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Review
. 2007 May;85(5):427-36.
doi: 10.1007/s00109-006-0152-3. Epub 2007 Jan 10.

The role of STATs in lung carcinogenesis: an emerging target for novel therapeutics

Affiliations
Review

The role of STATs in lung carcinogenesis: an emerging target for novel therapeutics

Michalis V Karamouzis et al. J Mol Med (Berl). 2007 May.

Abstract

The signal transducer and activator of transcription (STAT) proteins are a family of latent cytoplasmic transcription factors, which form dimers when activated by cytokine receptors, tyrosine kinase growth factor receptors as well as non-receptor tyrosine kinases. Dimeric STATs translocate to the nucleus, where they bind to specific DNA-response elements in the promoters of target genes, thereby inducing unique gene expression programs often in association with other transcription regulatory proteins. The functional consequence of different STAT proteins activation varies, as their target genes play diverse roles in normal cellular/tissue functions, including growth, apoptosis, differentiation and angiogenesis. Certain activated STATs have been implicated in human carcinogenesis, albeit only few studies have focused into their role in lung tumours. Converging evidence unravels their molecular interplays and complex multipartite regulation, rendering some of them appealing targets for lung cancer treatment with new developing strategies.

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References

    1. Cancer. 2006 Jan 15;106(2):366-74 - PubMed
    1. Clin Cancer Res. 2005 Sep 1;11(17):6382-9 - PubMed
    1. J Biol Chem. 2004 Jan 9;279(2):821-4 - PubMed
    1. Proc Natl Acad Sci U S A. 2003 Apr 1;100(7):4138-43 - PubMed
    1. Clin Cancer Res. 2002 May;8(5):949-61 - PubMed

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