39 research outputs found
In vitro evidence for senescent multinucleated melanocytes as a source for tumor-initiating cells
Oncogenic signaling in melanocytes results in oncogene-induced senescence (OIS), a stable cell-cycle arrest frequently characterized by a bi- or multinuclear phenotype that is considered as a barrier to cancer progression. However, the long-sustained conviction that senescence is a truly irreversible process has recently been challenged. Still, it is not known whether cells driven into OIS can progress to cancer and thereby pose a potential threat. Here, we show that prolonged expression of the melanoma oncogene N-RAS61K in pigment cells overcomes OIS by triggering the emergence of tumor-initiating mononucleated stem-like cells from senescent cells. This progeny is dedifferentiated, highly proliferative, anoikis-resistant and induces fast growing, metastatic tumors. Our data describe that differentiated cells, which are driven into senescence by an oncogene, use this senescence state as trigger for tumor transformation, giving rise to highly aggressive tumor-initiating cells. These observations provide the first experimental in vitro evidence for the evasion of OIS on the cellular level and ensuing transformation
The role of caretakers in disease dynamics
One of the key challenges in modeling the dynamics of contagion phenomena is
to understand how the structure of social interactions shapes the time course
of a disease. Complex network theory has provided significant advances in this
context. However, awareness of an epidemic in a population typically yields
behavioral changes that correspond to changes in the network structure on which
the disease evolves. This feedback mechanism has not been investigated in
depth. For example, one would intuitively expect susceptible individuals to
avoid other infecteds. However, doctors treating patients or parents tending
sick children may also increase the amount of contact made with an infecteds,
in an effort to speed up recovery but also exposing themselves to higher risks
of infection. We study the role of these caretaker links in an adaptive network
models where individuals react to a disease by increasing or decreasing the
amount of contact they make with infected individuals. We find that pure
avoidance, with only few caretaker links, is the best strategy for curtailing
an SIS disease in networks that possess a large topological variability. In
more homogeneous networks, disease prevalence is decreased for low
concentrations of caretakers whereas a high prevalence emerges if caretaker
concentration passes a well defined critical value.Comment: 8 pages, 9 figure
Inclusive eta' Production from the Upsilon(1S)
Using the CLEO II detector at CESR, we measure the eta' - gluon - gluon
form-factor in Y(1S) decays. This form-factor especially at large eta' energies
may provide an explanation of the large rate for B -> Xs eta'. Our data do not
support a large anomalous coupling at higher q^2 and thus the large eta' rate
remains a mystery, possibly requiring a non-Standard Model explanation.Comment: 14 pages postscript, also available through
http://w4.lns.cornell.edu/public/CLNS, submitted to PR
Study of the q^2-Dependence of B --> pi ell nu and B --> rho(omega)ell nu Decay and Extraction of |V_ub|
We report on determinations of |Vub| resulting from studies of the branching
fraction and q^2 distributions in exclusive semileptonic B decays that proceed
via the b->u transition. Our data set consists of the 9.7x10^6 BBbar meson
pairs collected at the Y(4S) resonance with the CLEO II detector. We measure
B(B0 -> pi- l+ nu) = (1.33 +- 0.18 +- 0.11 +- 0.01 +- 0.07)x10^{-4} and B(B0 ->
rho- l+ nu) = (2.17 +- 0.34 +0.47/-0.54 +- 0.41 +- 0.01)x10^{-4}, where the
errors are statistical, experimental systematic, systematic due to residual
form-factor uncertainties in the signal, and systematic due to residual
form-factor uncertainties in the cross-feed modes, respectively. We also find
