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Pan-cancer analysis reveals GGPS1 plays an important role in tumorigenesis in multiple tumor types
1School of Marine and Biological Engineering, Yancheng Teachers University, Yancheng, Jiangsu, China.
Abstract:
The deletion of geranylgeranyl diphosphate synthase 1 (GGPS1) has been reported to inhibit the proliferation of multiple cells. Although emerging evidence has demonstrated a correlation between GGPS1 and cancer, no pan-cancer analysis has been conducted to date. This study explored the potential tumorigenesis of GGPS1 using data from the cancer genome atlas human clinical database. GGPS1 expression was considerably upregulated at both the RNA and protein levels in several cancer types, especially in breast carcinoma (BRCA), (liver) hepatocellular carcinoma (LIHC/HCC) and lung adenocarcinoma (LUAD). Amplification is the most common form of genetic alteration observed in invasive BRCA, ovarian epithelial tumor and HCC. Additionally, elevated GGPS1 expression was markedly related to poor patient prognosis and overall survival in several cancer types including LIHC. GGPS1 expression was also linked to cancer-associated fibroblasts (CAFs) infiltration in several cancer types, such as BRCA and LUAD. Moreover, GGPPS-interacting proteins and GGPS1-correlated genes in cancers were functionally enriched in terpenoid backbone biosynthesis, steroid biosynthesis, and metabolic pathways. These results indicate that GGPS1 may play a role in promoting the tumorigenesis and tumor development, particularly in BRCA and LUAD, and may play a role in steroid biosynthesis and metabolic pathways.
Insights
Geranylgeranyl diphosphate synthase 1 (GGPS1) is upregulated in multiple cancers, correlating with poor prognosis and linked to cancer-associated fibroblasts. GGPS1 may promote tumorigenesis and impact metabolic pathways.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Geranylgeranyl diphosphate synthase 1 (GGPS1) inhibition affects cell proliferation.
- Emerging evidence suggests a link between GGPS1 and cancer, but a comprehensive pan-cancer analysis is lacking.
Purpose of the Study:
- To investigate the role of GGPS1 in tumorigenesis across various cancer types.
- To analyze GGPS1 expression, genetic alterations, and prognostic significance in a pan-cancer context.
Main Methods:
- Utilized The Cancer Genome Atlas (TCGA) database for human clinical data analysis.
- Examined GGPS1 RNA and protein expression levels.
- Assessed genetic alterations, including amplification.
- Correlated GGPS1 expression with patient prognosis and cancer-associated fibroblast (CAF) infiltration.
- Performed functional enrichment analysis of GGPS1-interacting and correlated genes.
Main Results:
- GGPS1 was significantly upregulated in multiple cancer types at both RNA and protein levels, notably in breast carcinoma (BRCA), hepatocellular carcinoma (LIHC/HCC), and lung adenocarcinoma (LUAD).
- Gene amplification was the predominant genetic alteration in BRCA, ovarian tumors, and HCC.
- Elevated GGPS1 expression correlated with poorer patient prognosis and overall survival in several cancers, including LIHC.
- GGPS1 expression was associated with CAF infiltration in BRCA and LUAD.
- Functional enrichment analysis revealed involvement in terpenoid backbone biosynthesis, steroid biosynthesis, and metabolic pathways.
Conclusions:
- GGPS1 plays a potential role in promoting tumorigenesis and tumor progression, particularly in BRCA and LUAD.
- GGPS1 is implicated in steroid biosynthesis and metabolic pathways.
- Further research into GGPS1's function in cancer is warranted.
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