Ray Swapan K
Department of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Building 2, Room C11, 6439 Garners Ferry Road, Columbia, SC 29209; Tel.: 803-216-3420.
For Immunopathol Dis Therap. 2016;7(1-2):127-139. doi: 10.1615/ForumImmunDisTher.2016017227.
The () gene is located on chromosome 9q31. All of the currently known 17 KLF transcription regulators that have similarity with members of the specificity protein family are distinctly characterized by the Cys/His zinc finger motifs at their carboxyl terminals for preferential binding to the GC/GT box or the CACCC element of the gene promoter and enhancer regions. KLF4 is a transcriptional regulator of cell proliferation, differentiation, apoptosis, migration, and invasion, emphasizing its importance in diagnosis and prognosis of particular tumors. KLF4 has been implicated in tumor progression as well as in tumor suppression, depending on tumor types and contexts. Different studies so far strongly suggest that KLF4 acts as an oncogene in glioblastoma, which is the most malignant and prevalent brain tumor in human adult. It is now well established that the presence of glioblastoma stem cells (GSCs) in glioblastoma causes therapy resistance and progressive growth of the tumor. Because KLF4 is one of the key stemness factors in GSCs, it is likely that KLF4 contributes significantly to the survival of GSCs and the recurrence of glioblastoma. On the other hand, recent studies show that KLF4 can act as a tumor suppressor in human malignant neuroblastoma, which is a deadly tumor mostly in children, by inhibiting the cell cycle and activating the cell differentiation and death pathways. Our increasing understanding of the molecular mechanisms of the contrasting roles of KLF4 in glioblastoma and neuroblastoma is useful for superior diagnosis, therapy, and prognosis of these tumors of the nervous system.
()基因位于9号染色体的q31区域。目前已知的17种与特异性蛋白家族成员相似的KLF转录调节因子,其羧基末端均具有Cys/His锌指基序,这使其能够优先结合基因启动子和增强子区域的GC/GT盒或CACCC元件,从而具有独特的特征。KLF4是细胞增殖、分化、凋亡、迁移和侵袭的转录调节因子,突显了其在特定肿瘤诊断和预后中的重要性。根据肿瘤类型和背景情况,KLF4既与肿瘤进展有关,也与肿瘤抑制有关。目前不同的研究强烈表明,KLF4在胶质母细胞瘤(这是成人中最恶性且最常见的脑肿瘤)中作为一种癌基因发挥作用。现已明确,胶质母细胞瘤中胶质母细胞瘤干细胞(GSCs)的存在会导致肿瘤产生治疗抗性并不断生长。由于KLF4是GSCs中的关键干性因子之一,KLF4很可能对GSCs的存活以及胶质母细胞瘤的复发有显著影响。另一方面,最近的研究表明,KLF4在人类恶性神经母细胞瘤(这主要是一种儿童致命肿瘤)中可作为肿瘤抑制因子,通过抑制细胞周期并激活细胞分化和死亡途径来发挥作用。我们对KLF4在胶质母细胞瘤和神经母细胞瘤中相反作用的分子机制的认识不断加深,这有助于对这些神经系统肿瘤进行更优的诊断、治疗和预后评估。