| Our data demonstrate that FOXP3 is an X-linked breast cancer suppressor gene and an important regulator of the HER-2/ErbB2 oncogene. | breast, |
| FOXP3 is an X-linked prostate tumor suppressor in the male. Because the male has only one X chromosome, our data represent a paradigm of single genetic hit inactivation-mediated carcinogenesis. | prostate, |
| Identification of a tumor suppressor relay between the FOXP3 and the Hippo pathways in breast and prostate cancers. | breast,prostate, |
| According to this review, FoxP3 is an important tumor suppressor gene in carcinomas and has putative cancer suppressor gene function in cutaneous melanoma as well. | skin, |
| CD4, IL-17and Foxp3 may be involved in the tumor suppression caused by host immune response, and are related with non-small cell lung cancer invasion and metastasis. | lung, |
| these data here suggest that although FOXP3 is upregulated in gastric cancer, its tumor suppressor role has been dampened due to the inflammation environment. | gastric, |
| FOXP3 exhibits tumor suppressor activity in glioblastomas. | glioblastoma, |
| we argue that tumoral FOXP3 has a potential oncogenic function in conjunction with the p53 tumor suppressor protein and infiltrated Tregs in human breast carcinomas. | breast, |
| Tumoral FOXP3 expression is associated with favorable clinicopathological variables and good prognosis in gastric adenocarcinoma: the tumor suppressor function of tumoral FOXP3 is related with the P21 expression in gastric adenocarcinoma | gastric, |
| Nuclear galectin-1-FOXP3 interaction dampens the tumor-suppressive properties of FOXP3 in breast cancer | breast, |
| FOXP3 as an X-linked tumor suppressor. | None |
| FOXP3 is a negative regulator of NF-kappaB activity and thus plays a tumor suppressor role by reducing cell metastasis. | None |
| Linking the tumor suppressor function of FOXP3 to NF-kappaB activation reveals a potential therapeutic approach for cancers with FOXP3 defects. | None |
| a novel role of FOXP3 as a tumor suppressor in T-ALL through modulation of TAL1 transcriptional activity. | None |
| we argue that tumoral FOXP3 has a potential oncogenic function in conjunction with the p53 tumor suppressor protein and infiltrated Tregs in human breast carcinomas. | breast, |