Similar to SEMA4C, SEMA7A (which showed a 3-fold increase, albeit insignificant, in our RNA-seq dataset) has been reported to have an effect on cells of other epithelial cancer types, for instance, to stimulate migration of oral tongue squamous cell carcinoma by regulating TGFβ-induced EMT signaling [103] and to orchestrate macrophage-mediated lymphatic vessel remodeling to drive metastasis in breast cancer [104]. Here, SEMA7A is linked to breast cancer.