RGD Reference Report - TGF-β-induced IRAK-M expression in tumor-associated macrophages regulates lung tumor growth. - Rat Genome Database

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TGF-β-induced IRAK-M expression in tumor-associated macrophages regulates lung tumor growth.

Authors: Standiford, T J  Kuick, R  Bhan, U  Chen, J  Newstead, M  Keshamouni, V G 
Citation: Standiford TJ, etal., Oncogene. 2011 May 26;30(21):2475-84. doi: 10.1038/onc.2010.619. Epub 2011 Jan 31.
RGD ID: 36049796
Pubmed: PMID:21278795   (View Abstract at PubMed)
PMCID: PMC3102782   (View Article at PubMed Central)
DOI: DOI:10.1038/onc.2010.619   (Journal Full-text)

Tumor-associated macrophages (TAMs) constitute a major component of the immune cell infiltrate observed in the tumor microenvironment (TME). Factors present in the TME, including tumor growth factor-β (TGF-β), allow tumors to circumvent host-mediated immune responses to promote tumor progression. However, the molecular mechanism(s) involved are not clear. Toll-like receptors (TLRs) are important mediators of innate immune responses by immune cells, whose activation triggers the production of molecules required for anti-tumoral responses. Interleukin (IL) receptor-associated kinase (IRAK)-M is an inactive serine/threonine kinase, predominantly expressed in macrophages and is a potent negative regulator of TLR signaling. In this study, we show that TAMs express significantly higher levels of IRAK-M compared with peritoneal macrophages in a syngeneic mouse model of lung cancer. Subcutaneous implantation of Lewis lung carcinoma cells in IRAK-M(-/-) mice resulted in a five-fold reduction in tumor growth as compared with tumors in wild-type (WT) animals. Furthermore, compared with WT TAMs, TAMs isolated from IRAK-M(-/-) mice displayed features of a classically activated (M1) rather than alternatively activated (M2) phenotype, as manifest by greater expression of IL-12, interferon-γ (IFN-γ) and inducible nitric oxide synthase. Human lung cancer cells induced IRAK-M expression in human peripheral blood mononuclear cells (PBMCs) when co-cultured together. Tumor cell-induced expression of IRAK-M was dependent on the activation of TGF-β pathway. Similarly, treatment of human PBMCs or mouse macrophage cell line, RAW 264.4, with TGF-β, induced IRAK-M expression. Interestingly, IRAK-M gene expression in 439 human lung adenocarcinoma tumors correlated with poor survival in patients with lung cancer. Together, our data demonstrates that TGF-β-dependent induction of IRAK-M expression is an important, clinically relevant mechanism by which tumors may circumvent anti-tumor responses of macrophages.



RGD Manual Disease Annotations    Click to see Annotation Detail View

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
IRAK3HumanCarcinoma, Lewis Lung  IMP  RGD 
Irak3RatCarcinoma, Lewis Lung  ISOIRAK3 (Homo sapiens) RGD 
Irak3MouseCarcinoma, Lewis Lung  ISOIRAK3 (Homo sapiens) RGD 
IRAK3Humanlung adenocarcinoma  HEP mRNA:increased expression:lung (human)RGD 

Objects Annotated

Genes (Rattus norvegicus)
Irak3  (interleukin-1 receptor-associated kinase 3)

Genes (Mus musculus)
Irak3  (interleukin-1 receptor-associated kinase 3)

Genes (Homo sapiens)
IRAK3  (interleukin 1 receptor associated kinase 3)


Additional Information