Search Results (592)

Deciphering the coloration mechanism of natural-colored cocoons in the domestic silkworm (Bombyx mori) is of great importance for the green and sustainable development of the sericulture industry. In this study, 14 silkworm strains were selected for studying differences in the coloration mechanism of diverse cocoon colors, and the present research carried out integrated investigations from three aspects: pigment content, differences in gene expression levels, and gene structural variation. The results demonstrated that pigment accumulation presented distinct tissue-specific and strain-specific characteristics. The middle silk gland (MSG) acts as the primary locus for pigment deposition: silkworm strains forming yellow or red cocoons accumulate carotenoids at high levels in this tissue, whereas those producing green cocoons show abundant flavonoid enrichment here. Analysis of gene expression profiles indicated that the expression patterns of core transporter genes are highly correlated with the spatial distribution of pigments. The expression level of CBP gene in the MSG is over 10-fold higher than that in the midgut (MG) among yellow/red cocoon strains. The pivotal glycosylation gene UGT86 displayed remarkably elevated expression in the MSG relative to other tissues across all green cocoon silkworm strains. The CBP gene acts as a core regulatory factor governing the transport of carotenoid pigments, and notable disparities existed in the coding region of the gene among silkworm strains with different cocoon colors. In contrast to yellow and red cocoon strains, the transcription start site of CBP gene is displaced in silkworm varieties that form green or white cocoons. In summary, this study clarified the expression patterns and variations in key pigment deposition-related genes at the population level for the first time and provided data references for the study of the biological basis and coloration mechanism of diverse cocoon colors. Full article

As digital transformation accelerates, artificial intelligence (AI) has become a central driver of social media ecosystems. Drawing on Uses and Gratifications Theory (UGT) and Consumer–Brand Relationship Theory, this study employs a quantitative research design based on questionnaire data and Partial Least Squares Structural Equation Modeling (PLS-SEM) to examine how AI-empowered social media functionalities influence the sustainability of consumer–brand relationships among Generation Z. The analysis incorporates key constructs, including AI-empowered functionalities, user engagement behaviors (information seeking, social interaction, and content co-creation), flow experience, user satisfaction, brand loyalty, and brand value co-creation. The results indicate that AI-empowered social media applications significantly enhance user engagement behaviors. However, user engagement does not directly affect consumer–brand relationship outcomes; instead, its influence operates indirectly through flow experience and user satisfaction. Notably, flow experience emerges as a critical mediating mechanism linking AI-empowered user engagement to both brand loyalty and brand value co-creation. This research provides empirical evidence for the development of sustainable consumer–brand relationships in AI-empowered social media environments and offers practical insights for fashion brands to optimize their social media strategies when targeting Generation Z users. Full article

Bactrocera dorsalis (Hendel) is a major fruit-feeding pest that poses a severe and persistent threat to the horticulture industry in tropical and subtropical regions. Methyl eugenol (ME) is a powerful male-specific attractant phytochemical and pheromone precursor that has been widely exploited in lure-and-kill pest management programs. Upon ingestion, ME is metabolized (E)-coniferyl alcohol (E-CF) and 2-allyl-4,5-dimethoxyphenol (DMP), which are stored in the male rectal glands and released during courtship to attract females. Despite its ecological significance, the fundamental molecular mechanism underlying ME perception remains poorly understood. Here, we performed a comparative transcriptomic analysis of ME-responsive and ME-non-responsive male B. dorsalis across four tissues (head, gut, midleg, and wing). A total of 15,727 genes were annotated, of which 970 were associated with odorant-binding proteins (OBPs), odorant receptors (ORs), gustatory receptors (GRs), ionotropic receptors (IRs), and chemosensory proteins (CSPs), as well as detoxification families comprising cytochrome P450s (CYPs), carboxylesterases (CaEs), glutathione S-transferases (GSTs), and uridine diphosphate (UDP)-glycosyltransferases (UGTs), and the stress-related heat shock proteins (HSPs) genes. Differential expression analysis identified 7222, 7763, and 6105 differentially expressed genes (DEGs) in the head, gut, and wings/midlegs, respectively, between ME-responsive and ME-non-responsive males. Notably, CYPs, UGTs, and HSPs involved in detoxification and stress response were significantly downregulated. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses revealed that CYPs were significantly enriched in metabolic detoxification pathways. These findings reveal a complex molecular interplay between olfaction and detoxification and suggest that ME induces coordinated genetic pathways supporting survival, reproduction, and environmental adaptability. This knowledge provides a foundation for the development of eco-friendly pest management strategies targeting these molecular mechanisms. Full article

