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We study the genuine tripartite nonlocality (GTN) and the genuine tripartite entanglement (GTE) of Dirac fields in the background of a Schwarzschild black hole. We find that the Hawking radiation degrades both the physically accessible GTN and the physically accessible GTE. The former suffers from “sudden death” at some critical Hawking temperature, and the latter approaches to the nonzero asymptotic value in the limit of infinite Hawking temperature. We also find that the Hawking effect cannot generate the physically inaccessible GTN, but can generate the physically inaccessible GTE for fermion fields in curved spacetime. These results show that on the one hand the GTN cannot pass through the event horizon of black hole, but the GTE do can, and on the other hand the surviving physically accessible GTE and the generated physically inaccessible GTE for fermions in curved spacetime are all not nonlocal. Some monogamy relations between the physically accessible GTE and the physically inaccessible GTE are found.

Epstein-Barr virus (EBV)-associated epithelial cancers, including nasopharyngeal carcinoma (NPC) and approximately 10% of gastric cancers, termed EBVaGC, represent 80% of all EBV-related malignancies. However, the exact role of EBV in epithelial cancers remains elusive. Here, we report that EBV functions in vasculogenic mimicry (VM). Epithelial cancer cells infected with EBV develop tumor vascular networks that correlate with tumor growth, which is different from endothelial-derived angiogenic vessels and is VEGF-independent. Mechanistically, activation of the PI3K/AKT/mTOR/HIF-1α signaling cascade, which is partly mediated by LMP2A, is responsible for EBV-induced VM formation. Both xenografts and clinical samples of NPC and EBVaGC exhibit VM histologically, which are correlated with AKT and HIF-1α activation. Furthermore, although anti-VEGF monotherapy shows limited effects, potent synergistic antitumor activities are achieved by combination therapy with VEGF and HIF-1α-targeted agents. Our findings suggest that EBV creates plasticity in epithelial cells to express endothelial phenotype and provides a novel EBV-targeted antitumor strategy.

Using two different types of quantification for quantum steering, we study the influence of Hawking radiation on quantum steering for fermionic fields in Schwarzschild spacetime. The degradation for the steering between physically accessible observers and the generation for the steering between physically accessible and inaccessible observers induced by Hawking radiation are studied. We also reveal the difference between the two types of quantification for steering, and find some monogamy relations between steering and entanglement. Furthermore, we show the different properties between fermionic steering and bosonic steering in Schwarzschild spacetime.

Many double-stranded DNA viruses, such as Epstein-Barr virus, can establish persistent infection, but the underlying virus–host interactions remain poorly understood. Here we report that in human airway epithelial cells Epstein-Barr virus induces TRIM29, a member of the TRIM family of proteins, to inhibit innate immune activation. Knockdown of TRIM29 in airway epithelial cells enhances type I interferon production, and in human nasopharyngeal carcinoma cells results in almost complete Epstein-Barr virus clearance. TRIM29 is also highly induced by cytosolic double-stranded DNA in myeloid dendritic cells. TRIM29 −/− mice have lower adenovirus titers in the lung, and are resistant to lethal herpes simplex virus-1 infection due to enhanced production of type I interferon. Mechanistically, TRIM29 induces K48-linked ubiquitination of Stimulator of interferon genes, a key adaptor in double-stranded DNA-sensing pathway, followed by its rapid degradation. These data demonstrate that Epstein-Barr virus and possible other double-stranded DNA viruses use TRIM29 to suppress local innate immunity, leading to the persistence of DNA virus infections. Proteins of the TRIM family have regulatory functions in immune signaling, often via ubiquitination of target proteins. Here, the authors show that TRIM29 is induced upon infection with DNA viruses, resulting in degradation of STING, decreased interferon signaling and increased pathogenicity in mice.

