CDKN2A/B homozygous deletion is associated with early recurrence in meningiomas
Genes, p16
Homozygote
2804 Cellular and Molecular Neuroscience
610 Medicine & health
10040 Clinic for Neurology
3. Good health
2734 Pathology and Forensic Medicine
03 medical and health sciences
2728 Neurology (clinical)
0302 clinical medicine
Correspondence
Meningeal Neoplasms
Humans
Gene Deletion [MeSH] ; Homozygote [MeSH] ; Genes, p16/physiology [MeSH] ; Meningeal Neoplasms/genetics [MeSH] ; Humans [MeSH] ; Sequence Deletion/genetics [MeSH] ; Pathology ; Meningioma/genetics [MeSH] ; Neurosciences ; Cyclin-Dependent Kinase Inhibitor p16/genetics [MeSH] ; Correspondence
Meningioma
Cyclin-Dependent Kinase Inhibitor p16
Gene Deletion
Sequence Deletion
DOI:
10.1007/s00401-020-02188-w
Publication Date:
2020-07-08T05:33:39Z
AUTHORS (25)
ABSTRACT
Soon after birth, the regenerative capacity of the mammalian heart is lost, cardiomyocytes withdraw from the cell cycle and demonstrate a minimal proliferation rate. Despite improved treatment and reperfusion strategies, the uncompensated cardiomyocyte loss during injury and disease results in cardiac remodeling and subsequent heart failure. The promising field of regenerative medicine aims to restore both the structure and function of damaged tissue through modulation of cellular processes and regulatory mechanisms involved in cardiac cell cycle arrest to boost cardiomyocyte proliferation. Non-coding RNAs (ncRNAs), such as microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) are functional RNA molecules with no protein-coding function that have been reported to engage in cardiac regeneration and repair. In this review, we summarize the current understanding of both the biological functions and molecular mechanisms of ncRNAs involved in cardiomyocyte proliferation. Furthermore, we discuss their impact on the structure and contractile function of the heart in health and disease and their application for therapeutic interventions.
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