Searches / Cellular And Molecular Biology (Noisy-le-Grand, France)[JOURNAL]

Cellular And Molecular Biology (Noisy-le-Grand, France)[JOURNAL]

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Effect of traction force during surgery on physical integrity and histological changes in peripheral nerves: experimental study on rabbits.

Mohammed RH, Khrwatany KAK, Hassan SMA

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976918 · Publisher ↗

Sensory and motor nerve damage is a common complication of maxillofacial surgery and trauma. Procedures such as orthognathic surgery, tumor resection, and salivary gland interventions can damage peripheral nerves when th... Sensory and motor nerve damage is a common complication of maxillofacial surgery and trauma. Procedures such as orthognathic surgery, tumor resection, and salivary gland interventions can damage peripheral nerves when the surrounding soft tissue or the nerve itself is manipulated. The purpose of this study was to evaluate the histological changes in the sciatic and median nerves of albino rabbits following traction-induced nerve injury. Nine albino rabbits were included in the study and divided equally into three groups, with three rabbits per group. In each rabbit, four peripheral nerves were exposed: the right and left sciatic nerves and the right and left median nerves. In Group A, varying traction forces (0.5 N, 1 N, 1.5 N, and a control of 0 N) were applied to each nerve for 5 minutes. The same traction forces used in Group A were applied to Groups B and C for 10 minutes and 15 minutes, respectively. Nerve fiber abnormalities, as well as damage to the axons, myelin sheath, and connective tissue layers, were assessed through histological examination. Histopathological evaluation of the injured nerves revealed Grade I and Grade II nerve injuries in Group A, while Grade IV and Grade V nerve injuries were noted in Groups B and C, respectively, based on the criteria established by the histopathologist.

Effect of vgb gene on microbial chondroitin sulfate production in recombinant Escherichia coli pETM6-PACF-vgb and physicochemical characterization of produced chondroitin sulfate.

Erenler AS, Unver T, Ceylan AF … +2 more , Ozcan I, Geckil H

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976917 · Publisher ↗

Chondroitin Sulfate (CS) is an essential component of the extracellular matrix and is a sulfated glycosaminoglycan structurally composed of a polysaccharide chain consisting of N-acetyl galactosamine and glucuronic acid.... Chondroitin Sulfate (CS) is an essential component of the extracellular matrix and is a sulfated glycosaminoglycan structurally composed of a polysaccharide chain consisting of N-acetyl galactosamine and glucuronic acid. The use of CS of animal origin is common in pharmacological research. The disadvantages of traditional sources and methods used in the production of CS, which is used in various applications in the medicine, veterinary, pharmacy, and cosmetic sectors, have made microbial production a vital alternative. In this study, recombinant Escherichia coli (pETM6-PACF-vgb) strain, in which kfoA, kfoC, kfoF and vgb gene regions are co-expressed, and E. coli pETM6-PACF strain, which does not contain the vgb gene, were used in the microbial production of CS. The vgb gene is the region responsible for expressing the bacterial protein Vitreoscilla hemoglobin (VtHb). This study investigated the effect of the expression of VtHb in E. coli on increasing bacterial cell respiration and, therefore, how ATP production would affect cell growth and the acquisition of chondroitin and microbial chondroitin sulfate (MCS) from biomass. The analysis results determined a 23.07% increase in the amount of MCS produced from the vgb+ strain. The presence of vgb had positively affected culture age and reproductive kinetics. Spectrophotometric measurements, NMR, HPLC, FT-IR, TGA, DTA, and DSC analyses for the reproductive values ​​and physicochemical characterization of the obtained MCS were applied to discuss this production process. For more detailed results on this subject, future research focused on optimization is needed.

Long non-coding RNA LINC00520 promotes malignant progression of gastric adenocarcinoma through miR-519b-3p/HIF1A axis.

