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The impact of chromosomal translocation locus and fusion oncogene coding sequence in synovial sarcomagenesis.
Synovial sarcomas are aggressive soft-tissue malignancies that express chromosomal translocation-generated fusion genes, SS18-SSX1 or SS18-SSX2 in most cases. Here, we report a mouse sarcoma model expressing SS18-SSX1, complementing our prior model expressing SS18-SSX2. Exome sequencing identified no recurrent secondary mutations in tumors of either genotype. Most of the few mutations identified in single tumors were present in genes that were minimally or not expressed in any of the tumors. Chromosome 6, either entirely or around the fusion gene expression locus, demonstrated a copy number gain in a majority of tumors of both genotypes. Thus, by fusion oncogene coding sequence alone, SS18-SSX1 and SS18-SSX2 can each drive comparable synovial sarcomagenesis, independent from other genetic drivers. SS18-SSX1 and SS18-SSX2 tumor transcriptomes demonstrated very few consistent differences overall. In direct tumorigenesis comparisons, SS18-SSX2 was slightly more sarcomagenic than SS18-SSX1, but equivalent in its generation of biphasic histologic features. Meta-analysis of human synovial sarcoma patient series identified two tumor-gentoype-phenotype correlations that were not modeled by the mice, namely a scarcity of male hosts and biphasic histologic features among SS18-SSX2 tumors. Re-analysis of human SS18-SSX1 and SS18-SSX2 tumor transcriptomes demonstrated very few consistent differences, but highlighted increased native SSX2 expression in SS18-SSX1 tumors. This suggests that the translocated locus may drive genotype-phenotype differences more than the coding sequence of the fusion gene created. Two possible roles for native SSX2 in synovial sarcomagenesis are explored. Thus, even specific partial failures of mouse genetic modeling can be instructive to human tumor biology
The evolution of rotating stars
First, we review the main physical effects to be considered in the building
of evolutionary models of rotating stars on the Upper Main-Sequence (MS). The
internal rotation law evolves as a result of contraction and expansion,
meridional circulation, diffusion processes and mass loss. In turn,
differential rotation and mixing exert a feedback on circulation and diffusion,
so that a consistent treatment is necessary.
We review recent results on the evolution of internal rotation and the
surface rotational velocities for stars on the Upper MS, for red giants,
supergiants and W-R stars. A fast rotation is enhancing the mass loss by
stellar winds and reciprocally high mass loss is removing a lot of angular
momentum. The problem of the ``break-up'' or -limit is critically
examined in connection with the origin of Be and LBV stars. The effects of
rotation on the tracks in the HR diagram, the lifetimes, the isochrones, the
blue to red supergiant ratios, the formation of W-R stars, the chemical
abundances in massive stars as well as in red giants and AGB stars, are
reviewed in relation to recent observations for stars in the Galaxy and
Magellanic Clouds. The effects of rotation on the final stages and on the
chemical yields are examined, as well as the constraints placed by the periods
of pulsars. On the whole, this review points out that stellar evolution is not
only a function of mass M and metallicity Z, but of angular velocity
as well.Comment: 78 pages, 7 figures, review for Annual Review of Astronomy and
Astrophysics, vol. 38 (2000
Coherent quantum state storage and transfer between two phase qubits via a resonant cavity
A network of quantum-mechanical systems showing long lived phase coherence of
its quantum states could be used for processing quantum information. As with
classical information processing, a quantum processor requires information bits
(qubits) that can be independently addressed and read out, long-term memory
elements to store arbitrary quantum states, and the ability to transfer quantum
information through a coherent communication bus accessible to a large number
of qubits. Superconducting qubits made with scalable microfabrication
techniques are a promising candidate for the realization of a large scale
quantum information processor. Although these systems have successfully passed
tests of coherent coupling for up to four qubits, communication of individual
quantum states between qubits via a quantum bus has not yet been demonstrated.
Here, we perform an experiment demonstrating the ability to coherently transfer
quantum states between two superconducting Josephson phase qubits through a
rudimentary quantum bus formed by a single, on chip, superconducting
transmission line resonant cavity of length 7 mm. After preparing an initial
quantum state with the first qubit, this quantum information is transferred and
stored as a nonclassical photon state of the resonant cavity, then retrieved at
a later time by the second qubit connected to the opposite end of the cavity.
