A pan-cancer analysis of the oncogenic and immunological roles of THOC3 in human cancer

There is a Limited number of studies on THO Complex Subunit 3 (THOC3) in tumors. The purpose of this study is to conduct a comprehensive analysis of various types of tumors to determine the role of THOC3 in tumor progression and to investigate its impact on immunity. Retrieved THOC3 expression data from various cancers in the TCGA database and analyzed it using R software (version 3.6.4) and its related packages; explored the differential expression of THOC3 in tumors, its correlation with prognosis, functional enrichment, and its relationship with tumor heterogeneity. The study also aimed to uncover the correlation between THOC3 and tumor immunity. THOC3 is differentially expressed in various tumors and normal samples, and is correlated with overall survival and progression-free time. The study found that THOC3 expression is strongly associated with tumor mutational burden, microsatellite deletion, and immune response. The expression of THOC3 is significantly correlated with immune cell infiltration, and THOC3 can regulate transcription output and mRNA splicing. Therefore, we speculate that THOC3 could serve as a therapeutic target for future anticancer therapies. THOC3 can serve as a novel specific biomarker for diagnosis and prognosis in pan cancer.

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2025-10-16
DOI
https://doi.org/10.1038/s41598-025-20257-6
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A pan-cancer analysis of the oncogenic and immunological roles of THOC3 in human cancer

Qi Zhao, Jidong Zhao, Xin Chen, Xing Cui et al.
Scientific Reports
RNA modifications and cancer
article

A pan-cancer analysis of the oncogenic and immunological roles of THOC3 in human cancer

Qi Zhao, Jidong Zhao, Xin Chen, Xing Cui, Jixin Zhang
article en

Abstract

There is a Limited number of studies on THO Complex Subunit 3 (THOC3) in tumors. The purpose of this study is to conduct a comprehensive analysis of various types of tumors to determine the role of THOC3 in tumor progression and to investigate its impact on immunity. Retrieved THOC3 expression data from various cancers in the TCGA database and analyzed it using R software (version 3.6.4) and its related packages; explored the differential expression of THOC3 in tumors, its correlation with prognosis, functional enrichment, and its relationship with tumor heterogeneity. The study also aimed to uncover the correlation between THOC3 and tumor immunity. THOC3 is differentially expressed in various tumors and normal samples, and is correlated with overall survival and progression-free time. The study found that THOC3 expression is strongly associated with tumor mutational burden, microsatellite deletion, and immune response. The expression of THOC3 is significantly correlated with immune cell infiltration, and THOC3 can regulate transcription output and mRNA splicing. Therefore, we speculate that THOC3 could serve as a therapeutic target for future anticancer therapies. THOC3 can serve as a novel specific biomarker for diagnosis and prognosis in pan cancer.

Scientific ReportsVol. 15(1)
Hebei Medical University (CN), Fourth Hospital of Hebei Medical University (CN)
Health Commission of Hebei Province
Openalex Percentile: Top 74%
RNA modifications and cancer
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

A pan-cancer analysis of the oncogenic and immunological roles of THOC3 in human cancer — Qi Zhao, Jidong Zhao, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS