High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer.
Yoshihisa TokumaruMariko AsaokaMasanori OshiEriko KatsutaLi YanSumana NarayananNobuhiko SugitoNobuhisa MatsuhashiManabu FutamuraYukihiro AkaoKazuhiro YoshidaKazuaki TakabePublished in: International journal of molecular sciences (2020)
microRNA-143(miR-143) is a well-known tumor suppressive microRNA that exhibits anti-tumoral function by targeting KRAS signaling pathways in various malignancies. We hypothesized that miR-143 suppresses breast cancer progression by targeting KRAS and its effector molecules. We further hypothesized that high expression of miR-143 is associated with a favorable tumor immune microenvironment of estrogen receptor (ER)-positive breast cancer patients which result in improved survival. Two major publicly available breast cancer cohorts; The Cancer Genome Atlas (TCGA) and Molecular Taxonomy of Breast Cancer International Consortium (METABRIC) were used. The miR-143 high expression group was associated with increased infiltration of anti-cancer immune cells and decreased pro-cancer immune cells, as well as enrichment of the genes relating to T helper (Th1) cells resulting in improved overall survival (OS) in ER-positive breast cancer patients. To the best of our knowledge, this is the first study to demonstrate that high expression of miR-143 in cancer cells associates with a favorable tumor immune microenvironment, upregulation of anti-cancer immune cells, and suppression of the pro-cancer immune cells, associating with better survival of the breast cancer patients.
Keyphrases
- estrogen receptor
- poor prognosis
- long non coding rna
- cell proliferation
- long noncoding rna
- papillary thyroid
- signaling pathway
- stem cells
- squamous cell
- induced apoptosis
- childhood cancer
- healthcare
- regulatory t cells
- gene expression
- binding protein
- pi k akt
- epithelial mesenchymal transition
- genome wide
- single cell
- immune response
- squamous cell carcinoma
- anti inflammatory
- cell death
- transcription factor
- wild type