EUVIMEDUpptäck EUVIMED
CrossrefInfokort

Loss of IGF ‐ 1R impairs DNA ‐ PKcs recruitment to chromatin leading to defective end‐joining

Matthew O. Ellis, Jack V. Mills, Wojciech Niedzwiedz, Valentine M. Macaulay

Molecular Oncology · 2026-11 · 20 (11) · 2876-2895

DOI: 10.1002/1878-0261.70266 ↗
AbstractBibliografiska uppgifter

Abstract

The insulin‐like growth factor (IGF) axis regulates cancer cell proliferation, growth, invasion, and therapy resistance. Elevated expression of the type 1 IGF receptor (IGF‐1R) is linked to radioresistance and biochemical recurrence in prostate cancer, yet the molecular mechanisms underlying IGF‐1R–mediated DNA damage responses remain unclear. We investigated the role of IGF‐1R in DNA double‐strand break (DSB) repair by assessing chromatin recruitment of DNA repair proteins, repair pathway usage, and therapeutic sensitivity in cancer cell models with altered IGF‐1R status. Loss of IGF‐1R impaired DNA‐dependent protein kinase catalytic subunit (DNA‐PKcs) localisation to chromatin, resulting in defective non‐homologous end‐joining (NHEJ) and a compensatory reliance on alternative repair pathways, including microhomology‐mediated end‐joining (MMEJ). Modulating IGF‐1R expression restored radiosensitivity in poly (ADP‐ribose) polymerase (PARP) inhibitor–resistant breast cancer cells. IGF‐1R inhibition compromises canonical DSB repair and re‐sensitises resistant cancer cells to therapy, supporting its potential as a therapeutic strategy in homologous recombination–deficient tumours. Furthermore, IGF‐1R mutant cancers may benefit from targeted inhibition of the MMEJ pathway.

Kunskap som passar ditt arbete.

Från en kostnadsfri start via personlig litteratursökning till hela Research Suite.

Visa priser →

Ingår alla förlagsfulltexter?

Nej. Bibliografiska poster, abstrakt och fulltexter är olika typer av innehåll. Om en fulltext är tillgänglig beror på källan, Open Access och dina befintliga licenser. En EUVIMED-plan ersätter inga ytterligare förlagsrättigheter.

Visa priser →