학술논문

Inactivation of axon guidance molecule netrin-1 in human colorectal cancer by an epigenetic mechanism.
Document Type
Article
Source
Biochemical & Biophysical Research Communications. Jun2022, Vol. 611, p146-150. 5p.
Subject
*COLORECTAL cancer
*DNA methylation
*INTESTINAL mucosa
*CELLULAR control mechanisms
*EPIGENETICS
Language
ISSN
0006-291X
Abstract
Netrin-1, the protein product of the NTN1 gene, is an axon guidance molecule implicated in regulation of cell survival and tumorigenesis. Expression of the netrin-1 receptors deleted in colorectal cancer (DCC) and uncoordinated 5 homolog (UNC5H) is frequently silenced in colorectal cancer (CRC) by either loss of heterozygosity or epigenetic mechanisms. However, netrin-1 expression and regulation in CRC are mostly unknown. Here, we report that NTN1 expression is significantly reduced in most CRC tissues compared to the adjacent normal intestinal mucosa, and that NTN1 DNA methylation is significantly higher in CRCs (24.6%) than in the adjacent normal intestinal mucosa (4.0%). In 6 CRC cell lines, NTN1 expression is low. Treatment with 5-Aza-2′-deoxycytidine increased expression of NTN1 in CRC cell lines, indicating that DNA methylation represses NTN1 transcription in CRCs. NTN1 DNA hypermethylation was significantly associated with advanced CRC disease. Median netrin-1 serum levels were significantly decreased in CRC patients (330.1 pg/mL) compared with normal individuals (438.6 pg/mL). Our results suggest that netrin-1 is a candidate biomarker for CRC. • Netrin-1 mRNA and protein levels are down-regulated in most CRCs. • Netrin-1 DNA methylation is higher in CRCs than in corresponding normal mucosa. • Hypermethylation of netrin-1 is associated with CRC patients with advanced TNM stage. • Serum levels of netrin-1 are significantly decreased in patients with CRC. [ABSTRACT FROM AUTHOR]