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Integrating the behavioral theory of the firm and social capital theory, this study examines how performance shortfalls and executive social relations jointly affect firms' trade-offs between the shared-control entry mode and full-control entry mode. This study argues that, for new overseas entries, performance shortfalls cause firms to prefer the shared-control entry mode. This is attributed to the fact that performance shortfalls increase firms' resource constraints and reduce their information search scope. This, in turn, leads decision-makers to prefer the shared-control entry mode, because that mode requires fewer resources, less information collection, and lower processing capabilities. In addition, guided by social capital theory, this study also finds that the positive effect of performance shortfalls on the shared-control entry mode is weakened when executives have social relations, either overseas or in banks. Further analysis shows that, compared with less-developed economies, firms facing a performance shortfall are more inclined to adopt the shared-control mode to enter developed economies. By clarifying the joint effect of performance shortfalls and executive social relations on firms' overseas equity entry modes, this study deepens the understanding of firms' choices of overseas equity entry modes. [ABSTRACT FROM AUTHOR]

Background: Previous studies involving risk–benefit analysis of trastuzumab deruxtecan (DS‐8201) have indicated the benefit of this treatment, although it may increase the risk of interstitial lung disease (ILD) and/or pneumonitis in certain patients. This study aimed to assess the safety of DS‐8201. Methods: A search was done for relevant articles in four electronic databases: PubMed, Embase, the Cochrane Library, and ClinicalTrials.gov. All reports published up until November 2, 2022, were included, and study types were restricted to clinical trials; the last search was then updated to January 10, 2023. We also assessed the quality of the literature with the Cochrane Handbook for Systematic Reviews of Interventions and the Methodological Index for Non‐Randomized Studies tool, and then performed a meta‐analysis with R version 4.2.1. Results: A total of 1428 patients reported in 13 articles were included in this study. The analysis revealed that the most common all‐grade treatment‐emergent adverse events (TEAEs) were nausea and fatigue. The most common TEAE of grade 3 or above (grade ≥3) was neutropenia. The incidences of ILD and/or pneumonitis for all‐grade and grade ≥3 TEAEs were 12.5% and 2.2%, respectively. Conclusions: This comprehensive summary of the incidence of TEAEs associated with DS‐8201 in clinical trials provides an important guide for clinicians. The most common TEAEs were gastrointestinal reactions and fatigue; meanwhile, the most common grade ≥3 TEAE was hematological toxicity. ILD and/or pneumonitis were specific adverse drug reactions associated with DS‐8201, of which physicians should be particularly aware for their higher morbidity and rates of grade ≥3 TEAEs. This study aimed to assess the safety of trastuzumab deruxtecan (DS‐8201) with a focus on interstitial lung disease and/or pneumonitis via the method of systematic review and single‐arm meta‐analysis. This comprehensive summary of the incidence of treatment‐emergent adverse events associated with DS‐8201 in clinical trials provides an important guide for clinicians. [ABSTRACT FROM AUTHOR]

Novel exohedral metalloborospherenes Al12Li20&B60 and Al20Li12&B60 with the classical fullerene-like borospherene B60 were theoretically predicted and their structures and properties were studied. Incredibly, the B60 cage (pull electron oxidizer) pulls 50 and 60e− from exohedral metal atoms, forming two super-reduced polyanionic states B6050− and B6060−, respectively. Next, the two super-reduced polyanionic states (push electron oxidizers) owing to their negative electric fields push out the remaining valence electrons of exohedral metal atoms. Accordingly, the metalloborospherenes convert to electride salt molecules 6e−&[(Al3+)12(Li+)20]&B6050− and 12e−&[(Al3+)20(Li+)12]&B6060− due to the pull–push electron oxidation relay. It is known that the loss of electrons by the reducing agent results in an oxidation effect. The mechanism of losing electrons involves not only the pull electron but also the push electron, which results in push electron oxidation. As long as there is enough reducing agents in oxidation–reduction electride systems, the unusual pull–push electron oxidation relay will occur, showing new physical insights. More interestingly, the B60x− (x = 50 or 60) polyanions can also display push electron oxidation for embedded calcium atoms, forming endohedral spherical electride molecules 14e−&[(Al3+)12(Li+)20]&[(Ca6)8+@B6050−] and 22e−&[(Al3+)20(Li+)12]&[(Ca6)10+@B6060−], in which the supernormal pull–push–push electron oxidizing ability of the B60 cage is reflected in the total number of pull–push electrons up to 64 and 82, respectively. Remarkably, these spherical electride molecules have extraordinarily small multiple ionization potential (VIPn, n = 1–22) values, demonstrating a nuclear large-scale effect of the superatomic model on VIPn. [ABSTRACT FROM AUTHOR]