B(B+ -> eta l+ nu) = (0.84 +- 0.31 +- 0.16 +- 0.09)x10^{-4}, consistent with
what is expected from the B -> pi l nu mode and quark model symmetries. We
extract |Vub| using Light-Cone Sum Rules (LCSR) for 0<= q^2<16 GeV^2 and
Lattice QCD (LQCD) for 16 GeV^2 <= q^2 < q^2_max. Combining both intervals
yields |Vub| = (3.24 +- 0.22 +- 0.13 +0.55/-0.39 +- 0.09)x10^{-3}$ for pi l nu,
and |Vub| = (3.00 +- 0.21 +0.29/-0.35 +0.49/-0.38 +-0.28)x10^{-3} for rho l nu,
where the errors are statistical, experimental systematic, theoretical, and
signal form-factor shape, respectively. Our combined value from both decay
modes is |Vub| = (3.17 +- 0.17 +0.16/-0.17 +0.53/-0.39 +-0.03)x10^{-3}.Comment: 45 pages postscript, also available through
http://w4.lns.cornell.edu/public/CLNS, submitted to PR
Search for CP Violation in D^0--> K_S^0 pi^+pi^-
We report on a search for CP violation in the decay of D0 and D0B to Kshort
pi+pi-. The data come from an integrated luminosity of 9.0 1/fb of e+e-
collisions at sqrt(s) ~ 10 GeV recorded with the CLEO II.V detector. The
resonance substructure of this decay is well described by ten quasi-two-body
decay channels (K*-pi+, K*0(1430)-pi+, K*2(1430)-pi+, K*(1680)-pi+, Kshort rho,
Kshort omega, Kshort f0(980), Kshort f2(1270), Kshort f0(1370), and the ``wrong
sign'' K*+ pi-) plus a small non-resonant component. We observe no evidence for
CP violation in the amplitudes and phases that describe the decay D0 to K_S^0
pi+pi-.Comment: 10 pages, 3 figures, also available at
http://w4.lns.cornell.edu/public/CLNS/, submitted to PR
Measurement of Lepton Momentum Moments in the Decay bar{B} \to X \ell \bar{\nu} and Determination of Heavy Quark Expansion Parameters and |V_cb|
We measure the primary lepton momentum spectrum in B-bar to X l nu decays,
for p_l > 1.5 GeV/c in the B rest frame. From this, we calculate various
moments of the spectrum. In particular, we find R_0 = [int(E_l>1.7)
(dGam/dE_sl)*dE_l] / [int(E_l>1.5) (dGam/dE_sl)*dE_l] = 0.6187 +/- 0.0014_stat
+/- 0.0016_sys and R_1 = [int(E_l>1.5) E_l(dGam/dE_sl)*dE_l] / [int(E_l>1.5)
(dGam/dE_sl)*dE_l] = (1.7810 +/- 0.0007_stat +/- 0.0009_sys) GeV. We use these
moments to determine non-perturbative parameters governing the semileptonic
width. In particular, we extract the Heavy Quark Expansion parameters
Lambda-bar = (0.39 +/- 0.03_stat +/- 0.06_sys +/- 0.12_th) GeV and lambda_1 =
(-0.25 +/- 0.02_stat +/- 0.05_sys +/- 0.14_th) GeV^2. The theoretical
constraints used are evaluated through order 1/M_B^3 in the non-perturbative
expansion and beta_0*alpha__s^2 in the perturbative expansion. We use these
parameters to extract |V_cb| from the world average of the semileptonic width
and find |V_cb| = (40.8 +/- 0.5_Gam-sl +/- 0.4_(lambda_1,Lambda-bar)-exp +/-
0.9_th) x 10^-3. In addition, we extract the short range b-quark mass m_b^1S =
(4.82 +/- 0.07_exp +/- 0.11_th) GeV/c^2. Finally, we discuss the implications
of our measurements for the theoretical understanding of inclusive semileptonic
processes.Comment: 21 pages postscript, also available through
http://w4.lns.cornell.edu/public/CLNS, submitted to PR
DarkSUSY 6: An advanced tool to compute dark matter properties numerically
The nature of dark matter remains one of the key science questions. Weakly Interacting Massive Particles (WIMPs) are among the best motivated particle physics candidates, allowing to explain the measured dark matter density by employing standard big-bang thermodynamics. Examples include the lightest supersymmetric particle, though many alternative particles have been suggested as a solution to the dark matter puzzle. We introduce here a radically new version of the widely used DarkSUSY package, which allows to compute the properties of such dark matter particles numerically. With DarkSUSY 6 one can accurately predict a large variety of astrophysical signals from dark matter, such as direct detection rates in low-background counting experiments and indirect detection signals through antiprotons, antideuterons, gamma rays and positrons from the Galactic halo, or high-energy