Santos André Azevedo Dos, Mafra Rodrigo Porpino, da Silva Leorik Pereira, Pinto Leão Pereira, Freitas Roseana de Almeida, de Souza Lélia Batista
Dentistry Sciences Postgraduate Program, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Oral Pathology Postgraduate Program, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Oral Surg Oral Med Oral Pathol Oral Radiol. 2023 Mar;135(3):396-409. doi: 10.1016/j.oooo.2022.09.038. Epub 2022 Sep 29.
This study aimed to compare the immunoexpression profile of tumor stem cell (TSC) biomarkers CD44, aldehyde dehydrogenase 1 (ALDH1), OCT4, and SOX2 in salivary gland tumors (SGTs).
Sixty tissue specimens of SGTs, including 20 pleomorphic adenomas, 20 adenoid cystic carcinomas (ACCs), and 20 mucoepidermoid carcinomas, in addition to 4 samples of normal glandular tissue, were subjected to immunohistochemistry. The expression of the biomarkers in the parenchyma and stroma was evaluated. Data were analyzed statistically by nonparametric tests (P < .05).
Higher parenchymal expression of ALDH1, OCT4, and SOX2 was observed in pleomorphic adenomas, ACCs, and mucoepidermoid carcinomas, respectively. Most ACCs did not express ALDH1. Higher immunoexpression of ALDH1 in major SGTs (P = .021) and of OCT4 in minor SGTs (P = .011) was found. Immunoexpression of SOX2 was related to lesions without myoepithelial differentiation (P < .001) and malignant behavior (P = .002). Furthermore, OCT4 was related to myoepithelial differentiation (P = .009). CD44 expression was related to a better prognosis. Stromal immunoexpressions of CD44, ALDH1, and OCT4 were higher in malignant SGTs.
Our findings suggest the participation of TSCs in the pathogenesis of SGTs. We emphasize the need for further investigations into the presence and role of TSCs in the stroma of these lesions.
本研究旨在比较肿瘤干细胞(TSC)生物标志物CD44、醛脱氢酶1(ALDH1)、八聚体结合转录因子4(OCT4)和性别决定区Y框蛋白2(SOX2)在涎腺肿瘤(SGT)中的免疫表达谱。
60例SGT组织标本,包括20例多形性腺瘤、20例腺样囊性癌(ACC)和20例黏液表皮样癌,另外还有4例正常腺组织样本,进行免疫组织化学检测。评估生物标志物在实质和间质中的表达。数据采用非参数检验进行统计学分析(P <.05)。
在多形性腺瘤、ACC和黏液表皮样癌中分别观察到ALDH1、OCT4和SOX2在实质中的较高表达。大多数ACC不表达ALDH1。发现在主要SGT中ALDH1的免疫表达较高(P = 0.021),在次要SGT中OCT4的免疫表达较高(P = 0.011)。SOX2的免疫表达与无肌上皮分化的病变(P <.001)和恶性行为(P = 0.002)有关。此外,OCT4与肌上皮分化有关(P = 0.009)。CD44表达与较好的预后有关。在恶性SGT中,CD44、ALDH1和OCT4的间质免疫表达较高。
我们的研究结果表明TSC参与了SGT的发病机制。我们强调需要进一步研究这些病变间质中TSC的存在及其作用。