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Hypoxia-induced alternative splicing in human diseases: the pledge, the turn, and the prestige

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 78, Issue 6, Pages 2729-2747

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-020-03727-0

Keywords

Hypoxia; Alternative splicing; Hallmarks of cancer; Cardiovascular disease; Neurodegenerative diseases; Splicing therapeutics

Funding

  1. DBT/Wellcome Trust India Alliance Fellowship [IA/I/16/2/502719]
  2. Department of Science and Technology, Ministry of Science and Technology
  3. Indian Institute of Science Education and Research Bhopal

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Maintenance of oxygen homeostasis is crucial for the existence of multicellular organisms, and disruption of this homeostasis can lead to pathological hypoxia in various conditions. Cellular adaptations include changes in gene expression, post-transcriptional modification of gene products, bioenergetics, and metabolism under hypoxic conditions. Hypoxia-induced alternative splicing events are associated with diseases like cancer, cardiovascular diseases, and neurological disorders, offering potential strategies for novel translational diagnosis and therapeutic interventions.
Maintenance of oxygen homeostasis is an indispensable criterion for the existence of multicellular life-forms. Disruption of this homeostasis due to inadequate oxygenation of the respiring tissues leads to pathological hypoxia, which acts as a significant stressor in several pathophysiological conditions including cancer, cardiovascular defects, bacterial infections, and neurological disorders. Consequently, the hypoxic tissues develop necessary adaptations both at the tissue and cellular level. The cellular adaptations involve a dramatic alteration in gene expression, post-transcriptional and post-translational modification of gene products, bioenergetics, and metabolism. Among the key responses to oxygen-deprivation is the skewing of cellular alternative splicing program. Herein, we discuss the current concepts of oxygen tension-dependent alternative splicing relevant to various pathophysiological conditions. Following a brief description of cellular response to hypoxia and the pre-mRNA splicing mechanism, we outline the impressive number of hypoxia-elicited alternative splicing events associated with maladies like cancer, cardiovascular diseases, and neurological disorders. Furthermore, we discuss how manipulation of hypoxia-induced alternative splicing may pose promising strategies for novel translational diagnosis and therapeutic interventions.

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