Arsenic-Induced NFkB Transactivation Through Erks- and JNKs-Dependent Pathways in Mouse Epidermal JB6 Cells
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2001/06/01
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Description:Tumor promoting effects of arsenic are believed to be associated with its transactivation activity on transcription factors, such as AP-1 and NFkappaB. However, the results from different groups studying the effects of arsenic on NFkappaB activation are contradictory in different cell models. Since arsenic is a strong skin carcinogen, we have investigated the activation of NFkappaB by arsenic in a mouse skin epidermal cell line, JB6 cells. Exposure of cells to arsenite or arsenate led to NFkappaB transactivation in mouse epidermal JB6 NFkappaB-luciferase reporter stable transfectants, C141 NFkappaB mass1. This induction of NFkappaB activity by arsenic was dose- and time-dependent. The transactivation of NFkappaB by arsenic appeared to be through activation of Erks and JNKs pathways because increased NFkappaB activity by arsenic could be dramatically inhibited by either pre-treatment of cells with PD98059 or overexpression of dominant negative JNK1. That Erks activation is required for arsenic-induced NFkappaB transactivation was further supported by the findings that arsenic-induced NFkappaB transactivation was impaired in JB6 30.7b cells, which were deficient in Erks. [Description provided by NIOSH]
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ISSN:0300-8177
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Pages in Document:29-34
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Volume:222
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Issue:1
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NIOSHTIC Number:nn:20021755
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Citation:Mol Cell Biochem 2001 Jun; 222(1-2):29-34
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Contact Point Address:Nelson Institute of Environmental Medicine, New York University School of Medicine, NY 10016
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Federal Fiscal Year:2001
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Peer Reviewed:True
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Source Full Name:Molecular and Cellular Biochemistry
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Main Document Checksum:urn:sha-512:16a8b8dff50876aa619d552fcd63bda2da86968023c1b975872b4395d11ba25162bdc6d7e6fdc12e674e75a5e6d54bbfcf713a86087531c2ec95f87826b6715b
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