We conducted a joint (pooled) analysis of three genome-wide association studies (GWAS) 1-3 of esophageal squamous cell carcinoma (ESCC) in ethnic Chinese (5,337 ESCC cases and 5,787 controls) with 9,654 ESCC cases and 10,058 controls for follow-up. In a logistic regression model adjusted for age, sex, study, and two eigenvectors, two new loci achieved genome-wide significance, marked by rs7447927 at 5q31.2 (per-allele odds ratio (OR) = 0.85, 95% CI 0.82-0.88; P=7.72x10−20) and rs1642764 at 17p13.1 (per-allele OR= 0.88, 95% CI 0.85-0.91; P=3.10x10−13). rs7447927 is a synonymous single nucleotide polymorphism (SNP) in TMEM173 and rs1642764 is an intronic SNP in ATP1B2, near TP53. Furthermore, a locus in the HLA class II region at 6p21.32 (rs35597309) achieved genome-wide significance in the two populations at highest risk for ESSC (OR=1.33, 95% CI 1.22-1.46; P=1.99x10−10). Our joint analysis identified new ESCC susceptibility loci overall as well as a new locus unique to the ESCC high risk Taihang Mountain region.

Nanostructured enzyme mimics are of great interest as promising alternatives to artificial enzymes for biomedical and catalytic applications. Studying the chemical interactions between antioxidants and nano-enzymes may result in a better understanding of the antioxidant capability of antioxidants and may help improve the function of artificial enzymes to better mimic natural enzymes. In this study, using Co3O4 nanoparticles (NPs) as peroxidase mimics to catalyze the oxidation of chromophoric substrates by H2O2, we developed a platform that acts as a biosensor for hydrogen peroxide and glucose and that can study the inhibitory effects of natural antioxidants on peroxidase mimics. This method can be applied specifically to glucose detection in real samples. Three natural antioxidants, gallic acid (GA), tannic acid (TA), and ascorbic acid (AA), were compared for their antioxidant capabilities. We found that these three antioxidants efficiently inhibit peroxidase-like activity with concentration dependence. The antioxidants showed different efficiencies, in the following order: tannic acid > gallic acid > ascorbic acid. They also showed distinct modes of inhibition based on different interaction mechanisms. This study serves as a proof-of-concept that nano-enzyme mimics can be used to evaluate antioxidant capabilities and to screen enzyme inhibitors.

The photoactivity of semiconductor nanostructures makes them potentially useful for environmental remediation and antibacterial applications. Understanding the mechanism underlying the photochemical and photobiological activities of photoexcited semiconductors is of great importance for developing applications and assessing associated risks. In the current work, using electron spin resonance spectroscopy coupled with spin trapping and spin labeling techniques, we comparatively and systematically investigate the abilities of ZnO and ZnS to generate hydroxyl radical, superoxide, singlet oxygen, photoinduced electrons, and oxygen consumption during irradiation. It was found that although ZnO and ZnS, when photoexcited, can produce hydroxyl radical, superoxide, and singlet oxygen, ZnO is more effective than ZnS in producing hydroxyl radical and singlet oxygen while ZnS is more effective than ZnO in generating superoxide. The characterization with ESR spin labeling and oximetry indicates ZnS is about 4 times more active than ZnO in production of photoinduced electrons and consumption of oxygen. We compared the photocatalytic and antibacterial activities of ZnO and ZnS and found that ZnO exhibits efficient and broad photocatalytic and antibacterial activity, conversely, ZnS is only effective in photodegradation of RhB and killing Staphylococcus aureus. The distinct photocatalytic activities of ZnO and ZnS nanoparticles were attributable to their unique capability to facilitate the generation of reactive oxygen species and charge carriers during photoirradiation. These results provide valuable information for understanding the photocatalytic mechanism of metal oxide and metal sulfides and for predicting their photocatalytic activities.

Identifying the dominantly active species and their reactive behaviors in semiconductor photocatalysis is important for developing a full understanding of their photochemical and photophysical properties. Here we report an effective method for studying the reactive oxygen species (ROS) and charge carriers generated by irradiating single crystalline CdS and Ag 2 S micro-nano structures (MNS). Our method, based on electron spin resonance spectroscopy (ESR) combined with spin trapping and spin labeling techniques, confirmed the generation of superoxide and charge carriers and their contribution to photocatalytic degradation of rhodamine B elicited by CdS and Ag 2 S MNS. The electronic band structures determined the reactivity of photogenerated holes/electrons and the generation of reactive oxygen species. Our comparison of CdS and Ag 2 S MNS showed that, because of the large difference between their band edge positions, these two sulfides differ greatly in ROS production and in the reactivity of photoinduced electrons and holes. Our ESR method not only provides specific mechanistic information, but also can predict the photocatalytic activity for metal sulfide and possible metal oxide micro-nano structures.

Recent studies have shown that long noncoding RNAs (lncRNAs) play pivotal roles in the initiation and progression of cancer, including esophageal squamous cell carcinoma (ESCC). The lncRNA HOX transcript antisense RNA (HOTAIR) was reported to be dysregulated and correlated with the progression of ESCC. However, the biological role and the underlying mechanism of HOTAIR in the development of ESCC remain unclear. Herein, we found that HOTAIR was aberrantly upregulated in ESCC cells and that HOTAIR depletion inhibited proliferation and led to G1 cell cycle arrest in ESCC cells. Besides, we found that HOTAIR acted as an endogenous sponge to downregulate miR-1 expression by directly binding to miR-1. Furthermore, HOTAIR overturned the effect of miR-1 on the proliferation and cell cycle profile in ESCC cells, which involved the derepression of cyclin D1 (CCND1) expression, a target of miR-1. Taken together, our study elucidated a novel HOTAIR /miR-1/CCND1 regulatory axis in which HOTAIR acted as a competing endogenous RNA by sponging miR-1 and upregulated CCND1 expression, thereby facilitating the tumorigenesis of ESCC. Investigation of this lncRNA/miRNA/mRNA pathway may contribute to a better understanding of ESCC pathogenesis and facilitate the development of lncRNA-directed therapy against this disease.