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.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 26 11 2018
accepted: 11 02 2020
entrez: 27 2 2020
pubmed: 27 2 2020
medline: 12 6 2020
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32101576
doi: 10.1371/journal.pone.0229577
pii: PONE-D-18-33807
pmc: PMC7043771
doi:

Substances chimiques

Biomarkers, Tumor 0
MIRN101 microRNA, human 0
MIRN1202 microRNA, human 0
MIRN548 microRNA, human 0
MicroRNAs 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0229577

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Yasuo Takashima (Y)

Laboratory of Molecular Target Therapy for Cancer, Graduate School for Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Atsushi Kawaguchi (A)

Center for Comprehensive Community Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Yasuo Iwadate (Y)

Department of Neurosurgery, Graduate School of Medical Sciences, Chiba University, Chiba, Japan.

Hiroaki Hondoh (H)

Departments of Neurosurgery, Toyama Prefectural Central Hospital, Toyama, Japan.

Junya Fukai (J)

Department of Neurological Surgery, Wakayama Medical University School of Medicine, Wakayama, Japan.

Koji Kajiwara (K)

Department of Neurosurgery, Graduate School of Medical Sciences, Yamaguchi University, Ube, Yamaguchi, Japan.

Azusa Hayano (A)

Laboratory of Molecular Target Therapy for Cancer, Graduate School for Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Ryuya Yamanaka (R)

Laboratory of Molecular Target Therapy for Cancer, Graduate School for Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

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Classifications MeSH