She joined the Polleux lab in 2014 and studies the role of the AMPK - ULK
kinase pathway in Alzheimer's Disease.
Role of the p38 Mitogen - Activated Protein
Kinase Pathway in the Generation of Arsenic Trioxide — Dependent Cellular Responses
Not exact matches
In contrast, HPV - inactive tumors often have mutations in the PIK3CA / PTEN / AKT pathway, indicating that AKT kinase inhibitors may be effective treatment options for these patients.&raqu
In contrast, HPV - inactive tumors often have mutations
in the PIK3CA / PTEN / AKT pathway, indicating that AKT kinase inhibitors may be effective treatment options for these patients.&raqu
in the PIK3CA / PTEN / AKT
pathway, indicating that AKT
kinase inhibitors may be effective treatment options for these patients.»
The authors also found that a novel small molecule inhibitor of the salvage
pathway enzyme deoxycytidine
kinase blocked leukemia growth
in mice
in combination with thymidine (to inhibit the de novo
pathway).
Researchers from the «Angiogenesis signaling
pathways» research group of the Institute of Biomedical Investigation of Bellvitge (IDIBELL), led by Dr. Mariona Graupera, have unveiled the potential therapeutic benefit of a selective inhibitior of the PI3 -
kinase (PI3K) protein
in pancreatic neuroendocrine tumors (PanNETs).
In his research, Juha Piltti has focused on a small molecule, which causes Rho - kinase inhibition and regulation of specific down - stream protein pathways involved in many physiological processe
In his research, Juha Piltti has focused on a small molecule, which causes Rho -
kinase inhibition and regulation of specific down - stream protein
pathways involved
in many physiological processe
in many physiological processes.
In this pathway, dopamine - and an adenosine 3 ′, 5 ′ - monophosphate (cAMP)-- regulated phospho - protein of 32 kilodaltons (DARPP - 32) is phosphorylated or dephosphorylated at three sites, in a pattern predicted to cause a synergistic inhibition of protein phosphatase — 1 and concomitant regulation of its downstream effector proteins glycogen synthesis kinase — 3 (GSK - 3), cAMP response element — binding protein (CREB), and c - Fo
In this
pathway, dopamine - and an adenosine 3 ′, 5 ′ - monophosphate (cAMP)-- regulated phospho - protein of 32 kilodaltons (DARPP - 32) is phosphorylated or dephosphorylated at three sites,
in a pattern predicted to cause a synergistic inhibition of protein phosphatase — 1 and concomitant regulation of its downstream effector proteins glycogen synthesis kinase — 3 (GSK - 3), cAMP response element — binding protein (CREB), and c - Fo
in a pattern predicted to cause a synergistic inhibition of protein phosphatase — 1 and concomitant regulation of its downstream effector proteins glycogen synthesis
kinase — 3 (GSK - 3), cAMP response element — binding protein (CREB), and c - Fos.
Half of all melanomas harbor an activating mutation
in the BRAF gene that turns on the cancer signaling
pathway in cells known as the MAP
kinase pathway.
Researchers found that genetically disrupting this
pathway, or using the FDA - approved Src
kinase inhibitor dasatinib, increases PUMA levels and decreases tumor progression and metastasis
in mice by up to fivefold.
Several years ago, researchers found that 80 percent of patients with uveal melanoma had mutations to GNAQ or GNA11, genes that activate signals
in the mitogen - activated protein
kinase (MAPK)
pathway.
Dr. Yaffe's research focuses on the biology of the complex signaling
pathways that cells use to respond to DNA damage and inflammation, particularly the role of protein
kinases and modular binding domains
in tumor development and anti-cancer therapeutics.
One option is an MEK inhibitor, which inhibits the mitogen - activated protein
kinase enzymes used to therapeutically affect the MAPK
pathway that is often overactive
in cancers.
Janus
kinases carry out important intracellular functions
in many organs — for instance, activating key signal
pathways in the systems which form new blood cells.
Astonishingly, sphingosine -1-phosphate is only released
in the macrophages if — alongside with the binding of dimer - GR to the DNA — a pro-inflammatory signalling
pathway is stimulated involving protein
kinases p38 and MSK1.
«For example, restoring the lost enzymes
in the two metabolic
pathways might slow tumor progression and reduce aggressiveness by inactivating oncogenic
kinases and activating immune responses,» says Chakravarti, who holds the Max Morehouse Chair
in Cancer Research.
