importantly, until now no report on examination of the expression patterns of ERp29 in osteosarcoma has been published.
In this study, an expression of ERp29 was examined in patient-derived osteosarcoma cells (7 cases) and normal bone graft-derived osteoblasts (7 cases) using western blotting. Expression profile of ERp29 in 94 osteosarcoma cases was investigated using immunohistochemically stained on formalin-fixed paraffin-embedded biopsied tissue. An association with clinicopathologic parameters and the patient survival was evaluated. The doubling time of five osteosarcoma cells lines expressing different levels of ERp29 was determined by a cell number along the exponential phase of the growth curve.
The results substantiate the outcome from the proteomic study in which ERp29 expression was significantly higher in primary osteosarcoma cells compared to osteoblastic cells. Immunohistochemical analysis found that expression of ERp29 was low in 79% of the cases (immunoreactive score (IRS) <6). A significant correlation was observed between expression of ERp29 and patient survival. Lower expression of ERp29 (IRS<6) was statistically significantly associated with shorter overall survival of the patients ( = 0.041). In addition, we found that osteosarcoma cells with low ERp29 expression had a higher growth rate compared with high-ERp29-expressing cells.
These findings suggest a tumor suppressive role of ERp29 in osteosarcoma. In addition, ERp29 might potentially be applied as a prognostic indicator in patients with osteosarcoma.
基因背景、蛋白质谱和生物学途径中的多种异常已成为阻碍骨肉瘤有效治疗方法发现的重要因素。在之前的一项研究中,我们采用蛋白质组学方法,通过原代细胞培养分析个体患者的蛋白质谱,以鉴定一些骨肉瘤相关蛋白。内质网蛋白29(ERp29)成为进一步研究的目标蛋白,因为越来越多的证据表明它在不同类型癌症的肿瘤发生中具有广泛功能。重要的是,迄今为止尚未有关于骨肉瘤中ERp29表达模式检测的报道。
在本研究中,使用蛋白质免疫印迹法检测了来源于患者的骨肉瘤细胞(7例)和正常骨移植来源的成骨细胞(7例)中ERp29的表达。采用免疫组织化学方法检测了94例骨肉瘤病例福尔马林固定石蜡包埋活检组织中ERp29的表达谱。评估其与临床病理参数及患者生存的相关性。通过生长曲线指数期的细胞数量测定了五种表达不同水平ERp29的骨肉瘤细胞系的倍增时间。
结果证实了蛋白质组学研究的结果,即原发性骨肉瘤细胞中ERp29的表达明显高于成骨细胞。免疫组织化学分析发现,79%的病例中ERp29表达较低(免疫反应评分(IRS)<6)。观察到ERp29表达与患者生存之间存在显著相关性。ERp29低表达(IRS<6)与患者较短的总生存期在统计学上显著相关(P = 0.041)。此外,我们发现与高表达ERp29的细胞相比,低表达ERp29的骨肉瘤细胞生长速度更快。
这些发现表明ERp29在骨肉瘤中具有肿瘤抑制作用。此外,ERp29可能有潜力作为骨肉瘤患者的预后指标。