Imatinib mesylate inhibits collagen synthesis in human breast stromal fibroblasts. Imatinib mesylate inhibits collagen synthesis in human breast stromal.

Slides:



Advertisements
Similar presentations
IL-18 Downregulates Collagen Production in Human Dermal Fibroblasts via the ERK Pathway  Hee Jung Kim, Seok Bean Song, Jung Min Choi, Kyung Moon Kim,
Advertisements

The Fumagillin Analogue TNP-470 Inhibits DNA Synthesis of Vascular Smooth Muscle Cells Stimulated by Platelet-Derived Growth Factor and Insulin-like Growth.
Inhibition of CR HCT-116 (A and B) or CR HT-29 cells (B) xenografts in EPA and/or FuOx-treated SCID mice. Inhibition of CR HCT-116 (A and B) or CR HT-29.
KG-501 suppresses NSCLC/IL-1β CM–induced migration of HUVECs by regulating IL-1β–induced CXC chemokine gene expression in NSCLC cells. KG-501 suppresses.
IL-1β stimulates CXCL5 and CXCL8 gene expression and protein secretion in A549 cells in a time- and dose-dependent manner. IL-1β stimulates CXCL5 and CXCL8.
سرطان الثدي Breast Cancer
Cyclic tensile stress of human annulus fibrosus cells induces MAPK activation: involvement in proinflammatory gene expression  H. Pratsinis, A. Papadopoulou,
Proline supplementation during P5CS protein knockdown suppressed GCN2 activation. Proline supplementation during P5CS protein knockdown suppressed GCN2.
Pioglitazone inhibits aromatase expression in human preadipocytes.
Collagen-dependent phosphorylation of eIF4E in PDAC cells.
The selective PI3K inhibitor A66 suppresses PIP3 accumulation, AKT phosphorylation at Thr308, and YAP/TAZ–regulated gene expression in PDAC cells. The.
p38 MAPK activation is required for phosphorylation of Akt at Ser473.
Overexpression of HGF decreases MET protein levels.
Mechanism of piperlongumine induced Sp downregulation.
Knocking down Wnt3 increases the cells' response to trastuzumab and reduces cells' invasiveness. Knocking down Wnt3 increases the cells' response to trastuzumab.
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.
Synergistic interaction of Activin and canonical Wnt/β-catenin signaling pathways in the anterior PS/endoderm specification during hES cell differentiation.
LSD1, a histone demethylase, is required for the assembly of the Notch repressor complex. LSD1, a histone demethylase, is required for the assembly of.
The lack of effect of denatonium to stimulate insulin release in the absence of extracellular Ca2+ or in the presence of 10 μmol/l nitrendipine. The lack.
BEZ235 induces MAPK signaling in a FOXO3A-dependent manner.
Adipocytes sequester daunorubicin (DNR).
Curcumin-generated ROS activates Chk1 and Chk2 kinases.
GA blocks HIF activity and reduces HIF target expression.
VHL-, oxygen-, and proteasome-dependent regulation of AUF1 expression in RCC and 293T cells. VHL-, oxygen-, and proteasome-dependent regulation of AUF1.
Gramicidin A (GA) decreases HIF protein expression in RCC cells.
CDCP1 is required for invadopodia formation and ECM degradation by human breast cancer cells. CDCP1 is required for invadopodia formation and ECM degradation.
Stimulatory effect induced by docetaxel, gefitinib, and cyclopamine on MMP (A) and (B) cytosolic cytochrome c level. Stimulatory effect induced by docetaxel,
The role of p53 in H2O2-mediated cell death of hOGG1-deficient H1299 lung carcinoma p53 null cells. The role of p53 in H2O2-mediated cell death of hOGG1-deficient.
A. A. XPCKD and KIN17KD HeLa cells grow poorly 2 weeks after transfection. Forty-eight hours after transfection, cells were plated at the same density.
DNA damage signaling regulates mutant p53 ubiquitination.
Imatinib mesylate inhibits PDGF-mediated ERK and Akt activation.
TGF-β1 modulates extracellular matrix–mediated MT1-MMP expression.
PELP1 regulates the expression and activities of MMPs in ER-negative cells. PELP1 regulates the expression and activities of MMPs in ER-negative cells.
Mitotic catastrophe symptoms caused by curcumin are followed by apoptosis. Mitotic catastrophe symptoms caused by curcumin are followed by apoptosis. A.
Expression of versican in mammary tumor stem/progenitor cells.
Matriptase-2 inhibited breast tumor development in vivo.
Effect of G9a on the expression of GSH synthesis enzymes.
SAF-1 expression in clinical breast cancer tissues.
Curcumin suppresses the expression of antiapoptotic proteins in multiple myeloma cells. Curcumin suppresses the expression of antiapoptotic proteins in.
