dc.contributor.author | Wang, L | en_US |
dc.contributor.author | Howell, MEA | en_US |
dc.contributor.author | McPeak, B | en_US |
dc.contributor.author | Riggs, K | en_US |
dc.contributor.author | Kohne, C | en_US |
dc.contributor.author | Yohanon, JU | en_US |
dc.contributor.author | Foxler, DE | en_US |
dc.contributor.author | Sharp, TV | en_US |
dc.contributor.author | Moorman, JP | en_US |
dc.contributor.author | Yao, ZQ | en_US |
dc.contributor.author | Ning, S | en_US |
dc.date.accessioned | 2018-05-14T10:07:24Z | |
dc.date.available | 2017-12-11 | en_US |
dc.date.issued | 2018-01-19 | en_US |
dc.date.submitted | 2018-05-10T16:06:37.112Z | |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/37943 | |
dc.description.abstract | LIMD1 (LIM domain-containing protein 1) is considered as a tumor suppressor, being deregulated in many cancers to include hematological malignancies; however, very little is known about the underlying mechanisms of its deregulation and its roles in carcinogenesis. Epstein-Barr Virus (EBV) is associated with a panel of malignancies of lymphocytic and epithelial origin. Using high throughput expression profiling, we have previously identified LIMD1 as a common marker associated with the oncogenic transcription factor IRF4 in EBV-related lymphomas and other hematological malignancies. In this study, we have identified potential conserved IRF4- and NFκB-binding motifs in the LIMD1 gene promoter, and both are demonstrated functional by promoter-reporter assays. We further show that LIMD1 is partially upregulated by EBV latent membrane protein 1 (LMP1) via IRF4 and NFκB in EBV latency. As to its role in the setting of EBV latent infection, we show that LIMD1 interacts with TRAF6, a crucial mediator of LMP1 signal transduction. Importantly, LIMD1 depletion impairs LMP1 signaling and functions, potentiates ionomycin-induced DNA damage and apoptosis, and inhibits p62-mediated selective autophagy. Taken together, these results show that LIMD1 is upregulated in EBV latency and plays an oncogenic role rather than that of a tumor suppressor. Our findings have identified LIMD1 as a novel player in EBV latency and oncogenesis, and open a novel research avenue, in which LIMD1 and p62 play crucial roles in linking DNA damage response (DDR), apoptosis, and autophagy and their potential interplay during viral oncogenesis. | en_US |
dc.description.sponsorship | This work was supported by NIH grants to SN
(1R15DE027314) and ZQY/JPM (R01DK093526;
R01AI114748; R15AG050456), an VA Merit Review
Award to ZQY/JPM (INFA-016-15S), and BBSRC, MRC
and CRUK grants (BB/L027755/1; MR/N009185/1;
CRUK-A12733 respectively) to TVS, and in part by the
NIH grant C06RR0306551. This publication is the result
of work supported with resources and the use of facilities
at the James H. Quillen Veterans Affairs Medical Center | en_US |
dc.format.extent | 6282 - 6297 | en_US |
dc.language | eng | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Oncotarget | en_US |
dc.rights | This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
dc.subject | DDR | en_US |
dc.subject | EBV | en_US |
dc.subject | LIMD1 | en_US |
dc.subject | autophagy | en_US |
dc.subject | p62 | en_US |
dc.title | LIMD1 is induced by and required for LMP1 signaling, and protects EBV-transformed cells from DNA damage-induced cell death. | en_US |
dc.type | Article | |
dc.rights.holder | (c) Wang et al. 2017. | |
dc.identifier.doi | 10.18632/oncotarget.23676 | en_US |
pubs.author-url | https://www.ncbi.nlm.nih.gov/pubmed/29464072 | en_US |
pubs.issue | 5 | en_US |
pubs.notes | Not known | en_US |
pubs.publication-status | Published online | en_US |
pubs.volume | 9 | en_US |
dcterms.dateAccepted | 2017-12-11 | en_US |