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A bstract We study the decoherence and thermalization of an Unruh-DeWitt detector linearly coupled to the free massless scalar field in flat spacetime with arbitrary dimensions d ≥ 2. The initial state of the detector is chosen to be a pure state consisting of a linear superposition of ground and excited states, and we calculate the time evolution of reduced density matrix of the detector. Using perturbation method, we analytically derive the transition rate of the detector (the rate of change of the diagonal elements in the density matrix) and the decoherence rate (the rate of change of the off-diagonal elements in the density matrix). We find that the results are not the same in odd and even dimensional spacetimes, but the unitarity of the qubit is preserved in both cases. The real part of the decoherence rate is related to the transition rate, while the imaginary part may contain different forms of divergence terms in different dimensions due to the temporal order product operator and the singularities of the Wightman function for quantum field theory. We derive the recurrence formula to obtain the divergence terms in each dimension and analyze the renormalization problem.

We give a general description of the system evolution under the interaction between qubit and quantum field theory up to the second order perturbation, which is also referred to as the simplified model of light-matter interaction. The results are classified into rotating and counter-rotating wave terms, the former corresponding to stimulated absorption and emission, and the latter to Unruh and anti-Unruh effects. We obtain not only the reduced density matrix of the qubit, but also the backreaction obtained by quantum field theory as the environment. The result shows that the energy variation of the quantum field theory is related to trajectory and the initial state of the qubit, the expectation values of the linear and quadratic field operators, and the temporal order product operator. When the qubit is in accelerated motion, the conventional Unruh effect causes the vacuum state to possess a “temperature”, which raises some doubts about the validity of Landauer’s principle. We prove that Landauer’s principle still holds for any state of motion.

Starting from Polchinski’s thought experiment on how to distinguish between pure and thermal states, we construct a specific system to study the interaction between qubit and cavity quantum field theory (QFT) in order to provide a more operational point of view. Without imposing any restrictions on the initial states of qubit and cavity QFT, we compute the evolution of the system order by order by the perturbation method. We choose Landauer’s principle, an important bound in quantum computation and quantum measurement, as the basis for the determination of the thermal state. By backtracking the initial state form, we obtain the conditions that must be satisfied by the cavity QFT: the expectation value of the annihilation operator should be zero, and the expectation value of the particle number operator should satisfy the Bose–Einstein distribution. We also discuss the difference between the thermal state and a possible alternative to the thermal state: the canonical thermal pure quantum (CTPQ) state.

BackgroundEmerging evidence suggested that miRNAs can function as oncogenes or tumor suppressors by regulating downstream target genes. miR-324-3p has been reported to function in several carcinomas, but its role in gastric cancer (GC) is still unknown. This study aims to explore the effects of miR-324-3p on the development of GC.MethodsExpression of miR-324-3p was examined in GC cells and tissues by qRT-PCR. Effects of miR-324-3p on GC cells were evaluated by cell vitality assay, colony formation assay, cell migration assay, and flow cytometric assay. The dual luciferase assay was used to verify whether miR-324-3p could interact with the potential target genes. Western blot was used to assess the expression level of Smad4 and beta-catenin. Intracellular ATP level was also examined. The tumor xenografts were established using nude mice. A gastric organoid model was made from fresh stomach tissue.ResultsmiR-324-3p was expressed at higher levels in the tumor tissues compared with adjacent normal tissues. Overexpression of miR-324-3p promoted cell growth, migration, and decreased apoptosis. miR-324-3p repressed the expression of Smad4, and loss of Smad4 activated the Wnt/beta-catenin signaling pathway. Overexpression of Smad4 rescued the effects of miR-324-3p on GC cells. The intracellular ATP level was upregulated with overexpression of miR-324-3p. miR-324-3p facilitated tumor cell colonization and growth in vivo and contributed to the growth of gastric organoids.ConclusionsThe results suggested that miR-324-3p promoted GC through activating the Smad4-mediated Wnt/beta-catenin signaling pathway. The miR-324-3p/Smad4/Wnt signaling axis may be a potential therapeutic target to prevent GC progression.

