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Background: The GINS complex is related to cancer development, invasion, and poor prognosis in multiple tumors. In the study, we attempted to investigate the prognostic value of in sarcoma patients.

Methods: We analyzed expression using Tumor IMmune Estimation Resource (TIMER) 2.0, Gene Expression Omnibus (GEO; GSE21122, GSE39262, and GSE21050), and The Cancer Genome Atlas (TCGA) databases. The prognostic value of was explored using the survival and survminer packages of R. Genetic alteration analysis was investigated using cBioPortal. The Cell-type Identification by Estimating Relative Subsets of RNA Transcripts (CIBERSORT) R script was used for the immunocyte infiltration analysis. MicroRNAs (miRNAs) targeting were predicted using GEO (GSE69470) and MicroRNA Target Prediction Database (miRDB).

Results: We found that was overexpressed in sarcoma, especially in metastatic samples, and was associated with a worse prognosis. High expression was a poor prognostic indicator for sarcoma patients. Moreover, alteration was associated with worse survival of sarcoma patients. Immune infiltration analysis indicated that expression was correlated with the infiltration of M0 and M2 macrophages in sarcoma. Finally, the miRNA hsa-miR-376a-3p was identified to potentially regulate in sarcoma.

Conclusions: These results indicate that may be a promising prognostic biomarker and therapeutic target for sarcoma.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174763PMC
http://dx.doi.org/10.21037/tcr-23-524DOI Listing

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