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The results suggest that MUC13 overexpression and loss of expression of AGR2 may predict the progression of Intraductal papillary mucinous neoplasm and an unfavorable prognosis in patients with Intraductal papillary mucinous neoplasm
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our study first demonstrated that USF1 could activate the transcription of MUC13, thereby enhancing the proliferation and self-renewal of glioblastoma stem cells
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MUC13 high expression is a novel independent adverse prognostic factor of clinical outcome in non-metastatic clear cell renal cell carcinoma patients after surgery.
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Luciferase assays and western blot confirmed MUC13 as a target gene of miR1323p.
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Results from this study demonstrate that MUC13 Functionally interacts and activates HER2 at p1248 in PDAC cells, leading to stimulation of HER2 signaling cascade, including ERK1/2, FAK, AKT and PAK1 as well as regulation of the growth, cytoskeleton remodeling and motility, invasion of PDAC cells-all collectively contributing to PDAC progression.
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High MUC13 expression is associated with renal cell carcinoma and drug resistance.
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A combination of MUC13/MUC20 expression was a potential prognostic marker for patients with ESCC, who received neoadjuvant chemotherapy followed by surgery.
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Results show that pancreatic ductal adenocarcinoma cells express higher levels of MUC13 and is associated with poor outcome when expressed at low level.
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Based on nasopharyngeal MUC13 gene expression in readily available Nasopharyngeal aspirate samples , we can discriminate between severity of disease in Respiratory syncytial virus infected infants.
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These results suggest miR-145 as a novel regulator of MUC13 in pancreatic cancer.
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Overexpression of MUC13 increased cell growth, colony formation, cell migration, and invasion in colon cancer cells.
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MUC13 is epigenetically regulated in ovarian cancer.
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Overexpression of MUC13 is associated with pancreatic neuroendocrine tumors.
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GALNT14 may contribute to ovarian carcinogenesis through aberrant glycosylation of MUC13.
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Metastatic colon cancer and liver metastasis tissue samples demonstrated significantly (p<0.05) higher cytoplasmic and nuclear MUC13 expression compared with non-metastatic colon cancer and adjacent normal colon samples.
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MUC13 overexpression caused a significant increase in cell motility, invasion, proliferation, and anchorage-dependent or -independent clonogenicity while decreasing cell-cell and cell-substratum adhesion in pancreatic cancer.
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The various functional domains of MUC13 may confer oncogenic potential to MUC13
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MUC13 is a good differentiation marker for gastrointestinal mucosa
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Aberrant intestinal expression and allelic variant MUC13 is associated with inflammatory bowel disease.
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Reflux laryngitis is associated with down-regulation of mucin gene expression.