Epimedium brevicornu is an important medicinal plant in China, whose main bioactive components are flavonoid glycosides. UDP-glycosyltransferases (UGTs) play key roles in flavonoid glycosylation and metabolic diversification. In this study, transcriptome data from four representative production regions in Gansu Province were used to systematically identify and analyze the UGT gene family in E. brevicornu. A total of 359 UGT members were identified, and 168 homologous genes with clear expression evidence were obtained from four geographical populations. Molecular evolutionary analysis showed that most UGT genes were under purifying selection, whereas UGT2, UGT52, UGT57, UGT241, UGT269, and UGT271 exhibited significant signals of positive selection in specific lineages (p < 0.05). Protein interaction analysis indicated that many UGT proteins were closely associated with key enzymes involved in flavonoid biosynthesis, including CHS (TT4), CHI (TT5), F3H, FLS, and DFR, suggesting their potential involvement in flavonoid metabolism. Promoter analysis further revealed a high enrichment of ERF (11,169 occurrences) and MYB (7673 occurrences) transcription factor binding sites in the upstream regions of UGT genes. In addition, UGT57 and UGT241 showed significantly higher expression levels in the QLH population. Molecular docking analysis indicated relatively strong binding affinities with quercetin, with binding energies of −7.23 kcal/mol and −4.62 kcal/mol, respectively. These results suggest that the sequence variation and differential expression of UGT genes may be associated with flavonoid glycosylation and ecological adaptation in Epimedium. This study provides a basis for understanding the evolutionary characteristics and expression patterns of the UGT gene family and offers candidate genes for future studies on flavonoid metabolism. Full article

Background/Objectives: Many chronic diseases, including cancer, can be developed in conjunction with excessive intracellular oxidative stress and persistent inflammation. The importance of preventive strategies is highlighted by the potential of phytochemical interventions to mitigate these diseases. The purpose of this study was to investigate how Citrus depressa leaf (CDL) extracts can prevent 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced carcinogenesis in JB6 P+ mouse skin epidermal cells. Methods: CDL extracts were prepared and characterized for their phenolic and flavonoid contents. Effects of the potent extract on cell viability, TPA-induced colony formation, intracellular reactive oxygen species (ROS) levels, and nuclear factor erythroid 2–related factor 2 (Nrf2)-related protein and mRNA expression, mediated by epigenetic modifications, were evaluated in JB6 P+ cells. Results: Both the water extract (CDL-WE) and the 95% ethanol extract (CDL-95EE) contain abundant flavonoids that inhibit TPA-induced cell transformation and colony formation without minimal cytotoxicity. Mechanistic studies indicated that CDL-95EE increased the gene expression of Nrf2-related detoxification and antioxidant enzymes, such as UDP-glucuronosyltransferase 1A (UGT1A) and heme oxygenase-1 (HO-1), and decreased intracellular ROS accumulation. Furthermore, CDL-95EE reduced the expression of epigenetic modifiers, including DNA methyltransferases (DNMTs) and histone deacetylases (HDACs), suggesting involvement in epigenetic regulation. Conclusions: These findings indicate that CDL, an agricultural by-product, may be useful in cancer prevention through antioxidant and epigenetic mechanisms. Full article

Background: Tamoxifen is widely used in the treatment of hormone receptor-positive breast cancer and has been shown to successfully reduce recurrence and mortality rates. Nonetheless, variability in patient response to tamoxifen treatment is observed with up to 40% of patients experiencing recurrence. Genetic polymorphisms in pharmacogenes encoding enzymes involved in tamoxifen metabolism have been linked to some of this observed interindividual variability. The pharmacogenetics of tamoxifen in populations of African descent remain understudied, creating difficulties in pinpointing the primary factors behind the observed variable response. To address this gap, this study aimed to investigate the role of genetic variation in tamoxifen treatment outcomes in a South African cohort. Methods: Participants included 166 Mixed and African Ancestry breast cancer patients who had received tamoxifen treatment. Genetic characterization was performed for 53 single nucleotide polymorphisms (SNPs) and two copy number variations across eight drug-metabolizing enzymes, including cytochrome P450s (CYP2D6, CYP3A4, CYP3A5, CYP2B6), UDP-glucuronosyltransferases (UGT1A4), and sulfotransferases (SULT1A1, SULT1E1, SULT2A1). The association between genotypes and disease-free survival (DFS) was evaluated using Cox proportional hazards regression models. Results: The CYP2B6*1/*6 or *4/*9 genotype showed a nominal association with improved DFS (p = 0.049), with a similar trend observed for UGT1A4 rs11888492. In contrast, SULT1E1 rs3775779 heterozygosity showed a nominal association with reduced DFS (p = 0.044). SULT1A1 SNPs (rs4149393, rs4149394, rs1042157) demonstrated trends toward reduced DFS. Conclusions: These exploratory findings highlight the need for more inclusive pharmacogenomic research and point to potential biomarkers for optimizing tamoxifen therapy in African populations. Full article

