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Repeated ionizing radiation exposure induces TRIP13 expression, conferring radioresistance in lung cancer cells

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Repeated ionizing radiation exposure induces TRIP13 expression, conferring radioresistance in lung cancer cells Abstract Radiation therapy is a common treatment modality for lung cancer, and resistance to radiation can significantly affect treatment outcomes. We recently described that lung cancer cells that express more germ cell cancer genes (GC genes, genes that are usually restricted to the germ line) can repair DNA double-strand breaks more rapidly, show higher rates of proliferation and are more resistant to ionizing radiation than cells that express fewer GC genes. The gene encoding TRIP13 appeared to play a large role in this malignant phenotype. However, the molecular regulatory mechanism of TRIP13 in radiation resistance remained largely unknown. Here, we show that TRIP13 is a key contributor to non-small cell lung cancer (NSCLC) treatment resistance, particularly in patients following radiation treatment, for whom levels of TRIP13 expression are correlated with a poor prognosis.
Period1 Jan 2025

Media contributions

1

Media contributions

  • TitleRepeated ionizing radiation exposure induces TRIP13 expression, conferring radioresistance in lung cancer cells
    Media name/outletScientific Reports
    Duration/Length/Size6646
    Date01/01/2025
    DescriptionRepeated ionizing radiation exposure induces TRIP13 expression, conferring radioresistance in lung cancer cells Abstract Radiation therapy is a common treatment modality for lung cancer, and resistance to radiation can significantly affect treatment outcomes. We recently described that lung cancer cells that express more germ cell cancer genes (GC genes, genes that are usually restricted to the germ line) can repair DNA double-strand breaks more rapidly, show higher rates of proliferation and are more resistant to ionizing radiation than cells that express fewer GC genes. The gene encoding TRIP13 appeared to play a large role in this malignant phenotype. However, the molecular regulatory mechanism of TRIP13 in radiation resistance remained largely unknown. Here, we show that TRIP13 is a key contributor to non-small cell lung cancer (NSCLC) treatment resistance, particularly in patients following radiation treatment, for whom levels of TRIP13 expression are correlated with a poor prognosis.
    PersonsWenqing Liu, Qijing Lei, Ans M.M. van Pelt, Geert Hamer