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May 9th, 2025
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Department of Biomedical Sciences, Seoul National University College of Medicine
cancer biology
biorxiv

Differential DNA damage response to WRN inhibition identifies a targetable vulnerability in ARID1A-mutated cancers

Kim, J.Open in Google Scholar•Oh, J.Open in Google Scholar•Jang, D.Open in Google Scholar•Shin, S.Open in Google Scholar•Lee, S.-J.Open in Google Scholar•Lee, S. E.Open in Google Scholar•Yang, Y.Open in Google Scholar•Kim, D.Open in Google Scholar•Choi, A.-J.Open in Google Scholar•Jung, H. R.Open in Google Scholaret al.

ARID1A, a key subunit of the SWI/SNF chromatin remodeling complex, is frequently mutated in cancers. However, effective clinical treatments for patients with this mutation are limited, highlighting a demand for new therapeutic strategies. Here, we establish Werner syndrome ATP-dependent helicase (WRN) as a critical vulnerability target in ARID1A-mutated cancers. Upon genetic and pharmacological inhibition of WRN, ARID1A-mutated cells had defective Chk1-mediated DNA damage signaling, resulting in compensatory Chk2 activation, leading to G1-phase arrest and apoptosis, whereas ARID1A-proficient cells underwent Chk1-dependent G2/M arrest. Additional p21 inhibition, combined with WRN suppression, drove G1-arrested cells to re-enter the cell cycle, triggering mitotic catastrophe. The anti-tumor efficacy of WRN inhibition was validated using in vivo cell lines and patient-derived xenograft mouse models. Our findings define WRN as a selective therapeutic target in ARID1A-mutated cancers and suggest a combinatorial strategy of WRN and p21 inhibition as a therapeutic approach.

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