No. 0 diesel oil may pose a serious threat to sea cucumber (Apostichopus japonicus) aquaculture by inducing skin ulceration. This study aimed to evaluate the protective efficacy and mechanism of a previously developed inhibitor composition against diesel-induced injury. The inhibitor composition significantly alleviated skin ulceration in the experimental group (Eg), reducing the lesion area to 14.44 ± 1.79% after 96 h, compared to 33.19 ± 2.94% in the diesel-exposed control group (Cg) (p < 0.05). It effectively suppressed the overactivation of autolytic enzymes (cathepsin L and B) while enhancing the activities of acetylcholinesterase, superoxide dismutase, and catalase. Transcriptomic profiling revealed 3137 differentially expressed genes, with functional enrichment in pathways related to Notch signaling, ECM–receptor interaction, glycosaminoglycan biosynthesis, and detoxification. The upregulation of genes such as HES-C, CYP1A1, GST, and UGT may be linked to the regulation of apoptosis inhibition, xenobiotic metabolism, and antioxidant defense. Furthermore, enhanced expression of NAD kinase and PNLIPRP may indicate a potential strengthening of energy metabolism and lipid utilization during stress adaptation. This study suggests that the inhibitor composition may exert a multi-level protective effect against diesel-induced injury by coordinating tissue repair, oxidative balance, and detoxification processes, offering a potential strategy to mitigate pollution impacts in sea cucumber aquaculture. Full article

Background/Objectives: Macrophages polarized into M1 and M2 phenotypes differentially regulate immune and drug responses. Despite their distinct functional roles, differences in UDP-glucuronosyltransferase (UGT) expression and enzymatic activity between M1 and M2 macrophages remain poorly understood. This study aimed to characterize differential UGT expression in M1 and M2 macrophages and to elucidate how UGT-mediated prostaglandin E₂ (PGE₂) glucuronidation modulates macrophage inflammatory responses. Methods: THP-1 cells were chemically differentiated into macrophages (M0) and subsequently polarized into M1 and M2 phenotypes. UGT expression profiles were assessed using RT-PCR, quantitative RT-PCR (qRT-PCR), and Western blot. UGT activity was compared by quantifying glucuronide metabolites derived from UGT-specific substrates using LC-MS/MS, along with measurement of free PGE₂ and PGE₂-glucuronide by ELISA. Pro-inflammatory cytokine expression and secretion in M1 macrophages were quantified using qRT-PCR and ELISA. Results: Expression of UGT1A1, UGT1A4, UGT1A5, UGT1A9, and UGT2B7 were markedly higher in M1 compared with M2 macrophages at both the mRNA and protein levels. Enhanced UGT activity in M1 macrophages was reflected by increased formation of estradiol-3-glucuronide and naloxone-3-glucuronide (both p < 0.01) and was attenuated in a concentration-dependent manner by diclofenac. Furthermore, PGE₂ glucuronidation was more pronounced in M1 macrophages, and inhibition of UGTs with atazanavir reduced PGE₂-glucuronide formation and pro-inflammatory cytokine production, including IL-1β, IL-6, and TNF-α. Conclusion: UGT-mediated PGE₂ glucuronidation in M1 macrophages contributes to the regulation of pro-inflammatory cytokine production. Collectively, these findings support a role for UGTs as modulators of inflammatory signaling, with differential expression and activity between M1 and M2 macrophages. Full article

UDP-glycosyltransferases (UGTs) represent a large multigene family that play a central role in glycosylating a highly diverse array of natural products, underscoring their critical importance in various biological processes. However, the functional roles of a substantial majority of UGTs remain to be elucidated. In the present study, we characterized the glycosyltransferase UGT78G3, a member of the UGT78 glycosyltransferase family in the model legume Medicago truncatula. Amino-acid sequence analysis revealed a conserved PSPG motif at the C-terminus of UGT78G3. Liquid chromatography-coupled tandem mass spectrometry (LC-MS/MS) analysis demonstrated that UGT78G3 catalyzes the formation of kaempferol 3-O-glucoside in vitro. However, neither UGT78G3 overexpression nor CRISPR/Cas9-mediated mutagenesis resulted in significant changes to the endogenous levels of kaempferol 3-O-glucoside, indicating that UGT78G3 does not play a predominant role in the biosynthesis of kaempferol 3-O-glucoside in vivo. Our findings identify a putative glycosyltransferase in M. truncatula and provide a target for biocatalyst design aimed at synthesizing flavonoid glucosides. Full article

