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|Title:||LRRK2 interacts with ATM and regulates Mdm2-p53 cell proliferation axis in response to genotoxic stress||Authors:||Chen Z.
|Issue Date:||2017||Publisher:||Oxford University Press||Citation:||Chen Z., Cao Z., Zhang W., Gu M., Zhou Z.D., Li B., Li J., Tan E.K., Zeng L. (2017). LRRK2 interacts with ATM and regulates Mdm2-p53 cell proliferation axis in response to genotoxic stress. Human Molecular Genetics 26 (22) : 4494-4505. ScholarBank@NUS Repository. https://doi.org/10.1093/hmg/ddx337||Abstract:||Pathogenic leucine-rich repeat kinase 2 (LRRK2) mutations are recognized as the most common cause of familial Parkinson's disease in certain populations. Recently, LRRK2 mutations were shown to be associated with a higher risk of hormonerelated cancers. However, how LRRK2 itself contributes to cancer risk remains unknown. DNA damage causes cancer, and DNA damage responses are among the most important pathways in cancer biology. To understand the role of LRRK2 in DNA damage response pathway, we induced DNA damage by applying genotoxic stress to the cells with Adriamycin. We found that DNA damage enhances LRRK2 phosphorylation at Serine 910, Serine 935 and Serine 1292. We further showed that LRRK2 phosphorylation is abolished in the absence of ATM, suggesting that LRRK2 phosphorylation requires ATM. It should also be noted that LRRK2 interacts with ATM. In contrast, overexpression or knockdown of LRRK2 does not affect ATM phosphorylation, indicating that LRRK2 is the downstream target of ATM in response to DNA damage. Moreover, we demonstrated that LRRK2 increases the expression of p53 and p21 by increasing the Mdm2 phosphorylation in response to DNA damage. Lossof- function in LRRK2 has the opposite effect to that of LRRK2. In addition, FACS analysis revealed that LRRK2 enhances cell cycle progression into S phase in response to DNA damage, a finding that was confirmed by 5-bromo-20-deoxyuridine immunostaining. Taken together, our findings demonstrate that LRRK2 plays an important role in the ATM-Mdm2-p53 pathway that regulates cell proliferation in response to DNA damage. � The Author 2017. Published by Oxford University Press. All rights reserved.||Source Title:||Human Molecular Genetics||URI:||http://scholarbank.nus.edu.sg/handle/10635/149001||ISSN:||9646906||DOI:||10.1093/hmg/ddx337|
|Appears in Collections:||Staff Publications|
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