RecruitingNCT07297134

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


Sponsor

Atlas University

Enrollment

160 participants

Start Date

Dec 1, 2025

Study Type

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

Sex: FEMALEMin Age: 18 Years

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)

Atlas University Faculty of Medicine

Istanbul, Istanbul, Turkey (Türkiye)

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NCT07297134


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