Tumor cells often reprogram their metabolism for rapid proliferation. The roles of long noncoding RNAs (lncRNAs) in metabolism remodeling and the underlying mechanisms remain elusive. Through screening, we found that the lncRNA Actin Gamma 1 Pseudogene ( AGPG ) is required for increased glycolysis activity and cell proliferation in esophageal squamous cell carcinoma (ESCC). Mechanistically, AGPG binds to and stabilizes 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3). By preventing APC/C-mediated ubiquitination, AGPG protects PFKFB3 from proteasomal degradation, leading to the accumulation of PFKFB3 in cancer cells, which subsequently activates glycolytic flux and promotes cell cycle progression. AGPG is also a transcriptional target of p53; loss or mutation of TP53 triggers the marked upregulation of AGPG . Notably, inhibiting AGPG dramatically impaired tumor growth in patient-derived xenograft (PDX) models. Clinically, AGPG is highly expressed in many cancers, and high AGPG expression levels are correlated with poor prognosis, suggesting that AGPG is a potential biomarker and cancer therapeutic target. PFKFB3 enhances glycolysis to promote cancer cell proliferation. Here, the authors identify a long noncoding RNA in esophageal squamous cell carcinoma, AGPG , which interacts with PFKFB3 and promotes its stability, leading to increased glycolysis and proliferation.

Emerging SARS-CoV-2 variants of concern (VOCs) harboring multiple mutations in the spike protein raise concerns on effectiveness of current vaccines that rely on the ancestral spike protein. Here, we design a quadrivalent mosaic nanoparticle vaccine displaying spike proteins from the SARS-CoV-2 prototype and 3 different VOCs. The mosaic nanoparticle elicits equivalent or superior neutralizing antibodies against variant strains in mice and non-human primates with only small reduction in neutralization titers against the ancestral strain. Notably, it provides protection against infection with prototype and B.1.351 strains in mice. These results provide a proof of principle for the development of multivalent vaccines against pandemic and potential pre-emergent SARS-CoV-2 variants. Emerging SARS-CoV-2 variants with multiple mutations raise concerns on vaccine effectiveness. Here, Kang et al . report that a quadrivalent mosaic nanoparticle vaccine displaying spike proteins from the SARS-CoV-2 prototype and three different VOCs confer protection against SARS-CoV-2 variants in mice.

A bstract Previous studies have shown that the Hawking effect always destroys quantum correlations and the fidelity of quantum teleportation in the Schwarzschild black hole. Here, we investigate the fidelity of quantum teleportation of Dirac fields between users in Schwarzschild spacetime. We find that, with the increase of the Hawking temperature, the fidelity of quantum teleportation can monotonically increase, monotonically decrease, or non-monotonically increase, depending on the choice of the initial state, which means that the Hawking effect can create net fidelity of quantum teleportation. This striking result banishes the extended belief that the Hawking effect of the black hole can only destroy the fidelity of quantum teleportation. We also find that quantum steering cannot fully guarantee the fidelity of quantum teleportation in Schwarzschild spacetime. This new unexpected source may provide a new idea for the experimental evidence of the Hawking effect.

We study the acceleration effect on the genuine tripartite entanglement for one or two accelerated detector(s) coupled to the vacuum field. Surprisingly, we find that the increase and decrease in entanglement have no definite correspondence with the Unruh and anti-Unruh effects. Specifically, Unruh effect can not only decrease but also enhance the tripartite entanglement between detectors; also, anti-Unruh effect can not only enhance but also decrease the tripartite entanglement. We give an explanation of this phenomenon. Finally, we extend the discussion from tripartite to N -partite systems.

To investigate the influence of the fissure morphology on the dynamic mechanical properties of the rock and the crack propagation, a drop hammer impact test device was used to conduct impact failure tests on sandstones with different fissure numbers and fissure dips, simultaneously recorded the crack growth after each impact. The box fractal dimension is used to quantitatively analyze the dynamic change in the sandstone cracks and a fractal model of crack growth over time is established based on fractal theory. The results demonstrate that under impact test conditions of the same mass and different heights, the energy absorbed by sandstone accounts for about 26.7% of the gravitational potential energy. But at the same height and different mass, the energy absorbed by the sandstone accounts for about 68.6% of the total energy. As the fissure dip increases and the number of fissures increases, the dynamic peak stress and dynamic elastic modulus of the fractured sandstone gradually decrease. The fractal dimensions of crack evolution tend to increase with time as a whole and assume as a parabolic. Except for one fissure, 60° and 90° specimens, with the extension of time, the increase rate of fractal dimension is decreasing correspondingly.