Regulator of telomere elongation helicase 1 gene and its association with malignancy

Cancer Rep (Hoboken). 2023 Jan;6(1):e1735. doi: 10.1002/cnr2.1735. Epub 2022 Oct 17.

Abstract

Background: With the progression of next-generation sequencing technologies, researchers have identified numerous variants of the regulator of telomere elongation helicase 1 (RTEL1) gene that are associated with a broad spectrum of phenotypic manifestations, including malignancies. At the molecular level, RTEL1 is involved in the regulation of the repair, replication, and transcription of deoxyribonucleic acid (DNA) and the maintenance of telomere length. RTEL1 can act both as a promotor and inhibitor of tumorigenesis. Here, we review the potential mechanisms implicated in the malignant transformation of tissues under conditions of RTEL1 deficiency or its aberrant overexpression.

Recent findings: A major hemostatic challenge during RTEL1 dysfunction could arise from its unbalanced activity for unwinding guanine-rich quadruplex DNA (G4-DNA) structures. In contrast, RTEL1 deficiency leads to alterations in telomeric and genome-wide DNA maintenance mechanisms, ribonucleoprotein metabolism, and the creation of an inflammatory and immune-deficient microenvironment, all promoting malignancy. Additionally, we hypothesize that functionally similar molecules could act to compensate for the deteriorated functions of RTEL1, thereby facilitating the survival of malignant cells. On the contrary, RTEL1 over-expression was directed toward G4-unwinding, by promoting replication fork progression and maintaining intact telomeres, may facilitate malignant transformation and proliferation of various pre-malignant cellular compartments.

Conclusions: Therefore, restoring the equilibrium of RTEL1 functions could serve as a therapeutic approach for preventing and treating malignancies.

Keywords: G-quadruplex; RTEL1; dyskeratosis congenita; glioma; malignancy; telomere length.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA
  • DNA Helicases* / genetics
  • Humans
  • Neoplasms* / genetics
  • Telomere* / genetics
  • Tumor Microenvironment

Substances

  • DNA
  • RTEL1 protein, human
  • DNA Helicases