An J, Niu Y, Liu W

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976916 · Publisher ↗

Gastric cancer is a prevalent malignant tumor, characterized by high morbidity and mortality rates globally. Long non-coding RNAs (lncRNAs), a class of transcripts exceeding 200 nucleotides in length, are non-protein-cod... Gastric cancer is a prevalent malignant tumor, characterized by high morbidity and mortality rates globally. Long non-coding RNAs (lncRNAs), a class of transcripts exceeding 200 nucleotides in length, are non-protein-coding molecules that exert crucial regulatory functions in cellular biology. Investigating the regulatory mechanisms of lncRNAs in gastric cancer is essential. This study aimed to elucidate the functional role and molecular mechanisms of LINC00520 in gastric cancer. Initially, the GEO database was screened for differentially expressed genes associated with the malignant progression of gastric cancer. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was utilized to ascertain the LINC00520 expression in gastric cancer tissues. Subsequently, cellular functional assays were conducted to investigate the potential effects of LINC00520 on cellular behavior. The interaction between LINC00520, miR-519b-3p, and HIF1A was examined through bioinformatics analysis, and their binding interactions were confirmed using dual-luciferase reporter gene assays and RNA immunoprecipitation (RIP) assays. Our findings revealed a marked increase in the LINC00520 expression in gastric cancer tissues. Overexpression of LINC00520 was observed to enhance the malignant progression of gastric cancer cells. Through bioinformatics analysis, dual-luciferase reporter assays, and RIP assays, we demonstrated that LINC00520 upregulated HIF1A expression by competitively binding to miR-519b-3p, thereby acting as a molecular sponge. In conclusion, this study indicates that LINC00520, which is highly expressed in gastric cancer, exerts its effects by targeting the miR-519b-3p/HIF1A axis. These insights provide a foundation for developing diagnostic and therapeutic strategies for gastric cancer.

Notch/IL33/ST2 signaling was involved in the maintenance of intestinal epithelial barrier through regulating tight junction after LPS stimulation.

Zhang Y, Xu C, Li F … +1 more , Chen G

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976915 · Publisher ↗

Interleukin-33(IL33), an alarm cytokine of the IL-1 family, is expressed mainly in epithelial cells of barrier tissues and is involved in the repair of epithelia to maintain barrier function. However, the mechanisms regu... Interleukin-33(IL33), an alarm cytokine of the IL-1 family, is expressed mainly in epithelial cells of barrier tissues and is involved in the repair of epithelia to maintain barrier function. However, the mechanisms regulating IL33 expression and the mechanisms by which IL33 regulates the intestinal barrier function are not fully clarified. In this study, Caco-2 cells and siRNA were applied to investigate the role of Notch/IL33/ST2 Signaling in regulating intestinal epithelial barrier function, which was demonstrated by protein expression of tight junctions and trans-epithelial resistance (TER) assay. Our results revealed that Notch signaling pathway was activated and IL33 expression was up-regulated after LPS stimulation. After blocking Notch signaling with DPAT or siRNA for Notch1, IL33 expression was significantly down-regulated in Caco-2 cells. The protein expression of tight junctions (ZO-1, occludin, and claudin-1) was down-regulated after siRNA for IL33 in Caco-2 cells with LPS stimulation. Also, the intestinal epithelial TER was down-regulated after siRNA for IL33 with LPS stimulation or not. Exogeneous IL33 promoted the tight junction protein expression and increased the TER. Finally, our data further showed that IL33 regulates intestinal epithelial barrier function through the ST2 receptor. In conclusion, our results indicated that IL33/ST2 axis, which was activated by the Notch signaling, maintains intestinal epithelial barrier function through regulating tight junction protein expression under inflammatory conditions. This study provides a new therapeutic pathway of regulating intestinal epithelial barrier dysfunction.

Comparative renoprotective effect of Tamarix dioica leaf extracts and metformin against acetaminophen-induced renal toxicity in Swiss albino mice: Novel insights on renoprotection and therapeutic potential.

