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Literature summary for 2.4.1.155 extracted from

  • Lee, J.H.; Kang, J.G.; Song, K.J.; Jeon, S.K.; Oh, S.; Kim, Y.S.; Ko, J.H.
    N-Acetylglucosaminyltransferase V triggers overexpression of MT1-MMP and reinforces the invasive/metastatic potential of cancer cells (2013), Biochem. Biophys. Res. Commun., 431, 658-663.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
gene MGAT5, quantitative real-time PCR enzyme expression analysis Homo sapiens

Protein Variants

Protein Variants Comment Organism
additional information enzyme downregulation in cancer cells by specific shRNA expression Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
Golgi apparatus
-
Homo sapiens 5794
-

Organism

Organism UniProt Comment Textmining
Homo sapiens Q09328 gene MGAT5
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Source Tissue

Source Tissue Comment Organism Textmining
Colo-205 cell
-
Homo sapiens
-
colon
-
Homo sapiens
-
colon cancer cell
-
Homo sapiens
-
HeLa cell
-
Homo sapiens
-
Hep-G2 cell
-
Homo sapiens
-
MDA-MB-231 cell
-
Homo sapiens
-
MKN-45 cell
-
Homo sapiens
-
additional information quantitative enzyme expression analysis in cancer cells, overview Homo sapiens
-
WiDr cell
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
GnT-V
-
Homo sapiens
N-acetylglucosaminyltransferase V
-
Homo sapiens

General Information

General Information Comment Organism
physiological function enzyme that catalyzes the formation of a beta1,6-N-acetylglucosamine side chain to a core mannosyl residue in N-linked glycoproteins. Besides its direct function of producing aberrant glycoproteins, it promotes cancer progression by its involvement in the stimulation of oncoproteins. Enzyme GnT-V guides the transcriptional activation of membrane-type matrix metalloproteinase-1 (MT1-MMP) in cancer cells. The activated MT1-MMP expression has dual effects on cancer progression. It not only promotes proteolytic activity for cancer cells per se, but also leads to the activation of MMP-2. Consequently, the activation of the two MMPs triggered by GnT-V intensifies the invasive potential. Cancer invasion is stimulated by GnT-V-induced activation of both MT1-MMP and MMP-2 Homo sapiens