# Prognostic and clinicopathological value of dbc1 expression in human cancers: a systematic review and meta-analysis

**Authors:** Haojia Wang, Xinhong Cheng, Bruce Xianzhuo Zhang, Yong Wang, Shuo Gao, Fanghui Ding, Xiaojing Song, Dandan Li, Haixu Ni, Yang Luo, Xun Li

PMC · DOI: 10.3389/fonc.2025.1584622 · Frontiers in Oncology · 2025-07-07

## TL;DR

DBC1 overexpression in cancer patients is linked to worse survival and worse cancer features, suggesting it could help predict cancer outcomes.

## Contribution

This study provides a meta-analysis showing DBC1 overexpression is a potential prognostic marker in cancer.

## Key findings

- DBC1 overexpression is associated with shorter overall and recurrence-free survival in cancer patients.
- High DBC1 levels correlate with worse TNM stage, metastasis, and histologic grade in cancers.
- The study highlights DBC1 as a possible predictive marker for cancer prognosis.

## Abstract

DBC1 is a large nuclear protein that is thought to influence the development of several human cancers. However, further research has revealed that the relationship between DBC1 and the prognosis and pathological characteristics of cancer patients is controversial. The aim of this paper is to explore the significance of DBC1 in cancer through the method of meta-analysis.

A systematic search of the PubMed, Web of Science, Embase, CNKI, and Wanfang databases was conducted, resulting in the identification of 25 studies encompassing 4014 patients. The Hazard Ratio (HR) and ratio ratios (RR) were combined using STATA 14.0 software, and 95% confidence intervals (CI) were obtained to assess the association of DBC1 with prognostic and pathologic characteristics of cancer patients.

Meta-analysis of the combined results demonstrated that patients with cancer who exhibited DBC1 overexpression exhibited shorter overall survival (OS) (n = 17, HR = 1.948, 95%CI: [1.280-2.964], P = 0.002, I2
 = 88.6) and recurrence-free survival (RFS) (n = 11, HR = 2.182, 95%CI: [1.430-3.330], P = 0.000, I2
 = 87.8) rates. In terms of pathological features, elevated DBC1 expression was indicative of poor TNM stage (n = 23, RR = 1.245, 95%CI: [1.012-1.531], P = 0.038, I2
 = 79.3), distant metastasis (n = 11, RR = 1.987, 95%CI: [1.021-3.866], P = 0.043, I2
 = 63.8), and histologic grade (n = 18, RR = 1.433, 95%CI: [1.115-1.843], P = 0.005, I2
 = 79.2).

DBC1 overexpression is associated with poor survival cycle and pathologic features in cancer patients, and it has the potential to be a predictive prognostic marker for cancer. However, more high-quality prospective studies are still needed to validate our conclusions.

https://www.crd.york.ac.uk/prospero/, identifier CRD42023426104.

## Linked entities

- **Genes:** BRINP1 (BMP/retinoic acid inducible neural specific 1) [NCBI Gene 1620]

## Full-text entities

- **Genes:** CCAR2 (cell cycle and apoptosis regulator 2) [NCBI Gene 57805] {aka DBC-1, DBC1, KIAA1967, NET35, p30 DBC, p30DBC}
- **Diseases:** metastasis (MESH:D009362), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12278428/full.md

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Source: https://tomesphere.com/paper/PMC12278428