Non-Coding RNA: An Emerging Modulator of ꞵ-Globin Regulation and ꞵ-Hemoglobinopathies
DOI:
https://doi.org/10.55627/mmc.002.002.0147Keywords:
ncRNA, hematopoiesis, ꞵ-thalassemia, sickle cell anemia, fetal hemoglobin, therapeutic targetsAbstract
ꞵ-Hemoglobinopathies, including ꞵ-thalassemia and sickle cell anemia, are the most common autosomal receiver disorders, globally. Non-coding RNAs (ncRNAs) are derived from exons or introns of protein-coding genes or intronic regions of non-coding genes. There is significant evidence that these ncRNAs may act as protein decoys to impact a variety of biological functions, signaling, transcriptional regulators, cell differentiation, morphogenesis, and developmental regulation. The aberrant regulation of ncRNA expression serves as a hallmark of many hematological disorders, and there is solid evidence that these RNA species can play key roles in the pathogenesis of ꞵ-hemoglobinopathies. In the present review, we provide a summary of recent research findings about the role of ncRNA in globin gene regulation and ꞵ-hemoglobinopathies and their potential as therapeutic targets or prognostic and diagnostic biomarkers.
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Copyright (c) 2022 Hamad Ali, Faisal Khan

This work is licensed under a Creative Commons Attribution 4.0 International License.