Albalawi AE, Aggad WS, Alharbi FKR … +10 more , Almuhimed RM, Alhuwaymil Z, Almohaimeed HM, Mohammedsaleh ZM, Alhasani RH, Alsharif I, Al-Abbas NS, A Shaer N, Mavromatis C, Soliman MH

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976914 · Publisher ↗

Nephrotoxicity is characterized by the adverse effects on kidney function caused by various substances, including hazardous chemicals and drugs. This study aimed to investigate the neuroprotective properties of aqueous,... Nephrotoxicity is characterized by the adverse effects on kidney function caused by various substances, including hazardous chemicals and drugs. This study aimed to investigate the neuroprotective properties of aqueous, methanolic, and ethanolic extracts of Tamarix dioica leaf against acetaminophen-induced kidney damage and compare their efficacy with metformin, a known neuroprotective agent. Thirty-six albino mice were randomly divided into six groups, including a standard control group, an acetaminophen-toxified group, a positive control group treated with metformin (at a dose of 200 mg/kg body weight), and three experimental groups treated with aqueous, methanolic, and ethanolic T. dioica extracts (at a dose of 400 mg/kg body weight each). The neuroprotective potential of the T. dioica extracts was assessed by evaluating hematological markers, electrolyte levels (Na+, K+, Cl-), antioxidant enzymes (CAT, SOD, MDA), renal function tests (urea and creatinine), and toxicity markers (SGOT and SGPT). Additionally, histopathological analysis was conducted to observe any pathological changes in kidney tissues stained with hematoxylin and eosin. The results demonstrated that the T. dioica leaf extracts effectively restored all the indicators and antioxidant enzyme levels to normal, significantly differing from the elevated levels observed in the acetaminophen control group (p < 0.05). Furthermore, histopathological examination revealed regeneration of glomeruli and renal tubules in the stained tissues. These findings suggest that T. dioica leaf extracts can potentially mitigate acetaminophen-induced nephrotoxicity.

Genome-wide identification: molecular characterization and evolutionary aspects of Sox genes in Nile tilapia.

Khan MF, Sultana M, Parveen S … +8 more , Hassan W, Tayyab M, Mashahour Fawwaz Alenazi, Alanazi Khalid Zabena, Xu Y, Hong Z, Zhu P, Shafique L

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976913 · Publisher ↗

Nile tilapia has become one the most significant species in global aquaculture due to its exceptional adaptability, rapid growth and high reproductive capacity. Role of Sox genes in reproduction and development made atte... Nile tilapia has become one the most significant species in global aquaculture due to its exceptional adaptability, rapid growth and high reproductive capacity. Role of Sox genes in reproduction and development made attention to further investigate the role of these genes. Based on N. tilapia importance in aquaculture industry and role of Sox genes in the development of tissues and organs during embryogenesis, this study systematically analyzed Sox genes functionality in N. tilapia by using computational tools. In our study, phylogenetic analysis revealed that N. tilapia is most closely related to blue tilapia compared to other species. Sox genes are conserved in nature and share both acidic and basic properties as well as thermostable and hydrophobic in nature. The subcellular localization in N. tilapia indicated that majority of the Sox proteins are expressed in the Nucleus and Cytoplasm. Enrichment analysis explains the Sox genes' role in cell differentiation, and biosynthesis process and acts as a molecular functional regulator. Significant differences in transcription binding sites were observed, highlighting the potential role of these regulatory regions in the regulation of Sox genes in N. tilapia. First time it is reported that Sox genes in N. tilapia have four major recombinant breakpoints that revealed phylogenetic segregation across several recombination fragments. In this primer, we aim to provide the reader with a comprehensive overview of Sox gene family in N. tilapia and to provide the functional properties of Sox genes for better follow-up in upcoming experiments for futuristic research.

Combined use of WNT signal pathway inhibitor FH535 and docetaxel causes mitotic catastrophism and antiproliferative effect in non-small cell lung cancer.

