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10.1093/carcin/bgt220

http://scihub22266oqcxt.onion/10.1093/carcin/bgt220
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23784082!ä!23784082

suck abstract from ncbi


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pmid23784082      Carcinogenesis 2013 ; 34 (11): 2655-63
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  • Activation of NF-kappaB by SOD2 promotes the aggressiveness of lung adenocarcinoma by modulating NKX2-1-mediated IKKbeta expression #MMPMID23784082
  • Chen PM; Wu TC; Wang YC; Cheng YW; Sheu GT; Chen CY; Lee H
  • Carcinogenesis 2013[Nov]; 34 (11): 2655-63 PMID23784082show ga
  • Magnesium superoxide dismutase (SOD2) has been shown to cause dysfunction of p53 transcriptional activity, whereas, in turn, SOD2 expression is regulated by p53 to modulate lung tumorigenesis. In this study, we found that the level of SOD2 expression in a panel of lung cancer cells was negatively correlated with that of NK2 homeobox 1 (NKX2-1) but was not associated with p53 status. Mechanistic studies indicated that a decrease in NKX2-1 caused by SOD2-activated IKKbeta transcription was achieved by derepression of binding of Sp1 to the IKKbeta promoter. Immunoprecipitation, glutathione S-transferase pull-down experiments and electrophoretic mobility shift assays demonstrated a direct interaction between NKX2-1 and Sp1, blocking Sp1-mediated IKKbeta transcription. SOD2-mediated nuclear factor-kappaB activation, via elevation of IKKbeta transcription, promoted anchorage-independent soft-agar growth, invasion and xenograft tumor formation, because of development of the epithelial-to-mesenchymal transition. The expression level of NKX2-1 messenger RNA was negatively associated with the extent of SOD immunostaining and the IKKbeta messenger RNA expression level in lung tumors. The extent of SOD2 immunostaining and IKKbeta messenger RNA levels may independently predict overall survival and relapse-free survival in lung adenocarcinoma patients. In summary, we found that SOD2 activates nuclear factor-kappaB signaling by increasing IKKbeta transcription, which results in progression of lung adenocarcinoma and poorer patient outcomes. We suggest that IKKbeta may potentially be targeted to improve outcomes in patients with SOD2-positive tumors.
  • |Adenocarcinoma/metabolism/mortality/*pathology[MESH]
  • |Animals[MESH]
  • |Blotting, Western[MESH]
  • |Cell Adhesion[MESH]
  • |Cell Movement[MESH]
  • |Cell Proliferation[MESH]
  • |Chromatin Immunoprecipitation[MESH]
  • |Electrophoretic Mobility Shift Assay[MESH]
  • |Epithelial-Mesenchymal Transition[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |I-kappa B Kinase/*genetics/metabolism[MESH]
  • |Immunoenzyme Techniques[MESH]
  • |Luciferases/metabolism[MESH]
  • |Lung Neoplasms/metabolism/mortality/*pathology[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]
  • |Mice, Nude[MESH]
  • |NF-kappa B/genetics/*metabolism[MESH]
  • |Nuclear Proteins/genetics/*metabolism[MESH]
  • |Promoter Regions, Genetic[MESH]
  • |RNA, Messenger/genetics[MESH]
  • |Real-Time Polymerase Chain Reaction[MESH]
  • |Reverse Transcriptase Polymerase Chain Reaction[MESH]
  • |Superoxide Dismutase/genetics/*metabolism[MESH]
  • |Thyroid Nuclear Factor 1[MESH]
  • |Transcription Factors/genetics/*metabolism[MESH]
  • |Tumor Cells, Cultured[MESH]


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