Long non-coding RNA Lnc-LALC facilitates colorectal cancer liver metastasis via epigenetically silencing LZTS1.

Abstract

Colorectal cancer (CRC) is one of the most common cancers around the world and endangers human health seriously. Liver metastasis is an important factor affecting the long-term prognosis of CRC and the specific mechanism of CRLM (colorectal cancer with liver metastasis) is not fully understood. LZTS1 has been found dysregulated in many cancers, especially in CRC. Theories suggested that hypermethylation of the promoter regions of LZTS1 was responsible for LZTS1 abnormal expression in multiple malignant tumors. Although the role of LZTS1 in CRC cell proliferation has been reported, its role in CRLM remains unclear. Numerous studies reported Long non-coding RNA (lncRNA) could regulate the gene expression level by regulating gene methylation status in many tumors. However, whether there were lncRNAs could change the methylation status of LZTS1 or not in CRLM was unknown. In this study, we aimed to investigate whether there are lncRNAs can regulate the expression of LZTS1 through affecting DNA methylation in CRLM. We found that upregulated Lnc-LALC in CRC was negatively correlated with LZTS1 expression, and Lnc-LALC could regulate LZTS1 expression in both mRNA and protein level in our study. Functionally, Lnc-LALC enhanced the CRC cells metastasis ability in vitro and vivo through inhibiting the expression of LZTS1. Furthermore, the precise mechanisms exploration showed that lnc-LALC could recruit DNA methyltransferases (DNMTs) to the LZTS1 promoter by combining with Enhancer of zeste homolog 2(EZH2) and then altered the expression of LZTS1 via DNMTs-mediated DNA methylation. Collectively, our data demonstrated the important role of Lnc-LALC/ LZTS1 axis in CRLM development.

• Authors: Chuan Zhang, Lu Wang, Chi Jin, Jiahui Zhou, Chaofan Peng, Yong Wang, Ziwei Xu, Dongsheng Zhang, Yuanjian Huang, Yue Zhang, Dongjian Ji, Wen Peng, Kangpeng Jin, Junwei Tang, Yifei Feng, Yueming Sun
• Journal: Cell death & disease (Cell Death Dis) Vol. 12 Issue 2 Pg. 224 (02 26 2021) ISSN: 2041-4889 [Electronic] England
• PMID: 33637680 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA-Binding Proteins
• LZTS1 protein, human
• RNA, Long Noncoding
• Tumor Suppressor Proteins
• DNA (Cytosine-5-)-Methyltransferases
• EZH2 protein, human
• Enhancer of Zeste Homolog 2 Protein

Topics

• Adenocarcinoma (genetics, metabolism, secondary)
• Aged
• Animals
• Caco-2 Cells
• Cell Movement
• Colorectal Neoplasms (genetics, metabolism, pathology)
• DNA (Cytosine-5-)-Methyltransferases (genetics, metabolism)
• DNA Methylation
• DNA-Binding Proteins (genetics, metabolism)
• Enhancer of Zeste Homolog 2 Protein (genetics, metabolism)
• Epithelial-Mesenchymal Transition
• Female
• Gene Expression Regulation, Neoplastic
• Gene Silencing
• HCT116 Cells
• HT29 Cells
• Humans
• Liver Neoplasms (genetics, metabolism, secondary)
• Male
• Mice, Inbred BALB C
• Mice, Nude
• Middle Aged
• Neoplasm Invasiveness
• Promoter Regions, Genetic
• RNA, Long Noncoding (genetics, metabolism)
• Tumor Suppressor Proteins (genetics, metabolism)
• Mice