Avşar EN, Çetin İ

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976912 · Publisher ↗

The development of treatment methods used in the treatment of non-small cell lung cancer (NSCLC) is important to prevent problem of increasing mortality. However, the treatment methods used in clinical settings at the cl... The development of treatment methods used in the treatment of non-small cell lung cancer (NSCLC) is important to prevent problem of increasing mortality. However, the treatment methods used in clinical settings at the clinic are insufficient to eliminate this problem. For this purpose, it was aimed to determine whether the combination of docetaxel (DTX) and FH535 can be used as an anticancer agent candidate in A549 cells and whether it is a candidate drug combination that can be used in clinical treatment after in vivo studies. FH535 is a WNT signaling pathway inhibitor and is known to be overactive in NSCLC. In this study, the effects of DTX and WNT signaling pathway inhibitor FH535 used in NSCLC treatment on A549 and BEAS-2B cell lines were evaluated at the cellular level. While increasing the anticancer activity in A549 cells, the doses showing minimum toxic effect in BEAS-2B cells were determined by Real Time Cell Analysis method. Mitotic activity, BrdU cell proliferation assay and caspase 3,7 activity assay were performed for detailed analysis of the combination dose at cellular level. The results show that the combined dose had an antimitotic effect on A549 cells, causing mitotic catastrophism, while in BEAS-2B cells neither agent was more toxic than either agent alone, reducing mitotic activity and BrdU activity, leading the cell to mitotic catastrophism, while caspase 3,7 activity was unchanged. This study demonstrated for the first time the effects of the combination of DTX and FH535 on A549 and BEAS-2B cell lines.

Exploring IFN-γ +874T/A gene polymorphisms among suspected tuberculosis cases in Ouagadougou, Burkina Faso.

Sagna T, Sana WYA, Traore L … +15 more , Compaore TR, Soubeiga ST, Kekoura I, Zabre P, Kiemde SN, Zida S, Cisse K, Kambire D, Ouedraogo O, Traore IMA, Ky Ba A, Combary A, Ouedraogo HG, Kouanda S, Simpore J

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976911 · Publisher ↗

Interferon-gamma (IFN-γ) plays a crucial role in resistance to mycobacterial infections, as it is a regulatory cytokine that acts as a pro-inflammatory mediator. Consequently, variants in the gene encoding this cytokine... Interferon-gamma (IFN-γ) plays a crucial role in resistance to mycobacterial infections, as it is a regulatory cytokine that acts as a pro-inflammatory mediator. Consequently, variants in the gene encoding this cytokine may be associated with a high risk of contracting pulmonary tuberculosis. The present study aimed to investigate the genetic susceptibility of polymorphisms in the gene coding for IFN-γ to infection by Mycobacterium tuberculosis in Burkina Faso. This cross-sectional study was conducted from May 2023 to January 2024. Venous blood was collected from suspected cases. Tuberculosis was confirmed by GeneXpert (CEPHEID). Human genomic DNA was extracted using the salting-out extraction technique, followed by the amplification and genotyping of IFN-γ gene polymorphisms,through the conventional PCR. Statistical analyses were performed using the SPSS and Epi info software. A total of 168 participants were included in the study, with an average age of 38.58 ±14.88, the majority of whom were men (76.19%). In our study population, 73.2% (123/168) were confirmed positive for tuberculosis. Some 46.4% (78/168) of the previous cases were contacts. Of these contact cases, 82.05% (64/78) were GeneXpert positive. The genotypic frequencies of the IFN-γ gene were distributed as follows: 73.3% (AA), 21.8% (AT) and 4.9% (TT), with a frequency of 84.2% for the A allele versus 15.8% for the mutated T allele. No statistically significant association was found between IFN-γ gene polymorphisms and M. tuberculosis infection in Burkina Faso. IFN-γ gene polymorphisms (IFN +874T/A) do not appear to be associated with M. tuberculosis infection in Burkina Faso.

Impact of metformin therapy on serum visfatin levels in polycystic ovary syndrome: a systematic review and randomized permuted meta-analysis.

