lncRNA FOXD3-AS1 is associated with clinical progression and regulates cell migration and invasion in breast cancer.
Yaoyao GuanAdheesh BhandariErjie XiaFan YangJingjing XiangOu-Chen WangPublished in: Cell biochemistry and function (2019)
For women, breast cancer is the most commonly diagnosed cancer and the leading cause of women deaths due to cancer. In recent years, increasing long noncoding RNA (lncRNA) has been discovered to be related to tumorigenesis, progression, and prognosis. FOXD3-AS1 is a lncRNA and has been identified as a cancer-promoting gene in glioma. By analysing the FOXD3-AS1 expression in The Cancer Genome Atlas (TCGA) database, we found that FOXD3-AS1 has significantly high expression in breast cancer tumour comparing with the normal tissue. And patients with low FOXD3-AS1 expression had greater survival probability, smaller tumour size, and less distant metastasis. This leads us to peep inquisitively biological function of FOXD3-AS1 in breast cancer. Biological assays demonstrated that silenced FOXD3-AS1 impaired cell proliferation and inhibited cell migration and invasion in breast cancer cell lines (BT549, MDA-MB-231). These results suggest that FOXD3-AS1 could play a potential diagnostics or prognostic biomarker for patients with breast cancer. SIGNIFICANCE OF THE STUDY: We demonstrated that lncRNA FOXD3-AS1 has significantly high expression in breast cancer cell lines comparing with the normal tissue. Besides, our findings suggested that lncRNA FOXD3-AS1 could play a potential diagnostics or prognostic biomarker for patients with breast cancer.
Keyphrases
- long noncoding rna
- poor prognosis
- papillary thyroid
- long non coding rna
- childhood cancer
- squamous cell
- cell proliferation
- single cell
- breast cancer risk
- polycystic ovary syndrome
- binding protein
- lymph node metastasis
- type diabetes
- emergency department
- stem cells
- cell therapy
- squamous cell carcinoma
- genome wide
- young adults
- signaling pathway
- adipose tissue
- risk assessment
- copy number
- dna methylation
- bone marrow
- insulin resistance
- cell death
- transcription factor
- electronic health record