Semaphorins play important regulatory roles in diverse processes such as axon guidance, angiogenesis and immune responses. We find that semaphorin-3C (sema3C) induces the collapse of the cytoskeleton of lymphatic endothelial cells (LEC) in a neuropilin-2, plexin-D1 and plexin-A1 dependent manner, while most other semaphorins, including anti-angiogenic semaphorins such as sema3A do not. Sema3C is cleaved, like other class-3 semaphorins, by furin like pro-protein convertases (FPPC). Cleaved sema3C (p65-Sema3C) was unable to induce the collapse of the cytoskeleton of LEC. FPPC are strongly up-regulated in tumor cells. In order to examine the effects of full length sema3C on tumor progression we therefore generated an active point mutated furin cleavage resistant sema3C (FR-sema3C). FR-sema3C inhibited potently proliferation of LEC and to a lesser extent proliferation of umbilical vein derived endothelial cells (HUVEC). FR-sema3C also inhibited VEGF-C induced phosphorylation of VEGFR-3, ERK1/2 and AKT. Expression of recombinant FR-sema3C in metastatic, triple negative LM2-4 breast cancer cells did not affect their migration or proliferation in-vitro. However, tumors derived from FR-sema3C expressing LM2-4 cells implanted in mammary fat pads developed at a slower rate, contained a lower concentration of blood vessels and lymph vessels, and metastasized much less effectively to lymph nodes. Interestingly, p65-Sema3C, but not FR-sema3C, rendered A549 lung cancer cells resistant to serum deprivation suggesting that previously reported pro-tumorigenic activities of sema3C may be due to p65-Sema3C produced by tumor cells. Our observations suggest that FR-sema3C may be further developed into a novel anti-tumorigenic drug.


