Acid
sphingomyelinase (ASM) regulates the homeostasis of sphingolipids, including
ceramides and sphingosine-1-phosphate (S1P). These sphingolipids regulate
carcinogenesis and proliferation, survival, and apoptosis of cancer cells.
However, the role of ASM in host defense against liver metastasis remains
unclear. In this study, the involvement of ASM in liver metastasis of colon
cancer was examined using Asm-/- and Asm+/+ mice that were inoculated with SL4
colon cancer cells to produce metastatic liver tumors. Asm-/- mice demonstrated
enhanced tumor growth and reduced macrophage accumulation in the tumor,
accompanied by decreased numbers of hepatic myofibroblasts (hMFs), which
express tissue inhibitor of metalloproteinase 1 (TIMP1), around the tumor
margin. Tumor growth was increased by macrophage depletion or by Timp1
deficiency, but was decreased by hepatocyte-specific ASM overexpression, which
was associated with increased S1P production. S1P stimulated macrophage
migration and TIMP1 expression in hMFs in vitro. These findings indicate that
ASM in the liver inhibits tumor growth through cytotoxic macrophage
accumulation and TIMP1 production by hMFs in response to S1P. Targeting ASM may
represent a new therapeutic strategy for treating liver metastasis of colon
cancer.
Source: Liver acid
sphingomyelinase inhibits growth of metastatic colon cancer. Osawa Y, Suetsugu
A, Matsushima-Nishiwaki R, Yasuda I, Saibara T, Moriwaki H, Seishima M, Kozawa
O (osawa-gif@umin.ac.jp). J Clin
Invest. 2013 Jan 9.
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