Literature DB >> 20110692

Interleukin-6 increases expression and secretion of cathepsin B by breast tumor-associated monocytes.

Mona M Mohamed1, Dora Cavallo-Medved, Deborah Rudy, Arulselvi Anbalagan, Kamiar Moin, Bonnie F Sloane.   

Abstract

In the tumor microenvironment, monocytes respond to paracrine stimuli from breast cancer cells by secreting molecules that participate in breast cancer growth, invasion, intravasation and metastasis. Here we examined the effects of media conditioned by MDA-MB-231 human breast carcinoma cells (231-CM) on expression and secretion of proteases and secretion of cytokines by U937 human monocytes. We found that 231-CM increased U937: 1) proliferation; 2) expression, activity and secretion of the cysteine protease cathepsin B (CTSB); 3) secretion of matrix metalloproteinases (MMP)-2 and -9; and 4) secretion of interleukin-6 (IL-6) and insulin-like growth factor binding protein-1 (IGFBP-1). We further demonstrated by western blotting and enzymatic activity assays that the increases in CTSB secretion and activity induced by 231-CM could be reduced by neutralizing antibodies against IL-6. Our data suggest a role for IL-6 in increased monocyte expression and secretion of CTSB in response to soluble factors secreted by breast cancer cells. Copyright 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20110692      PMCID: PMC3030463          DOI: 10.1159/000276564

Source DB:  PubMed          Journal:  Cell Physiol Biochem        ISSN: 1015-8987


  61 in total

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4.  Imaging proteolysis by living human breast cancer cells.

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  28 in total

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Review 5.  Proteolytic networks in cancer.

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Review 6.  Leukocytes as paracrine regulators of metastasis and determinants of organ-specific colonization.

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8.  STAT3 and STAT6 Signaling Pathways Synergize to Promote Cathepsin Secretion from Macrophages via IRE1α Activation.

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9.  Cytokines secreted by macrophages isolated from tumor microenvironment of inflammatory breast cancer patients possess chemotactic properties.

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