The sugar beet (Beta vulgaris L.) industry in China occupies a pivotal position in the national sugar supply, yet drought in its major cultivation areas has become a key limiting factor for its high-quality development. Glycosyltransferases (GTs) play a pivotal role in plant responses to abiotic stress, particularly in the regulation of drought resistance. However, the systematic identification of the BvUGT90 gene family in sugar beet and the functional characterization of its members under drought stress remain largely unexplored. In this study, drought stress was simulated in the sugar beet cultivar ‘HI0466’ using the weighing method to regulate soil moisture. Samples were collected at different stress durations and after rewatering for subsequent experimental analyses. In this study, 121 members of the BvUGT90 family were identified in sugar beet, and a comprehensive analysis was conducted on their gene structures, phylogenetic relationships, promoter cis-acting elements and expression patterns under drought stress. The results showed that these 121 members were unevenly distributed across 9 chromosomes. The proteins they encode had an average amino acid length of 474, with molecular weights ranging from 10.78 to 99.10 kDa and theoretical isoelectric points (pI) from 4.68 to 8.69 (with an average of 5.76). Notably, 110 of these members (accounting for 90.91%) were identified as hydrophilic proteins. Synteny analysis indicated a high degree of homology between the BvUGT90 family members in sugar beet and their orthologous genes in Arabidopsis thaliana. Analysis of promoter cis-acting elements revealed the presence of six major categories of core elements in the promoter regions of BvUGT90 genes, including hormone-responsive elements, stress-responsive elements and pathway regulatory elements. Transcriptomic data showed that 45 BvUGT90 family members exhibited significant responsiveness to drought stress. Proteomic analysis demonstrated that 10 of these members were significantly upregulated at the protein level under drought stress, and these results were further validated by quantitative real-time polymerase chain reaction (qRT-PCR). Integrated transcriptomic and proteomic analyses identified Bv_005070_jjst.t1 and Bv6_140060_stjc.t1 as the family members with the most prominent responses to drought stress. Furthermore, transgenic transformation of sugar beet was performed, which confirmed that Bv_005070_jjst.t1 plays an important role in drought stress resistance. The findings of this study provide direct candidate genes from this family for drought-tolerant sugar beet breeding. Full article

Resveratrol is a promising ingredient in functional food products, but its low bioavailability and solubility hinder its application. Polydatin, a 3-OH glycosylation of resveratrol, has been shown to exhibit enhanced bioavailability and more favorable physicochemical properties. In this work, a continuous-flow microreactor was developed to synthesize polydatin using resveratrol and a mutant glycosyltransferase (UGT_BS) as the substrate and biocatalyst, respectively. All reaction orders were determined to elucidate the possible reaction mechanism. To further reduce the process costs, a dual enzyme coupling reaction system was developed to enable the in situ regeneration of UDP-Glc. Full article

Emodin, a trihydroxy-methyl anthraquinone abundant in rhubarb, Polygonum species, and other medicinal plants, exemplifies the therapeutic potential and translational complexity of the broader anthraquinone scaffold. Anthraquinone derivatives have demonstrated antiproliferative, anti-inflammatory, metabolic, cardiovascular, antifibrotic, and immunomodulatory effects, consistently reported across diverse preclinical models, targeting pathways such as NF-κB, PI3K/AKT, MAPKs, AMPK, PPARs, NLRP3, and ferroptosis-related axes. Despite strong preclinical efficacy, clinical development has been limited by unfavorable absorption, distribution, metabolism, and excretion (ADME) characteristics, including poor aqueous solubility, extensive first-pass glucuronidation, and active efflux via intestinal and hepatic transporters. These features result in low and variable systemic exposure, while high local concentrations, particularly in the gastrointestinal tract, contribute to context-dependent toxicity signals that complicate risk assessment. The present review integrates pharmacological, toxicological, and formulation-focused evidence to provide a unified assessment of emodin and the anthraquinone scaffold. Particular emphasis is placed on bidirectional, dose- and context-dependent effects on the liver and kidney; the modulation of cytochrome P450 enzymes, UGTs, and transporters; and emerging preclinical formulation strategies that aim to decouple intrinsic bioactivity from pharmacokinetic limitations. Full article

