Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/121742
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Type: Journal article
Title: Interleukin-11 is the dominant Il-6 family cytokine during gastrointestinal tumorigenesis and can be targeted therapeutically
Author: Putoczki, T.L.
Thiem, S.
Loving, A.
Busuttil, R.A.
Wilson, N.J.
Ziegler, P.K.
Nguyen, P.M.
Preaudet, A.
Farid, R.
Edwards, K.M.
Boglev, Y.
Luwor, R.B.
Jarnicki, A.
Horst, D.
Boussioutas, A.
Heath, J.K.
Sieber, O.M.
Pleines, I.
Kile, B.T.
Nash, A.
et al.
Citation: Cancer Cell, 2013; 24(2):257-271
Publisher: Cell Press
Issue Date: 2013
ISSN: 1535-6108
1878-3686
Statement of
Responsibility: 
Tracy L.Putoczki, Stefan Thiem, Andrea Loving, Rita A.Busuttil, Nicholas J.Wilson ... Benjamin T. Kile ... et al.
Abstract: Among the cytokines linked to inflammation-associated cancer, interleukin (IL)-6 drives many of the cancer "hallmarks" through downstream activation of the gp130/STAT3 signaling pathway. However, we show that the related cytokine IL-11 has a stronger correlation with elevated STAT3 activation in human gastrointestinal cancers. Using genetic mouse models, we reveal that IL-11 has a more prominent role compared to IL-6 during the progression of sporadic and inflammation-associated colon and gastric cancers. Accordingly, in these models and in human tumor cell line xenograft models, pharmacologic inhibition of IL-11 signaling alleviated STAT3 activation, suppressed tumor cell proliferation, and reduced the invasive capacity and growth of tumors. Our results identify IL-11 signaling as a potential therapeutic target for the treatment of gastrointestinal cancers.
Keywords: Molecular Targeted Therapy
Rights: © 2013 Elsevier Inc.
DOI: 10.1016/j.ccr.2013.06.017
Grant ID: http://purl.org/au-research/grants/nhmrc/1008614
http://purl.org/au-research/grants/nhmrc/487922
http://purl.org/au-research/grants/nhmrc/1016647
Published version: http://dx.doi.org/10.1016/j.ccr.2013.06.017
Appears in Collections:Aurora harvest 8
Medical Sciences publications

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