Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 6.1.1.6 extracted from

  • Nam, S.H.; Kim, D.; Lee, M.S.; Lee, D.; Kwak, T.K.; Kang, M.; Ryu, J.; Kim, H.J.; Song, H.E.; Choi, J.; Lee, G.H.; Kim, S.Y.; Park, S.H.; Kim, D.G.; Kwon, N.H.; Kim, T.Y.; Thiery, J.P.; Kim, S.; Lee, J.W.
    Noncanonical roles of membranous lysyl-tRNA synthetase in transducing cell-substrate signaling for invasive dissemination of colon cancer spheroids in 3D collagen I gels (2015), Oncotarget, 6, 21655-21674 .
    View publication on PubMedView publication on EuropePMC

Inhibitors

Inhibitors Comment Organism Structure
additional information the complex formation among KRS, p67LR, and integrins alpha6 and beta1 upon cell adhesion can be disrupted by YH16899 treatment. SW620 cells with inhibitors U1026 or YH16899 blocks dissemination. Blockade of dissemination of KRS-suppressed cells is relieved by ERK1/2 and/or paxillin expression Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
cytosol
-
Homo sapiens 5829
-
plasma membrane
-
Homo sapiens 5886
-

Organism

Organism UniProt Comment Textmining
Homo sapiens Q15046
-
-

Source Tissue

Source Tissue Comment Organism Textmining
colon cancer cell
-
Homo sapiens
-
HCT-116 cell
-
Homo sapiens
-
SW-620 cell
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
KRS
-
Homo sapiens
Lysyl-tRNA synthetase
-
Homo sapiens

Expression

Organism Comment Expression
Homo sapiens the complex formation among KRS, p67LR, and integrins alpha6 and beta1 upon cell adhesion can be disrupted by YH16899 treatment. SW620 cells with inhibitors U1026 or YH16899 blocks dissemination. Blockade of dissemination of KRS-suppressed cells is relieved by ERK1/2 and/or paxillin expression additional information

General Information

General Information Comment Organism
malfunction KRS-suppressed HCT-116 cells show increased mesenchymal markers and decreased epithelial markers 24 h after embedding of colon cancer spheroids in 3D collagen I gels. KRS-positive cells are sensitive to laminin treatment for p67LR stabilization, KRS-suppressed cells are insensitive to the laminin treatment. KRS-expressing parental cells show disseminative margins that are positive for E-cadherin expression, whereas KRS-suppressed cells show neither. Specific effect of KRS suppression on paxillin. KRS suppression decreases the phosphorylations of vinculin Tyr822 and tensin2 Tyr483, but not of talin Ser425. KRS-suppression decreases ERK1/2 phosphorylation, ERK1/2 phosphorylation is increased by KRS overexpression. Treating SW620 cells with inhibitors U1026 or YH16899 blocks dissemination Homo sapiens
additional information noncanonical roles of membranous lysyl-tRNA synthetase in transducing cell-substrate signaling for invasive dissemination of colon cancer spheroids in 3D collagen I gels Homo sapiens
physiological function KRS at the plasma membrane is important for cancer metastasis, canonical roles of cytosolic KRS in protein translation. KRS and its downstream effectors promote the metastatic migration. Complex formation among KRS, p67LR, and integrins alpha6 and beta1 upon cell adhesion, KRS/p67LR/integrin alpha6beta1 linkage correlates for ERK1/2 activation, KRS-dependent ERK1/2 activation. KRS has prometastatic roles at the invasive margins of KRS-/+ mouse breast tumor and human colon tumor tissues Homo sapiens