首页> 外文期刊>Biochimica et biophysica acta: BBA: International journal of biochemistry, biophysics and molecular biololgy. Proteins and Proteomics >Discoidin, CUB and LCCL domain-containing protein 2 (DCBLD2) is a novel biomarker of myxofibrosarcoma invasion identified by global protein expression profiling
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Discoidin, CUB and LCCL domain-containing protein 2 (DCBLD2) is a novel biomarker of myxofibrosarcoma invasion identified by global protein expression profiling

机译:迪诺蛋白,幼崽和LCCL域域的蛋白2(DCBLD2)是通过全球蛋白表达分析鉴定的麦克热肌瘤侵袭的新型生物标志物

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摘要

Myxofibrosarcoma (MFS) is a mesenchymal malignancy characterized by frequent recurrence even after radical wide resection. To optimize therapy for MFS patients, we aimed to identify candidate tissue biomarkers of MFS invasion potential. Invasion characteristics of MFS were evaluated by magnetic resonance imaging and protein expression profiling of primary tumor tissues performed using two-dimensional difference gel electrophoresis (2D-DIGE). Protein expression profiles were compared between invasive and non-invasive tumors surgically resected from 11 patients. Among the 3453 protein spots observed, 59 demonstrated statistically significant difference in intensity (>= 2-fold) between invasive and non-invasive tumors (p < 0.01 by Wilkoxon test), and were identified by mass spectrometry as 47 individual proteins. Among them, we further focused on discoidin, CUB and LCCL domain-containing protein 2 (DCBLD2), a receptor tyrosine kinase with aberrant expression in malignant tumors. Immunohistochemistry analysis of 21 additional MFS cases revealed that higher DCBLD2 expression was significantly associated with invasive properties of tumor cells. DCBLD2 sensitivity and specificity, and positive and negative predictive values for MFS invasion were 69.2%, 87.5%, 90%, and 63.6%, respectively. The expression level of DCBLD2 was consistent in different portions of tumor tissues. Thus, DCBLD2 expression can be a useful biomarker to evaluate invasive properties of MFS. Further validation studies based on multi-institutional collaboration and comprehensive analysis of DCBLD2 biological functions in MFS are required to confirm its prognostic utility for clinical application.
机译:Myxofibrosarcoma(MFS)是一种间充质恶性肿瘤,其特征在于即使在激进的广泛切除后甚至经常复发。优化MFS患者的治疗,我们旨在鉴定MFS侵袭潜力的候选组织生物标志物。通过使用二维差异凝胶电泳(2D-Dige)进行的原发性肿瘤组织的磁共振成像和蛋白表达分析评估MFS的侵袭特性。比较从11名患者的侵袭性和非侵入性肿瘤之间比较蛋白表达谱。在观察到的3453个蛋白斑点中,59在侵袭性和非侵入性肿瘤之间的强度(> = 2倍)的强度(> = 2倍)差异(P <0.01通过Wilkoxon试验),并通过质谱法鉴定为47个单独的蛋白质。其中,我们进一步专注于盘状蛋白,幼崽和LCCL结构域的蛋白2(DCBLD2),受体酪氨酸激酶,恶性肿瘤中具有异常表达的受体酪氨酸激酶。 21例额外MFS病例的免疫组化分析表明,较高的DCBLD2表达与肿瘤细胞的侵袭性显着相关。 DCBLD2的敏感性和特异性,MFS侵袭的正负预测值分别为69.2%,87.5%,90%和63.6%。 DCBLD2的表达水平在肿瘤组织的不同部分中一致。因此,DCBLD2表达可以是有用的生物标志物,以评估MFS的侵入性。需要基于多制度合作的进一步验证研究和MFS中DCBLD2生物学功能的综合分析,以确认其对临床应用的预后效用。

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