Artas Gokhan, Ozturk Sait, Kuloglu Tuncay, Dagli Adile Ferda, Gonen Murat, Artas Hakan, Aydin Suleyman, Erol Fatih Serhat
Firat University, School of Medicine, Department of Pathology, Elazig, Turkey.
Turk Neurosurg. 2018;28(6):989-994. doi: 10.5137/1019-5149.JTN.22022-17.2.
To investigate the possible role of ELABELA (ELA) in the histopathological grading of gliomas.
We retrospectively assessed pathological specimens of patients who underwent surgery for intracranial space-occupying lesions. Only primary glioma specimens were included in this study. We enrolled 11 patients histologically diagnosed with low-grade glioma and 22 patients with high-grade glioma. The ELA antibody was applied to 4?6-?m-thick sections obtained from paraffin blocks. Histoscores were calculated using the distribution and intensity of staining immunoreactivity. An independent sample t-test was used for two-point inter-group assessments, whereas one-way analysis of variance was used for the other assessments. p < 0.05 was considered statistically significant.
The histoscores of the control brain, low-grade glioma, and high-grade glioma tissues were found to be 0.08, 0.37, and 0.92, respectively. The difference in ELA immunoreactivity between the control brain tissue and glioma tissue was statistically significant (p < 0.05). In addition, a statistically significant increase was observed in ELA immunoreactivity in high-grade glioma tissues compared with that in low-grade glioma tissues (p < 0.05).
ELA has an angiogenetic role in the progression of glial tumors. ELA, which is an endogenous ligand of the apelin receptor, activates the apelinergic system and causes the progression of glial tumors. Further studies with a large number of patients are necessary to investigate the angiogenetic role of ELA in glial tumors.
探讨ELABELA(ELA)在胶质瘤组织病理学分级中的可能作用。
我们回顾性评估了接受颅内占位性病变手术患者的病理标本。本研究仅纳入原发性胶质瘤标本。我们纳入了11例经组织学诊断为低级别胶质瘤的患者和22例高级别胶质瘤患者。将ELA抗体应用于从石蜡块中获取的4-6微米厚的切片。使用免疫反应性染色的分布和强度计算组织学评分。两组间两点评估采用独立样本t检验,其他评估采用单因素方差分析。p<0.05被认为具有统计学意义。
发现对照脑组织、低级别胶质瘤组织和高级别胶质瘤组织的组织学评分分别为0.08、0.37和0.92。对照脑组织与胶质瘤组织之间ELA免疫反应性的差异具有统计学意义(p<0.05)。此外,与低级别胶质瘤组织相比,高级别胶质瘤组织中ELA免疫反应性有统计学意义的增加(p<0.05)。
ELA在胶质肿瘤进展中具有血管生成作用。ELA作为apelin受体的内源性配体,激活apelin能系统并导致胶质肿瘤进展。有必要对大量患者进行进一步研究以探讨ELA在胶质肿瘤中的血管生成作用。