Macrophage Migration Inhibitory Factor Promotes Tumor Invasion and Metastasis via the Rho-Dependent Pathway
Purpose: Macrophage migration inhibitory factor (MIF) plays an important role not only in the immune system but also in tumorigenesis. In this study, we investigated the potential role of MIF in association with tumor invasion and metastasis. Methods: To assess the function of MIF, we knocked down t...
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Veröffentlicht in: | Clinical cancer research 2005-02, Vol.11 (3), p.1050-1058 |
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Zusammenfassung: | Purpose: Macrophage migration inhibitory factor (MIF) plays an important role not only in the immune system but also in tumorigenesis.
In this study, we investigated the potential role of MIF in association with tumor invasion and metastasis.
Methods: To assess the function of MIF, we knocked down the MIF mRNA using small interfering RNA (siRNA). Twenty-one base siRNA specific
for the mRNA sequence of mouse MIF was introduced to a murine colon cancer cell line, colon 26. Tumor cell invasion was evaluated
using a transwell method (8-μm pores) coated with Matrigel on the upperside membrane and with fibronectin on the underside
membrane. Moreover, we investigated the signal transduction of lysophosphatidic acid (LPA) relevant to the Rho-dependent pathway
and further examined the effect of MIF siRNA on this signal transduction system. In vivo , the tumor cells were pretreated with MIF siRNA and injected into the portal vein, and the effects on metastasis to the liver
were evaluated.
Results: We found that MIF siRNA markedly reduced the invasion of the cells from the upperside to lowerside membranes. We revealed
that the Rho-dependent pathway activated by LPA was suppressed by MIF siRNA. Next, we found that the tyrosine-phosphorylation
of focal adhesion kinase and LPA-induced expressions of integrin β1 were significantly suppressed by MIF siRNA. In vivo , metastasis to the liver was significantly inhibited by pretreatment of the cells with MIF siRNA.
Conclusion: Taken together, these results suggest that MIF promotes tumor invasion and metastasis via the Rho-dependent pathway. |
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ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.1050.11.3 |