Long noncoding RNA LINC01594 inhibits the CELF6-mediated splicing of oncogenic CD44 variants to promote colorectal cancer metastasis

被引:3
|
作者
Liu, Bowen [1 ,2 ]
Song, Angxi [2 ]
Gui, Pengkun [2 ]
Wang, Jin [3 ]
Pan, Yaojie [4 ]
Li, Chao [1 ,2 ]
Li, Shuai [1 ,2 ]
Zhang, Yi [1 ,2 ]
Jiang, Tao [1 ,2 ]
Xu, Yixin [1 ,2 ]
Pei, Dongsheng [3 ]
Song, Jun [1 ,2 ]
机构
[1] Xuzhou Med Univ, Dept Gen Surg, Affiliated Hosp, 99 Huaihai West Rd, Xuzhou 221006, Peoples R China
[2] Xuzhou Med Univ, Inst Digest Dis, 84 Huaihai West Rd, Xuzhou 221002, Peoples R China
[3] Xuzhou Med Univ, Dept Pathol, 209 Tongshan Rd, Xuzhou 221004, Peoples R China
[4] Zhejiang Prov Peoples Hosp, Dept Med Oncol, 158 Shangtang Rd, Hangzhou 310000, Zhejiang, Peoples R China
关键词
PROTEINS; EXPRESSION; TRANSCRIPTION; BINDING; REGULATOR; CARCINOMA; INTERACTS; ZMAT3;
D O I
10.1038/s41419-023-05924-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long noncoding RNAs (lncRNAs) play critical roles in tumorigenesis and tumor metastasis. However, the underlying mechanisms of lncRNAs in colorectal cancer (CRC) need further exploration. By using data from The Cancer Genome Atlas (TCGA) and GEO databases, we identified a novel CRC-related lncRNA, LINC01594, that is significantly upregulated in CRC and associated with poor prognosis. In vitro and in vivo, gain- and loss-of-function experiments demonstrated that LINC01594 promotes metastasis in CRC. LINC01594 functions as a DNMT1 scaffold, increasing the level of CELF6 promoter methylation. LINC01594 also competitively binds the transcription factor p53, decreasing CELF6 expression. This inhibited the exon skipping of CD44 V4-V7 induced by CELF6. In summary, this study highlights a novel CRC biomarker and therapeutic target, LINC01594, and the findings suggest that the LINC01594-CELF6-CD44 axis might serve as a biomarker and therapeutic target in CRC.
引用
收藏
页数:16
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