# Expression of Cyclin D1 and Claudin-1 in Invasive Breast Carcinoma and Their Correlation with Clinicopathological Parameters

**Authors:** Roopali Sehrawat, Vishesh Dhawan, Maitrayee Roy, Ayushi Kediya, Vijay Shrawan Nijhawan

PMC · DOI: 10.30699/ijp.2024.2028643.3299 · 2024-10-02

## TL;DR

This study examines how cyclin D1 and claudin-1 protein levels in breast cancer tissues relate to patient outcomes and tumor characteristics.

## Contribution

The study identifies cyclin D1 as a potential prognostic marker and suggests claudin-1's role in breast cancer subtypes.

## Key findings

- Cyclin D1 expression is significantly linked to nodal status and luminal-type breast cancer.
- Claudin-1 is expressed in both luminal and HER2/neu-positive tumors but shows no strong correlations.
- Cyclin D1 positivity may indicate better prognostic factors in breast cancer patients.

## Abstract

Evidence-based medicine has shown that patients with similar risk factors, stages, and therapy often have different clinical outcomes, highlighting the heterogeneity of breast cancer. In a quest for a better, cost-effective approach, researchers proposed the selection of surrogate IHC markers such as cyclin D1 and claudin-1 for the prognosis of breast cancer patients, supplementing the traditional ER, PR, and HER2/neu receptor.

This retrospective study was conducted in a tertiary care hospital in northern India and included 50 cases of invasive breast carcinoma obtained from mastectomies, wide local excisions, and biopsies diagnosed over 4 years. In addition to ER, PR, and Her2/neu, claudin-1 and cyclin D1 IHC expression was assessed.

Cyclin D1 expression exhibited a statistically significant correlation with nodal status involvement (P=0.011) and with luminal-type breast carcinoma (P=0.023). Though there was no significant statistical correlation between claudin-1 and various clinic pathological features, it was seen to be positive in both luminal and HER2/neu-positive tumors.

Our findings advocated the expression of IHC namely, cyclin D1 and claudin-1, in cases of breast cancer. Cyclin D1 positivity may show a significant association with better prognostic determinants while claudin-1 negative tumors may tend to be more often triple negative. Thus, IHC can be used in resource-constraint settings to substitute expensive molecular techniques.

## Linked entities

- **Genes:** ccnd1.S (cyclin D1 S homeolog) [NCBI Gene 379161], CLDN7 (claudin 7) [NCBI Gene 1366]
- **Proteins:** EREG (epiregulin), PGR (progesterone receptor), ERBB2 (erb-b2 receptor tyrosine kinase 2)
- **Diseases:** breast cancer (MONDO:0004989), triple negative breast cancer (MONDO:0005494)

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** nodal (MESH:D013611), tumors (MESH:D009369), Breast Carcinoma (MESH:D001943)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11872039/full.md

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Source: https://tomesphere.com/paper/PMC11872039