GEOapplication/xmlftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE330nnn/GSE330548/primaryOK200TranscriptomicsMus musculusExpression profiling by high throughput sequencinghttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE330548GEOGSEfalseMulti-Omics Integration Identifies Critical Molecular Drivers and Alternative Splicing Events in Small Cell Lung Cancer IISmall cell lung cancer (SCLC) remains a highly aggressive malignancy and a therapeutic challenge in clinical oncology. Here, we conducted an integrated multi-omics analysis of treatment-naïve human SCLC tissues along with paired adjacent tissues (NAT, n = 12), including transcriptomic, proteomic, phosphoproteomic, and glycoproteomic profiling to identify novel prognostic markers and therapeutic targets. Integration of these datasets revealed significant enrichment of RNA splicing pathway in SCLC. We systematically characterized aberrant alternative splicing events (AASEs), identifying 6,972 events with exon skipping representing the most prevalent type. These AASEs were regulated by RNA-binding proteins and predominantly enriched in pathways related to tumor proliferation and metastasis. We further identified four splicing-related proteins (THOC1, MAGOHB, RBM8A, and TXNL4A) that were markedly overexpressed in SCLC, correlated with proliferation, and predicted poor prognosis. Functional validation showed that THOC1 knockdown suppressed tumor growth in vivo, potentially through enhanced anti-tumor immunity. Additionally, we present the first N-glycoproteomic atlas of SCLC implicating glycosylated CEACAM proteins as potential biomarkers and revealing aberrantly glycosylated sites and proteins associated with SCLC. Our study unveils novel molecular features underlying SCLC pathogenesis and provides insights for developing therapeutic strategies targeting RNA splicing and protein glycosylation.2026/05/14GSE330548GSM9728549GSM9728548GSM9728550GSM9728552GSM9728551GSM972855324247330548Mus musculus