neutrinos from the center of the Earth or of the Sun. For thermally produced dark matter like WIMPs, high-precision tools are provided for the computation of the relic density in the Universe today, as well as for the size of the smallest dark matter protohalos. Furthermore, the code allows to calculate dark matter self-interaction rates, which may affect the distribution of dark matter at small cosmological scales. Compared to earlier versions, DarkSUSY 6 introduces many significant physics improvements and extensions. The most fundamental new feature of this release, however, is that the code has been completely re-organized and brought into a highly modular and flexible shape. Switching between different pre-implemented dark matter candidates has thus become straight-forward, just as adding new - WIMP or non-WIMP - particle models or replacing any given functionality in a fully user-specified way. In this article, we describe the physics behind the computer package, along with the main structure and philosophy of this major revision of DarkSUSY. A detailed manual is provided together with the public release at www.darksusy.org
NEOTROPICAL XENARTHRANS: a data set of occurrence of xenarthran species in the Neotropics
Xenarthrans â anteaters, sloths, and armadillos â have essential functions for ecosystem maintenance, such as insect control and nutrient cycling, playing key roles as ecosystem engineers. Because of habitat loss and fragmentation, hunting pressure, and conflicts with 24 domestic dogs, these species have been threatened locally, regionally, or even across their full distribution ranges. The Neotropics harbor 21 species of armadillos, ten anteaters, and six sloths. Our dataset includes the families Chlamyphoridae (13), Dasypodidae (7), Myrmecophagidae (3), Bradypodidae (4), and Megalonychidae (2). We have no occurrence data on Dasypus pilosus (Dasypodidae). Regarding Cyclopedidae, until recently, only one species was recognized, but new genetic studies have revealed that the group is represented by seven species. In this data-paper, we compiled a total of 42,528 records of 31 species, represented by occurrence and quantitative data, totaling 24,847 unique georeferenced records. The geographic range is from the south of the USA, Mexico, and Caribbean countries at the northern portion of the Neotropics, to its austral distribution in Argentina, Paraguay, Chile, and Uruguay. Regarding anteaters, Myrmecophaga tridactyla has the most records (n=5,941), and Cyclopes sp. has the fewest (n=240). The armadillo species with the most data is Dasypus novemcinctus (n=11,588), and the least recorded for Calyptophractus retusus (n=33). With regards to sloth species, Bradypus variegatus has the most records (n=962), and Bradypus pygmaeus has the fewest (n=12). Our main objective with Neotropical Xenarthrans is to make occurrence and quantitative data available to facilitate more ecological research, particularly if we integrate the xenarthran data with other datasets of Neotropical Series which will become available very soon (i.e. Neotropical Carnivores, Neotropical Invasive Mammals, and Neotropical Hunters and Dogs). Therefore, studies on trophic cascades, hunting pressure, habitat loss, fragmentation effects, species invasion, and climate change effects will be possible with the Neotropical Xenarthrans dataset
K-Shell photodetachment of Liâ: Experiment and theory
We have measured the first and second moments of the hadronic mass-squared distribution in BâXclv, for Plepton>1.5 GeV/c. We find(MX 2âMD â2)= 0.251 ± 0.66 GeV2,((MX 2âMX 2)2)=0.576 ± 0.170 GeV4, where MÂŻ Dis the spin-averaged D meson mass. From that first moment and the first moment of the photon energy spectrum in bâs Îł, we find the heavy quark effective theory parameter λ1(in the modified minimal subtraction renormalization scheme, to order 1/MB 3and Îł0αs 2) to be â0.24±0.11GeV2. Using these first moments and the B semileptonic width, and assuming parton-hadron duality, we obtain|Vcb|=0.0404±0.0013