Hebei Medical University
ORCID: 0000-0002-6282-0237Publishes on Cancer Immunotherapy and Biomarkers, Endometrial and Cervical Cancer Treatments, Ovarian cancer diagnosis and treatment. 565 papers and 12.1k citations.
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A major challenge facing all law-enforcement and intelligence-gathering organizations is accurately and efficiently analyzing the growing volumes of crime data. Detecting cybercrime can likewise be difficult because busy network traffic and frequent online transactions generate large amounts of data, only a small portion of which relates to illegal activities. Data mining is a powerful tool that enables criminal investigators who may lack extensive training as data analysts to explore large databases quickly and efficiently. We present a general framework for crime data mining that draws on experience gained with the Coplink project, which researchers at the University of Arizona have been conducting in collaboration with the Tucson and Phoenix police departments since 1997.
Tumor immune microenvironment (TIME) include tumor cells, immune cells, cytokines, etc. The interactions between these components, which are divided into anti-tumor and pro-tumor, determine the trend of anti-tumor immunity. Although the immune system can eliminate tumor through the cancer-immune cycle, tumors appear to eventually evade from immune surveillance by shaping an immunosuppressive microenvironment. Immunotherapy reshapes the TIME and restores the tumor killing ability of anti-tumor immune cells. Herein, we review the function of immune cells within the TIME and discuss the contribution of current mainstream immunotherapeutic approaches to remolding the TIME. Changes in the immune microenvironment in different forms under the intervention of immunotherapy can shed light on better combination treatment strategies.
We calculated bolometric temperature (T<SUB>bol</SUB>) and luminosity (L<SUB>bol</SUB>) for 128 young stellar objects (YSOs) in Taurus, 74 in the Ophiuchus 'core', and 33 in the Ophiuchus 'off-core' region. We have constructed the bolometric luminosity-temperature (BLT) diagram, the log-log plot of L<SUB>bol</SUB> versus T<SUB>bol</SUB>, for the three samples. T<SUB>bol</SUB> is defined as the temperature of a blackbody having the same frequency as the observed continuum spectrum. It measures the redness (or coldness) of an astronomical source. The BLT diagram is analogous to the H-R diagram and allows for a direct and quantitative comparison of YSOs at a wide variety of evolutionary states, ranging from the most deeply embedded stars to T Tauri stars nearly on the main sequence. We found (1) T<SUB>bol</SUB> increases monotonically from embedded sources (approximately 60-500 K) to classical T Tauri stars (approximately 1000-3000 K) to weak-line T Tauri stars (approximately 2000-5000 K); (2) T<SUB>bol</SUB> correlates reasonably well with the age inferred from the evolutionary models of pre-main-sequence stars and protostars for embedded 'protostars' and weak-line T Tauri stars. There is no significant correlation for the classical T Tauri stars. These results can be understood in terms of dissipation of circumstellar dust envelope and disk during the early stages of stellar evolution. Sources in the three regions have different distributions in the BLT diagram. The Ophiuchus core has the highest fraction of cold sources among the three regions. These cold sources are also more luminous than the YSOs in the other regions. The Ophiuchus off-core sample is dominated by the more evolved pre-main-sequence stars. The Taurus sources have distributions intermediate in L<SUB>bol</SUB>, T<SUB>bol</SUB>, and age between the Ophiuchus core and off-core distributions. These may suggest differences in the star formation history, and possibly in the stellar masses and mass accretion rates in these star-forming regions.
Complete loss of BRCA1 or BRCA2 function is associated with sensitivity to DNA damaging agents. However, not all BRCA1 and BRCA2 germline mutation-associated tumors respond. Herein we report analyses of 160 BRCA1 and BRCA2 germline mutation-associated breast and ovarian tumors. Retention of the normal BRCA1 or BRCA2 allele (absence of locus-specific loss of heterozygosity (LOH)) is observed in 7% of BRCA1 ovarian, 16% of BRCA2 ovarian, 10% of BRCA1 breast, and 46% of BRCA2 breast tumors. These tumors have equivalent homologous recombination deficiency scores to sporadic tumors, significantly lower than scores in tumors with locus-specific LOH (ovarian, P = 0.0004; breast P < 0.0001, two-tailed Student's t-test). Absence of locus-specific LOH is associated with decreased overall survival in ovarian cancer patients treated with platinum chemotherapy (P = 0.01, log-rank test). Locus-specific LOH may be a clinically useful biomarker to predict primary resistance to DNA damaging agents in patients with germline BRCA1 and BRCA2 mutations.Most tumours associated with germline BRCA1/BRCA2 loss of function mutations respond to DNA damaging agents, however, some do not. Herein, the authors identify that a subset of breast/ovarian tumors retain a normal allele, which is associated with decreased overall survival after DNA damage-inducing platinum chemotherapy.