1,550 research outputs found
The Dynamics of Sustained Reentry in a Loop Model with Discrete Gap Junction Resistance
Dynamics of reentry are studied in a one dimensional loop of model cardiac
cells with discrete intercellular gap junction resistance (). Each cell is
represented by a continuous cable with ionic current given by a modified
Beeler-Reuter formulation. For below a limiting value, propagation is found
to change from period-1 to quasi-periodic () at a critical loop length
() that decreases with . Quasi-periodic reentry exists from
to a minimum length () that is also shortening with .
The decrease of is not a simple scaling, but the bifurcation can
still be predicted from the slope of the restitution curve giving the duration
of the action potential as a function of the diastolic interval. However, the
shape of the restitution curve changes with .Comment: 6 pages, 7 figure
Inhibition of the PI3K/AKT/mTOR pathway activates autophagy and compensatory Ras/Raf/MEK/ERK signalling in prostate cancer
The PI3K/AKT/mTOR pathway is frequently activated in advanced prostate cancer, due to loss of the tumour suppressor PTEN, and is an important axis for drug development. We have assessed the molecular and functional consequences of pathway blockade by inhibiting AKT and mTOR kinases either in combination or as individual drug treatments. In established prostate cancer cell lines, a decrease in cell viability and in phospho-biomarker expression was observed. Although apoptosis was not induced, a G1 growth arrest was observed in PTEN null LNCaP cells, but not in BPH1 or PC3 cells. In contrast, when the AKT inhibitor AZD7328 was applied to patient-derived prostate cultures that retained expression of PTEN, activation of a compensatory Ras/MEK/ERK pathway was observed. Moreover, whilst autophagy was induced following treatment with AZD7328, cell viability was less affected in the patient-derived cultures than in cell lines. Surprisingly, treatment with a combination of both AZD7328 and two separate MEK1/2 inhibitors further enhanced phosphorylation of ERK1/2 in primary prostate cultures. However, it also induced irreversible growth arrest and senescence.Ex vivo treatment of a patient-derived xenograft (PDX) of prostate cancer with a combination of AZD7328 and the mTOR inhibitor KU-0063794, significantly reduced tumour frequency upon re-engraftment of tumour cells.The results demonstrate that single agent targeting of the PI3K/AKT/mTOR pathway triggers activation of the Ras/MEK/ERK compensatory pathway in near-patient samples. Therefore, blockade of one pathway is insufficient to treat prostate cancer in man
Measurement of the Total Active 8B Solar Neutrino Flux at the Sudbury Neutrino Observatory with Enhanced Neutral Current Sensitivity
The Sudbury Neutrino Observatory (SNO) has precisely determined the total
active (nu_x) 8B solar neutrino flux without assumptions about the energy
dependence of the nu_e survival probability. The measurements were made with
dissolved NaCl in the heavy water to enhance the sensitivity and signature for
neutral-current interactions. The flux is found to be 5.21 +/- 0.27 (stat) +/-
0.38 (syst) x10^6 cm^{-2}s^{-1}, in agreement with previous measurements and
standard solar models. A global analysis of these and other solar and reactor
neutrino results yields Delta m^{2} = 7.1^{+1.2}_{-0.6}x10^{-5} ev^2 and theta
= 32.5^{+2.4}_{-2.3} degrees. Maximal mixing is rejected at the equivalent of
5.4 standard deviations.Comment: Submitted to Phys. Rev. Let
Direct Search for Charged Higgs Bosons in Decays of Top Quarks
We present a search for charged Higgs bosons in decays of pair-produced top
quarks in pbar p collisions at sqrt(s) = 1.8 TeV using 62.2 pb^-1 of data
recorded by the D0 detector at the Fermilab Tevatron collider. No evidence is
found for signal, and we exclude at 95% confidence most regions of the (M
higgs, tan beta) parameter space where the decay t->H b has a branching
fraction greater than 0.36 and B(H -> tau nu) is large.Comment: 11 pages, 4 figures, submitted to Phys. Rev. Let
Limits on Anomalous WWgamma and WWZ Couplings
Limits on the anomalous WWgamma and WWZ couplings are presented from a
simultaneous fit to the data samples of three gauge boson pair final states in
pbar-p collisions at sqrt(s)=1.8 TeV: Wgamma production with the W boson
decaying to enu or munu, W boson pair production with both of the W bosons
decaying to enu or munu, and WW or WZ production with one W boson decaying to
enu and the other W boson or the Z boson decaying to two jets. Assuming
identical WWgamma and WWZ couplings, 95 % C.L. limits on the anomalous
couplings of -0.30<Delta kappa<0.43 (lambda = 0) and -0.20<lambda<0.20 (Delta
kappa = 0) are obtained using a form factor scale Lambda = 2.0 TeV. Limits
found under other assumptions on the relationship between the WWgamma and WWZ
couplings are also presented.Comment: 13 pages, 3 figures, submitted to Physical Review
A review of uncertainties in global temperature projections over the twenty-first century