Background: The predominant immune cells in solid tumors are M2-like tumor-associated macrophages (M2-like TAMs), which significantly impact the promotion of epithelial-mesenchymal transition (EMT) in tumors, enhancing stemness and facilitating tumor invasion and metastasis. However, the contribution of M2-like TAMs to tumor progression in gallbladder cancer (GBC) is partially known. Methods: Immunohistochemistry was used to evaluate the expression of M2-like TAMs and cancer stem cell (CSC) markers in 24 pairs of GBC and adjacent noncancerous tissues from patients with GBC. Subsequently, GBC cells and M2-like TAMs were co-cultured to examine the expression of CSC markers, EMT markers, and migratory behavior. Proteomics was performed on the culture supernatant of M2-like TAMs. The mechanisms underlying the induction of EMT, stemness, and metastasis in GBC by M2-like TAMs were elucidated using proteomics and transcriptomics. GBC cells were co-cultured with undifferentiated macrophages (M0) and analyzed. The therapeutic effect of gemcitabine combined with a chemokine (C-C motif) receptor 2 (CCR2) antagonist on GBC was observed in vivo. Results: The expression levels of CD68 and CD163 in M2-like TAMs and CD44 and CD133 in gallbladder cancer stem cells (GBCSCs) were increased and positively correlated in GBC tissues compared with those in neighboring noncancerous tissues. M2-like TAMs secreted a significant amount of chemotactic cytokine ligand 2 (CCL2), which activated the MEK/extracellular regulated protein kinase (ERK) pathway and enhanced SNAIL expression after binding to the receptor CCR2 on GBC cells. Activation of the ERK pathway caused nuclear translocation of ELK1, which subsequently led to increased SNAIL expression. GBCSCs mediated the recruitment and polarization of M0 into M2-like TAMs within the GBC microenvironment via CCL2 secretion. In the murine models, the combination of a CCR2 antagonist and gemcitabine efficiently inhibited the growth of subcutaneous tumors in GBC. Conclusions: The interaction between M2-like TAMs and GBC cells is mediated by the chemokine CCL2, which activates the MEK/ERK/ELK1/SNAIL pathway in GBC cells, promoting EMT, stemness, and metastasis. A combination of a CCR2 inhibitor and gemcitabine effectively suppressed the growth of subcutaneous tumors. Consequently, our study identified promising therapeutic targets and strategies for treating GBC. [ABSTRACT FROM AUTHOR]

The utilization of resources plays a crucial role in mitigating the environmental pollution issue that improper disposal of construction and demolition waste (CDW) causes. However, the slow growth of the recycled building materials market limits the development of CDW resource utilization. Green value co-creation among remanufacturers, construction enterprises, and the public in CDW resource utilization projects is an effective way to address the issue. This study, based on the theory of value co-creation, uses the evolutionary game method to construct an evolutionary game model for CDW resource utilization projects. The main conclusions are as follows: (1) When the degree of green value co-creation is 0.1 or 0.5, the remanufacturer, the construction enterprise, and the public cannot maintain a state of green value co-creation; when the degree of green value co-creation is 0.9, the remanufacturer, the construction enterprise, and the public in the CDW resource utilization project finally reach a stable state of green value co-creation. (2) When the degree of green value co-creation is 0.5, enhancing the green value co-creation willingness of the remanufacturer or the public can lead other CDW resource utilization project stakeholders to participate in green value co-creation. This study contributes to the promotion of stakeholder cooperation in CDW resource utilization projects, thus providing implications for the promotion of CDW resources. [ABSTRACT FROM AUTHOR]

Association of circulating glycoprotein acetyls (GlycA), a systemic inflammation biomarker, with lung function and respiratory diseases remain to be investigated. We examined the genetic correlation, shared genetics, and potential causality of GlycA (N = 115,078) with lung function and respiratory diseases (N = 497,000). GlycA showed significant genetic correlation with FEV1 (rg = −0.14), FVC (rg = −0.18), asthma (rg = 0.21) and COPD (rg = 0.31). We consistently identified ten shared loci (including chr3p21.31 and chr8p23.1) at both SNP and gene level revealing potential shared biological mechanisms involving ubiquitination, immune response, Wnt/β-catenin signaling, cell growth and differentiation in tissues or cells including blood, epithelium, fibroblast, fetal thymus, and fetal intestine. Genetically elevated GlycA was significantly correlated with lung function and asthma susceptibility (354.13 ml decrement of FEV1, 442.28 ml decrement of FVC, and 144% increased risk of asthma per SD increment of GlycA) from MR analyses. Our findings provide insights into biological mechanisms of GlycA in relating to lung function, asthma, and COPD. Here, the authors observed significant genetic correlation of GlycA with lung function, asthma and COPD and identified ten shared loci revealing potential shared biological mechanisms involving ubiquitination and Wnt/β-catenin signaling. [ABSTRACT FROM AUTHOR]

