Author
Listed:
- Tian-Wei Chen
(Chinese Academy of Sciences
Chinese Academy of Sciences
Fengxian Hospital Affiliated to Southern Medical University)
- Fen-Fen Yin
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Yan-Mei Yuan
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Dong-Xian Guan
(Chinese Academy of Sciences)
- Erbin Zhang
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Feng-Kun Zhang
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Hao Jiang
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Ning Ma
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Jing-Jing Wang
(Chinese Academy of Sciences)
- Qian-Zhi Ni
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Lin Qiu
(Chinese Academy of Sciences)
- Jing Feng
(Fengxian Hospital Affiliated to Southern Medical University)
- Xue-Li Zhang
(Fengxian Hospital Affiliated to Southern Medical University)
- Ying Bao
(Huzhou University)
- Kang Wang
(Second Military Medical University)
- Shu-Qun Cheng
(Second Military Medical University)
- Xiao-Fan Wang
(Duke University Medical Center)
- Xiang Wang
(Huzhou University)
- Jing-Jing Li
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Dong Xie
(Chinese Academy of Sciences
Chinese Academy of Sciences
China National Center for Food Safety Risk Assessment
ShanghaiTech University)
Abstract
Metastasis-associated recurrence is the major cause of poor prognosis in hepatocellular carcinoma (HCC), however, the underlying mechanisms remain largely elusive. In this study, we report that expression of choroideremia-like (CHML) is increased in HCC, associated with poor survival, early recurrence and more satellite nodules in HCC patients. CHML promotes migration, invasion and metastasis of HCC cells, in a Rab14-dependent manner. Mechanism study reveals that CHML facilitates constant recycling of Rab14 by escorting Rab14 to the membrane. Furthermore, we identify several metastasis regulators as cargoes carried by Rab14-positive vesicles, including Mucin13 and CD44, which may contribute to metastasis-promoting effects of CHML. Altogether, our data establish CHML as a potential promoter of HCC metastasis, and the CHML-Rab14 axis may be a promising therapeutic target for HCC.
Suggested Citation
Tian-Wei Chen & Fen-Fen Yin & Yan-Mei Yuan & Dong-Xian Guan & Erbin Zhang & Feng-Kun Zhang & Hao Jiang & Ning Ma & Jing-Jing Wang & Qian-Zhi Ni & Lin Qiu & Jing Feng & Xue-Li Zhang & Ying Bao & Kang W, 2019.
"CHML promotes liver cancer metastasis by facilitating Rab14 recycle,"
Nature Communications, Nature, vol. 10(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10364-0
DOI: 10.1038/s41467-019-10364-0
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