Current Biotechnology ›› 2026, Vol. 16 ›› Issue (3): 706-718.DOI: 10.19586/j.2095-2341.2026.0016

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Transcriptomic Analysis of the Role of NFIA in HER2-positive Breast Cancer Brain Metastasis

Mengjie DONG1(), Peiwen FAN2, Ruozheng WANG2,3()   

  1. 1.Affiliated Cancer Hospital of Xinjiang Medical University,Urumqi 830011,China
    2.Xinjiang Key Laboratory of Oncology,Affiliated Cancer Hospital of Xinjiang Medical University,Urumqi 830011,China
    3.Clinical Key Specialty of Radiotherapy of Xinjiang Uygur Autonomous Region,Urumqi 830011,China
  • Received:2026-01-23 Accepted:2026-03-31 Online:2026-05-25 Published:2026-07-14
  • Contact: Ruozheng WANG

Abstract:

This study systematically investigated the expression characteristics of NFIA in HER2-positive breast cancer brain metastasis (BCBM) and its association with patient prognosis, as well as its potential roles in the tumor microenvironment (TME), aiming to identify novel therapeutic targets. NFIA expression patterns and their prognostic relevance were analyzed using multiple public databases, and immunohistochemistry (IHC) validation was performed on paired clinical samples. Furthermore, by integrating public datasets with our single-cell transcriptomic data, we systematically analyzed the functional states of NFIA-high cell subpopulations and their interactions within the TME. The results demonstrated that NFIA was significantly upregulated in HER2-positive BCBM and that its high expression was closely associated with poor patient prognosis. Single-cell analyses further revealed that NFIA-high tumor epithelial cells exhibited pronounced genomic instability and highly malignant features, accompanied by activation of pathways related to invasion and proliferation. In addition, NFIA-high cells acted as key modulators within the TME by regulating angiogenesis, immune suppression, and extracellular matrix remodeling. Collectively, NFIA high expression defines a highly malignant tumor epithelial cell subpopulation in HER2-positive BCBM and promotes tumor progression through TME remodeling, providing a potential molecular target for precision therapy in HER2-positive breast cancer brain metastasis.

Key words: NFIA, HER2-positive breast cancer brain metastasis, single-cell transcriptome, tumor microenvironment

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