... Pathways andCellDeath in Breast Cancer, Edited by Rebecca L Aft p cm ISBN 978-953-51-0145-1 Contents Preface IX Part Breast Cancer CellDeath Chapter Estrogen-Induced Apoptosis in Breast Cancer Cells: ... and prostate cancers Targeting New Pathways andCellDeath in Breast Cancer was affiliated with significant systemic side effects, such as nausea, areola pigmentation, uterine bleeding, andedema ... glutamine, cysteine, and glycine It is the most abundant intracellular small molecule thiol present in mammalian cells and it serves as a potent intracellular antioxidant protecting cells from toxins...
... hand, in non-neuronal cells, cytoplasmic retention of ERK1 ⁄ is required for death- associated protein kinase-mediated celldeath [35] Thus, ERK1 ⁄ might promote celldeath depending upon the cell ... promote celldeath As discussed above, in PC12 cells a sustained ERK1 ⁄ activation induced by NGF promotes differentiation andcell survival Thus, the decision by sustained ERK1 ⁄ to induce celldeath ... neuronal death was mediated by ERK1 ⁄ [43] Together, these data suggest that ERK1 ⁄ 2-mediated features of neuronal death may differ depending on cell type anddeath stimulus, but in several cell death...
... negative selecting ligand Note the separate location of pJNK and pERK, and Ras-GRP1 ⁄ Grb2 ⁄ SOS ⁄ Ras ⁄ Raf at the plasma membrane lead to such distinct cell fates as survival anddeath Much is known ... problem Interestingly, JNK activity and subcellular location are the same regardless of the ligand strength, ERK location and T cell selection whereas ERK activity and location change depending of ... important for determining cell fate decisions in a diverse number of organisms andcell types (reviewed in [7,8]) In thymocytes, c-JunNH2-terminal kinase (JNK) [9], p38 [10] and extracellular signal-regulated...
... result of celldeathand not due to an inhibition of cell proliferation, as determined by cell counting as well as quantification of loss of cell integrity [22] Although the ERK prodeath effect ... J & Lenormand P (2009) Total ERK1 ⁄ activity regulates cell proliferation Cell Cycle 8, 705–711 ´ Lefloch R, Pouyssegur J & Lenormand P (2008) Single and combined silencing of ERK1 and ERK2 reveals ... cells [40] and in astrocytes This increase in turn leads to an increase in ROS and to mitochondrial impairment [41] Pretreatment with a calcium chelator reduced ROS production and increased cell...
... Pathways andCellDeath in Breast Cancer, Edited by Rebecca L Aft p cm ISBN 978-953-51-0145-1 Contents Preface IX Part Breast Cancer CellDeath Chapter Estrogen-Induced Apoptosis in Breast Cancer Cells: ... and prostate cancers Targeting New Pathways andCellDeath in Breast Cancer was affiliated with significant systemic side effects, such as nausea, areola pigmentation, uterine bleeding, andedema ... glutamine, cysteine, and glycine It is the most abundant intracellular small molecule thiol present in mammalian cells and it serves as a potent intracellular antioxidant protecting cells from toxins...
... precursors stimulate celldeath in plants and animals The mechanism by which sphingolipids promote celldeath is unknown and may be indirect via their impact on the functioning of celldeath effectors ... programmed celldeath during the plant innate immune response Cell 2005, 121(4):567-577 Gilchrist DG: Mycotoxins reveal connections between plants and animals in apoptosis and ceramide signaling CellDeath ... causes celldeath in both plants and animals and appears to target the same step in ceramide biosynthesis as fumonisin B1 [8,9] In addition, the acd5 and acd11 mutants, which exhibit constitutive cell...
... autophagy andcelldeath in TSC2-/- cells 93 Figure 3.12 Nutrients supplementation further sensitizes TSC2-/cells to celldeath 94 Figure 3.13 The involvement of TSC in the regulation of autophagy and ... “programmed celldeath (PCD) is the most common term used in the study of celldeath (Vaux, 2002), and was first coined by Lockshin and Williams (1965) to study developmental celldeath in insects ... immunity, inflammation and tumourigenesis (Fuchs and Steller, 2011; Takeda et al., 2007) There are three types of cell death, which are apoptosis, necrosis and autophagic celldeath (Clarke, 1990),...
... with death domain (FADD) induced caspaseindependent celldeath No DNA fragmentation was observed and dying cells showed neither condensation nor fragmentation of cells and nuclei, but the cells and ... autophagy and caspase-dependent celldeath pathways Camougrand and coworkers [133] showed in yeast that the expression of Bax induces celldeath with characteristics of both apoptosis and autophagy, ... inhibitors [94] Neuregulin (NRG; a ligand of ErbB), also activates ErbB-2/ErbB-3 heterodimers and induces celldeath of prostate cancer LNCaP cells Neuregulin-induced celldeath was not inhibited by broadspectrum...
... loss of ERK1 ⁄ and ⁄ or PKB signalling and, as a consequence, promote increased expression of BIM and BIM-dependent celldeath in tumour cells Here we review recent advances in understanding BIM ... promote celldeath [73] and there is now good evidence to indicate that (a) BIM is important in Myc-induced celldeathand (b) that this may be an arbiter of tumour progression B-lymphoid cells ... Furthermore, NSCLC cell lines expressing the secondary T790M mutant EGFR were resistant to gefitinib and erlotinib and failed to upregulate BIM; in such cases, BIM induction andcelldeath were re-imposed...
