Immunoprofile of some surface and cytoplasmic peripheral cell adhesion molecules in oral squamous cell carcinoma.

Ionuţ Octavian Ilie, Adrian Camen, Daniela Dumitrescu, Maria Cristina Munteanu, Marius Matei, Mircea Sebastian Şerbănescu, Claudiu Mărgăritescu
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Abstract

Despite the recent advances in diagnosis and treatment, oral squamous cell carcinoma (OSCC) continues to have a low overall survival rate (around 50%), being a tumor with high locoregional aggressiveness and high risk of lymph node (LN) dissemination. Such behavior can also be explained by the alteration of the expression of adhesion molecules, allowing tumor cells to invade surrounding tissues and make them capable of metastasizing. In this regard, we initiated a study on the immunohistochemical expression of Integrin alphavbeta6 (Integrin αvβ6), CD44 and Ezrin in OSCCs. A number of 39 such tumors with various locations in the oral cavity were investigated by enzymatic immunohistochemistry together with several samples of oral mucosa and oral dysplastic lesions. Using integrated optical density (IOD) as a method to quantify, we observed that the reactivity of these three markers decreased in the progression of dysplastic lesions and in the transition from well to moderately and poorly differentiated tumors. Also, in both conditions we noticed a shift of pattern reactivity from the continuous membrane to discontinuous membrane and cytoplasmic one, even to a nuclear pattern. In addition, the reactivity of the three markers was more evident in the invasion front and especially in these tumors with discohesive growth patterns. All this suggests the involvement of these adhesion molecules in the processes of transformation and malignant progression of OSCCs. It also explains their possible involvement in locoregional aggressiveness and LN dissemination.

口腔鳞状细胞癌中一些表面和细胞质外周细胞粘附分子的免疫谱分析。
尽管最近在诊断和治疗方面取得了进展,但口腔鳞状细胞癌(OSCC)的总生存率仍然很低(约50%),是一种具有高局部侵袭性和高淋巴结(LN)传播风险的肿瘤。这种行为也可以解释为粘附分子表达的改变,使肿瘤细胞能够侵入周围组织并使其具有转移能力。为此,我们开展了整合素αvβ6 (Integrin αvβ6)、CD44和Ezrin在OSCCs中的免疫组化表达研究。我们用酶免疫组化方法研究了39例不同位置的口腔肿瘤以及一些口腔黏膜和口腔发育不良病变的样本。利用综合光密度(IOD)作为量化方法,我们观察到这三种标志物的反应性在发育不良病变的进展以及从良好分化到中度分化和低分化肿瘤的转变过程中下降。此外,在这两种情况下,我们都注意到从连续膜到不连续膜和细胞质的模式反应性的转变,甚至到核模式。此外,这三种标记物的反应性在侵袭前沿更为明显,特别是在这些具有不粘连生长模式的肿瘤中。所有这些提示这些粘附分子参与了OSCCs的转化和恶性进展过程。这也解释了他们可能参与地方侵略性和LN传播。
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