Emerging roles and mechanisms of miR-206 in human disorders: a comprehensive review
Sheyda Khalilian, Seyedeh Zahra Hosseini Imani, Soudeh Ghafouri‐Fard
Abstract
As a member of the miR-1 family, miR-206 is located between IL-17 and PKHD1 genes in human. This miRNA has been shown to be involved in the pathogenic processes in a variety of human disorders including cancers, amyotrophic lateral sclerosis, Alzheimer's disease, atherosclerosis, bronchopulmonary dysplasia, coronary artery disease, chronic obstructive pulmonary disease, epilepsy, nonalcoholic fatty liver disease, Hirschsprung disease, muscular dystrophies, pulmonary arterial hypertension, sepsis and ulcerative colitis. In the current review, we summarize the role of miR-206 in both malignant and non-malignant situations and explain its possible therapeutic implications.
Topics & Concepts
MedicineDiseaseAmyotrophic lateral sclerosisNonalcoholic fatty liver diseasemicroRNACoronary artery diseaseDysplasiaUlcerative colitisBronchopulmonary dysplasiaSepsisEpilepsyInflammatory bowel diseaseBioinformaticsPathologyFatty liverGeneInternal medicineGeneticsBiologyGestational agePsychiatryPregnancyMicroRNA in disease regulationCircular RNAs in diseasesExtracellular vesicles in disease