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      NF-κB, an active player in human cancers.

      1 , 1 , 2
      Cancer immunology research

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          Abstract

          NF-κB comprises a family of five transcription factors that form distinct protein complexes, which bind to consensus DNA sequences at promoter regions of responsive genes regulating cellular processes. The past three decades have witnessed remarkable progress in understanding the NF-κB signaling pathway in physiologic and pathologic conditions. The role of NF-κB in human cancer initiation, development, metastasis, and resistance to treatment has drawn particular attention. A significant number of human cancers have constitutive NF-κB activity due to the inflammatory microenvironment and various oncogenic mutations. NF-κB activity not only promotes tumor cells' proliferation, suppresses apoptosis, and attracts angiogenesis, but it also induces epithelial-mesenchymal transition, which facilitates distant metastasis. In certain circumstances, NF-κB activation may also remodel local metabolism and anergize the immune system to favor tumor growth. Suppression of NF-κB in myeloid cells or tumor cells usually leads to tumor regression, which makes the NF-κB pathway a promising therapeutic target. However, because of its vital role in various biologic activities, components of the NF-κB pathway need to be carefully selected and evaluated to design targeted therapies.

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          Author and article information

          Journal
          Cancer Immunol Res
          Cancer immunology research
          2326-6074
          2326-6066
          Sep 2014
          : 2
          : 9
          Affiliations
          [1 ] Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, California.
          [2 ] Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, California. verma@salk.edu.
          Article
          2/9/823 NIHMS613931
          10.1158/2326-6066.CIR-14-0112
          4155602
          25187272
          2418e883-585e-4453-b5ad-5d00f22fcee6
          ©2014 American Association for Cancer Research.
          History

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