402 research outputs found
Bony metastases from breast cancer - a study of foetal antigen 2 as a blood tumour marker
Background : Foetal antigen 2 (FA-2), first isolated in the amniotic fluid, was shown to be the circulating form of the aminopropeptide of the alpha 1 chain of procollagen type I. Serum concentrations of FA-2 appeared to be elevated in a number of disorders of bone metabolism. This paper is the first report of its role as a marker of bone metabolism in metastatic breast cancer.
Methods: Serum FA-2 concentrations were measured by radioimmunoassay in 153 women with different stages of breast cancer and in 34 normal controls.
Results: Serum FA-2 was significantly elevated in women with bony metastases (p < 0.015). Its levels were not significantly different among women with non-bony metastases, with non-metastatic disease, as well as among normal controls.
Conclusions: FA-2 is a promising blood marker of bone metabolism. Further studies to delineate its role in the diagnosis and management of bony metastases from breast cancer are required
Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients
<p>Abstract</p> <p>Background</p> <p>Treacher Collins syndrome (TCS) is an autosomal dominant craniofacial disorder caused by frameshift deletions or duplications in the <it>TCOF1 </it>gene. These mutations cause premature termination codons, which are predicted to lead to mRNA degradation by nonsense mediated mRNA decay (NMD). Haploinsufficiency of the gene product (treacle) during embryonic development is the proposed molecular mechanism underlying TCS. However, it is still unknown if <it>TCOF1 </it>expression levels are decreased in post-embryonic human cells.</p> <p>Methods</p> <p>We have estimated <it>TCOF1 </it>transcript levels through real time PCR in mRNA obtained from leucocytes and mesenchymal cells of TCS patients (n = 23) and controls (n = 18). Mutational screening and analysis of NMD were performed by direct sequencing of gDNA and cDNA, respectively.</p> <p>Results</p> <p>All the 23 patients had typical clinical features of the syndrome and pathogenic mutations were detected in 19 of them. We demonstrated that the expression level of <it>TCOF1 </it>is 18-31% lower in patients than in controls (<it>p < 0.05</it>), even if we exclude the patients in whom we did not detect the pathogenic mutation. We also observed that the mutant allele is usually less abundant than the wild type one in mesenchymal cells.</p> <p>Conclusions</p> <p>This is the first study to report decreased expression levels of <it>TCOF1 </it>in TCS adult human cells, but it is still unknown if this finding is associated to any phenotype in adulthood. In addition, as we demonstrated that alleles harboring the pathogenic mutations have lower expression, we herein corroborate the current hypothesis of NMD of the mutant transcript as the explanation for diminished levels of <it>TCOF1 </it>expression. Further, considering that <it>TCOF1 </it>deficiency in adult cells could be associated to pathologic clinical findings, it will be important to verify if TCS patients have an impairment in adult stem cell properties, as this can reduce the efficiency of plastic surgery results during rehabilitation of these patients.</p
On soft singularities at three loops and beyond
We report on further progress in understanding soft singularities of massless
gauge theory scattering amplitudes. Recently, a set of equations was derived
based on Sudakov factorization, constraining the soft anomalous dimension
matrix of multi-leg scattering amplitudes to any loop order, and relating it to
the cusp anomalous dimension. The minimal solution to these equations was shown
to be a sum over color dipoles. Here we explore potential contributions to the
soft anomalous dimension that go beyond the sum-over-dipoles formula. Such
contributions are constrained by factorization and invariance under rescaling
of parton momenta to be functions of conformally invariant cross ratios.
Therefore, they must correlate the color and kinematic degrees of freedom of at
least four hard partons, corresponding to gluon webs that connect four eikonal
lines, which first appear at three loops. We analyze potential contributions,
combining all available constraints, including Bose symmetry, the expected
degree of transcendentality, and the singularity structure in the limit where
two hard partons become collinear. We find that if the kinematic dependence is
solely through products of logarithms of cross ratios, then at three loops
there is a unique function that is consistent with all available constraints.
