Kang Honggang, Ma Dan, Zhang Jing, Zhao Jun, Yang Mengxiang
Department of Oncology, Liaocheng People's Hospital, Liaocheng 252000, China.
Ann Transl Med. 2020 Apr;8(7):433. doi: 10.21037/atm.2020.03.195.
Pancreatic cancer is a devastating invasive disease. Understanding the molecular mechanism of metastasis of this cancer is basis for its treatment and prevention.
Pancreatic cancer tissues and normal adjacent tissues were collected from patients tour hospital. Western blotting and a sphere growth and invasion assay were performed to conduct analysis. Pancreatic ductal adenocarcinoma cell Line PANC-1 were cultured. To test the level of Raf-1 kinase inhibitor protein (RKIP), immunofluorescence analyses were performed.
In this study, we showed that expression of RKIP was downregulated in pancreatic cancer. RKIP can inhibit epithelial to mesenchymal transition (EMT) in PANC-1 cells. MicroRNA-181a (miR-181a) has a high expression in pancreatic cancer and can induce EMT phenotype by directly degrading RKIP in pancreatic cancer PANC-1 cells.
We concluded that miR-181a induces EMT phenotype through its regulation of RKIP in pancreatic cancer. MicroRNA-18a may be a novel target in the treatment of pancreatic cancer in future.
胰腺癌是一种具有毁灭性的侵袭性疾病。了解这种癌症转移的分子机制是其治疗和预防的基础。
从我院患者处收集胰腺癌组织和癌旁正常组织。进行蛋白质印迹法以及球形生长和侵袭试验以进行分析。培养胰腺导管腺癌细胞系PANC-1。为检测Raf-1激酶抑制蛋白(RKIP)的水平,进行了免疫荧光分析。
在本研究中,我们表明RKIP在胰腺癌中表达下调。RKIP可抑制PANC-1细胞中的上皮-间质转化(EMT)。微小RNA-181a(miR-181a)在胰腺癌中高表达,并且可通过直接降解胰腺癌PANC-1细胞中的RKIP来诱导EMT表型。
我们得出结论,miR-181a通过其在胰腺癌中对RKIP的调控诱导EMT表型。微小RNA-18a未来可能是胰腺癌治疗的新靶点。