543 research outputs found
Metallic monoclinic phase in VO induced by electrochemical gating: in-situ Raman study
We report in-situ Raman scattering studies of electrochemically top gated
VO thin film to address metal-insulator transition (MIT) under gating. The
room temperature monoclinic insulating phase goes to metallic state at a gate
voltage of 2.6 V. However, the number of Raman modes do not change with
electrolyte gating showing that the metallic phase is still monoclinic. The
high frequency Raman mode A(7) near 616 cm ascribed to V-O vibration
of bond length 2.06 \AA~ in VO octahedra hardens with increasing gate
voltage and the B(3) mode near 654 cm softens. This shows that the
distortion of the VO octahedra in the monoclinic phase decreases with
gating. The time dependent Raman data at fixed gate voltages of 1 V (for 50
minute, showing enhancement of conductivity by a factor of 50) and 2 V (for 130
minute, showing further increase in conductivity by a factor of 5) show similar
changes in high frequency Raman modes A(7) and B(3) as observed in
gating. This slow change in conductance together with Raman frequency changes
show that the governing mechanism for metalization is more likely to the
diffusion controlled oxygen vacancy formation due to the applied electric
field.Comment: 5 pages, 6 figure
Human Papillomavirus DNA in LEEP Plume
Objective: This study was undertaken to determine the prevalence of human papillomavirus (HPV)
in loop electrosurgical excision procedure (LEEP) plumes
Understanding the effect of stress hormones on ovarian cancer cells
Department of Cancer Systems Imaging Department of Gynecologic Oncology and Reproductive Medicinehttps://openworks.mdanderson.org/sumexp22/1022/thumbnail.jp
Anomalous Raman scattering from phonons and electrons of superconducting FeSe
We report interesting anomalies in the temperature dependent Raman spectra of
FeSe measured from 3K to 300K in the spectral range from 60 to 1800
cm and determine their origin using complementary first-principles
density functional calculations. A phonon mode near 100 cm exhibits a
sharp increase by 5% in frequency below a temperature T ( 100
K) attributed to strong spin-phonon coupling and onset of short-range
antiferromagnetic order. In addition, two high frequency modes are observed at
1350 cm and 1600 cm, attributed to electronic Raman scattering
from ()to / -orbitals of Fe.Comment: 19 pages, 4 figures, 1 tabl
Prediction and failure of anti-angiogenesis escape
Many clinical trials have demonstrated the benefit of anti-angiogenesis therapy in the treatment of gynecologic cancer. However, these benefits have often been in terms of progression-free rather than overall survival and in some cases, the magnitude of benefit demonstrated in the pivotal phase 3 trials has been disappointing when compared with the percentage of patients who responded in earlier phase 2 trials. Two potential explanations for this are the current inability to stratify patients according to chance of benefit and the development of resistance mechanisms within the tumor. In this article, we review the prediction of response and the proposed resistance and escape mechanisms involved in anti-angiogenesis therapy, including the up-regulation of alternative proangiogenic pathways, vascular co-option, and resistance to hypoxia. These insights may offer a personalized strategy for anti-angiogenesis therapy and help us to consider the best selection of other therapies that should be combined with anti-angiogenesis therapy to improve the outcome of patients with gynecologic cancer
Integrated Analysis of Gene Expression and Tumor Nuclear Image Profiles Associated with Chemotherapy Response in Serous Ovarian Carcinoma
Small sample sizes used in previous studies result in a lack of overlap between the reported gene signatures for prediction of chemotherapy response. Although morphologic features, especially tumor nuclear morphology, are important for cancer grading, little research has been reported on quantitatively correlating cellular morphology with chemotherapy response, especially in a large data set. In this study, we have used a large population of patients to identify molecular and morphologic signatures associated with chemotherapy response in serous ovarian carcinoma.A gene expression model that predicts response to chemotherapy is developed and validated using a large-scale data set consisting of 493 samples from The Cancer Genome Atlas (TCGA) and 244 samples from an Australian report. An identified 227-gene signature achieves an overall predictive accuracy of greater than 85% with a sensitivity of approximately 95% and specificity of approximately 70%. The gene signature significantly distinguishes between patients with unfavorable versus favorable prognosis, when applied to either an independent data set (P = 0.04) or an external validation set (P<0.0001). In parallel, we present the production of a tumor nuclear image profile generated from 253 sample slides by characterizing patients with nuclear features (such as size, elongation, and roundness) in incremental bins, and we identify a morphologic signature that demonstrates a strong association with chemotherapy response in serous ovarian carcinoma.A gene signature discovered on a large data set provides robustness in accurately predicting chemotherapy response in serous ovarian carcinoma. The combination of the molecular and morphologic signatures yields a new understanding of potential mechanisms involved in drug resistance
Recommended from our members
Mechanisms of nuclear content loading to exosomes.
Exosome cargoes are highly varied and include proteins, small RNAs, and genomic DNA (gDNA). The presence of gDNA suggests that different intracellular compartments contribute to exosome loading, resulting in distinct exosome subpopulations. However, the loading of gDNA and other nuclear contents into exosomes (nExo) remains poorly understood. Here, we identify the relationship between cancer cell micronuclei (MN), which are markers of genomic instability, and nExo formation. Imaging flow cytometry analyses reveal that 10% of exosomes derived from cancer cells and <1% of exosomes derived from blood and ascites from patients with ovarian cancer carry nuclear contents. Treatment with genotoxic drugs resulted in increased MN and nExos both in vitro and in vivo. We observed that multivesicular body precursors and exosomal markers, such as the tetraspanins, directly interact with MN. Collectively, this work provides new insights related to nExos, which have implications for cancer biomarker development
- …