Abstract

Background: Long noncoding RNA (lncRNA) ST7-AS1 can be observed in various cancers, but its role in breast cancer (BRC) remains unclear. Our aim is to, on the basis of The Cancer Genome Atlas (TCGA) database, prove the correlation between lncRNA ST7-AS1 and BRC. Methods: The lncRNA ST7-AS1 expression and its roles in the prognosis of BRC were explored using data from the TCGA database. The expression level of lncRNA ST7-AS1 in BRC samples was detected using RT-PCR. The 1-, 3-, or 5-year survival rate was predicted using a nomogram established through Cox proportional hazard regression. At last, the biological function was explored through gene ontology (GO) analysis and gene set enrichment analysis (GSEA). The hallmark pathways significantly involved in hub genes were described through functional enrichment analysis. The correlation between lncRNA ST7-AS1 expression and immune infiltration was analyzed through single-sample GSEA (ssGSEA). Results: LncRNA ST7-AS1 expression was downregulated in BRC. Decreased lncRNA ST7-AS1 expression in BRC was correlated with advanced clinical pathologic characteristics (high grade, histological type, age, menopause status, and HER2 status), survival time, and poor prognosis. The nomogram was established for using lncRNA ST7-AS1 to predict 1-, 3-, or 5-year survival in patients with BRC. In addition, GO and pathway analyses suggested the involvement of lncRNA ST7-AS1 in cell cycle, DNA repair, and immune cell infiltration in the BRC immune microenvironment. We found the correlation of lncRNA ST7-AS1 with T helper cells and DC cells. Conclusion: Low expression of lncRNA ST7-AS1 indicates poor prognosis and has an impact on cell cycle, DNA repair, and proportion of infiltrating immune cells in the BRC microenvironment. Therefore, lncRNA ST7-AS1 can be used as a protective prognostic marker and a potential treatment target for BRC.

Highlights

  • Breast cancer is most commonly observed in female patients with cancer, which is a main cause of death induced by cancer

  • To further evaluate the difference of Long noncoding RNA (lncRNA) ST7-antisense RNA 1 (AS1) expression in breast cancer (BRC), 1,065 patients’ clinical and gene expression data were downloaded from The Cancer Genome Atlas (TCGA) (Table 1)

  • Decreased lncRNA ST7-AS1 expression in BRC was correlated with advanced clinical pathologic characteristics, survival time, and poor prognosis

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Summary

Introduction

Breast cancer is most commonly observed in female patients with cancer, which is a main cause of death induced by cancer. The proportion of BRC in all newly diagnosed cancers (Balasubramanian et al, 2019) in women reaches 30%, and cancers result in 15% of deaths in women (Siegel et al, 2019). As breast tumors are heterogeneous, BRC are classified according to their expression of key proteins ER, PR, HER2, etc., for individual therapy (Klinge, 2018). These biomarkers are not satisfactory for diagnosis or prognosis due to poor sensitivity and specificity. Long noncoding RNA (lncRNA) ST7-AS1 can be observed in various cancers, but its role in breast cancer (BRC) remains unclear. On the basis of The Cancer Genome Atlas (TCGA) database, prove the correlation between lncRNA ST7-AS1 and BRC

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