Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:O76050 (
neu
)
3,969
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
In a previous study it was found that the therapeutic effects of QLT0267, a small molecule inhibitor of integrin-linked kinase (ILK), were influenced by Her2/
neu
expression. To understand how inhibition or silencing of ILK influences Her2/
neu
expression, Her2/
neu
signaling was evaluated in six Her2/
neu
-positive breast cancer cell lines (LCC6(Her2), MCF7(Her2), SKBR3, BT474, JIMT-1 and KPL-4). Treatment with QLT0267 engendered suppression (32-87%) of total Her2/
neu
protein in these cells. Suppression of Her2/
neu
was also observed following small interfering RNA-mediated silencing of ILK expression. Time course studies suggest that ILK inhibition or silencing caused transient decreases in P-AKT(ser473), which were not temporally related to Her2/
neu
downregulation. Attenuation of ILK activity or expression was, however, associated with decreases in
YB-1
(Y-box binding protein-1) protein and transcript levels.
YB-1
is a known transcriptional regulator of Her2/
neu
expression, and in this study it is demonstrated that inhibition of ILK activity using QLT0267 decreased
YB-1
promoter activity by 50.6%. ILK inhibition was associated with changes in
YB-1
localization, as reflected by localization of cytoplasmic
YB-1
into stress granules. ILK inhibition also suppressed TWIST (a regulator of
YB-1
expression) protein expression. To confirm the role of ILK on
YB-1
and TWIST, cells were engineered to overexpress ILK. This was associated with a fourfold increase in the level of
YB-1
in the nucleus, and a 2- and 1.5-fold increase in TWIST and Her2/
neu
protein levels, respectively. Taken together, these data indicate that ILK regulates the expression of Her2/
neu
through TWIST and
YB-1
, lending support to the use of ILK inhibitors in the treatment of aggressive Her2/
neu
-positive tumors.
...
PMID:Suppression of Her2/neu expression through ILK inhibition is regulated by a pathway involving TWIST and YB-1. 2083 84