MicroRNA-301a promotes pancreatic cancer invasion and metastasis through the JAK/STAT3 signaling pathway by targeting SOCS5

Author:

Hu Hui1,Zhang Qin12,Chen Weiqun134,Wu Tangwei1,Liu Shuiyi13,Li Xiaoyi1,Luo Bo5,Zhang Tianzhu12,Yan Ge12,Lu Hongda36,Lu Zhongxin1234

Affiliation:

1. Department of Medical Laboratory, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

2. School of Laboratory Medicine, Hubei University of Chinese Medicine, Wuhan, China

3. Cancer Research Institute of Wuhan, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

4. Key Laboratory for Molecular Diagnosis of Hubei Province, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

5. Department of Pathology, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

6. Department of Oncology, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

Abstract

AbstractPancreatic cancer is one of the most lethal digestive malignant tumors. We had previously found that microRNA-301a (miR-301a) is a oncogenic microRNA whose recognized conduce to nuclear factor-kappa B (NF-κB) activation in pancreatic cancer, yet the underlying mechanisms of miR-301a in promoting pancreatic cancer invasion and migration is obscure. In this work we found that high expression of miR-301a in human pancreatic cancer patients is related to poor survival. Overexpression of miR-301a enhances pancreatic cancer cell invasion, angiogenesis and migration, whereas inhibition of miR-301a suppresses pancreatic cancer cell invasion and reduces orthotopic pancreatic tumor growth and metastasis. Furthermore, suppressor of cytokine signaling 5 (SOCS5) is identified as a target gene of miR-301a. We found that miR-301a suppressed the expression of SOCS5 leads to janus kinase/signal transducer and activator of transcription 3 (JAK/STAT3) activation and is related to poor overall survival of pancreatic cancer patients. Taken together, our data show for the first time that the feedback loop between miR-301a and JAK/STAT3 pathway may play a significant role in pancreatic cancer invasion and metastasis. Targeting the loop may prove beneficial to prevent metastasis and provide a more effective therapeutic strategy for pancreatic cancer.

Funder

Key project of Natural Sciences Foundation of Hubei Province

Science and technology support program (foreign scientific and technological cooperation) of Hubei Province

Yellow CraneTalent Plan Foundation, Research Fund of Wuhan Public Health Bureau

Youth Foundation of Wuhan Central Hospital

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,General Medicine

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