miR-216a may inhibit pancreatic tumor growth by targeting JAK2.

نویسندگان

  • Bao-hua Hou
  • Zhi-xiang Jian
  • Peng Cui
  • Shao-jie Li
  • Rui-qing Tian
  • Jin-rui Ou
چکیده

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.

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عنوان ژورنال:
  • FEBS letters

دوره 589 17  شماره 

صفحات  -

تاریخ انتشار 2015