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Regulating the regulators: long non-coding RNAs as autophagic controllers in chronic disease management
Aviral Kumar1, Kenneth Chun-Hong Yap2,3, Bandari BharathwajChetty1
1Cancer Biology Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati (IITG), Guwahati, Assam, 781039, India.
Abstract:
The increasing prevalence of chronic diseases and their associated morbidities demands a deeper understanding of underlying mechanism and causative factors, with the hope of developing novel therapeutic strategies. Autophagy, a conserved biological process, involves the degradation of damaged organelles or protein aggregates to maintain cellular homeostasis. Disruption of this crucial process leads to increased genomic instability, accumulation of reactive oxygen species (ROS), decreased mitochondrial functions, and suppression of ubiquitination, leading to overall decline in quality of intracellular components. Such deregulation has been implicated in a wide range of pathological conditions such as cancer, cardiovascular, inflammatory, and neurological disorders. This review explores the role of long non-coding RNAs (lncRNAs) as modulators of transcriptional and post-transcriptional gene expression, regulating diverse physiological process like proliferation, development, immunity, and metabolism. Moreover, lncRNAs are known to sequester autophagy related microRNAs by functioning as competing endogenous RNAs (ceRNAs), thereby regulating this vital process. In the present review, we delineate the multitiered regulation of lncRNAs in the autophagic dysfunction of various pathological diseases. Moreover, by highlighting recent findings on the modulation of lncRNAs in different stages of autophagy, and the emerging clinical landscape that recognizes lncRNAs in disease diagnosis and therapy, this review highlights the potential of lncRNAs as biomarkers and therapeutic targets in clinical settings of different stages of autophagic process by regulating ATG and its target genes. This focus on lncRNAs could lead to breakthroughs in personalized medicine, offering new avenues for diagnosis and treatment of complex diseases.
Insights
Long non-coding RNAs (lncRNAs) regulate autophagy, a cellular process crucial for homeostasis. Dysfunctional autophagy is linked to diseases, and lncRNAs offer potential as diagnostic biomarkers and therapeutic targets.
Area of Science:
- Molecular Biology
- Cellular Biology
- Genetics
Background:
- Chronic diseases necessitate understanding underlying mechanisms for novel therapies.
- Autophagy maintains cellular homeostasis by degrading damaged components; its disruption is implicated in diseases like cancer and neurological disorders.
- Long non-coding RNAs (lncRNAs) are key regulators of gene expression and cellular processes.
Purpose of the Study:
- To review the multitiered regulation of lncRNAs in autophagic dysfunction across various pathological diseases.
- To highlight recent findings on lncRNA modulation in autophagy and their clinical potential.
- To explore lncRNAs as biomarkers and therapeutic targets for autophagy-related diseases.
Main Methods:
- Literature review focusing on lncRNAs, autophagy, and disease mechanisms.
- Analysis of lncRNA roles in transcriptional and post-transcriptional gene regulation.
- Examination of lncRNAs as competing endogenous RNAs (ceRNAs) sequestering microRNAs.
Main Results:
- lncRNAs modulate diverse physiological processes including proliferation, development, immunity, and metabolism.
- lncRNAs regulate autophagy by sequestering microRNAs and influencing autophagy-related genes (ATGs).
- Dysregulated lncRNAs are implicated in the pathogenesis of various diseases, including cancer and neurological disorders.
Conclusions:
- lncRNAs play a critical role in regulating autophagy and are implicated in disease pathogenesis.
- lncRNAs demonstrate significant potential as diagnostic biomarkers and therapeutic targets for autophagy-related diseases.
- Targeting lncRNAs may offer novel avenues for personalized medicine and treatment of complex diseases.
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