Aims: To explore the association of dietary vitamin intake from food and/or supplement with mortality in US adults with diabetes. Materials and Methods: This prospective cohort study was conducted on 5418 US adults with diabetes from the National Health and Nutrition Examination Survey 1999–2018. Vitamin intake from food and supplements was estimated via dietary recall. Sufficient intake from food or food + supplement was defined as ≥ estimated average requirement (EAR) and ≤ tolerable upper intake level (UL), insufficient intake, < EAR; and excess intake, > UL. Medium supplementary intake was classified as > median level and ≤75th percentile; low intake, ≤ median level; and high intake, >75th percentile, as reported by supplement users. Results: A total of 1601 deaths occurred among the participants over a median follow‐up of 11.0 years. Cox regression analysis of the single‐vitamin model demonstrated that sufficient vitamin A and folate intake from food and food + supplement and medium vitamin A and folate intake from supplement; sufficient riboflavin, niacin, and vitamin B6 intake from food and food + supplement; and sufficient thiamin and vitamin E intake from food + supplement were significantly associated with reduced all‐cause mortality (all p < 0.05). In the multivitamin model, sufficient vitamin A and folate intake from food and food + supplement, medium vitamin A and folate intake from the supplement, and sufficient niacin intake from food and food + supplement were inversely associated with mortality (all p < 0.05). Conclusions: Vitamin A and folate intake from food or supplement and niacin intake from food were significantly associated with reduced mortality in US adults with diabetes. [ABSTRACT FROM AUTHOR]

Background: Gallbladder cancer (GBC), a highly malignant gastrointestinal tumor, lacks effective therapies. Foxhead box A2 (FOXA2) is a tumor suppressor that is poorly expressed in various human malignancies. This study aimed to ascertain FOXA2 expression in GBC and its relevance to tumor metastasis, and to elucidate its regulatory mechanism with epithelial‐mesenchymal transition (EMT) as an entry point, in the hope of providing a potential therapeutic target for GBC. Methods: FOXA2 expression in GBC tissues was first detected using immunohistochemistry (IHC), followed by correlation analysis with clinicopathological characteristics and survival prognosis. Subsequently, the effects of FOXA2 on GBC cell migration and invasion, as well as EMT induction, were evaluated by scratch, Transwell, RT‐PCR, and Western blot assays, together with animal experimentation. Ultimately, mRNA sequencing was carried out to identify the key downstream target genes of FOXA2 in controlling the EMT process in GBC cells, and dual‐luciferase reporter and chromatin immunoprecipitation assays were used to determine its regulatory mechanism. Results: FOXA2 was underexpressed in GBC tissues and inversely correlated with tumor node metastasis stage, lymph node metastasis, and poor patient prognosis. FOXA2 exerts suppressive effects on EMT and metastasis of GBC in vivo and in vitro. FOXA2 can impede GBC cell migratory and invasive functions and EMT by positively mediating serine protein kinase inhibitor B5 (SERPINB5) expression. Conclusion: FOXA2 directly binds to the SERPINB5 promoter region to stimulate its transcription, thereby modulating the migration and invasion behaviors of GBC cells as well as the EMT process, which might be an effective therapeutic target against GBC. [ABSTRACT FROM AUTHOR]

Objective: To estimate the pooled prevalence, as well as the spatial and temporal distribution, of urolithiasis among subjects in China. Materials and Methods: We conducted a comprehensive search of both Chinese and English databases to retrieve literature pertaining to the prevalence of urolithiasis in the indigenous Chinese population. A random‐effects meta‐analysis model was employed to calculate the pooled prevalence of urolithiasis. Subgroup analyses were conducted based on factors such as time, region, gender, and sample size. Prevalence and spatial distribution maps were created based on provinces and latitude/longitude coordinates. Results: A total of 46 studies conducted in 22 provinces across China were included in this meta‐analysis and the pooled prevalence of urolithiasis, kidney stones, ureteric calculi, urethral and bladder stones were 8.1% (95% confidence interval [CI] 5.6–11.1%), 7.8% (95% CI 5.8–10.0%), 3.2% (95% CI 0.6–5.7%), 0.5% (95% CI 0.1–0.9%). Most of the urolithiasis prevalence screening in China was concentrated between 100° E and 120° E, with higher rates observed in low latitude areas. Subgroup analysis of kidney stones revealed that Guangdong (12.7%) and Guangxi (10.3%) had the highest prevalence, with the eastern developed area exhibiting higher rates compared to the west. The prevalence in males was higher than in females (odds ratio 1.67, 95% CI 1.46–1.92), although the gender gap has significantly reduced since 2006. Moreover, a greater sample size is associated with a decreased prevalence of urolithiasis. Conclusions: The prevalence of urolithiasis is increasing in China, and there are noteworthy regional or provincial disparities in occurrence. It is worth noting that the current number of screening studies in some areas is insufficient. Additional investigations with appropriate sample sizes should be supplemented in time. [ABSTRACT FROM AUTHOR]