BCR/ABL expression, tyrosine phosphorylation, and signaling in dasatinib- and imatinib-resistant cell lines and the ubiquitin inhibitor lactacystin modifies.

Slides:



Advertisements
Similar presentations
Supplementary Figure 1 Lapatinib nM mM pEGFR MDA-MB231 EGFR pEGFR
Advertisements

Lyn regulates BCR-ABL and Gab2 tyrosine phosphorylation and c-Cbl protein stability in imatinib-resistant chronic myelogenous leukemia cells by Ji Wu,
TGF-β1 induces ILK activity in renal tubular epithelial cells.
ARG tyrosine kinase activity is inhibited by STI571
Small-molecule inhibitor QLT-0267 suppresses ILK activity and inhibits its downstream signaling. Small-molecule inhibitor QLT-0267 suppresses ILK activity.
PGAM5 associates with and activates ASK1.
MEL23 and MEL24 inhibit Mdm2 and p53 ubiquitination in cells.
Pirh2 promotes p73 ubiquitination in vivo.
Combined inhibition of MAP kinase and KIT signaling destabilizes ETV1 protein and results in enhanced growth suppression of human GIST cells. Combined.
Expression and regulation of MD-2s.
AKT dependence of ovarian cancer cell lines.
FAS1 domain protein inhibits association of αvβ3 integrin with VEGFR-2 and attenuates VEGF165-induced VEGFR-2 phosphorylation. FAS1 domain protein inhibits.
FIP200 maintains microRNA1198-5p expression via Ago2 in naïve T cells.
NM-3 induces p21 levels and down-regulation of Cdk2 activity.
Involvement of PI3K activation in TCR/CD3-dependent HIF-1α protein expression. Involvement of PI3K activation in TCR/CD3-dependent HIF-1α protein expression.
p38 MAPK activation is required for phosphorylation of Akt at Ser473.
Role of HER2 in mediating acquired resistance to EGFR inhibition.
Mechanism of Smad1/5 activation by rapamycin.
pY-Tie2 (IP with anti-Tie2) Tie2 P-RET RET P-KIT KIT GAPDH P-AXL AXL
Tyrosine phosphorylations of both DAB1 and ABL are essential for invasion of colorectal cancer cells. Tyrosine phosphorylations of both DAB1 and ABL are.
Thiocolchicoside inhibits TNF-dependent IκBα phosphorylation, IκBα degradation, p65 phosphorylation, and p65 nuclear translocation. Thiocolchicoside inhibits.
Lapatinib reduces IGF-I signaling in trastuzumab-resistant cells.
P38 activation mediates chronic insulin-induced IRS1 and IRS2 degradation and is involved in myocardial insulin resistance in vitro. p38 activation mediates.
Expression of cGMP signaling components in polyps.
The p53 pathway is involved in the inhibition of cell proliferation observed in 15-LOX-1-overexpressing cells. The p53 pathway is involved in the inhibition.
eNOS regulated IR-induced NO generation and EGFR signal activation.
The dynamics of Akt activation in cultured human keratinocytes.
BCR–ABL kinase activity rewires GM-CSFR signaling and confers oncogene addiction in TF1 cells. BCR–ABL kinase activity rewires GM-CSFR signaling and confers.
PKM2 is tyrosine phosphorylated and inhibited by FGFR1 in cancer cells with oncogenic or overexpressed FGFR1. PKM2 is tyrosine phosphorylated and inhibited.
The effects of the FASN blocker C75 on cell growth and survival (A, E, and F), on expression/phosphorylation of PI3K and MAPK signaling proteins and on.
co-IP of LEDGF/p75 and MeCP2.
Silencing hOGG1 triggers caspase-3 and caspase-7 activation in response to H2O2 in GM00637 cells. Silencing hOGG1 triggers caspase-3 and caspase-7 activation.
Identification of NSC as a FADD-kinase inhibitor.
Protein expression profile in a dasatinib-resistant cell line.
DNA damage signaling regulates mutant p53 ubiquitination.
ALDH1A3 is mainly responsible for the ALDH activity in two human cholangiocarcinoma lines. ALDH1A3 is mainly responsible for the ALDH activity in two human.
Down-regulation of the erbB-2 receptor by trastuzumab decreases Akt kinase activation but not MAPK activation. Down-regulation of the erbB-2 receptor by.
Effects of visfatin on the cell proliferation and phosphorylation of ERK, Akt, and GSK-3β proteins in HCC cells. Effects of visfatin on the cell proliferation.
Discovery of Gö6976-related potent reversible EGFR T790M inhibitors.
A. A. Honokiol inhibits TNF-induced NF-κB activation, IκBα phosphorylation, and IκBα degradation. Honokiol inhibits TNF-induced activation of NF-κB. H1299.