Quantification of the uncertainties in future climate projections is crucial for the implementation of climate policies. Here a review of projections of global temperature change over the twenty-first century is provided for the six illustrative emission scenarios from the Special Report on Emissions Scenarios (SRES) that assume no policy intervention, based on the latest generation of coupled general circulation models, climate models of intermediate complexity, and simple models, and uncertainty ranges and probabilistic projections from various published methods and models are assessed. Despite substantial improvements in climate models, projections for given scenarios on average have not changed much in recent years. Recent progress has, however, increased the confidence in uncertainty estimates and now allows a better separation of the uncertainties introduced by scenarios, physical feedbacks, carbon cycle, and structural uncertainty. Projection uncertainties are now constrained by observations and therefore consistent with past observed trends and patterns. Future trends in global temperature resulting from anthropogenic forcing over the next few decades are found to be comparably well constrained. Uncertainties for projections on the century time scale, when accounting for structural and feedback uncertainties, are larger than captured in single models or methods. This is due to differences in the models, the sources of uncertainty taken into account, the type of observational constraints used, and the statistical assumptions made. It is shown that as an approximation, the relative uncertainty range for projected warming in 2100 is the same for all scenarios. Inclusion of uncertainties in carbon cycle–climate feedbacks extends the upper bound of the uncertainty range by more than the lower bound
Measurement of the Boson Mass
A measurement of the mass of the boson is presented based on a sample of
5982 decays observed in collisions at
= 1.8~TeV with the D\O\ detector during the 1992--1993 run. From a
fit to the transverse mass spectrum, combined with measurements of the
boson mass, the boson mass is measured to be .Comment: 12 pages, LaTex, style Revtex, including 3 postscript figures
(submitted to PRL
Second Generation Leptoquark Search in p\bar{p} Collisions at = 1.8 TeV
We report on a search for second generation leptoquarks with the D\O\
detector at the Fermilab Tevatron collider at = 1.8 TeV.
This search is based on 12.7 pb of data. Second generation leptoquarks
are assumed to be produced in pairs and to decay into a muon and quark with
branching ratio or to neutrino and quark with branching ratio
. We obtain cross section times branching ratio limits as a function
of leptoquark mass and set a lower limit on the leptoquark mass of 111
GeV/c for and 89 GeV/c for at the 95%\
confidence level.Comment: 18 pages, FERMILAB-PUB-95/185-
Search for First Generation Scalar Leptoquark Pairs in ppbar Collisions at sqrt(s)=1.8 TeV
We have searched for first generation scalar leptoquark (LQ) pairs in the
enu+jets channel using ppbar collider data (integrated luminosity= 115 pb^-1)
collected by the DZero experiment at the Fermilab Tevatron during 1992-96. The
analysis yields no candidate events. We combine the results with those from the
ee+jets and nunu+jets channels to obtain 95% confidence level (CL) upper limits
on the LQ pair production cross section as a function of mass and of beta, the
branching fraction to a charged lepton. Comparing with the next-to-leading
order theory, we set 95% CL lower limits on the LQ mass of 225, 204, and 79
GeV/c^2 for beta=1, 1/2, and 0, respectively.Comment: 14 pages, 4 figures, submitted to Physical Review Letters Replaced to
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Anti-cancer effects and mechanism of actions of aspirin analogues in the treatment of glioma cancer
INTRODUCTION: In the past 25 years only modest advancements in glioma treatment have been made, with patient prognosis and median survival time following diagnosis only increasing from 3 to 7 months. A substantial body of clinical and preclinical evidence has suggested a role for aspirin in the treatment of cancer with multiple mechanisms of action proposed including COX 2 inhibition, down regulation of EGFR expression, and NF-κB signaling affecting Bcl-2 expression. However, with serious side effects such as stroke and gastrointestinal bleeding, aspirin analogues with improved potency and side effect profiles are being developed. METHOD: Effects on cell viability following 24 hr incubation of four aspirin derivatives (PN508, 517, 526 and 529) were compared to cisplatin, aspirin and di-aspirin in four glioma cell lines (U87 MG, SVG P12, GOS – 3, and 1321N1), using the PrestoBlue assay, establishing IC50 and examining the time course of drug effects. RESULTS: All compounds were found to decrease cell viability in a concentration and time dependant manner. Significantly, the analogue PN517 (IC50 2mM) showed approximately a twofold increase in potency when compared to aspirin (3.7mM) and cisplatin (4.3mM) in U87 cells, with similar increased potency in SVG P12 cells. Other analogues demonstrated similar potency to aspirin and cisplatin. CONCLUSION: These results support the further development and characterization of novel NSAID derivatives for the treatment of glioma
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