Intertissue Flow of Gsh as a Tumor Growth Promoting Mechanism: Interleukin 6 Induces Gsh Release from Hepatocytes in Metastatic B16 Melanoma-bearing Mice

B16 melanoma F10 (B16-F10) cells with high glutathione (GSH) content show high metastatic activity in vivo. An intertissue flow of GSH, where the liver is the main reservoir, can increase GSH content in metastatic cells and promote their growth. We have studied here possible tumorderived molecular signals that could activate GSH release from hepatocytes. GSH efflux increases in hepatocytes isolated from mice bearing liver or lung metastases, thus suggesting a systemic mechanism. Fractionation of serum-free conditioned medium from cultured B16F10 cells, and monoclonal antibodiesinduced neutralization techniques, facilitated identification of interleukin 6 (IL-6) as a tumor-derived molecule promoting GSH efflux in hepatocytes. IL6 activates GSH release through a methionine-sensitive/organic anion transporter polypeptide 1and multidrug resistance protein 1-independent channel located on the sinusoidal site of hepatocytes. Specific siRNAs were used to knock-down key factors in the main signaling pathways activated by IL-6, which revealed a STAT3-dependent mechanism. Our results show that IL-6 (mainly of tumor origin in B16-F10bearing mice) may facilitate GSH release from hepatocytes and its interorgan transport to metastatic growing foci.