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KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling
KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling
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KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling
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KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling
KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling

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KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling
KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling
Journal Article

KIFC1 regulated by miR-532-3p promotes epithelial-to-mesenchymal transition and metastasis of hepatocellular carcinoma via gankyrin/AKT signaling

2019
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Overview
Hepatocellular carcinoma (HCC) is one of the most lethal cancers worldwide. The poor survival may be due to a high proportions of tumor recurrence and metastasis. Kinesin family member C1 (KIFC1) is highly expressed in a variety of neoplasms and is a potential marker for non-small cell lung cancer or ovarian adenocarcinoma metastasis. Nevertheless, the role of KIFC1 in HCC metastasis remains obscure. We investigated this in the present study using HCC cell lines and clinical specimens. Our results indicated that increased levels of KIFC1 were associated with poor prognosis and metastasis in HCC. In addition, KIFC1 induced epithelial-to-mesenchymal transition (EMT) and HCC metastasis both in vitro and in vivo. This tumorigenic effect depended on gankyrin; inhibiting gankyrin activity reversed EMT via activation of protein kinase B (AKT)/Twist family BHLH transcription factor 1 (AKT/TWIST1). We also found that KIFC1 was directly regulated by the microRNA miR-532-3p, whose downregulation was associated with metastatic progression in HCC. These results denote that a decrease in miR-532-3p levels results in increased KIFC1 expression in HCC, leading to metastasis via activation of the gankyrin/AKT/TWIST1 signaling pathway.
Publisher
Nature Publishing Group,Nature Publishing Group UK
Subject

Adenocarcinoma

/ AKT protein

/ Animals

/ Cancer

/ Cancer metastasis

/ Carcinoma

/ Carcinoma, Hepatocellular - genetics

/ Carcinoma, Hepatocellular - metabolism

/ Carcinoma, Hepatocellular - mortality

/ Carcinoma, Hepatocellular - secondary

/ Care and treatment

/ Cell Line, Tumor

/ Cellular signal transduction

/ Development and progression

/ Down-Regulation

/ Epithelial-Mesenchymal Transition - physiology

/ Gene expression

/ Genetic aspects

/ Health aspects

/ Helix-loop-helix proteins (basic)

/ Hepatocellular carcinoma

/ Heterografts

/ Humans

/ Kaplan-Meier Estimate

/ Kinases

/ Kinesin

/ Kinesins - antagonists & inhibitors

/ Kinesins - physiology

/ Liver cancer

/ Liver Neoplasms - genetics

/ Liver Neoplasms - metabolism

/ Liver Neoplasms - mortality

/ Liver Neoplasms - pathology

/ Lung cancer

/ Lung Neoplasms - physiopathology

/ Lung Neoplasms - secondary

/ Male

/ Medical prognosis

/ Mesenchyme

/ Metastases

/ Metastasis

/ Mice, Inbred BALB C

/ Mice, Nude

/ MicroRNA

/ MicroRNAs - biosynthesis

/ MicroRNAs - genetics

/ MicroRNAs - physiology

/ miRNA

/ Neoplasm Proteins - antagonists & inhibitors

/ Neoplasm Proteins - physiology

/ Non-small cell lung cancer

/ Non-small cell lung carcinoma

/ Nuclear Proteins - physiology

/ Ovarian cancer

/ Prognosis

/ Proteasome Endopeptidase Complex - physiology

/ Protein kinases

/ Proto-Oncogene Proteins - physiology

/ Proto-Oncogene Proteins c-akt - physiology

/ Recurrence (Disease)

/ RNA Interference

/ RNA, Neoplasm - biosynthesis

/ RNA, Neoplasm - genetics

/ RNA, Neoplasm - physiology

/ Signal Transduction

/ Small cell lung cancer

/ Stem cells

/ Tumors

/ Twist-Related Protein 1 - physiology