... of EDS1 ⁄ PAD4 ⁄ SAG101 and BON1 ⁄ BAP1 + in celldeathand plant pathogen resistance Whereas EDS1, PAD4 and SAG101 are positive regulators of cell death, BON1, BAP1 and BAP2 operate as negative ... C Reinbothe et al JA andcelldeath Fig Central role of JA in celldeath regulation in plants Animals respond to many external factors with a plethora of different celldeath pathways of which ... and JA-mediated celldeath in irradiated flu plants is likely to be a form of programmed celldeath (PCD) [29] In many aspects it resembles PCD and apoptosis in animals [95–99] This includes cell...
... proteins Bax and Bak, caspase activation andcelldeath [2,3] In addition, the physiological platelet agonist thrombin also induces Bid, Bax and Bak translocation to the mitochondria and endogenous ... analysis showing the intracellular distribution of CD47 molecule in zymosan-treated cells (central panel) and OPZ-treated cells (right panel) (E) DIC (Nomarski) micrographs showing cell aggregates in ... annexin V and 0.05% trypan blue for 10 at room temperature, and analyzed by fluorescenceactivated cell sorting (FACS) in the FL1 and FL3 channels to determine the percentage of dead cells The...
... L(1–2); loop between sheets b-1 and b-2; L(2–3), loop between sheets b-2 and b-3 Asp57, Glu197 and Glu201 are residues involved in chitosan substrate binding at )2, )1 and +2 subsite, respectively ... cell density We thus estimated the number of falsepositive colonies recovered on this medium by mixing various proportions of the V148T chitosanase-expressing cells and chitosanase-negative cells ... CsnN174 (GH46) C-end of a-1 helix b-1 strand E36 (alternative general base) D40b (general base) T45 (water positioning) Loop between b-1 and b2 strands b-2 strand Hen egg-white lysozyme (GH22) T japonica...
... cancer cells, by either inducing celldeath or preventing further proliferation; b) to explore the molecular mechanism of celldeath by Ruta + Ca3(PO4)2 treatment of brain cancer cells in vitro; and ... 37˚C, and the cells were harvested after 72 h following the standard air-drying techniques Cell harvesting and cytological preparations All drugtreated and control MGR1 cell cultures, B-lymphoid and ... 3(PO4) could induce celldeath in human (HL-60 and MGR1 glioma) and murine (K 1735 clone X-21) cancer cells and provide chemo-protection for normal human PBLs and B-lymphoid cells, by inducing...
... shown to participate in celldeath in response to various cytokine signals, including IFN-cinduced celldeath [2], TNF-a and FAS-induced celldeath [48], and TGF-b-induced celldeath [10] There are ... source maintaining cell survival, it has been proposed that autophagy can contribute to celldeath in a process DAPK and signal transduction termed autophagic (type II) celldeath Disturbance ... control andcell metabolism [15] In mammalian cells, two structurally and functionally distinct mTOR-containing complexes have been identified, mTORC1 and mTORC2 [15] mTORC1 directly regulates cell...
... apoptotic celldeath resemble those of ‘healthy’ cells Growth and retraction FEBS Journal 277 (2010) 58–65 ª 2009 The Authors Journal compilation ª 2009 FEBS 61 Blebbing in programmed celldeath ... not been examined in blebs of cells undergoing celldeath Although the proteins involved in the execution of blebbing appear similar in apoptotic and autophagic cell death, the upstream signals ... occurs as part of the normal cell growth process, and although blebbing is one of the characteristic hallmarks of programmed cell death, its exact contribution to celldeath remains unclear It has...
... ANT1 and ANT2-silencing on ADF cells (A) Cell growth curves analyzed by crystal violet assay in nontransfected ADF cells, and in Scramble- and ANT1 siRNA and ANT2 siRNA ADF-transfected cells ... BA, ATR and ANT1 siRNA on cell viability and glucose consumption (A,B) Cell growth curves analyzed by crystal violet assay in BA and vehicle-treated (A) and in ATR and vehicle-treated (B) cells ... U-87-MG cells, 24 and 48 h after transfection (C) Cell growth curves analyzed by crystal violet assay in nontransfected U87-MG cells, and in Scramble- and ANT1 siRNA U87-MG-transfected cells Each...
... going and now I I think we can more with it and look for more specialized areas What we cannot quite understand ZONAL CENTRIFUGATION OF BRAIN SUBCELLULAR FRACTIONS 11 in this methodology, and I ... enzymes from pigeon and guinea-pig brains the enzymes from rat and cat brains were distributed over a rather broader pH range The enzymes from rat brain (Malthe-Ssrenssen and Fonnum, 1971a) were ... endings This fits in with observations of Lenard and Singer (1968) on the red cell membrane and those of Condrea and Rosenberg (1968) and Rosenberg and Condrea (1968) on the squid giant axon From...
... augments H pyloriinduced celldeathand DNA fragmentation in gastric epithelial cells To investigate the relations of PAR-2 expression, cell death, and DNA fragmentation, cells were transfected ... apoptotic cell death, the expression of PAR-2, and the activation of MAPK in H pylori-infected gastric epithelial cells, cell viability and DNA fragmentation were determined in the cells transfected ... the cells without transfection and cultured in the presence of H pylori Figure Inhibition of PAR-2 expression augments H pyloriinduced celldeathand DNA fragmentation in AGS cells (A) AGS cells...
... avidity T cells, with excellent memory recall features, restricted migration and refractory to negative regulatory mechanisms => Expanding high avidity T cells, with broad functionality and widespread ... recombinant proteins, peptides, cells, or cell lysates), achieves alternating production of ‘central-memory’ low PD-1 cells and highly differentiated effector T cells, respectively Figure 4B is ... subsides, a minor subset of T cells down-regulate PD-1 and become memory cells, while the larger pool of effector cells extinguishes through a range of mechanisms leading to cellular apoptosis Conversely,...