| http://purl.uniprot.org/citations/35447102 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/35447102 | http://www.w3.org/2000/01/rdf-schema#comment | "Breast cancer, the most prevalent malignancy in women, is also the leading cause of cancer-related deaths in women worldwide. The activation of the Wnt pathway plays a pivotal role in the metastatic abilities of breast cancer. In this study, IL1F6, MRGPRX1, and SEC14L3 were significantly correlated to breast cancer patients'overall survival based on TCGA-BRCA dataset. Although IL1F6, MRGPRX1 and SEC14L3 high expression were associated with better survival in breast cancer patients, SEC14L3 had the biggest survival benefit for breast cancer; therefore, SEC14L3 was selected for the subsequent investigation. SEC14L3 mRNA expression and protein levels within breast cancer cell lines decreased compared with normal human breast epithelial cells. Overexpressing SEC14L3 in breast cancer cells inhibited the malignant phenotypes of cancer cells, including the capacity of cells to migrate and invade. SEC14L3 overexpression decreased the levels of mesenchymal markers, whereas SEC14L3 knockdown facilitated the malignant behaviors of breast cancer cells. SEC14L3 overexpression also inhibited Wnt/β-catenin activation. The Wnt agonist strengthened the malignant phenotypes of breast cancer cells; moreover, the anti-tumor effects of SEC14L3 overexpression were partially attenuated by the Wnt agonist. Conclusively, SEC14L3, which is underexpressed in breast cancer cells and tissues, could play a tumor-suppressive role in a Wnt/β-catenin-related way."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.org/dc/terms/identifier | "doi:10.1016/j.yexcr.2022.113161"xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "He Y."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "He X."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "Liu H."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "Zhang Y."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "Zhu Q."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "Lu L.L."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "Deng H.W."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/author | "Wan N.B."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/date | "2022"xsd:gYear |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/name | "Exp Cell Res"xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/pages | "113161"xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/title | "SEC14L3 plays a tumor-suppressive role in breast cancer through a Wnt/beta-catenin-related way."xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://purl.uniprot.org/core/volume | "417"xsd:string |
| http://purl.uniprot.org/citations/35447102 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/35447102 |
| http://purl.uniprot.org/citations/35447102 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/35447102 |
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