TRIP6 a potential diagnostic marker for colorectal cancer with glycolysis and immune infiltration association

• Published in: Scientific reports Vol. 14; no. 1; pp. 4042 - 13
• Main Authors: Liu, Xu-Sheng, Chen, Yu-Xuan, Wan, Hua-Bing, Wang, Ya-Lan, Wang, Yang-Yang, Gao, Yan, Wu, Li-Bing, Pei, Zhi-Jun
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 19.02.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/67; 631/67/1857; 631/67/2327; 631/67/69; Adaptor proteins; Angiogenesis; Colorectal cancer; Colorectal carcinoma; Correlation analysis; Gene set enrichment analysis; Glucose metabolism; Glycolysis; Humanities and Social Sciences; Immune cell infiltration; Immune checkpoint; Infiltration; Lymphocytes T; Metastases; multidisciplinary; Prognostic; Regression analysis; Science; Science (multidisciplinary); Therapeutic targets; Thyroid; TRIP6; Tumor cells; Glycolysis; Immune cell infiltration; Prognostic; TRIP6; Colorectal cancer
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-54670-0

Thyroid hormone receptor interactor 6 (TRIP6) it is an adaptor protein belonging to the zyxin family of LIM proteins, participating in signaling events through interactions with various molecules. Despite this, TRIP6's role in colorectal cancer (CRC), particularly its correlation with glucose metabolism and immune cell infiltration, remains unclear. Through the TCGA and GEO databases, we obtained RNA sequencing data to facilitate our in-depth study and analysis of TRIP6 expression. To investigate the prognostic value of TRIP6 in CRC, we also used univariate Cox regression analysis. In addition, this study also covered a series of analyses, including clinicopathological analysis, functional enrichment analysis, glycolysis correlation analysis, immunoinfiltration analysis, immune checkpoint analysis, and angiogenesis correlation analysis, to gain a comprehensive and in-depth understanding of this biological phenomenon. It has been found that TRIP6 expression is significantly upregulated in CRC and correlates with the stage of the disease. Its overexpression portends a worse survival time. Functional enrichment analysis reveals that TRIP6 is associated with focal adhesion and glycolysis. Mechanistically, TRIP6 appears to exert its tumorigenic effect by regulating the glycolysis-related gene GPI. A higher level of expression of TRIP6 is associated with an increase in the number of iDC immune cells and a decrease in the number of Th1 immune cells. Also, TRIP6 may promote angiogenesis in tumor cells by promoting the expression of JAG2. Our study uncovers the upregulation of TRIP6 in CRC, illuminating its prognostic and diagnostic value within this context. Furthermore, we examine the relationship between TRIP6 expression levels, glycolysis, angiogenesis and immune cell infiltration. This underscores its potential as a biomarker for CRC treatment and as a therapeutic target.