Journal
LABORATORY INVESTIGATION
Volume 85, Issue 4, Pages 512-521Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/labinvest.3700252
Keywords
anaplastic thyroid carcinoma; growth factors; interleukins; vasculature; xenograft tumors; soluble receptors
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A pathologically elevated interstitial fluid pressure (IFP) is a characteristic of both clinical and experimental carcinoma. The soluble TGF-beta receptor type II-murine Fc: IgG(2A) chimeric protein (Fc: T beta RII) lowers IFP in the KAT-4 experimental model for anaplastic thyroid carcinoma. Analyses of messenger RNA ( mRNA) expressions by Affymetrix microarrays and RNase protection assays, as well as of protein expressions identified tumor macrophages as targets for Fc: TbRII. Treatment with Fc: TbRII reduced albumin extravasation, increased coverage of alpha-smooth muscle actin- positive cells and reduced expression of NG2, a marker of activated pericytes, in KAT-4 carcinoma blood vessels. Specific inhibition of interleukin- 1 (IL-1), a major cytokine produced by activated macrophages, lowered carcinoma IFP to a similar degree as Fc: TbRII but had no significant effect on the parameters of blood vessel maturation. Neither Fc: TbRII nor inhibition of IL-1 changed blood vessel density. Finally, pretreatment of KAT-4 carcinomas with Fc: TbRII increased the antitumor efficacy of doxorubicin. Our data emphasize a potential role of tumor macrophages in carcinoma physiology and identify these cells as potential stromal targets for treatment aimed to improve efficacy of chemotherapy.
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