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Epstein-Barr virus latent membrane protein 1 increases chemo-resistance of cancer cells via cytoplasmic sequestration of Pim-1

Authors
Kim, JH[Kim, Joo Hyun]Kim, WS[Kim, Won Seog]Yun, Y[Yun, Yungdae]Park, C[Park, Chaehwa]
Issue Date
Dec-2010
Publisher
ELSEVIER SCIENCE INC
Keywords
LMP1; Pim-1; Epstein-Barr virus; Sequestration; Chemo-resistance; Cancer
Citation
CELLULAR SIGNALLING, v.22, no.12, pp.1858 - 1863
Indexed
SCIE
SCOPUS
Journal Title
CELLULAR SIGNALLING
Volume
22
Number
12
Start Page
1858
End Page
1863
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/72773
DOI
10.1016/j.cellsig.2010.07.013
ISSN
0898-6568
Abstract
Improved treatment of EBV positive lymphoma depends on the identification of molecular mechanism underlying chemo-resistance. LMP1 is an essential transmembrane protein for EBV-induced immortalization of hematopoietic cells. Herein, we show that an oncogenic Pim-1 is translocated to the cytoplasm by LMP1. Three lines of evidence indicate that cytoplasmic sequestration of Pim-1 may be required for LMP1-induced cancer cell survival. First, Pim-1 enhanced the survival of LMP1-overexpressing cells treated with doxorubicin. Second, nuclear export of Pim-1 was sufficient to increase the survival. Third, knockdown of Pim-1 effectively suppressed LMP-1-induced survival of cancer cells. Collectively, these data suggest that Pim-1 is a downstream target of LMP1, and that it contributes to the chemo-resistance of cancer cells. (C) 2010 Elsevier Inc. All rights reserved.
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