miR-4793-3p predicts poor prognosis and regulates ferroptosis and invasiveness of breast cancer via targeting RNF169
摘要
The prognosis prediction of breast cancer is a challenging problem in the clinic. Identifying reliable biomarkers and revealing the regulatory mechanism underlying the progression of breast cancer cells would benefit the treatment and outcomes of breast cancer patients.
ObjectivesThis study aims to explore a novel biomarker related with tumor progression and clinical prognosis, focusing on miR-4793-3p and its targets.
Materials and methodsThe study enrolled 133 patients with breast cancer, and tissue samples were obtained. Expression of miR-4793-3p and its clinical significance were evaluated from the perspective of molecular subtypes, disease development, and prognosis. The regulatory effect and mechanism of miR-4793-3p in the biological function of breast cancer cells were assessed.
ResultsSignificant downregulation of miR-4793-3p was observed in tumor tissues of patients with breast cancer, and lower miR-4793-3p levels were found in patients with more malignant subtypes. miR-4793-3p was closely associated with the differentiation, TNM stage, lymph node metastasis, subtypes, and poor prognosis of patients and was identified as an independent prognostic factor. miR-4793-3p significantly suppressed cell growth, metastatic potential, and promoted ferroptosis of breast cancer, and the negative regulation of RNF169 was revealed to mediate the function of miR-4793-3p. JAK2/STAT3 signaling was suppressed by miR-4793-3p, which suppressed cell growth and metastatic potential and promoted ferroptosis.
ConclusionmiR-4793-3p could act as a biomarker for breast cancer, indicating cancer development and predicting patients’ outcomes. miR-4793-3p modulated ferroptosis and therefore regulated tumor progression via suppressing JAK2/STAT3 signaling by targeting RNF169.