多数据库整合分析识别金属蛋白酶组织抑制剂 1 在结直肠癌中的表达及其与免疫微环境的关联

In recent decades, the incidence of colorectal cancer (CRC) has been rising worldwide. CRC ranks second in cancer-related mortality. The identification of reliable biomarkers for early diagnosis and prognosis prediction, along with a deeper understanding of the underlying molecular events, holds substantial promise for improving patient outcomes. The tissue inhibitor of the metalloproteinase 1 ( TIMP1 ) gene is overexpressed in various gastrointestinal malignancies and contributes to tumor progression. However, its role in regulating the CRC tumor immune microenvironment (TIME) and its potential as a clinically actionable prognostic biomarker remain unclear.

To probe how TIMP1 acts as a prognosis-related candidate biomarker in colorectal carcinoma, TCGA-derived datasets were adopted to conduct Kaplan-Meier survival assessment. We also investigated the connection between the expression abundance of TIMP1 and the infiltration of immune populations and intratumoral lymphocytes; furthermore, immune checkpoint-related genes were systematically assessed across multiple tumor types via the TISIDB and TIMER2.0 platforms, with particular emphasis on CRC. We adopted the ESTIMATE scoring system to figure out how TIMP1 gene expression correlates with the phenotypic properties of the colorectal-cancer TIME. We relied on the limma toolkit for the screening of differential transcripts from high- TIMP1 and low- TIMP1 cohorts. Enrichment assessments covering Gene Ontology terms and Kyoto Encyclopedia of Genes and Genomes entries were then carried out to predict the potential biological pathways associated with TIMP1 . We constructed the protein-protein interaction map for TIMP1 -interacting partners via the STRING repository. To further explore TIMP1 -correlated genes, we performed Venn diagram intersection analysis combined with Spearman's correlation test. Finally, quantitative reverse-transcription PCR was then implemented to detect TIMP1 messenger-RNA abundance inside the RKO colorectal carcinoma cell line as well as normal colonic epithelial CCD-18Co cells, which offered in vitro experimental verification for our bioinformatic outcomes.

According to outcome data, TIMP1 transcripts were markedly up-regulated in CRC specimens and cell lines relative to normal samples. Elevated TIMP1 expression served as a poor-prognosis indicator for overall survival (hazard ratio [HR] = 0.43, 95% confidence interval [CI] = 0.29-0.64, p < 0.001) and disease-specific survival (HR = 0.39, 95% CI = 0.22-0.68, p = 0.001) among colorectal-carcinoma patients. TIMP1 -high and TIMP1 -low groups exhibited notable differences in immune cell infiltration (CD8 + T, macrophage, mast, neutrophil, B, monocyte, dendritic, and CD4 + T cells). TIMP1 expression was also significantly correlated with tumor-infiltrating lymphocytes, key immune checkpoint genes (e.g., CD274 [ PD-L1 ] and CTLA4 ), and immunomodulatory chemokines (e.g., CCL3 and CCL5 ). Twelve TIMP1 -interacting DEGs were selected: COL5A1 , FN1 , PRG4 , and a cluster of nine MMPs ( MMP1 / 2 / 3 / 7 / 8 / 9 / 11 / 13 / 14 ), all of which showed significant positive correlations with TIMP1 (r = 0.31-0.63, all p < 0.001).

TIMP1 expression correlates with features of the tumor immune microenvironment and extracellular matrix remodeling in CRC, suggesting that TIMP1 shows potential as a candidate biomarker. However, its potential as a therapeutic target warrants further experimental investigation.