LncRNA LINC01207 Could Positively Regulate the Development of Colorectal Cancer

Gaowu Hu; Wenquan Chen; Wei Peng; Yongqing Cao

doi:10.1155/2023/7671917

LncRNA LINC01207 Could Positively Regulate the Development of Colorectal Cancer

J Oncol. 2023 Feb 24:2023:7671917. doi: 10.1155/2023/7671917. eCollection 2023.

Authors

Gaowu Hu¹, Wenquan Chen¹, Wei Peng¹, Yongqing Cao²

Affiliations

¹ Department of Anorectal Medicine, Shanghai Traditional Chinese and Western Medicine Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Floor 9, Building 5, No. 303, Changyang Road, Hongkou District, Shanghai, China.
² Department of Anorectal Medicine, Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 725 Wanping South Road, Shanghai, China.

Abstract

Background: LINC01207 expression is associated with colorectal cancer progression. However, the exact role of LINC01207 in colorectal cancer (CRC) is not clear, and further exploration is needed.

Methods: Gene expression data of the GSE34053 database were used to explore the differential expressed genes (DEGs) between colon cancer cells and normal cells. The gene expression profiling interactive analysis (GEPIA) was used to determine the differential expression of LINC01207 between CRC and normal tissues and the association between the expression of LINC01207 and survival in patients with CRC. The Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) analysis were performed to obtain the biological processes and pathways associated with DEGs and LINC01207 coexpressed genes in CRC. The qRT-PCR was used to determine the LINC01207 level in CRC cell lines and tissue samples. CCK-8 assay was employed to measure cell viability and Transwell assay to assess cell invasion and migration.

Results: In this study, a total of 954 DEGs were identified, including 282 upregulated and 672 downregulated genes. LINC01207 was significantly upregulated in CRC samples with a poor prognosis. LINC01207 was also associated with pathways such as ECM-receptor interaction, O-glycan processing, and TNF signaling pathway in CRC. Knockdown of LINC01207 inhibited the migration, invasion, and proliferation of CRC cells.

Conclusion: LINC01207 might act as an oncogene and promote the progression of CRC. Our study suggested that LINC01207 had the potential to be a novel biomarker for CRC detection and a therapeutic target for CRC treatment.