Loss of PTEN-assisted G2/M checkpoint impedes homologous recombination repair and enhances radio-curability and PARP inhibitor treatment response in prostate cancer
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-22289-7.pdf
Reference37 articles.
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3. Mansour, W. Y. et al. Hierarchy of nonhomologous end-joining, single-strand annealing and gene conversion at site-directed DNA double-strand breaks. Nucleic Acids Res 36, 4088–4098, https://doi.org/10.1093/nar/gkn347 (2008).
4. Bentley, J., Diggle, C. P., Harnden, P., Knowles, M. A. & Kiltie, A. E. DNA double strand break repair in human bladder cancer is error prone and involves microhomology-associated end-joining. Nucleic Acids Res 32, 5249–5259, https://doi.org/10.1093/nar/gkh842 (2004).
5. Kotter, A. et al. Inhibition of PARP1-dependent end-joining contributes to Olaparib-mediated radiosensitization in tumor cells. Mol Oncol 8, 1616–1625, https://doi.org/10.1016/j.molonc.2014.06.008 (2014).
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1. NHEJ is promoted by the phosphorylation and phosphatase activity of PTEN via regulation of DNA-PKcs;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2024-12
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4. Blocking lipid synthesis induces DNA damage in prostate cancer and increases cell death caused by PARP inhibition;Science Signaling;2024-04-09
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