Death-receptor O-glycosylation controls tumor-cell sensitivity to the proapoptotic ligand Apo2L/TRAIL
By K. Wagner, E. Punnoose, T. Januario, D. Lawrence, R. Pitti, Kate Lancaster, Dori Lee, M. Goetz, S. Yee, K. Totpal and 6 more. Nature Medicine, 2007
617 citations recorded by the source corpus.
Subfields: Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/8cadaeb8ca70bacf8121a8556d6f042587a55c12
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In Immunology
In Molecular Biology
Citations in the corpus
- Protein Glycosylation in Cancer (2015, background): “In addition, ppGalNAcT-14 is overexpressed in colorectal carcinoma and pancreatic cancer and is associated with altered sensitivity to TRAILinduced apoptosis through modulation of the O-glycosylation of death receptors on these tumor cells (138).”
- Control of mucin-type O-glycosylation: a classification of the polypeptide GalNAc-transferase gene family. (2012, background): “2009) and GALNT14 to resistance to death-receptor-mediated apoptosis (Wagner et al. 2007).”
- Life and death by death receptors (2009, background): “Elevated expression of O-glycosyltransferases, the enzymes responsible for O-glycosylation of the receptors, correlates with sensitivity to TRAIL-mediated apoptosis in a large number of tumor cell lines, and represent a potential new biomarker to screen cancer patients for TRAIL-based clinical trial”
- Cullin3-based polyubiquitination and p62-dependent aggregation of caspase-8 mediate extrinsic apoptosis signaling. (2009, positive): “Alternatively, O-glycosylation of the extracellular domains of DR4 and DR5 facilitates ligand-induced receptor clustering (Wagner et al., 2007).”
- A gene expression signature associated with "K-Ras addiction" reveals regulators of EMT and tumor cell survival. (2009, background): “Cell line Cell line APO2L/TRAIL sensitivity: top 10% overexpressed in highly sensitive (Wagner et al., 2007) 86 13.”
- The TRAIL apoptotic pathway in cancer onset, progression and therapy (2008, background): “This whole-genome screen indicated that genes encoding enzymes that initiate and carry out O -glycosylation, such as GALNT14 , GALNT3 , FUT6 and FUT3 , were significantly overrepresented in TRAIL-sensitive cell line”
- Poor-prognosis colon cancer is defined by a molecularly distinct subtype and develops from serrated precursor lesions (2013, methodology): “Finally, we used CRC cell line data from the Cancer Cell Line Encyclopaedia4 (CCLE, n = 55, GSE36133) and from Wagner et al.33 (n = 11, GSE8332).”