miR-101, miR-548b, miR-554, and miR-1202 are reliable prognosis predictors of the miRNAs associated with cancer immunity in primary central nervous system lymphoma.
Yasuo TakashimaAtsushi KawaguchiYasuo IwadateHiroaki HondohJunya FukaiKoji KajiwaraAzusa HayanoRyuya YamanakaPublished in: PloS one (2020)
MicroRNAs (miRNAs) inhibit protein function by silencing the translation of target mRNAs. However, in primary central nervous system lymphoma (PCNSL), the expression and functions of miRNAs are inadequately known. Here, we examined the expression of 847 miRNAs in 40 PCNSL patients with a microarray and investigated for the miRNA predictors associated with cancer immunity-related genes such as T helper cell type 1/2 (Th-1/Th-2) and regulatory T cell (T-reg) status, and stimulatory and inhibitory checkpoint genes, for prognosis prediction in PCNSL. The aim of this study is to find promising prognosis markers based on the miRNA expression in PCNSL. We detected 334 miRNAs related to 66 cancer immunity-related genes in the microarray profiling. Variable importance measured by the random survival forest analysis and Cox proportional hazards regression model elucidated that 11 miRNAs successfully constitute the survival formulae dividing the Kaplan-Meier curve of the respective PCNSL subgroups. On the other hand, univariate analysis shortlisted 23 miRNAs for overall survival times, with four miRNAs clearly dividing the survival curves-miR-101/548b/554/1202. These miRNAs regulated Th-1/Th-2 status, T-reg cell status, and immune checkpoints. The miRNAs were also associated with gene ontology terms as Ras/MAP-kinase, ubiquitin ligase, PRC2 and acetylation, CDK, and phosphorylation, and several diseases including acquired immunodeficiency syndrome, glioma, and those related to blood and hippocampus with statistical significance. In conclusion, the results demonstrated that the four miRNAs comprising miR-101/548b/554/1202 associated with cancer immunity can be a useful prognostic marker in PCNSL and would help us understand target pathways for PCNSL treatments.
Keyphrases
- papillary thyroid
- poor prognosis
- long non coding rna
- cell proliferation
- squamous cell carcinoma
- binding protein
- cell cycle
- gene expression
- transcription factor
- stem cells
- genome wide
- immune response
- mesenchymal stem cells
- bone marrow
- diffuse large b cell lymphoma
- blood brain barrier
- lymph node metastasis
- regulatory t cells
- protein kinase
- cell therapy
- dna methylation
- drug induced
- brain injury
- subarachnoid hemorrhage
- amino acid
- data analysis
- single molecule
- cerebral ischemia
- bioinformatics analysis