Yıldırım İbrahim Halil, Çakmak Ecir Ali, Camcı Celaleddin
Dicle University, Faculty of Veterinary Medicine, Department of Genetics, Diyarbakır, Türkiye.
Gaziantep University, Faculty of Medicine, Department of Medical Biology and Genetics, Konya, Türkiye.
Cell Mol Biol (Noisy-le-grand). 2018 Oct 30;64(13):6-9.
Pancreatic cancer is characterized by rapid metastasis and resistant to medical treatments. As the other cancers, mutations of tumor suppressor genes that involved in suppression of cell growth are observed in pancreatic cancers. ING4 protein is one of the proteins involved in the regulation of p53 tumor suppressor gene functions. ING4 involved in suppression of cell proliferation, chromosome rearrangement, cell migration, and angiogenesis. In this study, gene expressions and splicing variants of ING4 gene were investigated. Fresh tumor and normal specimens of the same pancreatic cancer patients were used. Gene expression study carried out by calculating the brightness of the bands on agarose gel and splicing variants were detected by direct sequencing. According to the results, three splice forms of ING4 and a decrease in gene expression of ING4 were determined. Splicing type of ING4 affects the translocation of ING4 proteins into the nucleus. To determine the gene expression of each splicing variant, will further clarify the role of ING4 in pancreatic cancers.
胰腺癌的特点是转移迅速且对医学治疗具有抗性。与其他癌症一样,在胰腺癌中观察到参与抑制细胞生长的肿瘤抑制基因发生了突变。ING4蛋白是参与调控p53肿瘤抑制基因功能的蛋白质之一。ING4参与抑制细胞增殖、染色体重排、细胞迁移和血管生成。在本研究中,对ING4基因的基因表达和剪接变体进行了研究。使用了同一胰腺癌患者的新鲜肿瘤和正常标本。通过计算琼脂糖凝胶上条带的亮度进行基因表达研究,并通过直接测序检测剪接变体。根据结果,确定了ING4的三种剪接形式以及ING4基因表达的降低。ING4的剪接类型影响ING4蛋白向细胞核的转运。为了确定每个剪接变体的基因表达,将进一步阐明ING4在胰腺癌中的作用。