94 research outputs found
The 2021 X-ray outburst of magnetar SGR J1935+2154 -- I. Spectral properties
Over a period of multiple active episodes between January 2021 and January
2022, the magnetar SGR J1935+2154 emitted a total of 82 bursts observed by
GECAM-B. Temporal and spectral analyses reveal that the bursts have an average
duration of 145 ms and a fluence ranging from $1.2 \times 10^{-8} \
\mathrm{erg \cdot cm^{-2}}3.7 \times 10^{-5} \ \mathrm{erg \cdot
cm^{-2}}E_{\mathrm{peak}}\alphakT_{\mathrm{min}} \sim 5$ keV of the MBB model, which is
consistent between GECAM-B and GBM-GECAM. This indicates that both samples
originated from similar magnetar bursts. We also reveal the spectra of magnetar
bursts tend to be soft. It indicates that magnetar bursts may be composed of
multiple low BB temperatures and the majority of the BB temperatures are
concentrated around the minimum temperature
Reactive Oxygen Species and Targeted Therapy for Pancreatic Cancer
Pancreatic cancer is the fourth leading cause of cancer-related death in the United States. Reactive oxygen species (ROS) are generally increased in pancreatic cancer cells compared with normal cells. ROS plays a vital role in various cellular biological activities including proliferation, growth, apoptosis, and invasion. Besides, ROS participates in tumor microenvironment orchestration. The role of ROS is a doubled-edged sword in pancreatic cancer. The dual roles of ROS depend on the concentration. ROS facilitates carcinogenesis and cancer progression with mild-to-moderate elevated levels, while excessive ROS damages cancer cells dramatically and leads to cell death. Based on the recent knowledge, either promoting ROS generation to increase the concentration of ROS with extremely high levels or enhancing ROS scavenging ability to decrease ROS levels may benefit the treatment of pancreatic cancer. However, when faced with oxidative stress, the antioxidant programs of cancer cells have been activated to help cancer cells to survive in the adverse condition. Furthermore, ROS signaling and antioxidant programs play the vital roles in the progression of pancreatic cancer and in the response to cancer treatment. Eventually, it may be the novel target for various strategies and drugs to modulate ROS levels in pancreatic cancer therapy
Reactive Oxygen Species and Targeted Therapy for Pancreatic Cancer
Pancreatic cancer is the fourth leading cause of cancer-related death in the United States. Reactive oxygen species (ROS) are generally increased in pancreatic cancer cells compared with normal cells. ROS plays a vital role in various cellular biological activities including proliferation, growth, apoptosis, and invasion. Besides, ROS participates in tumor microenvironment orchestration. The role of ROS is a doubled-edged sword in pancreatic cancer. The dual roles of ROS depend on the concentration. ROS facilitates carcinogenesis and cancer progression with mild-to-moderate elevated levels, while excessive ROS damages cancer cells dramatically and leads to cell death. Based on the recent knowledge, either promoting ROS generation to increase the concentration of ROS with extremely high levels or enhancing ROS scavenging ability to decrease ROS levels may benefit the treatment of pancreatic cancer. However, when faced with oxidative stress, the antioxidant programs of cancer cells have been activated to help cancer cells to survive in the adverse condition. Furthermore, ROS signaling and antioxidant programs play the vital roles in the progression of pancreatic cancer and in the response to cancer treatment. Eventually, it may be the novel target for various strategies and drugs to modulate ROS levels in pancreatic cancer therapy
Calibration of the Timing Performance of GECAM-C
As a new member of the Gravitational wave high-energy Electromagnetic
Counterpart All-sky Monitor (GECAM) after GECAM-A and GECAM-B, GECAM-C
(originally called HEBS), which was launched on board the SATech-01 satellite
on July 27, 2022, aims to monitor and localize X-ray and gamma-ray transients
from 6 keV to 6 MeV. GECAM-C utilizes a similar design to GECAM but
operates in a more complex orbital environment. In this work, we utilize the
secondary particles simultaneously produced by the cosmic-ray events on orbit
and recorded by multiple detectors, to calibrate the relative timing accuracy
between all detectors of GECAM-C. We find the result is 0.1 , which
is the highest time resolution among all GRB detectors ever flown and very
helpful in timing analyses such as minimum variable timescale and spectral
lags, as well as in time delay localization. Besides, we calibrate the absolute
time accuracy using the one-year Crab pulsar data observed by GECAM-C and
Fermi/GBM, as well as GECAM-C and GECAM-B. The results are and , respectively. Finally, we investigate the
spectral lag between the different energy bands of Crab pulsar observed by
GECAM and GBM, which is .Comment: submitte
Downregulation of Fat Mass and Obesity Associated (FTO) Promotes the Progression of Intrahepatic Cholangiocarcinoma
