In addition, we noted a highly significant increase in arginase-1 activity in endometrial carcinomas compared with normal endometria, which was not the case for uterine sarcomas.
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Mapping the immunosuppressive environment in uterine tumors: implications for immunotherapy.
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When gating on these different cell populations, a slightly higher percentage of membranous galectin-3 positivity on tumor cells versus fibroblasts and immune cells was found, although this did not reach statistical significance, shown in Fig. 3 c.