PTEN and Organ-Specific microRNAs in Metastatic Breast Cancer
Serum PTEN Levels and Organ-Specific microRNA Signatures as Predictors of Metastatic Patterns in Breast Cancer: A Prospective Observational Study
Atlas University
160 participants
Dec 1, 2025
OBSERVATIONAL
Conditions
Summary
This prospective observational study aims to evaluate serum levels of PTEN, a tumor suppressor gene, and organ-specific microRNAs (miRNAs) associated with metastatic patterns in breast cancer. Serum samples will be analyzed using quantitative reverse transcription polymerase chain reaction (qRT-PCR)-based miRNA profiling and enzyme-linked immunosorbent assay (ELISA)-based PTEN quantification. Three groups will be included: patients with metastatic breast cancer (n=80), patients with non-metastatic early-stage breast cancer (n=40), and healthy controls (n=40). The primary objective is to identify serum biomarkers that differentiate metastatic from non-metastatic disease. Secondary analyses will evaluate correlations between biomarker levels and organ-specific metastatic involvement, including bone, lung, liver, and brain metastases. Findings from this study may support the development of a noninvasive serum-based tool for predicting metastatic patterns in breast cancer.
Eligibility
Inclusion Criteria5
- Female individuals aged ≥18 years
- Ability to provide written informed consent
- Group I (Metastatic BC): Histopathologically confirmed breast cancer and radiologically or clinically proven distant organ metastasis at the time of enrollment
- Group II (Non-Metastatic BC): Histopathologically confirmed breast cancer with no evidence of distant metastasis
- Group III (Healthy Controls): Women ≥18 years with no known breast disease and no personal history of malignancy
Exclusion Criteria7
- History of any other primary malignancy
- Known breast disease or breast cancer diagnosis in Group III
- Immunosuppressive therapy that may alter immune or biomarker profiles
- Active infection or inflammatory condition that may alter biomarker levels
- Inability or unwillingness to provide informed consent
- Severe hepatic, renal, or hematologic dysfunction
- Current pregnancy or lactation
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07297134