» Articles » PMID: 33041245

Synthetic Lethal Interactions of RECQ Helicases

Overview
Journal Trends Cancer
Publisher Cell Press
Specialty Oncology
Date 2020 Oct 12
PMID 33041245
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

DNA helicases have risen to the forefront as genome caretakers. Their prominent roles in chromosomal stability are demonstrated by the linkage of mutations in helicase genes to hereditary disorders with defects in DNA repair, the replication stress response, and/or transcriptional activation. Conversely, accumulating evidence suggests that DNA helicases in cancer cells have a network of pathway interactions such that codeficiency of some helicases and their genetically interacting proteins results in synthetic lethality (SL). Such genetic interactions may potentially be exploited for cancer therapies. We discuss the roles of RECQ DNA helicases in cancer, emphasizing some of the more recent developments in SL.

Citing Articles

ATM, BLM, and CDH1 gene co-mutations in a high-grade endometrial stromal sarcoma patient with multiple abdominal cavity metastases: a case report and literature review.

Li N, Yan Y, Li Y, Yang Y, Dai C, Li N BMC Geriatr. 2024; 24(1):603.

PMID: 39009979 PMC: 11247777. DOI: 10.1186/s12877-024-05201-z.


Replication stress as a driver of cellular senescence and aging.

Herr L, Schaffer E, Fuchs K, Datta A, Brosh Jr R Commun Biol. 2024; 7(1):616.

PMID: 38777831 PMC: 11111458. DOI: 10.1038/s42003-024-06263-w.


Design and synthesis of N-aryl-2-trifluoromethyl-quinazoline-4-amine derivatives as potential Werner-dependent antiproliferative agents.

Li H, Yu J, Yu G, Cheng S, Wu H, Wei J Mol Divers. 2024; 29(1):195-214.

PMID: 38739229 DOI: 10.1007/s11030-024-10844-6.


New Facets of DNA Double Strand Break Repair: Radiation Dose as Key Determinant of HR versus c-NHEJ Engagement.

Mladenov E, Mladenova V, Stuschke M, Iliakis G Int J Mol Sci. 2023; 24(19).

PMID: 37834403 PMC: 10573367. DOI: 10.3390/ijms241914956.


PARP1 negatively regulates transcription of BLM through its interaction with HSP90AB1 in prostate cancer.

Huang M, Chen L, Guo Y, Ruan Y, Xu H J Transl Med. 2023; 21(1):445.

PMID: 37415147 PMC: 10324254. DOI: 10.1186/s12967-023-04288-z.


References
1.
Laud P, Multani A, Bailey S, Wu L, Ma J, Kingsley C . Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway. Genes Dev. 2005; 19(21):2560-70. PMC: 1276730. DOI: 10.1101/gad.1321305. View

2.
Mohindra A, Hays L, Phillips E, Preston B, Helleday T, Meuth M . Defects in homologous recombination repair in mismatch-repair-deficient tumour cell lines. Hum Mol Genet. 2002; 11(18):2189-200. DOI: 10.1093/hmg/11.18.2189. View

3.
Hills S, Diffley J . DNA replication and oncogene-induced replicative stress. Curr Biol. 2014; 24(10):R435-44. DOI: 10.1016/j.cub.2014.04.012. View

4.
Garner E, Kim Y, Lach F, Kottemann M, Smogorzewska A . Human GEN1 and the SLX4-associated nucleases MUS81 and SLX1 are essential for the resolution of replication-induced Holliday junctions. Cell Rep. 2013; 5(1):207-15. PMC: 3844290. DOI: 10.1016/j.celrep.2013.08.041. View

5.
de Lange T . T-loops and the origin of telomeres. Nat Rev Mol Cell Biol. 2004; 5(4):323-9. DOI: 10.1038/nrm1359. View