# Clinical relevance and mechanistic investigation of miR-1908-5p as a prognostic biomarker in colorectal cancer

**Authors:** Chenchen Yuan, Shaofei Chen, Qianli Liu, Riwei Wang

PMC · DOI: 10.1186/s41065-026-00645-2 · Hereditas · 2026-01-27

## TL;DR

This study shows that low levels of miR-1908-5p in colorectal cancer are linked to worse outcomes and that it helps control cancer cell growth by targeting SCAMP4.

## Contribution

The study identifies miR-1908-5p as a novel prognostic biomarker in colorectal cancer and reveals its functional role in suppressing tumor progression.

## Key findings

- miR-1908-5p is downregulated in CRC tumors and linked to poor prognosis and advanced disease stages.
- miR-1908-5p suppresses CRC cell proliferation, migration, and invasion by targeting SCAMP4.
- SCAMP4 is overexpressed in CRC and inversely correlated with miR-1908-5p levels.

## Abstract

Colorectal cancer (CRC) is characterized by a complex pathogenesis and substantial heterogeneity in prognosis.

This study aims to elucidate the clinical significance of miR-1908-5p in CRC, as well as its association with clinicopathological parameters and patient prognosis.

miR-1908-5p expression in tumor tissues was quantified by RT-qPCR. Survival outcomes were assessed using the Kaplan–Meier method. The chi-square (χ2) test and Cox regression analysis were employed to evaluate clinicopathological correlations and prognostic value.miR-1908-5p was compared between NCM460 and CRC lines (HT-29, HCT116), overexpressed, and functionally tested by CCK-8 and Transwell assays. TargetScan and luciferase assay verified the targeting of SCAMP4 3'-UTR. qPCR and Pearson analysis defined their correlation in CRC.

miR-1908-5p is downregulated in CRC tumors versus adjacent normal mucosal tissues. Low expression predicts poor prognosis and is associated with reduced survival rates in colorectal cancer, correlating with advanced TNM stage and elevated serum CA19-9 levels. CRC lines (HT-29 and HCT116) show reduced miR-1908-5p compared to NCM460. miR-1908-5p mimic suppresses proliferation, migration, and invasion. TargetScan-predicted binding to SCAMP4 3'-UTR was validated by dual-luciferase reporter assay. miR-1908-5p overexpression lowers SCAMP4, which is overexpressed in tumor tissues and exhibits an inverse correlation with miR-1908-5p.

miR-1908-5p is downregulated in CRC, correlates with TNM stage, nodal metastasis, elevated CA19-9 levels, and poor survival, and suppresses CRC cell proliferation, migration, and invasion by directly targeting SCAMP4, thereby qualifying as a potential prognostic biomarker for CRC.

## Linked entities

- **Genes:** SCAMP4 (secretory carrier membrane protein 4) [NCBI Gene 113178]
- **Diseases:** colorectal cancer (MONDO:0005575), CRC (MONDO:0005575)

## Full-text entities

- **Genes:** SCAMP4 (secretory carrier membrane protein 4) [NCBI Gene 113178] {aka SCAMP-4}
- **Diseases:** nodal metastasis (MESH:D009362), CRC (MESH:D015179), tumor (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12918142/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12918142/full.md

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Source: https://tomesphere.com/paper/PMC12918142