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Alternative Lengthening of Telomeres: Building Bridges To Connect Chromosome Ends.
- Source :
-
Trends in cancer [Trends Cancer] 2020 Mar; Vol. 6 (3), pp. 247-260. Date of Electronic Publication: 2020 Jan 23. - Publication Year :
- 2020
-
Abstract
- Alternative lengthening of telomeres (ALT) is a mechanism of telomere maintenance that is observed in many of the most recalcitrant cancer subtypes. Telomeres in ALT cancer cells exhibit a distinctive nucleoprotein architecture shaped by the mismanagement of chromatin that fosters cycles of DNA damage and replicative stress that activate homology-directed repair (HDR). Mutations in specific chromatin-remodeling factors appear to be key determinants of the emergence and survival of ALT cancer cells. However, these may represent vulnerabilities for the targeted elimination of ALT cancer cells that infiltrate tissues and organs to become devastating tumors. In this review we examine recent findings that provide new insights into the factors and mechanisms that mediate telomere length maintenance and survival of ALT cancer cells.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Subjects :
- Chromatin ultrastructure
Clonal Evolution
Co-Repressor Proteins antagonists & inhibitors
Co-Repressor Proteins physiology
DNA Damage
DNA Repair
DNA Replication
DNA, Neoplasm metabolism
DNA, Neoplasm ultrastructure
Histones physiology
Homologous Recombination
Humans
Models, Genetic
Molecular Chaperones antagonists & inhibitors
Molecular Chaperones physiology
Mutation
Neoplasm Proteins antagonists & inhibitors
Neoplasm Proteins genetics
Neoplasm Proteins physiology
Neoplasms ultrastructure
Nucleic Acid Conformation
Telomerase genetics
Telomerase physiology
X-linked Nuclear Protein antagonists & inhibitors
X-linked Nuclear Protein physiology
Neoplasms genetics
Telomere Homeostasis
Subjects
Details
- Language :
- English
- ISSN :
- 2405-8025
- Volume :
- 6
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Trends in cancer
- Publication Type :
- Academic Journal
- Accession number :
- 32101727
- Full Text :
- https://doi.org/10.1016/j.trecan.2019.12.009