If polylogarithms are allowed to appear as well, then at least two additional
structures are consistent with the available constraints.Comment: v2: revised version published in JHEP (minor corrections in Sec. 4;
added discussion in Sec. 5.3; refs. added); v3: minor corrections (eqs. 5.11,
5.12 and 5.29); 38 pages, 3 figure
On the renormalization of multiparton webs
We consider the recently developed diagrammatic approach to soft-gluon
exponentiation in multiparton scattering amplitudes, where the exponent is
written as a sum of webs - closed sets of diagrams whose colour and kinematic
parts are entangled via mixing matrices. A complementary approach to
exponentiation is based on the multiplicative renormalizability of intersecting
Wilson lines, and their subsequent finite anomalous dimension. Relating this
framework to that of webs, we derive renormalization constraints expressing all
multiple poles of any given web in terms of lower-order webs. We examine these
constraints explicitly up to four loops, and find that they are realised
through the action of the web mixing matrices in conjunction with the fact that
multiple pole terms in each diagram reduce to sums of products of lower-loop
integrals. Relevant singularities of multi-eikonal amplitudes up to three loops
are calculated in dimensional regularization using an exponential infrared
regulator. Finally, we formulate a new conjecture for web mixing matrices,
involving a weighted sum over column entries. Our results form an important
step in understanding non-Abelian exponentiation in multiparton amplitudes, and
pave the way for higher-loop computations of the soft anomalous dimension.Comment: 60 pages, 15 figure
Should red cell transfusion be individualized? Yes
SCOPUS: ed.jinfo:eu-repo/semantics/publishe
On form factors in N=4 sym
In this paper we study the form factors for the half-BPS operators
and the stress tensor supermultiplet
current up to the second order of perturbation theory and for the
Konishi operator at first order of perturbation theory in
SYM theory at weak coupling. For all the objects we observe the
exponentiation of the IR divergences with two anomalous dimensions: the cusp
anomalous dimension and the collinear anomalous dimension. For the IR finite
parts we obtain a similar situation as for the gluon scattering amplitudes,
namely, apart from the case of and the finite part has
some remainder function which we calculate up to the second order. It involves
the generalized Goncharov polylogarithms of several variables. All the answers
are expressed through the integrals related to the dual conformal invariant
ones which might be a signal of integrable structure standing behind the form
factors.Comment: 35 pages, 7 figures, LATEX2
University rankings:What do they really show?
University rankings as developed by the media are used by many stakeholders in higher education: students looking for university places; academics looking for university jobs; university managers who need to maintain standing in the competitive arena of student recruitment; and governments who want to know that public funds spent on universities are delivering a world class higher education system. Media rankings deliberately draw attention to the performance of each university relative to all others, and as such they are undeniably simple to use and interpret. But one danger is that they are potentially open to manipulation and gaming because many of the measures underlying the rankings are under the control of the institutions themselves. This paper examines media rankings (constructed from an amalgamation of variables representing performance across numerous dimensions) to reveal the problems with using a composite index to reflect overall performance. It ends with a proposal for an alternative methodology which leads to groupings rather than point estimates
Inhibition of APN/CD13 leads to suppressed progressive potential in ovarian carcinoma cells
<p>Abstract</p> <p>Background</p> <p>Aminopeptidase N (APN/CD13), a 150-kDa metalloprotease, is a multifunctional cell surface aminopeptidase with ubiquitous expression. Recent studies have suggested that APN/CD13 plays an important role in tumor progression of several human malignancies. In the current study, we investigated the role of APN/CD13 in ovarian carcinoma (OVCA) progression.</p> <p>Methods</p> <p>We first examined the expression of APN/CD13 at the protein level in a variety of OVCA cell lines and tissues. We subsequently investigated whether there was a correlation between APN/CD13 expression and invasive potential of various OVCA cell lines. Moreover, we investigated the function of APN/CD13 in OVCA cells using bestatin, an APN/CD13 inhibitor, or transfection of siRNA for APN/CD13.</p> <p>Results</p> <p>We confirmed that APN/CD13 was expressed in OVCA tissues and cell lines to various extents. There was a positive correlation between APN/CD13 expression and migratory potential in various OVCA cell lines with accordingly enhanced secretion of endogenous MMP-2. Subsequently, we found a significant decrease in the proliferative and migratory abilities of OVCA cells after the addition of bestatin or the inhibition of APN/CD13 expression by siRNA. Furthermore, in an animal model, daily intraperitoneal administration of bestatin after inoculation of OVCA cells resulted in a decrease of peritoneal dissemination and in prolonged survival of nude mice.</p> <p>Conclusion</p> <p>The current data indicate the possible involvement of APN/CD13 in the development of OVCA, and suggest that clinical use of bestatin may contribute to better prognosis for ovarian carcinoma patients.</p
Net primary productivity of forest stands in New Hampshire estimated from Landsat and MODIS satellite data
© 2007 Potter et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution Licens
Surface and Temporal Biosignatures
Recent discoveries of potentially habitable exoplanets have ignited the
prospect of spectroscopic investigations of exoplanet surfaces and atmospheres
for signs of life. This chapter provides an overview of potential surface and
temporal exoplanet biosignatures, reviewing Earth analogues and proposed
applications based on observations and models. The vegetation red-edge (VRE)
remains the most well-studied surface biosignature. Extensions of the VRE,
spectral "edges" produced in part by photosynthetic or nonphotosynthetic
pigments, may likewise present potential evidence of life. Polarization
signatures have the capacity to discriminate between biotic and abiotic "edge"
features in the face of false positives from band-gap generating material.
Temporal biosignatures -- modulations in measurable quantities such as gas
abundances (e.g., CO2), surface features, or emission of light (e.g.,
fluorescence, bioluminescence) that can be directly linked to the actions of a
biosphere -- are in general less well studied than surface or gaseous
biosignatures. However, remote observations of Earth's biosphere nonetheless
provide proofs of concept for these techniques and are reviewed here. Surface
and temporal biosignatures provide complementary information to gaseous
biosignatures, and while likely more challenging to observe, would contribute
information inaccessible from study of the time-averaged atmospheric
composition alone.Comment: 26 pages, 9 figures, review to appear in Handbook of Exoplanets.
Fixed figure conversion error
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