# Molecular and serological biomarkers to predict trastuzumab responsiveness in HER-2 positive breast cancer

**Authors:** Noor Abdullah, Loma Al-Mansouri, Naael Ali, Najah Rayish Hadi

PMC · DOI: 10.25122/jml-2023-0163 · 2023-11-01

## TL;DR

This study explores how CTLA-4 and IGF-1 levels in HER-2 positive breast cancer patients may predict response to trastuzumab treatment and influence outcomes.

## Contribution

The study identifies CTLA-4 and IGF-1 as potential biomarkers for trastuzumab responsiveness in HER-2 positive breast cancer.

## Key findings

- CTLA-4 expression in peripheral blood cells increased significantly during treatment cycles.
- High IGF-1 levels in newly diagnosed patients decreased significantly after trastuzumab therapy.
- Combining HER-2 and IGF-1 targeting may improve outcomes and reduce recurrence risk.

## Abstract

HER-2-positive breast cancer is characterized by its aggressive nature, poor prognosis, and reduced overall survival. The emergence of trastuzumab resistance is currently considered a global problem. The immune system plays a pivotal role in tumor progression and development. Cytotoxic T lymphocyte-associated protein-4 (CTLA-4) and other immune checkpoint proteins may be potential prognostic factors and therapeutic targets for breast cancer. This study aimed to determine the correlation between CTLA-4 expression in peripheral blood and insulin-like growth factor-1 (IGF-1) serum levels and their impact on trastuzumab responsiveness in HER-2-positive patients with breast cancer. CTLA-4 expression was analyzed in peripheral blood cells using quantitative PCR, while IGF-1 serum levels were assessed through electrochemiluminescence assays. There was a significant increase in CTLA-4 expression at cycle 9, which continued to increase until it reached 4.6 at cycle 17. High IGF-1 levels were observed in newly diagnosed HER-2 positive patients before trastuzumab therapy, significantly decreasing post-therapy (p=0.001). Co-targeting HER-2 and IGF-1 receptors may reduce the risk of recurrence and improve outcomes. In addition, targeted CTLA-4 molecules may improve patient survival and prevent recurrence.

## Linked entities

- **Genes:** CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493], IGF1 (insulin like growth factor 1) [NCBI Gene 3479]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}
- **Diseases:** breast cancer (MESH:D001943), tumor (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10893566/full.md

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Source: https://tomesphere.com/paper/PMC10893566