Mozalbat Shiraz, Nashef Aysar, Maalouf Naseem, Abdol-Elraziq Murad, El-Naaj Imad Abu, Tadmor Hagar, Ghantous Yasmin
Molecular Biology of Oral Cancer Laboratory, Tzafon Medical Center, Azrieli Faculty of Medicine, Bar-Ilan University, Safed 1311502, Israel.
Department of Oral and Maxillofacial Surgery, Tzafon Medical Center, Faculty of Medicine, Bar-Ilan University, Ramat Gan 5290002, Israel.
Cancers (Basel). 2025 May 23;17(11):1761. doi: 10.3390/cancers17111761.
Oral squamous cell carcinoma (OSCC) is a prevalent malignancy with a poor prognosis. Surgical removal of the primary tumor and regional lymph nodes (LNs) remains the fundamental treatment for OSCC, although 40% of patients are negative for LN metastasis. The epithelial-mesenchymal transition (EMT) plays a crucial role in OSCC progression by enabling epithelial cells to acquire mesenchymal traits, thereby facilitating migration and metastasis. Smad4, a tumor suppressor protein, is known to mediate EMT and is associated with poor prognosis and metastasis; however, its precise pro-metastatic role in OSCC via EMT remains unclear. We hypothesize that EMT and Smad4 could serve as practical diagnostic tools for personalized OSCC treatment. In this study, we analyzed 23 OSCC samples from Tzafon Medical Center, comparing the expression of Smad4 and EMT markers with clinical and histopathological data. Additionally, an OSCC cell model with and without Smad4 mutation was used to investigate tumor phenotypes, including proliferation and invasion, in relation to EMT markers. Our findings reveal a strong correlation between EMT markers, Smad4 expression, and OSCC pathological staging, with the cell model further confirming the link between Smad4 and EMT markers. The combined influence of Smad4 and EMT markers on OSCC progression highlights their potential as diagnostic tools and as guides for personalized treatment strategies.
口腔鳞状细胞癌(OSCC)是一种常见的恶性肿瘤,预后较差。手术切除原发肿瘤和区域淋巴结(LN)仍然是OSCC的基本治疗方法,尽管40%的患者淋巴结转移呈阴性。上皮-间质转化(EMT)通过使上皮细胞获得间质特征,在OSCC进展中起关键作用,从而促进迁移和转移。Smad4是一种肿瘤抑制蛋白,已知其介导EMT,并与预后不良和转移相关;然而,其通过EMT在OSCC中的确切促转移作用仍不清楚。我们假设EMT和Smad4可作为个性化OSCC治疗的实用诊断工具。在本研究中,我们分析了来自Tzafon医疗中心的23份OSCC样本,将Smad4和EMT标志物的表达与临床和组织病理学数据进行比较。此外,使用具有和不具有Smad4突变的OSCC细胞模型来研究与EMT标志物相关的肿瘤表型,包括增殖和侵袭。我们的研究结果揭示了EMT标志物、Smad4表达与OSCC病理分期之间存在密切相关性,细胞模型进一步证实了Smad4与EMT标志物之间的联系。Smad4和EMT标志物对OSCC进展的综合影响突出了它们作为诊断工具和个性化治疗策略指导的潜力。