In this mechanism, proteases are released into the immune synapse, where they travel through the perforin pores into target cells generating pro-apoptotic effectors, granzyme A and granzyme B. Tumor cells are able to prevent elimination from the perforin/granzyme pathway by abnormally eradicating granzyme expression or increasing intrinsic granzyme inhibitors, called serpins [107]. Here, GZMA is linked to neoplasm.