Kobayashi Takahiko, Ishida Junich, Shimizu Yuichi, Kawakami Hiroshi, Suda Goki, Muranaka Tetsuhito, Komatsu Yoshito, Asaka Masahiro, Sakamoto Naoya
Department of Gastroenterology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Tumour Biol. 2017 Mar;39(3):1010428317694547. doi: 10.1177/1010428317694547.
RNA-binding motif 5 is a putative tumor suppressor gene that modulates cell cycle arrest and apoptosis. We recently demonstrated that RNA-binding motif 5 inhibits cell growth through the p53 pathway. This study evaluated the clinical significance of RNA-binding motif 5 expression in gastric cancer and the effects of altered RNA-binding motif 5 expression on cancer biology in gastric cancer cells. RNA-binding motif 5 protein expression was evaluated by immunohistochemistry using the surgical specimens of 106 patients with gastric cancer. We analyzed the relationships of RNA-binding motif 5 expression with clinicopathological parameters and patient prognosis. We further explored the effects of RNA-binding motif 5 downregulation with short hairpin RNA on cell growth and p53 signaling in MKN45 gastric cancer cells. Immunohistochemistry revealed that RNA-binding motif 5 expression was decreased in 29 of 106 (27.4%) gastric cancer specimens. Decreased RNA-binding motif 5 expression was correlated with histological differentiation, depth of tumor infiltration, nodal metastasis, tumor-node-metastasis stage, and prognosis. RNA-binding motif 5 silencing enhanced gastric cancer cell proliferation and decreased p53 transcriptional activity in reporter gene assays. Conversely, restoration of RNA-binding motif 5 expression suppressed cell growth and recovered p53 transactivation in RNA-binding motif 5-silenced cells. Furthermore, RNA-binding motif 5 silencing reduced the messenger RNA and protein expression of the p53 target gene p21. Our results suggest that RNA-binding motif 5 downregulation is involved in gastric cancer progression and that RNA-binding motif 5 behaves as a tumor suppressor gene in gastric cancer.
RNA结合基序5是一种假定的肿瘤抑制基因,可调节细胞周期停滞和细胞凋亡。我们最近证明,RNA结合基序5通过p53途径抑制细胞生长。本研究评估了RNA结合基序5在胃癌中表达的临床意义,以及RNA结合基序5表达改变对胃癌细胞生物学行为的影响。使用106例胃癌患者的手术标本,通过免疫组织化学评估RNA结合基序5蛋白的表达。我们分析了RNA结合基序5表达与临床病理参数及患者预后的关系。我们进一步探讨了短发夹RNA下调RNA结合基序5对MKN45胃癌细胞生长和p53信号传导的影响。免疫组织化学显示,106例胃癌标本中有29例(27.4%)RNA结合基序5表达降低。RNA结合基序5表达降低与组织学分化、肿瘤浸润深度、淋巴结转移、肿瘤-淋巴结-转移分期及预后相关。在报告基因检测中,RNA结合基序5沉默增强了胃癌细胞增殖并降低了p53转录活性。相反,在RNA结合基序5沉默的细胞中,恢复RNA结合基序5表达可抑制细胞生长并恢复p53反式激活。此外,RNA结合基序5沉默降低了p53靶基因p21的信使核糖核酸和蛋白表达。我们的结果表明,RNA结合基序5下调参与胃癌进展,且RNA结合基序5在胃癌中发挥肿瘤抑制基因的作用。