The exceptional adaptability of insects to diverse food sources is central to their survival and evolutionary success. However, the molecular mechanisms underlying this rapid adaptation remain largely uncharacterized. In this study, adaptive phenotypic, transcriptomic, and metabolomic differences in silkworms fed mulberry leaves versus artificial diets were investigated. The results showed that dietary changes induced enrichment of multiple detoxification pathways in the fat body, midgut, and Malpighian tubules, accompanied by significant accumulation of secondary metabolites and xenobiotics such as flavonoids, terpenoids and saponins in these tissues. Stimulation experiments with nine upregulated metabolites in silkworm BmE cells revealed that most metabolites inhibited cell viability and induced detoxification genes such as GST, UGT and CYP upregulated, with flavonoids like genistein and daidzin exhibiting obvious inductive effects. Among the upregulated genes, GSTd2 frequently responded and was significantly upregulated in artificial diet-fed silkworms. Notably, overexpressing GSTd2 in BmE cells enhanced cell tolerance to genistein and daidzin. Furthermore, silkworms overexpressing GSTd2 showed higher flavonoid tolerance and better adaptability to artificial diets. In conclusion, this study provides valuable genetic targets for improving silkworm rearing efficiency on artificial diets, providing reference to optimize feed formulations and theoretical basis for understanding metabolic adaptation mechanisms to artificial diets in silkworms. Full article

Browning is the major physiological cause of quality loss in lotus root. This study explored the effects of temperature (4 °C, 25 °C, 35 °C) or ethylene (ET) on quality, especially browning, as well as polyphenol and starch metabolism in lotus root. Low temperature (4 °C) reduced browning and color changes (L*, a*), while retaining water and vitamin C (Vc) content. ET maintained Vc and soluble protein, while high temperature (35 °C) promoted total soluble solids (TSS) and soluble sugar accumulation. ET or 35 °C upregulated polyphenol metabolism-related genes including NnPAL1/4, NnCHS1, NnF3H and NnANR, increased total phenolic and flavonoid content, and enhanced antioxidant capacity. Moreover, 35 °C increased PAL activity, and ET also upregulated NnUGT88B1. Furthermore, 4 °C downregulated NnGBE1-1/2, promoted starch accumulation, while ET upregulated NnSSI, downregulated NnGBE1-1/2, and delayed starch decline. Meanwhile, ET elevated NnETR and NnEBF1-2 and mediated ethylene signaling transduction. In conclusion, 4 °C storage was optimal for delaying browning and starch metabolism of lotus root. Meanwhile, ET treatment or 35 °C were more beneficial to obtain more phenolics and flavonoids. Full article

Background/Objectives: Sacituzumab govitecan (SG) releases SN-38, the same active metabolite as irinotecan, thereby sharing key metabolic pathways and toxicity mechanisms. The clearance of SN-38 is strongly influenced by UGT1A1 polymorphisms, particularly the UGT1A1*28 allele. While UGT1A1*28 genotyping routinely guides irinotecan dosing, no such recommendations exist for SG. This study describes the relationship between UGT1A1*28 and severe SG-related toxicity in real-world practice, identifying early safety signals and exploring the clinical and economic impact. Methods: This retrospective observational study (2021–2025) included patients with metastatic breast cancer treated with SG and patients with advanced gastrointestinal malignancies treated with irinotecan at a tertiary hospital. In the SG cohort, genotyping followed grade ≥3 toxicity; in the irinotecan cohort, it was performed prospectively. Toxicity (Common Terminology Criteria for Adverse Events version 5.0) and healthcare costs related to hospitalizations were estimated using official institutional tariffs. Results: All nine SG patients with severe toxicity (100%) carried the UGT1A1*28 allele. In the irinotecan cohort (n = 74), which was managed with genotype-guided dosing, severe toxicity and hospitalization were less frequent. SG was associated with higher mean costs per treated patient (€2817.01 vs. €1233.63), driven by toxicity-related admissions (33.3% vs. 10.8%). Genotyping costs (€10.51) were negligible compared to daily hospitalization expenses (up to €1984.90). Conclusions: Severe SG-related toxicity reveals a consistent UGT1A1*28-associated vulnerability. Given the drug’s recent approval in Spain, these data represent an urgent real-world safety signal. The marked disparity between low genotyping costs and high hospitalization expenses supports implementing preventive UGT1A1 testing to optimize the safety and sustainability of sacituzumab govitecan therapy. Full article