# Alternative splicing factor RAB3IP as a novel risk signature to predict the prognosis of colorectal cancer

**Authors:** Zhengwei Zhou, Fei Gao, Han Lei, Haixuan Wen, Jiaxi Tang, Yulong Peng, Lili Fan, Lu Xu, Guang Shu

PMC · DOI: 10.7150/jca.110271 · Journal of Cancer · 2025-06-23

## TL;DR

This study identifies RAB3IP, an alternative splicing factor, as a new biomarker for predicting the prognosis of colorectal cancer.

## Contribution

The study introduces RAB3IP as a novel independent prognostic marker for colorectal cancer based on splicing factor analysis.

## Key findings

- RAB3IP shows a significant positive correlation with favorable prognosis in colorectal cancer.
- RAB3IP is linked to key cancer-related pathways like Cell Cycle, WNT, and Spliceosome.
- Four splicing factors, including RAB3IP, were identified as the most predictive markers for CRC prognosis.

## Abstract

Emerging evidence suggests that aberrant alternative splicing plays a vital role in the development of tumors. However, the expression of splicing factors (SF) in colorectal cancer and its relationship with prognosis is still unclear. Here, we divided patients into high-risk and low-risk groups through univariate COX analysis and LASSO regression analysis, and selected 13 alternative splicing factors that are highly correlated with prognosis for subsequent analysis. We systematically analyzed the prognostic value of transcription levels of SFs in colorectal cancer (CRC) and found that RAB3A interacting protein (RAB3IP), programmed cell death 4 (PDCD4), golgin B1 (GOLGB1), and neuregulin 4 (NRG4) as the most predictive markers for the prognosis of CRC. After comparing the expression of four splicing factors in cancer tissues with normal tissues as well as OS analysis, it is strongly indicated that only RAB3IP demonstrates a significant positive correlation with favorable prognosis. Accordingly, we established a risk signature of transcription levels of RAB3IP as an independent prognostic marker for CRC. Moreover, by the Gene Set Enrichment Analysis (GSEA), we demonstrated that the RAB3IP was correlated to Cell Cycle, WNT pathway and Spliceosome in cancer. In conclusion, our findings demonstrate that SFs play a critical role in CRC pathogenesis, and identify RAB3IP as a novel prognostic biomarker for CRC.

## Linked entities

- **Genes:** RAB3IP (RAB3A interacting protein) [NCBI Gene 117177], PDCD4 (programmed cell death 4) [NCBI Gene 27250], GOLGB1 (golgin B1) [NCBI Gene 2804], NRG4 (neuregulin 4) [NCBI Gene 145957]
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** PDCD4 (programmed cell death 4) [NCBI Gene 27250] {aka H731}, RAB3IP (RAB3A interacting protein) [NCBI Gene 117177] {aka RABIN3, RABIN8}, NRG4 (neuregulin 4) [NCBI Gene 145957] {aka HRG4}, GOLGB1 (golgin B1) [NCBI Gene 2804] {aka GCP, GCP372, GOLIM1}
- **Diseases:** cancer (MESH:D009369), CRC (MESH:D015179)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12244333/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12244333/full.md

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Source: https://tomesphere.com/paper/PMC12244333