Pouloudi Despoina, Manou Maria, Sarantis Panagiotis, Tsoukalas Nikolaos, Tsourouflis Gerasimos, Dana Eougken, Karamouzis Michalis V, Klijanienko Jerzy, Theocharis Stamatios
First Department of Pathology, Medical School, National and Kapodistrian University of Athens, 115 27 Athens, Greece.
Department of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, 115 27 Athens, Greece.
Diagnostics (Basel). 2021 Mar 14;11(3):517. doi: 10.3390/diagnostics11030517.
Salivary gland tumors (SGTs) comprise a group of rare neoplasms. Locally aggressive, recurrent and/or metastatic SGTs are notorious for their resistance to systemic therapy, making the need for carefully designed, prospective and randomized trials with useful predictive markers mandatory to define new effective therapeutic protocols. Histone Deacetylases (HDACs), are thought to play a crucial role in carcinogenesis. They affect the DNA structure, being also able to regulate its transcription, repair, and replication. This study aimed to evaluate-to our knowledge for the first time-the HDAC-1, -2, -4 and -6 immunohistochemical expression in SGTs and their potential use as prognostic biomarkers. Medical records and archival histopathological material of 58 (36 benign and 22 malignant) SGT patients were included in this study. The -score was statistically correlated with the clinicopathological characteristics for all cases and patients' survival rate in malignant SGTs. HDAC-2 positivity was significantly associated with more prolonged overall survival (OS) of patients with malignant SGTs ( = 0.028), while HDAC-2 positivity and no HDAC-6 expression were associated with prolonged OS of patients with HG malignant SGT ( = 0.003 and = 0.043, respectively). Additionally, a high HDAC-2 H-score was significantly associated with longer OS for HG malignant SGT patients ( = 0.027). In our study, HDAC-2 expression is a marker for good prognosis, whereas HDAC-6 expression indicated poor prognosis; thus, an inhibitor of HDAC-6 may be used to improve patients' survival.
涎腺肿瘤(SGTs)是一组罕见的肿瘤。局部侵袭性、复发性和/或转移性SGTs因其对全身治疗的耐药性而声名狼藉,因此需要精心设计、具有前瞻性和随机性的试验,并带有有用的预测标志物,以确定新的有效治疗方案。组蛋白去乙酰化酶(HDACs)被认为在致癌过程中起关键作用。它们影响DNA结构,还能够调节其转录、修复和复制。本研究旨在首次评估HDAC-1、-2、-4和-6在SGTs中的免疫组化表达及其作为预后生物标志物的潜在用途。本研究纳入了58例(36例良性和22例恶性)SGT患者的病历和存档组织病理学材料。对所有病例的 -评分与临床病理特征以及恶性SGTs患者的生存率进行了统计学相关性分析。HDAC-2阳性与恶性SGTs患者更长的总生存期(OS)显著相关( = 0.028),而HDAC-2阳性且无HDAC-6表达与高级别(HG)恶性SGT患者的OS延长相关(分别为 = 0.003和 = 0.043)。此外,HDAC-2高H评分与HG恶性SGT患者更长的OS显著相关( = 0.027)。在我们的研究中,HDAC-2表达是预后良好的标志物,而HDAC-6表达表明预后不良;因此,HDAC-6抑制剂可用于提高患者生存率。