OLR1 is closely related to poor prognosis and immune cell infiltration in gastric cancer

Oxidized low-density lipoprotein receptor 1 (OLR1) in gastric cancer (GC) progression and immune cell infiltration remains unclear. This study aimed to investigate the impact of OLR1 on GC progression and to elucidate its association with immune cell infiltration in GC. OLR1 expression profiles in GC and paired normal tissues were analyzed using datasets from the TCGA, GTEx, and GEO databases, with validation conducted through quantitative real-time PCR (qPCR) and immunohistochemistry (IHC). Differentially expressed genes (DEGs) associated with OLR1 were identified through gene set enrichment analysis (GSEA) and functional enrichment analysis. We evaluated the role of OLR1 in GC immune cell infiltration. In addition, Cox regression and Kaplan-Meier analyses were conducted on OLR1 for its prognostic significance and correlation with clinical variables. We evaluated the role of OLR1 in gastric cancer cell invasion and migration via Transwell and wound-healing assays following OLR1 knockdown and overexpression. Finally, survival probabilities in GC patients were predicted by nomogram construction. OLR1 expression in GC tissues significantly increased relative to that in matched normal samples (P < 0.001), as confirmed by qPCR and IHC (both P < 0.05). There were 268 DEGs associated with Staphylococcus aureus infection, protein digestion and absorption signaling, and the estrogen signaling pathway. OLR1 expression was positively related to macrophage infiltration (r = 0.742, P < 0.001, as validated by IHC). Additionally, OLR1 expression was strongly related to histological grade (P < 0.001), histological type (P < 0.05), T stage (P < 0.01), pathological stage (P < 0.05), and unfavorable overall survival (OS, P < 0.05). In vitro findings indicate that OLR1 enhances the invasive and migratory abilities of gastric cancer cells. Our established nomogram effectively predicted the 1-, 3-, and 5-year OS probabilities in patients with GC (C-index [95% CI] = 0.649 [0.624-0.675]). OLR1 is strongly associated with a dismal prognostic outcome and immune cell infiltration in patients with GC.

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Journal
Scientific Reports
Published
2025-11-24
DOI
https://doi.org/10.1038/s41598-025-25552-w
Primary Topic
Atherosclerosis and Cardiovascular Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

OLR1 is closely related to poor prognosis and immune cell infiltration in gastric cancer

Qiaofeng Chen, Zhenzhen Yang, Bo Jiang, Qingzi Fu et al.
Scientific Reports
Atherosclerosis and Cardiovascular Diseases
article

OLR1 is closely related to poor prognosis and immune cell infiltration in gastric cancer

Qiaofeng Chen, Zhenzhen Yang, Bo Jiang, Qingzi Fu, Shiyu Zhang, Peng Chen, Meixia Zhang
article en

Abstract

Oxidized low-density lipoprotein receptor 1 (OLR1) in gastric cancer (GC) progression and immune cell infiltration remains unclear. This study aimed to investigate the impact of OLR1 on GC progression and to elucidate its association with immune cell infiltration in GC. OLR1 expression profiles in GC and paired normal tissues were analyzed using datasets from the TCGA, GTEx, and GEO databases, with validation conducted through quantitative real-time PCR (qPCR) and immunohistochemistry (IHC). Differentially expressed genes (DEGs) associated with OLR1 were identified through gene set enrichment analysis (GSEA) and functional enrichment analysis. We evaluated the role of OLR1 in GC immune cell infiltration. In addition, Cox regression and Kaplan-Meier analyses were conducted on OLR1 for its prognostic significance and correlation with clinical variables. We evaluated the role of OLR1 in gastric cancer cell invasion and migration via Transwell and wound-healing assays following OLR1 knockdown and overexpression. Finally, survival probabilities in GC patients were predicted by nomogram construction. OLR1 expression in GC tissues significantly increased relative to that in matched normal samples (P < 0.001), as confirmed by qPCR and IHC (both P < 0.05). There were 268 DEGs associated with Staphylococcus aureus infection, protein digestion and absorption signaling, and the estrogen signaling pathway. OLR1 expression was positively related to macrophage infiltration (r = 0.742, P < 0.001, as validated by IHC). Additionally, OLR1 expression was strongly related to histological grade (P < 0.001), histological type (P < 0.05), T stage (P < 0.01), pathological stage (P < 0.05), and unfavorable overall survival (OS, P < 0.05). In vitro findings indicate that OLR1 enhances the invasive and migratory abilities of gastric cancer cells. Our established nomogram effectively predicted the 1-, 3-, and 5-year OS probabilities in patients with GC (C-index [95% CI] = 0.649 [0.624-0.675]). OLR1 is strongly associated with a dismal prognostic outcome and immune cell infiltration in patients with GC.

Scientific ReportsVol. 15(1)
First Affiliated Hospital of Jiangxi Medical College (CN), Suizhou Central Hospital (CN), Jiangxi Maternal and Child Health Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangxi Province
Openalex Percentile: Top 60%
Atherosclerosis and Cardiovascular Diseases
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