Antisense lncRNA LDLRAD4-AS1 promotes metastasis by decreasing the expression of LDLRAD4 and predicts a poor prognosis in colorectal cancer

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作者
Shaobo Mo
Long Zhang
Weixing Dai
Lingyu Han
Renjie Wang
Wenqiang Xiang
Zhimin Wang
Qingguo Li
Jun Yu
Jihang Yuan
Sanjun Cai
Guoxiang Cai
机构
[1] Fudan University Shanghai Cancer Center,Department of Colorectal Surgery
[2] Fudan University,Department of Oncology, Shanghai Medical College
[3] Fudan University Shanghai Cancer Center,Department of Cancer Institute
[4] Fudan University,Shanghai
[5] Chinese National Human Genome Center and Shanghai Industrial Technology Institute (SITI),MOST Key Laboratory of Health and Disease Genomics
[6] Johns Hopkins University School of Medicine,Department of Surgery
[7] Second Military Medical University,Department of Medical Genetics
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Long noncoding RNAs (lncRNAs) have been revealed to play critical roles in tumor initiation and progression. The antisense lncRNA LDLRAD4-AS1 is the longest lncRNA of LDLRAD4, and its expression levels, cellular localization, precise function, and mechanism in colorectal cancer (CRC) remain unknown. In this study, we observed that lncRNA LDLRAD4-AS1 was located in the nucleus of CRC cells and that lncRNA LDLRAD4-AS1 was upregulated in most CRC specimens and cell lines. Overexpression of lncRNA LDLRAD4-AS1 was correlated with poor prognosis in CRC patients. LncRNA LDLRAD4-AS1 upregulation enhanced the migration and invasion of CRC cells in vitro and facilitated CRC metastasis in vivo. Mechanistic investigations suggested that lncRNA LDLRAD4-AS1 could decrease the expression of LDLRAD4 by disrupting the stability of LDLRAD4 mRNA, resulting in epithelial-to-mesenchymal transition (EMT) through upregulating Snail, thereby promoting metastasis in CRC. Our results demonstrated a previously unrecognized LDLRAD4-AS1-LDLRAD4-Snail regulatory axis involved in epigenetic and posttranscriptional regulation that contributes to CRC progression and metastasis.
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