# ERCC3 Gene Associated with Breast Cancer: A Genetic and Bioinformatic Study

**Authors:** Xiangyu Chen, Heng Xiao, Shuangcheng Ning, Bang Liu, Huashan Zhou, Ting Fu

PMC · DOI: 10.1155/2024/7278636 · The Breast Journal · 2024-07-14

## TL;DR

This study investigates the ERCC3 gene's role in breast cancer, identifying a mutation linked to increased risk in the Han-Chinese population.

## Contribution

A novel ERCC3 mutation (p.Y116X) is identified as a potential breast cancer risk factor in Han-Chinese populations.

## Key findings

- The ERCC3 mutation p.Y116X was found in a breast cancer family, suggesting a link to increased cancer risk.
- ERCC3 expression was negatively associated with hormone receptors and specific cancer subtypes.
- ERCC3 mutations showed decreased expression in tumor tissues, supporting its role as a potential diagnostic biomarker.

## Abstract

Female breast cancer is the most common and the fifth deadliest cancer worldwide. It is influenced by a combination of genetic, hormonal, and environmental factors. The excision repair cross-complementation group 3 gene (ERCC3) has recently been identified as a breast cancer susceptibility gene in various cohorts of different geographical and ethnic origin. To explore the role of ERCC3 mutations in breast cancer development and pathological diagnosis, genetic analysis was conducted in 291 patients and 291 controls from mainland China. Bioinformatic analysis and immunohistochemistry (IHC) were performed. A novel ERCC3 mutation p.Y116X was identified in a breast cancer family, while no frequency bias for the genotype and allele of rs754010782 and rs371627165 was observed (all P > 0.05). Bioinformatic analysis revealed that ERCC3 expression was negatively associated with estrogen receptor (ER), progesterone receptor (PR), nontriple-negative status, and nodal status of breast cancers. ERCC3 amplifications and deep deletions primarily occurred in breast invasive cancer not otherwise specified (NOS) and metaplastic breast cancer, respectively. The decreased ERCC3 expression in tumor tissues of patient with p.Y116X mutation was found by IHC. The ERCC3 mutation p.Y116X may increase breast cancer risk in the Han-Chinese population. ERCC3 exhibits potential as a biomarker for the pathological diagnosis of breast cancer.

## Linked entities

- **Genes:** ERCC3 (ERCC excision repair 3, TFIIH core complex helicase subunit) [NCBI Gene 2071]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, ERCC3 (ERCC excision repair 3, TFIIH core complex helicase subunit) [NCBI Gene 2071] {aka BTF2, GTF2H, RAD25, Ssl2, TFIIH, TTD2}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** Breast Cancer (MESH:D001943), NOS (MESH:C536665), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** p.Y116X, rs371627165, rs754010782

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11260512/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC11260512/full.md

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Source: https://tomesphere.com/paper/PMC11260512