Sharma Aarti E, Olivas Andrea, Parilla Megan, Yassan Lindsay, Wang Hanlin, Zhang Sharon S, Weber Christopher, Keutgen Xavier M, Hart John, Krausz Thomas, Setia Namrata
Department of Pathology.
Department of Pathology, Loyola University, Chicago, IL.
Appl Immunohistochem Mol Morphol. 2022 Feb 1;30(2):e11-e15. doi: 10.1097/PAI.0000000000000982.
Dysregulation of epigenetic mechanisms, reflected by loss of expression of 5-hydroxymethylcytosine (5-hmC) is being increasingly recognized as a marker of aggressive behavior in several neoplasms; however, the role of such epigenetic modifiers in pancreatic neuroendocrine tumors (PanNETs) has not been studied. Annotated cohort of 60 PanNETs was evaluated for 5-hmC expression using immunohistochemistry. Univariable and multivariable analyses were performed. To determine intratumor heterogeneity of 5-hmC expression, 26 additional synchronous metastatic deposits of PanNETs from 8 patients were evaluated for 5-hmC expression. 5-hmC level showed significant association with the presence of distant metastases (P=0.02), female sex (P=0.04), and Ki-67 proliferation index (P=0.002). A multivariate model created using the stepwise logistic regression analysis showed the presence of nodal metastases (odds ratio=6.15), lymphovascular invasion (odds ratio=4.07) and lack of 5-hmC expression (odds ratio=5.34) were predictive of the risk of distant metastasis in PanNETs with a c-statistic of 0.845. Epigenetic intratumoral heterogeneity of 5-hmC expression was seen in 37.5% cases (3/8). Our work provides evidence that epigenetic regulators are involved in the pathobiology of PanNETs and immunohistochemical analysis of 5-hmC may be able to refine prognostic evaluation of these tumors.
表观遗传机制失调表现为5-羟甲基胞嘧啶(5-hmC)表达缺失,这在多种肿瘤中越来越被视为侵袭性行为的标志物;然而,此类表观遗传修饰因子在胰腺神经内分泌肿瘤(PanNETs)中的作用尚未得到研究。使用免疫组织化学方法对60例PanNETs的注释队列进行5-hmC表达评估。进行了单变量和多变量分析。为了确定5-hmC表达的肿瘤内异质性,对来自8例患者的另外26个PanNETs同步转移灶进行了5-hmC表达评估。5-hmC水平与远处转移的存在(P=0.02)、女性性别(P=0.04)和Ki-67增殖指数(P=0.002)显著相关。使用逐步逻辑回归分析创建的多变量模型显示,存在淋巴结转移(比值比=6.15)、淋巴管侵犯(比值比=4.07)和缺乏5-hmC表达(比值比=5.34)可预测PanNETs远处转移的风险,c统计量为0.845。在37.5%的病例(3/8)中观察到5-hmC表达的表观遗传肿瘤内异质性。我们的工作提供了证据,表明表观遗传调节因子参与了PanNETs的病理生物学过程,5-hmC的免疫组织化学分析可能能够完善这些肿瘤的预后评估。