Mostafa Rahma Gamal, Hashim Mohammad Ibrahim, Bawahab Ahmed Abdulwahab, Baloush Razan Abed A, Abdelwahed Mohammed S, Hasan Abdulkarim, Ismail Khadiga A, Abd-Elhameed Nageh Rady, Embaby Ahmed, Sharfeldeen Abd El Rahman M
Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Assiut University, Assiut 71524, Egypt.
Department of Basic Medical Sciences, College of Medicine, University of Jeddah, Jeddah 23218, Saudi Arabia.
Medicina (Kaunas). 2025 Mar 21;61(4):557. doi: 10.3390/medicina61040557.
: Glucose Transporter-1 (GLUT1) is the key target gene for hypoxia-inducible factor (HIF), which helps cells uptake glucose during cell division, malignant transformation, and nutrient depletion. Cancer hypoxia is a well-known condition caused by an oxygen imbalance in the cancer microenvironment. During chronic hypoxia, certain cancer cells can survive and adapt. These cellular alterations can make cancer more aggressive, causing invasion and metastasis. The study investigated the presence of GLUT1 in oral epithelial dysplasia (OED) and various histopathological grades of oral squamous cell carcinoma (OSCC) to assess the significance of GLUT1 as a prognostic indicator. : A total of 40 samples of tissue blocks, including 5 cases of normal oral mucosa, 5 cases of epithelial dysplasia, and 30 cases of OSCC with 10 cases each of well-differentiated, moderately differentiated, and poorly differentiated OSCCs, these cases were diagnosed using the Hematoxylin and Eosin (H&E) staining technique. GLUT1 expression was assessed using immunohistochemical staining, which involved evaluating the location of the stain and the percentage of staining. : The mean area percent was highest in poorly differentiated cases (47.37) and lowest in well-differentiated cases (13.42). In poorly differentiated cases, diffuse expression was observed in almost all malignant cells, exhibiting membrane, cytoplasmic and nuclear staining. A significant difference ( < 0.001) between all groups in regard to immunostaining was detected. GLUT1 expression increased from oral epithelial dysplasia to oral squamous cell carcinoma histological grades. GLUT1 in actively dividing cells may reflect the tumor's aggressiveness and treatment response. Hypoxia increases this marker's expression, indicating division and proliferation.
葡萄糖转运蛋白1(GLUT1)是缺氧诱导因子(HIF)的关键靶基因,在细胞分裂、恶性转化和营养耗竭过程中帮助细胞摄取葡萄糖。癌症缺氧是癌症微环境中氧失衡导致的一种众所周知的情况。在慢性缺氧期间,某些癌细胞能够存活并适应。这些细胞改变会使癌症更具侵袭性,导致侵袭和转移。该研究调查了口腔上皮发育异常(OED)和不同组织病理学分级的口腔鳞状细胞癌(OSCC)中GLUT1的存在情况,以评估GLUT1作为预后指标的意义。
共收集40个组织块样本,包括5例正常口腔黏膜、5例上皮发育异常以及30例OSCC,其中高分化、中分化和低分化OSCC各10例,这些病例均采用苏木精和伊红(H&E)染色技术进行诊断。使用免疫组织化学染色评估GLUT1的表达,包括评估染色位置和染色百分比。
低分化病例的平均面积百分比最高(47.37),高分化病例最低(13.42)。在低分化病例中,几乎所有恶性细胞均观察到弥漫性表达,呈现膜、细胞质和细胞核染色。检测到所有组之间免疫染色存在显著差异(<0.001)。GLUT1表达从口腔上皮发育异常到口腔鳞状细胞癌的组织学分级逐渐增加。活跃分裂细胞中的GLUT1可能反映肿瘤的侵袭性和治疗反应。缺氧会增加该标志物的表达,表明细胞分裂和增殖。