In this paper, we study and predict flow observables in 2.76 and 5.02 A TeV Pb + Pb collisions, using the iEBE-VISHNU hybrid model with TRENTo and AMPT initial conditions and with different forms of the QGP transport coefficients. With properly chosen and tuned parameter sets, our model calculations can nicely describe various flow observables in 2.76 A TeV Pb + Pb collisions, as well as the measured flow harmonics of all charged hadrons in 5.02 A TeV Pb + Pb collisions. We also predict other flow observables, including v n ( p T ) of identified particles, event-by-event v n distributions, event-plane correlations, (normalized) symmetric cumulants, non-linear response coefficients and p T -dependent factorization ratios, in 5.02 A TeV Pb + Pb collisions. We find many of these observables to remain approximately the same values as the ones in 2.76 A TeV Pb + Pb collisions. Our theoretical studies and predictions could shed light to the experimental investigations in the near future.

Hepatocellular carcinoma (HCC), the most prevalent malignancy of the digestive tract, is characterized by a high mortality rate and poor prognosis, primarily due to its initial diagnosis at an advanced stage that precludes any surgical intervention. Recent advancements in systemic therapies have significantly improved oncological outcomes for intermediate and advanced‐stage HCC, and the combination of locoregional and systemic therapies further facilitates tumor downstaging and increases the likelihood of surgical resectability for initially unresectable cases following conversion therapies. This shift toward high conversion rates with novel, multimodal treatment approaches has become a principal pathway for prolonged survival in patients with advanced HCC. However, the field of conversion therapy for HCC is marked by controversies, including the selection of potential surgical candidates, formulation of conversion therapy regimens, determination of optimal surgical timing, and application of adjuvant therapy post‐surgery. Addressing these challenges and refining clinical protocols and research in HCC conversion therapy is essential for setting the groundwork for future advancements in treatment strategies and clinical research. This narrative review comprehensively summarizes the current strategies and clinical experiences in conversion therapy for advanced‐stage HCC, emphasizing the unresolved issues and the path forward in the context of precision medicine. This work not only provides a comprehensive overview of the evolving landscape of treatment modalities for conversion therapy but also paves the way for future studies and innovations in this field. Setting a foundation for future research and advancements in HCC treatment, aligning with the emerging paradigm of precision medicine; addressing the need for a holistic approach in managing advanced‐stage HCC, and advocating for a balance between aggressive treatment and quality of life considerations.

C-reactive protein (CRP) is a plasma protein that is evolutionarily conserved, found in both vertebrates and many invertebrates. It is a member of the pentraxin superfamily, characterized by its pentameric structure and calcium-dependent binding to ligands like phosphocholine (PC). In humans and various other species, the plasma concentration of this protein is markedly elevated during inflammatory conditions, establishing it as a prototypical acute phase protein that plays a role in innate immune responses. This feature can also be used clinically to evaluate the severity of inflammation in the organism. Human CRP (huCRP) can exhibit contrasting biological functions due to conformational transitions, while CRP in various species retains conserved protective functions in vivo . The focus of this review will be on the structural traits of CRP, the regulation of its expression, activate complement, and its function in related diseases in vivo .

A bstract We study Ising Field Theory (the scaling limit of Ising model near the Curie critical point) in pure imaginary external magnetic field. We put particular emphasis on the detailed structure of the Yang-Lee edge singularity. While the leading singular behavior is controlled by the Yang-Lee fixed point (= minimal CFT M 2 / 5 ), the fine structure of the subleading singular terms is determined by the effective action which involves a tower of irrelevant operators. We use numerical data obtained through the “Truncated Free Fermion Space Approach” to estimate the couplings associated with two least irrelevant operators. One is the operator T T ¯ , and we use the universal properties of the T T ¯ deformation to fix the contributions of higher orders in the corresponding coupling parameter α . Another irrelevant operator we deal with is the descendant L_ 4 L ¯ _ 4 ϕ of the relevant primary ϕ in M 2 / 5 . The significance of this operator is that it is the lowest dimension operator which breaks integrability of the effective theory. We also establish analytic properties of the particle mass M (= inverse correlation length) as the function of complex magnetic field.