Beyond simple communication, these results suggest that a high quality factor
superconducting cavity could also function as a long term memory element. The
basic architecture presented here is scalable, offering the possibility for the
coherent communication between a large number of superconducting qubits.Comment: 17 pages, 4 figures (to appear in Nature
Health plan administrative records versus birth certificate records: quality of race and ethnicity information in children
<p>Abstract</p> <p>Background</p> <p>To understand racial and ethnic disparities in health care utilization and their potential underlying causes, valid information on race and ethnicity is necessary. However, the validity of pediatric race and ethnicity information in administrative records from large integrated health care systems using electronic medical records is largely unknown.</p> <p>Methods</p> <p>Information on race and ethnicity of 325,810 children born between 1998-2008 was extracted from health plan administrative records and compared to birth certificate records. Positive predictive values (PPV) were calculated for correct classification of race and ethnicity in administrative records compared to birth certificate records.</p> <p>Results</p> <p>Misclassification of ethnicity and race in administrative records occurred in 23.1% and 33.6% children, respectively; the majority due to missing ethnicity (48.3%) and race (40.9%) information. Misclassification was most common in children of minority groups. PPV for White, Black, Asian/Pacific Islander, American Indian/Alaskan Native, multiple and other was 89.3%, 86.6%, 73.8%, 18.2%, 51.8% and 1.2%, respectively. PPV for Hispanic ethnicity was 95.6%. Racial and ethnic information improved with increasing number of medical visits. Subgroup analyses comparing racial classification between non-Hispanics and Hispanics showed White, Black and Asian race was more accurate among non-Hispanics than Hispanics.</p> <p>Conclusions</p> <p>In children, race and ethnicity information from administrative records has significant limitations in accurately identifying small minority groups. These results suggest that the quality of racial information obtained from administrative records may benefit from additional supplementation by birth certificate data.</p
Combinatorial discovery of polymers resistant to bacterial attachment
Bacterial attachment and subsequent biofilm formation are key challenges to the long term performance of many medical devices. Here, a high throughput approach coupled with the analysis of surface structure-property relationships using a chemometics approach has been developed to simultaneously investigate the interaction of bacteria with hundreds of polymeric materials on a microarray format. Using this system, a new group of materials comprising ester and hydrophobic moieties are identified that dramatically reduce the attachment of clinically relevant, pathogenic bacteria (Pseudomonas aeruginosa, Staphylococcus aureus and uropathogenic Escherichia coli). Hit materials coated on silicone catheters resulted in up to a 30 fold reduction in coverage compared to a commercial silver embedded catheter, which has been proven to half the incidence of clinically acquired infection. These polymers represent a new class of materials resistant to bacterial attachment that could not have been predicted from the current understanding of bacteria-surface interactions
Non-Linear Elasticity of Extracellular Matrices Enables Contractile Cells to Communicate Local Position and Orientation
Most tissue cells grown in sparse cultures on linearly elastic substrates typically display a small, round phenotype on soft substrates and become increasingly spread as the modulus of the substrate increases until their spread area reaches a maximum value. As cell density increases, individual cells retain the same stiffness-dependent differences unless they are very close or in molecular contact. On nonlinear strain-stiffening fibrin gels, the same cell types become maximally spread even when the low strain elastic modulus would predict a round morphology, and cells are influenced by the presence of neighbors hundreds of microns away. Time lapse microscopy reveals that fibroblasts and human mesenchymal stem cells on fibrin deform the substrate by several microns up to five cell lengths away from their plasma membrane through a force limited mechanism. Atomic force microscopy and rheology confirm that these strains locally and globally stiffen the gel, depending on cell density, and this effect leads to long distance cell-cell communication and alignment. Thus cells are acutely responsive to the nonlinear elasticity of their substrates and can manipulate this rheological property to induce patterning
ICG fluorescence-guided sentinel node biopsy for axillary nodal staging in breast cancer
Molecular mechanism for 3:1 subunit stoichiometry of rod cyclic nucleotide-gated ion channels
Molecular determinants of ion channel tetramerization are well characterized, but those involved in heteromeric channel assembly are less clearly understood. The heteromeric composition of native channels is often precisely controlled. Cyclic nucleotide-gated (CNG) channels from rod photoreceptors exhibit a 3:1 stoichiometry of CNGA1 and CNGB1 subunits that tunes the channels for their specialized role in phototransduction. Here we show, using electrophysiology, fluorescence, biochemistry, and X-ray crystallography, that the mechanism for this controlled assembly is the formation of a parallel 3-helix coiled-coil domain of the carboxy-terminal leucine zipper region of CNGA1 subunits, constraining the channel to contain three CNGA1 subunits, followed by preferential incorporation of a single CNGB1 subunit. Deletion of the carboxy-terminal leucine zipper domain relaxed the constraint and permitted multiple CNGB1 subunits in the channel. The X-ray crystal structures of the parallel 3-helix coiled-coil domains of CNGA1 and CNGA3 subunits were similar, suggesting that a similar mechanism controls the stoichiometry of cone CNG channels
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