Fyn cooperates with Src to increase the tumorigenic potential of PTB-independent ShcA signaling complexes. Fyn cooperates with Src to increase the tumorigenic.
Biological effects of BRAF silencing: growth curves of A375 (A) and ARO (B) cell lines in the absence or presence of doxycycline. Biological effects of.
Effect of IL24 on phosphorylation of eIF2α and proliferation in cancer cells. Effect of IL24 on phosphorylation of eIF2α and proliferation in cancer cells.
The AKT–mTOR pathway controls PD-L1 protein expression.
Role of MAPKs on DPP-23-induced autophagy and apoptosis.
Drug interaction signatures for GIST and benign osteoma cell lines representing all combinatorial data compiled in a 9 × 9 drug matrix. Drug interaction.
A, P causes G2-M arrest with apoptosis in asynchronous population of PC-3 when exposed to 1.5 and 5 μmol/L P for various time points. A, P
Nested RT-PCR of Mammaglobin and CK19 mRNA in plasma and circulating cells of controls (C) and patients (T) with breast cancer. Nested RT-PCR of Mammaglobin.
ABT-100 inhibits PI3K activity and p85 tyrosine phosphorylation.
Changes in signal transduction pathway induced by gefitinib.
The combination of trastuzumab and SU11274 abrogate Akt phosphorylation. The combination of trastuzumab and SU11274 abrogate Akt phosphorylation. Serum-starved.
Osteoactivin expression is required for the invasive phenotype of in vivo selected bone metastatic 4T1 breast cancer cells. Osteoactivin expression is.
Identification of compounds that enhance TMZ cytotoxicity in melanoma cells by screening the Spectrum Collection library. Identification of compounds that.
Pdcd4 expression inhibits AP-1 transactivation.
Induction of apoptosis by statins in NB4 cells and NB4 variant cell lines. Induction of apoptosis by statins in NB4 cells and NB4 variant cell lines. A,
Enhanced expression of Cap43 gene by nickel in breast cancer cell lines. Enhanced expression of Cap43 gene by nickel in breast cancer cell lines. Expression.
Lapatinib cooperates with PLX4032 to inhibit BRAF-mutant thyroid cancer cell growth. Lapatinib cooperates with PLX4032 to inhibit BRAF-mutant thyroid cancer.
Functional SLC6A3 in ccRCC cell lines KMRC3 and SNU-349, but not in conventional cell lines. Functional SLC6A3 in ccRCC cell lines KMRC3 and SNU-349, but.
A, DMA and Ral significantly inhibit estrone methyl ether (MeOE1) formation in MCF-10A cells. A, DMA and Ral significantly inhibit estrone methyl ether.
AKT activation in HCC2429 is SRC- but not Notch-dependent.
Apoptotic cell debris induces AXL-dependent cell migration.
ER stress mediates postslippage AMPK activation.
Effect of MIF siRNA on the production of MMP-13 induced by LPA
Establishment of HeLa/rtTAA/TRE-N1-IC cell line.
ABT-888 sensitizes multiple ovarian cancer cell lines but not normal cells to FdUrd. ABT-888 sensitizes multiple ovarian cancer cell lines but not normal.
IAP antagonists enhance osteoclastogenesis in vitro.
Elevated STAT3 phosphorylation and RANTES levels in tamoxifen-treated breast cancer cells. Elevated STAT3 phosphorylation and RANTES levels in tamoxifen-treated.
Effect of SFN on the total activity and protein expression of HDACs in JB6 P+ cells. Effect of SFN on the total activity and protein expression of HDACs.
I3C reduces the level of Cdc25A protein in breast cancer cells.
Loss of NQO1 expression inhibits invasion of NSCLC
Inhibition of stromal cell–induced survival of primary B-CLL cells by cyclopamine in vitro. Inhibition of stromal cell–induced survival of primary B-CLL.
Presentation transcript:

Imatinib mesylate inhibits collagen synthesis in human breast stromal fibroblasts. Imatinib mesylate inhibits collagen synthesis in human breast stromal fibroblasts. A. Confluent breast fibroblast cultures, arrested in DMEM containing 0.2% FCS in the presence of tritiated proline (5 μCi/mL), were treated with 10 μmol/L imatinib. Forty-eight hours later, collagen synthesis was estimated as described in Materials and Methods. Columns, average of eight separate experiments. B. Confluent breast fibroblast cultures, arrested in DMEM containing 0.2% FCS, were treated with 10 μmol/L imatinib. Cell lysates were collected at 6 and 24 h later in the absence (C6 and C24, respectively) or presence (I6 and I24, respectively) of imatinib, and RNA was isolated and subjected to real-time PCR, as described in Materials and Methods. Columns, average of three separate experiments. *, P < 0.05; **, P < 0.01. Vassiliki Gioni et al. Mol Cancer Res 2008;6:706-714 ©2008 by American Association for Cancer Research