2,187 research outputs found
MUSTANG 3.3 Millimeter Continuum Observations of Class 0 Protostars
We present observations of six Class 0 protostars at 3.3 mm (90 GHz) using
the 64-pixel MUSTANG bolometer camera on the 100-m Green Bank Telescope. The
3.3 mm photometry is analyzed along with shorter wavelength observations to
derive spectral indices (S_nu ~ nu^alpha) of the measured emission. We utilize
previously published dust continuum radiative transfer models to estimate the
characteristic dust temperature within the central beam of our observations. We
present constraints on the millimeter dust opacity index, beta, between 0.862
mm, 1.25 mm, and 3.3 mm. Beta_mm typically ranges from 1.0 to 2.4 for Class 0
sources. The relative contributions from disk emission and envelope emission
are estimated at 3.3 mm. L483 is found to have negligible disk emission at 3.3
mm while L1527 is dominated by disk emission within the central beam. The
beta_mm^disk <= 0.8 - 1.4 for L1527 indicates that grain growth is likely
occurring in the disk. The photometry presented in this paper may be combined
with future interferometric observations of Class 0 envelopes and disks.Comment: 19 pages, 3 figures, AJ accepted, in pres
From survival to survivorship: late side effects become an issue in high-grade glioma.
“For many patients, controlling neurological symptoms, preventing cognitive dysfunction and maintaining functional independence are just as important as prolonging survival.
Toxicity of Phase I Radiation Oncology Trials: Worldwide Experience
Introduction: Informed consent involves understanding the risks and benefits of trial enrollment. This is challenging in the phase I setting since true quantitative information is never known. We therefore performed an analysis of published radiation oncology (RO) phase I trials emphasizing patient outcomes. To our knowledge, no such systemic analysis has previously been published.
American Society for Therapeutic Radiation Oncology (ASTRO) 52nd Annual Meeting October 31 - November 4, San Diego, C
Effects of EGFR Expression on Anti-tumor Efficacy of Vandetanib or Cediranib Combined with Radiotherapy (RT) in U87 Human Glioblastoma (GBM) Xenografts
Introduction: Vandetanib is a receptor tyrosine kinase inhibitor (RTKI) with activity against vascular endothelial growth factor receptor-2 (VEGFR-2) and epidermal growth factor receptor (EGFR). Cediranib is a highly potent VEGF RTKI that inhibits all three VEGF receptors. In this study we investigated the effect of exogenous overexpression of EGFR on sensitivity of human GBM U87 xenografts to vandetanib or cediranib, alone or in combination with RT.
American Association for Cancer Research (AACR) 101st Annual Meeting April 17-21, Washington, DC
Combination of Vorinostat with Whole-brain Radiotherapy in the Treatment of Brain Metastases
Background: A third of patients with solid malignancies develop brain metastases. Expected overall survival is 4-7 months depending on age, performance status, and extracranial disease. Standard treatment is controversial; however, the majority of patients receive wholebrain radiation therapy at some point. Vorinostat (suberoylanilide hydroxamic acid, SAHA), an FDA-approved HDAC inhibitor, has been demonstrated to radiosensitize tumor cells in vitro, as assessed by both radiation-induced DNA damage and clonogenic cell survival (Munshi et al. Molecular Cancer Therapeutics 5, 1967-1974, 2006). We have shown that vorinostat downregulates key genes involved in double-strand DNA repair (Rad50, Rad51, XRCC2, XRCC3, XRCC6), as assessed by quantitative PCR. This suggests that the drug’s mechanism of radiosensitization is epigenetic coordinated inhibition of the DNA repair process. We hypothesize that the combination of vorinostat with whole-brain radiation therapy will be both safe and efficacious.
American Society of Clinical Oncology (ASCO) 46th Annual Meeting June 4-8, Chicago, IL
CMB observations with the Jodrell Bank - IAC interferometer at 33 GHz
The paper presents the first results obtained with the Jodrell Bank - IAC
two-element 33 GHz interferometer. The instrument was designed to measure the
level of the Cosmic Microwave Background (CMB) fluctuations at angular scales
of 1 - 2 degrees. The observations analyzed here were taken in a strip of the
sky at Dec = +41 deg with an element separation of 16.7 lambda, which gives a
maximum sensitivity to ~1.6 deg structures on the sky. The data processing and
calibration of the instrument are described. The sensitivity achieved in each
of the two channels is 7 micro K per resolution element. A reconstruction of
the sky at Dec = +41 deg using a maximum entropy method shows the presence of
structure at a high level of significance. A likelihood analysis, assuming a
flat CMB spatial power spectrum, gives a best estimate of the level of CMB
fluctuations of Delta Tl = 43 (+13,-12) micro K for the range l = 109 +/- 19;
the main uncertainty in this result arises from sample variance. We consider
that the contamination from the Galaxy is small. These results represent a new
determination of the CMB power spectrum on angular scales where previous
results show a large scatter; our new results are in agreement with the
theoretical predictions of the standard inflationary cold dark matter models.Comment: 11 pages, 11 figures. Web site at
http://www.jb.man.ac.uk/research/cmb/ Accepted for publication in MNRA
Evolving Role of Vorinostat Combined with Radiation Therapy in the Treatment of Brain Tumors, from the Lab to the Clinic
Purpose/Objective(s): Radiation therapy (RT) is a critical element in the treatment of both brain metastases and glioblastoma (GBM). Temozolomide (TMZ) has an established role in the upfront treatment of GBM. Down-regulated mismatch repair (MMR) is a known mechanism of resistance to TMZ. Vorinostat (SAHA), an HDAC inhibitor, has successfully been combined with a number of cytotoxic agents, including ionizing radiation (IR). We performed a series of preclinical and clinical studies to examine the role of SAHA in the treatment of brain tumors.
American Society for Therapeutic Radiation Oncology (ASTRO) 52nd Annual Meeting October 31 - November 4, San Diego, C
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