Ontology highlight
ABSTRACT: Background
Colorectal cancer (CRC) is the leading cause of cancer deaths, and treatment, especially in the metastatic stage, is challenging. Immune checkpoint inhibitors (ICIs) have revolutionized CRC treatment, but response varies, emphasizing the need for effective biomarkers. This study explores SPEN mutations as potential biomarkers.Methods
Using data from the Memorial Sloan Kettering Cancer Center (MSKCC) and The Cancer Genome Atlas (TCGA)-Colorectal Cancer, this research applied bioinformatics tools and statistical analysis to SPEN (Split Ends) mutant and wild-type CRC patients treated with ICIs. Focus areas included mutation rates, immune cell infiltration, and DNA damage response pathways.Results
The SPEN mutation rate was found to be 13.8% (15/109 patients)
SUBMITTER: Dong Y
PROVIDER: S-EPMC10890329 | biostudies-literature | 2024 Jan
REPOSITORIES: biostudies-literature