Department of Oral and Maxillofacial Surgery, Xiangya Hospital of Central South University, Changsha, 410008, China.
Center of Stomatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Curr Med Sci. 2019 Jun;39(3):410-414. doi: 10.1007/s11596-019-2051-1. Epub 2019 Jun 17.
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3 (PFKFB3), an enzyme producing fructose 2, 6-bisphosphate (F-2, 6-BP), serves as a switch to activate phosphofructokinase-1, and is a critical enzyme for endothelial glycolysis, mediating circadian control of carcinogenesis. Also, tumor-associated macrophages (TAMs) play an important role in the progression and prognosis of numerous cancers. However, the role and clinical significance of PFKFB3 and TAMs in oral squamous cell carcinoma (OSCC) have not been elucidated. The present study was designed to investigate the correlation between PFKFB3 expression, CD163+ TAMs infiltration and tumor angiogenesis in OSCC by tissue microarray. Tissue microarrays containing 117 OSCC specimens and 56 matched paracarcinoma tissues were studied by immunohistochemistry. The expression levels of PFKFB3, CD163 and CD31 were significantly increased in OSCC specimens as compared with normal oral mucosa (P<0.05), and PFKFB was signifcantly correlated with tumor differentiation and tumor size (P<0.05), and CD163 was significantly correlated with areca nut chewing habit among OSCC tissues (P<0.05). Furthermore, Pearson's correlation analysis revealed that PFKFB3 was signifcantly correlated with both CD163 and CD31 (P<0.05), meanwhile CD163 was signifcantly correlated with CD31 (P<0.001), suggesting PFKFB3 may promote angiogenesis in tumor progression and metastases by regulating CD163+ TAMs infiltration in OSCC.
6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶 3(PFKFB3)是一种产生果糖 2,6-二磷酸(F-2,6-BP)的酶,作为激活磷酸果糖激酶-1 的开关,是内皮细胞糖酵解的关键酶,介导致癌作用的昼夜节律控制。此外,肿瘤相关巨噬细胞(TAMs)在许多癌症的进展和预后中发挥重要作用。然而,PFKFB3 和 TAMs 在口腔鳞状细胞癌(OSCC)中的作用和临床意义尚未阐明。本研究旨在通过组织微阵列研究 PFKFB3 表达、CD163+TAMs 浸润与 OSCC 肿瘤血管生成之间的相关性。通过免疫组织化学研究了包含 117 例 OSCC 标本和 56 例配对癌旁组织的组织微阵列。与正常口腔黏膜相比,OSCC 标本中 PFKFB3、CD163 和 CD31 的表达水平显著升高(P<0.05),PFKFB 与肿瘤分化和肿瘤大小显著相关(P<0.05),CD163 与 OSCC 组织中的槟榔咀嚼习惯显著相关(P<0.05)。此外,Pearson 相关分析显示 PFKFB3 与 CD163 和 CD31 均显著相关(P<0.05),同时 CD163 与 CD31 显著相关(P<0.001),提示 PFKFB3 可能通过调节 OSCC 中 CD163+TAMs 浸润促进肿瘤进展和转移中的血管生成。