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This paper generalizes the structural Markov properties for undirected decomposable graphs to arbitrary ones. This helps us to exploit the conditional independence properties of joint prior laws to analyze and compare multiple graphical structures, while being able to take advantage of the common conditional independence constraints. This work provides a theoretical support for full Bayesian posterior updating about the structure of a graph using data from a certain distribution. We further investigate the ratio of graph law so as to simplify the acceptance probability of the Metropolis–Hastings sampling algorithms. [ABSTRACT FROM AUTHOR]

Malignant ascites is a common complication of some advanced cancers. Although intraperitoneal (IP) administration of chemotherapy drugs is routinely used to treat cancerous ascites, conventional drugs have poor retention and therefore need to be administered frequently to maintain a sustained anti-tumor effect. In this study, a thermosensitive hydrogel composite loaded with norethindrone nanoparticles (NPs) and oxaliplatin (N/O/Hydrogel) was developed to inhibit ascites of hepatocellular carcinoma (HCC) through IP injection. N/O/Hydrogel induced apoptosis in the H22 cells in vitro, and significantly inhibited ascites formation, tumor cell proliferation and micro-angiogenesis in a mouse model of advanced HCC with ascites, and prolonged the survival of tumor-bearing mice. Histological examination of the major organs indicated that the hydrogel system is safe. Taken together, the N/O/Hydrogel system is a promising platform for in-situ chemotherapy of malignant ascites. [ABSTRACT FROM AUTHOR]

Chemotherapy is the primary treatment for advanced non-small-cell lung cancer (NSCLC). However, related dose-dependent toxicity limits its clinical use. Therefore, it is necessary to explore new strategies for improving the clinical outcomes while reducing the side effects of chemotherapy in the treatment of NSCLC. In this study, we designed and synthesized epidermal growth factor (EGF)-modified doxorubicin nanoparticles (EGF@DOX-NPs) that selectively targets the epidermal growth factor receptor (EGFR) overexpressed in lung tumor cells. When administered in combination with low-dose X-ray radiotherapy (RT), the NPs preferentially accumulated at the tumor site due to radiation-induced outburst of the local intra-tumoral blood vessels. Compared with DOX alone, EGF@DOX-NPs significantly decreased the viability and migration and enhanced the apoptosis rates of tumor cells in vitro. Also, the EGF@DOX-NPs significantly inhibited tumor growth in vivo, increasing the survival of the tumorbearing mice without apparent systemic toxic effects through RT-induced aggregation. The tumor cell proliferation was greatly inhibited in the RTþEGF@DOX-NPs group. Contrarily, the apoptosis of tumor cells was significantly higher in this group. These results confirm the promising clinical application of radiotherapy in combination with EGF@DOX-NPs for lung cancer treatment. [ABSTRACT FROM AUTHOR]

• Multitude advances were found for V-rich Bi 2 S 3 nanowire than pristine Bi 2 S 3 photoelectrode. • V-rich Bi 2 S 3 nanowires achieve excellent photocurrent density for water splitting under visible light. • Deep insights on how the V-rich feature affects the PEC performance of Bi 2 S 3. Bi 2 S 3 is a n-type (negative type) semiconductor that has a narrow band gap and an ideal band edge position for hydrogen generation. However, high charge recombination rate, low photoelectrochemical (PEC) efficiency and poor stability are of major concerns of Bi 2 S 3 as a photoelectrode. Herein, we report an efficient Vanadium-rich Bi 2 S 3 nanowires (atomic ratio of V to Bi is 1/22) that have been prepared on fluorine-doped tin oxide (FTO) substrate by an in-situ solution-processed reaction with BiVO 4 film as precursor. The resulting V-rich photoelectrode demonstrates notably high charge separation efficiency and fast charge transport with respect to pristine Bi 2 S 3 nanowires. As a result, the photocurrent density of ca. 10 mA·cm−2 at -0.2 V vs Ag/AgCl is obtained under visible light illumination. In addition, V-rich Bi 2 S 3 generates IPCE (incident photocurrent-to-current conversion efficiency) of 50% at 460 nm and 45% at 760 nm, demonstrating a 2.0 and 2.8-fold increase, respectively, when compared with pristine Bi 2 S 3. This enhancement is probably due to increased light absorption, less charge recombination, and faster charge transfer. More importantly, in contrast to pristine Bi 2 S 3 sample that suffers detrimental photocorrosion in sulfide containing electrolyte, V-rich Bi 2 S 3 nanowires retain 84.6% of its initial photocurrent over the course of 1 h. These findings are expected to shed light on engineering high-performance and robust metal sulfide materials for photoelectrochemical application. [ABSTRACT FROM AUTHOR]

The role of c-Jun N-terminal kinases (JNKs) in the pathogenesis of cancer is well-known due to their involvement in carcinogenesis. Although previous studies have discussed different functions of JNKs depending on cell type, the present study aimed to investigate the function of JNKs in nasopharyngeal carcinoma (NPC) cells, as well as their involvement in chemotherapy sensitivity to Adriamycin. The present results showed that Adriamycin administration reduced cell viability and led to elevated expressions of c-Jun, phosphorylated JNK and phosphorylated c-Jun, indicating an activated JNK pathway. Notably, JNK inhibition by SP600125 also reduced cell growth. Thus, Adriamycin treatment combined with SP600125 was more effective on cell growth inhibition than each agent alone. The apoptosis analysis confirmed the reduction in cell growth. Therefore, these data provide evidence that the JNK pathway activity is negatively associated with cell viability, and its decline could sensitize NPC cells to Adriamycin. [ABSTRACT FROM AUTHOR]