Intrahepatic cholangiocarcinoma (ICC) ranks as the second most malignant type of primary liver cancer with a high degree of incidence and a very poor prognosis. Fat mass and obesity-associated protein (FTO) functions as an eraser of the RNA m6A modification, but its roles in ICC tumorigenesis and development remain unknown. We showed here that the protein level of FTO was downregulated in clinical ICC samples and cell lines and that FTO expression was inversely correlated with the expression of CA19-9 and micro-vessel density (MVD). A Kaplan-Meier survival analysis showed that a low expression of FTO predicted poor prognosis in ICC. in vitro, decreased endogenous expression of FTO obviously reduced apoptosis of ICC cells. Moreover, FTO suppressed the anchorage-independent growth and mobility of ICC cells. Through mining the database, FTO was found to regulate the integrin signaling pathway, inflammation signaling pathway, epidermal growth factor receptor (EGFR) signaling pathway, angiogenesis, and the pyrimidine metabolism pathway. RNA decay assay showed that oncogene TEAD2 mRNA stability was impaired by FTO. In addition, the overexpression of FTO suppressed tumor growth in vivo. In conclusion, our study demonstrated the critical roles of FTO in ICC
The Minimum Variation Timescales of X-ray bursts from SGR J1935+2154
The minimum variation timescale (MVT) of soft gamma-ray repeaters can be an
important probe to estimate the emission region in pulsar-like models, as well
as the Lorentz factor and radius of the possible relativistic jet in gamma-ray
burst (GRB)-like models, thus revealing their progenitors and physical
mechanisms. In this work, we systematically study the MVTs of hundreds of X-ray
bursts (XRBs) from SGR J1935+2154 observed by {\it Insight}-HXMT, GECAM and
Fermi/GBM from July 2014 to Jan 2022 through the Bayesian Block algorithm. We
find that the MVTs peak at 2 ms, corresponding to a light travel time
size of about 600 km, which supports the magnetospheric origin in pulsar-like
models. The shock radius and the Lorentz factor of the jet are also constrained
in GRB-like models. Interestingly, the MVT of the XRB associated with FRB
200428 is 70 ms, which is longer than that of most bursts and implies
its special radiation mechanism. Besides, the median of MVTs is 7 ms, shorter
than the median MVTs of 40 ms and 480 ms for short GRBs or long GRBs,
respectively. However, the MVT is independent of duration, similar to GRBs.
Finally, we investigate the energy dependence of MVT and suggest that there is
a marginal evidence for a power-law relationship like GRBs but the rate of
variation is at least about an order of magnitude smaller. These features may
provide an approach to identify bursts with a magnetar origin.Comment: accepted for publication in ApJ
Detection of the Diffuse Supernova Neutrino Background with JUNO
As an underground multi-purpose neutrino detector with 20 kton liquid scintillator, Jiangmen Underground Neutrino Observatory (JUNO) is competitive with and complementary to the water-Cherenkov detectors on the search for the diffuse supernova neutrino background (DSNB). Typical supernova models predict 2-4 events per year within the optimal observation window in the JUNO detector. The dominant background is from the neutral-current (NC) interaction of atmospheric neutrinos with 12C nuclei, which surpasses the DSNB by more than one order of magnitude. We evaluated the systematic uncertainty of NC background from the spread of a variety of data-driven models and further developed a method to determine NC background within 15\% with {\it{in}} {\it{situ}} measurements after ten years of running. Besides, the NC-like backgrounds can be effectively suppressed by the intrinsic pulse-shape discrimination (PSD) capabilities of liquid scintillators. In this talk, I will present in detail the improvements on NC background uncertainty evaluation, PSD discriminator development, and finally, the potential of DSNB sensitivity in JUNO
Potential of Core-Collapse Supernova Neutrino Detection at JUNO
JUNO is an underground neutrino observatory under construction in Jiangmen, China. It uses 20kton liquid scintillator as target, which enables it to detect supernova burst neutrinos of a large statistics for the next galactic core-collapse supernova (CCSN) and also pre-supernova neutrinos from the nearby CCSN progenitors. All flavors of supernova burst neutrinos can be detected by JUNO via several interaction channels, including inverse beta decay, elastic scattering on electron and proton, interactions on C12 nuclei, etc. This retains the possibility for JUNO to reconstruct the energy spectra of supernova burst neutrinos of all flavors. The real time monitoring systems based on FPGA and DAQ are under development in JUNO, which allow prompt alert and trigger-less data acquisition of CCSN events. The alert performances of both monitoring systems have been thoroughly studied using simulations. Moreover, once a CCSN is tagged, the system can give fast characterizations, such as directionality and light curve
Efficient Quantum-Dot Light-Emitting Diodes Employing Thermally Activated Delayed Fluorescence Emitters as Exciton Harvesters
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