Gain-of-function conferred by RNF31 SNPs
Role of MAPKs on DPP-23-induced autophagy and apoptosis.
CDCP1 links Ras and SFK signaling and regulates anoikis resistance, cell migration, and invasion in NSCLC cells. CDCP1 links Ras and SFK signaling and.
TET2 interacts with KLF1 transcription factor.
PTB-independent ShcA pools employ distinct domains to hyperactivate mTOR and Src signaling. PTB-independent ShcA pools employ distinct domains to hyperactivate.
PKCζ is tyrosine phosphorylated by EGF and contributes to EGF-induced activation of ERK in Mef cells. PKCζ is tyrosine phosphorylated by EGF and contributes.
Treatment with DZNep depletes expression of PRC2 proteins EZH2, SUZ12, and associated 3MeK27H3 levels in cultured human MCL cells. Treatment with DZNep.
ABT-100 inhibits PI3K activity and p85 tyrosine phosphorylation.
Met is expressed in Her2-overexpressing cell lines and Her2 (+) breast tumors. Met is expressed in Her2-overexpressing cell lines and Her2 (+) breast tumors.
Activation of multiple RTKs in chondrosarcoma cells.
The combination of trastuzumab and SU11274 abrogate Akt phosphorylation. The combination of trastuzumab and SU11274 abrogate Akt phosphorylation. Serum-starved.
ODC protein expression in paired benign and cancer tissue obtained from patients with PCA. The protein expression was measured by immunoblot analysis in.
Immunoblot analysis in PANC1 and MSTO-211H cells.
The effects of AZD1775 and olaparib on DNA damage response signaling.
AKT activation in HCC2429 is SRC- but not Notch-dependent.
Effect of bevacizumab on the proliferation of A2780 cells.
Induction of PARP cleavage (A) and activation of caspases (B) after treatment with a combination of TRAIL and cisplatin. Induction of PARP cleavage (A)
Effect of MIF siRNA on the production of MMP-13 induced by LPA
Posttranslational phosphorylation of p53 by platinum drugs in ovarian tumor cells. Posttranslational phosphorylation of p53 by platinum drugs in ovarian.
RA-9 induces G2–M cell-cycle arrest and caspase-mediated apoptosis in ovarian cancer cells. RA-9 induces G2–M cell-cycle arrest and caspase-mediated apoptosis.
Blockade of cell cycle at G2-M phase in Bel-7402 cells treated with IG-105. Blockade of cell cycle at G2-M phase in Bel-7402 cells treated with IG-105.
LUBAC is essential for NF-κB activity in ABC DLBCL
Mechanism by which flavopiridol induces cell cycle arrest and apoptosis in rhabdoid tumor cells. Mechanism by which flavopiridol induces cell cycle arrest.
MTOR kinase inhibition–induced reactivation of AKT substrates is HER2 and PI3K dependent. mTOR kinase inhibition–induced reactivation of AKT substrates.
BME treatment increases cytotoxic activity of NK3
Identification of the molecular regulators of FLP formation.
Depletion of murine Dnmt proteins after 5-Aza-CdR treatment.
Inhibition of HDACs disrupts DNMT1 association with Hsp90.
Inhibition of BCR-mediated signaling by ARQ 531.
TCTP enhances the protein stability of Pim-3 by blocking the ubiquitin–proteasome degradation of Pim-3. TCTP enhances the protein stability of Pim-3 by.
Presentation transcript:

BCR/ABL expression, tyrosine phosphorylation, and signaling in dasatinib- and imatinib-resistant cell lines and the ubiquitin inhibitor lactacystin modifies the BCR/ABL protein. BCR/ABL expression, tyrosine phosphorylation, and signaling in dasatinib- and imatinib-resistant cell lines and the ubiquitin inhibitor lactacystin modifies the BCR/ABL protein. Protein tyrosine phosphorylation and abl (A), phosphorylation of Lyn, Lck, p21WAF, Akt, mitogen-activated protein kinase, actin (D) levels were analyzed by an immunoblotting protein (30 μg) from cell lysates. B, K562 BMS-R cells were treated with or without lactacystin for 24 h. Cell lysates were immunoprecipitated (IP) with anti-Abl Ab and immunoblotted (WB) with the ubiquitin or Abl Abs. C, K562 BMS-R cells were treated lactacystin for indicated hours. Cell viability was evaluated through the trypan blue exclusion and cell lysates were immunoblotted with Abl or actin Abs. Seiichi Okabe et al. Clin Cancer Res 2008;14:6181-6186 ©2008 by American Association for Cancer Research