«We started at the mTORC1
kinase and are building the
pathway up piece by piece to identify who is talking to whom
in the
pathway and to understand how each of those proteins is relaying information about the availability of nutrients
in the cell.»
Effect of Saturated Stearic Acid on MAP
Kinase and ER Stress Signaling
Pathways during Apoptosis Induction
in Human Pancreatic ß - Cells Is Inhibited by Unsaturated Oleic Acid.
Wang, H, Gai, Q, Yang, X, Li, Z, Linders, B, Santoro, S, Zutter, M. Role of the a1 and a2 integrin cytoplasmic domains
in cell morphology, motility and responsiveness to stimulation by the protein
kinase C
pathway.
We are focusing on a few key molecular
pathways including; 1) Polycomb - mediated epigenetic gene silencing
in the tumor initiation, maintenance, and invasion, 2) c - Met (receptor tyrosine
kinase) signal transduction
pathways in stemness and migration of these tumor cells, 3) Novel mitogenic signaling
pathways that are specific to GSCs, and 4) Identification of radio - and chemo - sensitizing
pathway to maximize therapeutic efficacy.
PACAP regulates immediate catecholamine release from adrenal chromaffin cells
in an activity - dependent manner through a protein
kinase C - dependent
pathway.
Apolipoprotein (a), through Its Strong Lysine - binding Site
in KIV10, Mediates Increased Endothelial Cell Contraction and Permeability via a Rho / Rho
Kinase / MYPT1 - dependent
Pathway.
In the last decade the identification of genetic drivers of melanoma cell which regulate proliferation and survival - such as BRAF and other activators of the MAP - kinase pathway - along with the recent development of immunotherapy has taken away in many cases the invasive treatment of melanoma as an optio
In the last decade the identification of genetic drivers of melanoma cell which regulate proliferation and survival - such as BRAF and other activators of the MAP -
kinase pathway - along with the recent development of immunotherapy has taken away
in many cases the invasive treatment of melanoma as an optio
in many cases the invasive treatment of melanoma as an option.
Tobias Heckel (Hoflack, TUD)-- «Revealing Src tyrosine
kinase - dependent signaling
pathways in osteoclasts: Implications on actin organization and cell polarity» (2008)
Synapses are regulated by the cytoplasmic tyrosine
kinase Fer
in a
pathway mediated by p120catenin, Fer, SHP - 2, and β - catenin.
It is known that one of the
pathways involved
in cutaneous cancer is mediated through CDKN2A which is a gene associated with melanoma dysregulation through its pro-oncogenic products p16INK4a (Cyclin - Dependent
Kinase Inhibitor P16) and p14ARF (P14 alternate open reading frame)[28].
Regulation of heme oxygenase - 1 expression by demethoxy curcuminoids through Nrf2 by a PI3 -
kinase / Akt - mediated
pathway in mouse β - cells.
In this new paper, the researchers reveal more about that mechanism, showing that without the protective ability of BRCA1, breaks in the DNA strands go unfixed, prompting the molecule ATM kinase to activate a cellular «suicide» pathway involving a protein called p5
In this new paper, the researchers reveal more about that mechanism, showing that without the protective ability of BRCA1, breaks
in the DNA strands go unfixed, prompting the molecule ATM kinase to activate a cellular «suicide» pathway involving a protein called p5
in the DNA strands go unfixed, prompting the molecule ATM
kinase to activate a cellular «suicide»
pathway involving a protein called p53.
[48] Mutations
in GNAQ or GNA11 occur
in the majority of uveal melanomas and drive oncogenesis via activation of the phospholipase C / protein
kinase C (PKC), Rho / Rac, and Yes - associated protein
pathways.
These receptors have been used
in bacterial biosensors, where re-designed PBPs were linked to gene expression through a histidine
kinase signaling
pathway [5].
Activation of Mammalian Target of Rapamycin Signaling
Pathway Contributes to Tumor Cell Survival
in Anaplastic Lymphoma
Kinase — Positive Anaplastic Large Cell Lymphoma
One of the relatively new findings is the recurrence of mutations
in MAP3K1, a serine - threonine
kinase that activates the ERK and JNK
kinase pathways.
The basal and B - RAF - stimulated
kinase activities of a third variant are unaltered but its activation by RAS is significantly reduced, suggesting that it may act
in a dominant - negative manner to modulate
pathway signaling.
