Pinpointing Functionally Relevant miRNAs in Classical Hodgkin Lymphoma Pathogenesis.
Yujia PanRoza CengizJoost KluiverArjan DiepstraAnke van den BergPublished in: Cancers (2024)
Classical Hodgkin lymphoma (cHL) is a hematological malignancy of B-cell origin. The tumor cells in cHL are referred to as Hodgkin and Reed-Sternberg (HRS) cells. This review provides an overview of the currently known miRNA-target gene interactions. In addition, we pinpointed other potential regulatory roles of microRNAs (miRNAs) by focusing on genes related to processes relevant for cHL pathogenesis, i.e., loss of B-cell phenotypes, immune evasion, and growth support. A cHL-specific miRNA signature was generated based on the available profiling studies. The interactions relevant for cHL were extracted by comprehensively reviewing the existing studies on validated miRNA-target gene interactions. The miRNAs with potential critical roles included miR-155-5p, miR-148a-3p, miR-181a-5p, miR-200, miR-23a-3p, miR-125a/b, miR-130a-3p, miR-138, and miR-143-3p, which target, amongst others, PU.1, ETS1, HLA-I, PD-L1, and NF-κB component genes. Overall, we provide a comprehensive perspective on the relevant miRNA-target gene interactions which can also serve as a foundation for future functional studies into the specific roles of the selected miRNAs in cHL pathogenesis.
Keyphrases
- hodgkin lymphoma
- genome wide identification
- genome wide
- cell proliferation
- long non coding rna
- transcription factor
- long noncoding rna
- copy number
- genome wide analysis
- case control
- induced apoptosis
- signaling pathway
- dna methylation
- oxidative stress
- gene expression
- cell cycle arrest
- pi k akt
- single cell
- climate change
- current status
- inflammatory response
- risk assessment
- cell death