Hou Bao-hua, Jian Zhi-xiang, Cui Peng, Li Shao-jie, Tian Rui-qing, Ou Jin-rui
Department of General Surgery, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, PR China.
Department of General Surgery, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, PR China.
FEBS Lett. 2015 Aug 4;589(17):2224-32. doi: 10.1016/j.febslet.2015.06.036. Epub 2015 Jul 3.
This study was aimed to investigate miR-216a expression in pancreatic cancer and determine its effects on proliferation. miR-216a was found downregulated in pancreatic cancer tissues as compared to benign pancreatic lesions. JAK2 was identified as a miR-216a gene target. Further, in vivo treatment of PANC-1 tumors with miR-216a reduced JAK2 protein levels in the tumor and reduced tumor volume. In conclusion, miR-216a may function as a tumor suppressor regulating pancreatic cancer cells by targeting the JAK/STAT pathway. Further studies with a larger number of patient samples are necessary to fully explore the diagnostic and therapeutic potential of miR-216a for pancreatic cancer.
本研究旨在调查miR-216a在胰腺癌中的表达,并确定其对增殖的影响。与良性胰腺病变相比,发现miR-216a在胰腺癌组织中表达下调。JAK2被确定为miR-216a的基因靶点。此外,用miR-216a对PANC-1肿瘤进行体内治疗可降低肿瘤中JAK2蛋白水平并减小肿瘤体积。总之,miR-216a可能作为一种肿瘤抑制因子,通过靶向JAK/STAT途径调节胰腺癌细胞。需要对更多患者样本进行进一步研究,以充分探索miR-216a在胰腺癌诊断和治疗方面的潜力。