# Expression and clinical significance of CCN5 and the oestrogen receptor in advanced breast cancer

**Authors:** Guofeng Zhou, Wei Qu, Liu Yang, Aili Huang, Xinxing Gui

PMC · DOI: 10.1186/s12905-025-03608-3 · 2025-02-27

## TL;DR

This study explores how CCN5 and estrogen receptor expression in breast cancer tissues relates to disease progression and treatment response.

## Contribution

The study identifies a positive correlation between CCN5 and ER expression in ductal carcinoma in situ and their potential role in breast cancer progression.

## Key findings

- CCN5 and ER show high expression in DCIS but low in invasive carcinoma tissues.
- CCN5 expression correlates with PR, HER-2, Ki-67, and other clinical markers in advanced breast cancer.
- CCN5 and ER may help predict endocrine therapy effectiveness in advanced breast cancer.

## Abstract

The aim of this study was to investigate the expression and clinical implications of CCN family member 5 (CCN5) and the oestrogen receptor (ER) in advanced breast cancer (BC).

A total of 130 patients with advanced BC were selected for the study. Samples of normal breast tissue, ductal carcinoma in situ (DCIS), and invasive carcinoma were collected. The expression levels of CCN5 and ER in these tissues were examined using immunohistochemical methods. The correlation between expression of CCN5 and ER in different tissues and also differences in expression in invasive carcinoma were analysed. In addition, the relationship between CCN5 expression in advanced BC tissues and clinical pathological features was examined.

CCN5 and ER had low expression in normal breast tissues and invasive carcinoma tissues, but high expression in DCIS, with this difference being statistically significant (X2 = 119.899, P < 0.001; X2 = 113.524, P < 0.001, respectively). The expression of CCN5 and ER in different tissues of patients with advanced BC showed a positive correlation. Significant differences were also observed in the positive and negative expression of CCN5 and ER (X2 = 56.358, P < 0.001). Moreover, the expression of CCN5 protein in advanced BC showed a statistically significant associations (P < 0.05) with the expression of the progesterone receptor (PR), human epidermal growth factor receptor 2 (HER-2), Ki-67, and P53, tumor diameter, histological grade, lymph node metastasis, pathological molecular subtype, and clinical staging.

High expression of CCN5 and ER was observed in DCIS tissues of patients with advanced BC, with their expression being positively correlated. These findings suggest that CCN5 and ER may have a potential synergistic role in the progression of BC that influences the progression of advanced BC and can also be used to predict the effectiveness of endocrine therapy.

## Linked entities

- **Genes:** CCN5 (cellular communication network factor 5) [NCBI Gene 8839], EREG (epiregulin) [NCBI Gene 2069], PGR (progesterone receptor) [NCBI Gene 5241], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064], Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345], TP53 (tumor protein p53) [NCBI Gene 7157]
- **Diseases:** breast cancer (MONDO:0004989), ductal carcinoma in situ (MONDO:0005023), invasive carcinoma (MONDO:0040677)

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, CCN5 (cellular communication network factor 5) [NCBI Gene 8839] {aka CT58, CTGF-L, WISP2}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** lymph node metastasis (MESH:D008207), DCIS (MESH:D002285), invasive carcinoma (MESH:D009361), tumor (MESH:D009369), BC (MESH:D001943)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11866700/full.md

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Source: https://tomesphere.com/paper/PMC11866700