The chromatin regulator HELLS mediates SSB repair and responses to DNA alkylation damage

The SNF2 family chromatin remodeler HELLS has emerged as an important regulator of cell proliferation, genome stability, and several cancer pathways. Significant upregulation of HELLS has been reported in 33 human cancer types. While HELLS has been implicated in DNA damage response, its function in DNA repair is poorly understood. Here, we report a new regulatory link between HELLS and single-strand break (SSB) repair in cellular responses to DNA alkylation damage. We found that loss of HELLS impairs SSB repair and selectively sensitizes cells to DNA alkylating agents and PARP inhibitors (PARPi). Our data reveal non-epistatic interactions between HELLS and PARP1 and suggest that HELLS functionally compensates for PARP1 deficiency in promoting cell survival in response to DNA alkylation damage. Furthermore, we found that HELLS is co-expressed with PARP1 in cancer cells, and its loss is synthetic lethal with homologous recombination deficiency (HRD). This work unveils new functions of HELLS in modulating SSB repair and responses to clinically relevant DNA alkylation damage, thus offering new insights into the potential therapeutic value of targeting HELLS in cancer.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-10-21
DOI
https://doi.org/10.1093/nar/gkaf1201
Citations
1
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
1.05
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article

The chromatin regulator HELLS mediates SSB repair and responses to DNA alkylation damage

Beverly K. Jones, Zachary Lewis, Estanislao Peixoto, Arko Sen et al.
1 citations
Nucleic Acids Research
PARP inhibition in cancer therapy
1.05
article

The chromatin regulator HELLS mediates SSB repair and responses to DNA alkylation damage

Beverly K. Jones, Zachary Lewis, Estanislao Peixoto, Arko Sen, Rafael Contreras-Galindo, Wioletta Czaja, Sergio A. Gradilone, Aaiyas Mujawar, Etsuko Shibata, Joyous T. Joseph, Imtiaz Ali, Yanfeng Zhang, Asad Ullah Khan, Yong Li, Christine Wright, Bo-Ruei Chen, Saba Tufail, Jason S Romero Neidigk, Olivia Decker, Krishna Reethika Kadali
article en
1 citations

Abstract

The SNF2 family chromatin remodeler HELLS has emerged as an important regulator of cell proliferation, genome stability, and several cancer pathways. Significant upregulation of HELLS has been reported in 33 human cancer types. While HELLS has been implicated in DNA damage response, its function in DNA repair is poorly understood. Here, we report a new regulatory link between HELLS and single-strand break (SSB) repair in cellular responses to DNA alkylation damage. We found that loss of HELLS impairs SSB repair and selectively sensitizes cells to DNA alkylating agents and PARP inhibitors (PARPi). Our data reveal non-epistatic interactions between HELLS and PARP1 and suggest that HELLS functionally compensates for PARP1 deficiency in promoting cell survival in response to DNA alkylation damage. Furthermore, we found that HELLS is co-expressed with PARP1 in cancer cells, and its loss is synthetic lethal with homologous recombination deficiency (HRD). This work unveils new functions of HELLS in modulating SSB repair and responses to clinically relevant DNA alkylation damage, thus offering new insights into the potential therapeutic value of targeting HELLS in cancer.

Nucleic Acids ResearchVol. 53(22)
University of Minnesota (US), University of Georgia (US), Washington University in St. Louis (US), Hormel (United States) (US), University of Alabama at Birmingham (US), University of Florida (US), Mayo Clinic in Florida (US)
Openalex Percentile: Top 16%
PARP inhibition in cancer therapy
1.05
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