Abstract

Wilms tumor gene on the X chromosome (WTX) is a putative tumor suppressor gene in Wilms tumor, but its expression and functions in other tumors are unclear. Colorectal cancer (CRC) is the third leading cause of cancer-related deaths in women and the second leading cause in men in the United States. We demonstrated that WTX frequently lost in CRC which was highly correlated with cell proliferation, tumor invasion and metastasis. Mechanistically, WTX loss disrupts the interaction between RhoGDIα and CDC42 by losing of the binding with RhoGDIα and triggers the activation of CDC42 and its downstream cascades, which promotes CRC development and liver metastasis. The aberrant upregulation of miR-20a/miR-106a were identified as the reason of WTX loss in CRC both in vivo and in vitro. These study defined the mechanism how miR-20a/miR-106a-mediated WTX loss regulates CRC progression and metastasis, and provided a potential therapeutic target for preventing CRC progression.

Wilms tumor gene on the X chromosome (WTX) is commonly downregulated in human cancers. Here the authors show that in colorectal cancer (CRC) WTX expression is downregulated via miR20a and miR160a and its loss promotes tumor development and liver metastasis by disrupting the interaction between RhoGDIα and CDC42 leading to the activation of the CDC42 downstream cascades.

Details

Title
RETRACTED ARTICLE: Mir20a/106a-WTX axis regulates RhoGDIa/CDC42 signaling and colon cancer progression
Author
Zhu, Gui-fang 1   VIAFID ORCID Logo  ; Xu, Yang-wei 1 ; Li, Jian 1 ; Niu, Hui-lin 1 ; Ma, Wen-xia 1 ; Xu, Jia 2 ; Zhou, Pei-rong 3 ; Liu, Xia 1 ; Ye, Dan-li 1 ; Liu, Xiao-rong 1   VIAFID ORCID Logo  ; Yan, Tao 3 ; Zhai, Wei-ke 1 ; Xu, Zhi-jun 3 ; Liu, Chun 3 ; Wang, Lei 4 ; Wang, Hao 3 ; Luo, Jia-mao 3 ; Liu, Li 5 ; Li, Xuan-qi 6 ; Guo, Suiqun 7 ; Jiang, Hui-ping 7 ; Shen, Peng 8 ; Lin, Hui-kuan 9   VIAFID ORCID Logo  ; Yu, Di-hua 10 ; Ding, Yan-qing 1 ; Zhang, Qing-ling 1 

 Southern Medical University, Department of Pathology, Nanfang Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Department of Pathology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Key Laboratory of Molecular Tumor Pathology of Guangdong Province, Guangzhou, China (GRID:grid.284723.8) 
 Icahn School of Medicine at Mount Sinai, Department of Oncological Sciences, New York, USA (GRID:grid.59734.3c) (ISNI:0000 0001 0670 2351) 
 Southern Medical University, Department of Pathology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Nanfang Hospital/First clinical Medical School, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471) 
 Southern Medical University, Department of Pathology, Nanfang Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Department of Pathology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471) 
 Southern Medical University, Hepatology Unit and Department of Infectious Diseases, Nanfang Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471) 
 Southern Medical University, Department of Pathology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471) 
 Southern Medical University, Department of Obstetrics and Gynecology, The Third Affiliated Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471) 
 Southern Medical University, Department of Oncology, Nanfang Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471) 
 Wake Forest Baptist Medical Center, Cancer Biology Comprehensive Cancer Center, Winston-Salem, USA (GRID:grid.412860.9) (ISNI:0000 0004 0459 1231) 
10  The University of Texas, MD Anderson Cancer Center, Department of Molecular & Cellular Oncology, Houston, USA (GRID:grid.240145.6) (ISNI:0000 0001 2291 4776) 
Pages
112
Publication year
2019
Publication date
2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2865943912
Copyright
© The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.