Pathways involved
in inflammation, glycan metabolism, cancer, Wnt signaling, and mitogen - activated protein
kinase signaling were among those significantly enriched (Fig. 2J and Supplementary Table 13).
Title: A genome - wide RNAi screen reveals MAP
kinase phosphatases as key ERK
pathway regulators during embryonic stem cell differentiation (
IN PRESS, Oct 2012) Authors: Sharrocks A, Yang S - H, Kalkan T, Haslam C, Smith A Date:
IN PRESS, Oct 2012 Publication Details: PLoS Genetics
GSK3 (Glycogen Synthase
Kinase - 3) is a signaling mediator involved
in a variety of different signaling
pathways including WNT, growth factors, insulin, and Hedgehog
pathways.
Metlakunta AS, Sahu M, Sahu A. Hypothalamic phosphatidylinositol 3 -
kinase pathway of leptin signaling is impaired during the development of diet - induced obesity
in FVB / N mice.
[41] Approximately 50 % of cutaneous melanomas have an activating BRAF mutation, with an additional 10 % to 20 % having an activating mutation
in NRAS; NRAS is an upstream partner of BRAF that also activates the phosphatidylinositol 3 -
kinase (PI3K) / Akt / mammalian target of rapamycin (mTOR)
pathway.
«So a cell that rewires its metabolism early on to scarf up nutrients from the environment is more likely to do what the tyrosine
kinase pathway sets
in motion; it's more likely to have all the things it needs to become a tumor.»
Mairet - Coello G., Courchet J., Pierault S., Courchet, V., Maximov A., Polleux F. (2013) The CAMKK2 - AMPK
kinase pathway mediates the synaptotoxic effects of Aβ oligomers
in vivo through Tau phosphorylation.
In the cytoplasm, lethal toxin is a zinc metalloprotease that cleaves a number of identified proteins, including members of mitogen - activated protein
kinase (MAPK) signaling
pathways [33] and the inflammasome - activating sensor NLRP1B [34].
In addition to inhibiting STAT5 signaling, we found that depletion of ABL kinases decreased the expression of the Hippo pathway mediator TAZ and downstream target genes in triple - negative and HER2 + breast cancer cell
In addition to inhibiting STAT5 signaling, we found that depletion of ABL
kinases decreased the expression of the Hippo
pathway mediator TAZ and downstream target genes
in triple - negative and HER2 + breast cancer cell
in triple - negative and HER2 + breast cancer cells.
Interestingly, PDGF - BB overexpression by modified hDPSCs enhanced the recruitment of hDPSCs both
in vitro and
in vivo via the activation of the phosphatidylinositol 3
kinase (PI3K) / Akt signaling
pathway and,
in combination with secreted vascular endothelial growth factor (VEGF), enhanced
in vitro angiogenesis.
To evaluate whether the TAZ and STAT5
pathways promote breast cancer bone metastasis downstream of the ABL
kinases, we expressed the constitutively active mutants TAZ S89A and STAT5 *
in ABL1 / ABL2 knockdown cells.
ABL
kinases regulate the expression of genes
in the JAK / STAT and Hippo
pathway signatures
in metastatic breast cancer cells.
This is a very important lipid, that actually is involved
in signaling, to many other
kinases, and the key
kinase that through this
pathway gets activated is Akt; and Akt is a very important
kinase that regulates many other factors.
We showed that inactivation of the ABL
kinases in breast cancer cells resulted
in decreased expression of genes
in the JAK / STAT and cytokine / cytokine receptor
pathway signatures, which may be due to decreased STAT5A mRNA expression and reduced STAT5 phosphorylation
in ABL1 / ABL2 - depleted breast cancer cells.
The allosteric inhibitors specific for ABL
kinases (which are currently
in clinical trials) provide a potentially useful tool for selectively targeting ABL
kinases in metastatic breast cancer types with an increase
in the ABL
pathway signature (58).
Here, we uncovered a role for the ABL
kinases in promoting breast cancer bone metastasis through the regulation of distinct
pathways required for tumor colonization and survival
in the bone microenvironment.
MEK1 / 2 and MKK3 / 6 are MAPK
kinases upstream of several MAPK
pathways, including ERK1 / 2 and p38, respectively, and have well described roles
in many immune cells [48], but this has not been studied
in IL -23-stimulated ILC3s.
Further, inactivation of the ABL
kinases resulted
in decreased expression of the genes
in the Hippo, Janus
kinase (JAK) / STAT, and cytokine / cytokine receptor
pathway signatures (Fig. 6B).