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editorial
. 2015 Sep 14;2(10):797–798. doi: 10.18632/oncoscience.248

Figure 1. Crosstalk between ovarian cancers and O-ASCs in tumor microenvironment.

Figure 1

O-ASCs supply cancer cells with the pool of L-arginine for NO synthesis. The conversion of L-arginine into citrulline is through nitric oxide synthase (NOS). Moreover, secreted citrulline by cancer cells is consumed by O-ASCs and enhances adipogenicity of O-ASCs. The generated NO may induce s-nitrosylation of metabolic enzymes and may alter ovarian cancer cell metabolism.