Chithravel Vadivalagan

Hepatocellular Carcinoma (HCC) arising from Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is an increasing public health burden with high mortality, highlighting the need for improved early detection strategies. Current surveillance tools, including Alpha-fetoprotein (AFP) and ultrasound, lack sufficient sensitivity for early-stage HCC detection. We analyzed serum samples from 131 patients, including 58 with cirrhosis and 73 with MASLD-related HCC (42 early-stage, 31 late-stage), using an nLC-stepped HCD-PRM-MS/MS workflow for targeted N-glycome profiling of glycopeptides derived from haptoglobin and vitronectin. Combining targeted glycopeptides with AFP significantly improved HCC detection compared with AFP alone. The optimal panel for all HCC versus cirrhosis (AFP + VTNC_169_A2G2F0S1 + VTNC_242_A3G3F2S2) achieved an AUC of 0.859 and 76.7% sensitivity at 90% specificity. For early-stage HCC, AFP + HP_184_A3G3F1S3 + VTNC_169_A2G2F0S1 yielded an AUC of 0.890 with 66.7% sensitivity at 1% specificity. A SHAP-selected Gaussian Naive Bayes model based on seven molecular/glycopeptide features, without demographic variables, further improved performance, achieving ROC-AUC values of 0.9985 in training and 1.0000 in independent testing cohorts, with accuracies of 98.1% and 100.0%, respectively. GRAPHICAL

Coenzyme Q₀ (CoQ₀), a quinone derivative from Antrodia camphorata, has antitumor capabilities. This study investigated the antitumor effect of noncytotoxic CoQ₀, which included NLRP3 inflammasome inhibition, anti-EMT/metastasis, and metabolic reprogramming via HIF-1α inhibition, in HNSCC cells under normoxia and hypoxia. CoQ₀ suppressed hypoxia-induced ROS-mediated HIF-1α expression in OECM-1 and SAS cells. Under normoxia and hypoxia, the inflammatory NLRP3, ASC/caspase-1, NFκB, and IL-1β expression was reduced by CoQ₀. CoQ₀ reduced migration/invasion by enhancing epithelial marker E-cadherin and suppressing mesenchymal markers Twist, N-cadherin, Snail, and MMP-9, and MMP-2 expression. CoQ₀ inhibited glucose uptake, lactate accumulation, GLUT1 levels, and HIF-1α-target gene (HK-2, PFK-1, and LDH-A) expressions that are involved in aerobic glycolysis. Notably, CoQ₀ reduced ECAR as well as glycolysis, glycolytic capability, and glycolytic reserve and enhanced OCR, basal respiration, ATP generation, maximal respiration, and spare capacity in OECM-1 cells. Metabolomic analysis using LC-ESI-MS showed that CoQ₀ treatment decreased the levels of glycolytic intermediates, including lactate, 2/3-phosphoglycerate, fructose 1,6-bisphosphate, and phosphoenolpyruvate, and increased the levels of TCA cycle metabolites, including citrate, isocitrate, and succinate. HIF-1α silencing reversed CoQ₀-mediated anti-metastasis (N-Cadherin, Snail, and MMP-9) and metabolic reprogramming (GLUT1, HK-2, and PKM-2) under hypoxia. CoQ₀ prevents cancer stem-like characteristics (upregulated CD24 expression and downregulated CD44, ALDH1, and OCT4) under normoxia and/or hypoxia. Further, in IL-6-treated SG cells, CoQ₀ attenuated fibrosis by inhibiting TGF-β and Collagen I expression and suppressed EMT by downregulating Slug and upregulating E-cadherin expression. Interesting, CoQ₀ inhibited the growth of OECM-1 tumors in xenografted mice. Our results advocate CoQ₀ for the therapeutic application against HNSCC.

Biosurfactant is a biodegradation accelerator that improves bioavailability and facilitates degradation by microorganisms. The study was meant to produce a novel biosurfactant molecule from Bacillussafensis YKS2. An efficient biosurfactant-producing strain, namely, Bacillus safensis YKS2, was selected using hemolytic activity, drop collapsing test, oil spreading test and blue agar plate methods in four oil-degrading strains isolated from a soil sample. Biosurfactant production in the optimization of bacteria culture conditions by RSM is a statistical grouping technique that is analyzed using the AVOVA approach to surface tention. In addition, the study was characterized by UV spectrophotometer FT-IR, HR-SEM, and GC-MS analyses to explain its structural and chemical details. Wastewater treatment was monitored for pH, EC, turbidity, alkalinity, chemical oxygen demand (COD), biochemical oxygen demand (BOD) and dissolved oxygen (DO) in order to justify the efficacy of the biosurfactant during wastewater treatment. The results of the UV spectrophotometer showed absorption at 530 nm, and the FT-IR analyzed carboxylic acids, alcohol and phenols groups, whichthe GC-MS analysis indicated were lipopeptide purified by hexadecanoic andtetradecanoic processes, respectively. The results show that the wastewater removal efficiency of 70% wasachieved within 24 h. In comparison, metagenomics was conducted during the treatment process to identify changes in the microbial load and diversity, which essentially indicatethe biosurfactant performance of the wastewater treatment process. The microbial load in the treated biosurfactant wastewater (84,374 sequences) was greatly decreased compared to untreated wastewater (139,568 sequences). It was concluded that B. safensis YKS2, producing a glycolipid form of biosurfactant, has possible benefits in the remediation of wastewater, and can be used for large-scale processing inbiosurfactant industries.

Recent evidences have demonstrated that bio‐macromolecule assisted nanomaterials syntheses have been widely used for cancer treatment. The aim of this study was to investigate the effects and cellular mechanisms of silymarin‐routed synthesis of selenium nanowires (SeNWs) on cytotoxic and cell migration inhibitory potential against triple negative breast cancer (MDA‐MB‐231) cells. Characterizations of SeNWs were detected by XRD, scanning electron microscopy, and Raman spectrum. Cell proliferation and migration of MDA‐MB‐231 cells were evaluated by MTT and wound assays respectively. The study revealed that SeNWs significantly suppressed the cell viability and cell migration potential compared with the control group. Moreover, SeNWs significantly induce the apoptotic induction in triple negative breast cancer cells. Overall, the current findings highlight the potential cancer therapeutic applications of SeNWs in in vitro condition.

Leucinodes orbonalis Guenée is serious quarantine pest occurring globally, studies are needed to enlighten the genetic complexities associated with the species. India is considered to be the origin of the L. orbonalis, therefore availability of species records from this region enable to analyse the genetic differences and dispersal of the lineages. The results of the study reported 47 haplotypes in four clusters pertaining to their ancestral lineage. The transition/transversion bias (R) was observed to be higher with 1.238 and 1.312 in the first and third codon positions respectively. The overall intraspecies divergence was found to be 0.302. AMOVA revealed that the total variations were then as reported 67.15 among the south-east countries but our studies reported the total variation to be 77.25% (Germany, India, South east and Australia). F_ST and Mantel’s test indicated that there was no correlation between the genetic variation and geographical distance. The overall haplotype diversity was 0.852, where the nucleotide diversity of H31 (0.00593) was highest and H1 (0.00087) was lowest. The genetic diversity indices Tajima D and Fu's Fs static for H1, H13 and H31 had negative values which possibly inferred for the bottle neck effect. The ML tree was constituted the branch length of 5.0157 with one out-group. The tree was formed with ten distinctive clades with the haplotypes congregated together based on similar genetic composition.