Reddy EP, Thangappazham HR, Patnaik N … +7 more , Duggina P, Kumar KL, Varshney S, Grover A, Gupta P, Mishra KG, Varikasuvu SR

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976910 · Publisher ↗

Visfatin, an, is associated with reproductive and metabolic disorders like polycystic ovary syndrome (PCOS). Although visfatin levels are known to be elevated in PCOS, the effect of metformin treatment on these levels re... Visfatin, an, is associated with reproductive and metabolic disorders like polycystic ovary syndrome (PCOS). Although visfatin levels are known to be elevated in PCOS, the effect of metformin treatment on these levels remains unclear. This meta-analysis aimed to assess changes in circulating visfatin levels before and after metformin intervention in PCOS patients. Relevant studies were identified through comprehensive searches, and a random-effects meta-analysis was conducted to calculate standardized mean differences (SMDs) with 95% confidence intervals (CIs). Sensitivity analysis and randomized permuted meta-analyses (with 1,000, 10,000, and 100,000 iterations) were performed to validate the findings. The analysis included four studies and showed a significant reduction in visfatin levels following metformin treatment (SMD: -0.45, 95% CI: -0.76 to -0.14, p = 0.0043). These results highlight metformin's impact on visfatin levels in PCOS, though larger trials are needed to further explore visfatin's role as a therapeutic target in PCOS.

Biological effects of L-carnitine on ovine oocyte maturation and embryo development.

Darzi Nia A, Zandi M, Ghaedrahmati A

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976909 · Publisher ↗

This study was conducted to determine the effects of L-carnitine on in vitro ovine maturation and early embryo development. In the first experiment, oocytes were matured in TCM-199 medium with different concentrations of... This study was conducted to determine the effects of L-carnitine on in vitro ovine maturation and early embryo development. In the first experiment, oocytes were matured in TCM-199 medium with different concentrations of L-carnitine (0, 0.125, 0.25, 0.5, 1, 2, and 4 mM) and after fertilization, presumptive zygotes were cultured for 9 days on mCR2aa medium. In the second experiment, oocytes were matured in a maturation medium with various concentrations of L-carnitine (0, 0.125, 0.25, 0.5, 1, 2, and 4 mM). After fertilization, presumptive zygotes were cultured in a culture medium containing various L-carnitine concentrations (0, 0.125, 0.25, 0.5, 1, 2, and 4 mM).  In vitro maturation (IVM) was carried out in a humid atmosphere of 5% CO2, 5% O2, and 90% N2 at 38.5 °C, and for in vitro culture (IVC), the concentration of O2 decreased to 5%. Morula and blastocyst development was evaluated on days 5 and 9, respectively. The results of the first experiment showed that the concentrations of 0.125, and 0.25 mM L-carnitine numerically led to an increase in the percentage of morula, blastocyst, and hatched blastocyst compared with control. The percentage of blastocyst formation increased at concentrations of 0.125 mM and 0.25 mM (31.97 ± 0.74 and 31.60 ± 1.39, respectively) compared with the control treatment (29.44 ± 2.42) (p>0.05). The results of the second experiment showed that the different concentrations of L-carnitine, simultaneously in the maturation and culture media of ovine embryos, similar results were observed when it was used only in the maturation medium, and the percentage of blastocyst formation increased at concentrations of 0.125 mM and 0.25 mM (35.62 ± 0.45 and 35.04 ± 1.70, respectively) compared to the control treatment (31.56 ± 3.39) (p>0.05). In conclusion, the use of L-carnitine in the media for oocyte maturation and embryo culture is recommended.

Prenatal DEHP exposure induces hippocampal neurotoxicity in male offspring via PTEN dysregulation and impaired Akt/mTOR and NMDA signaling.

Kiknadze N, Zhuravliova E, Mikeladze D

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976908 · Publisher ↗

Widespread human exposure to phthalates is caused by their intensive usage in industrial and consumer plastic products. DEHP (di(2-ethylhexyl) phthalate) is one of the most often used phthalates and is presented not only... Widespread human exposure to phthalates is caused by their intensive usage in industrial and consumer plastic products. DEHP (di(2-ethylhexyl) phthalate) is one of the most often used phthalates and is presented not only in food and fluids but also in the air and dust contact with plastic products. Regrettably, phthalates easily migrate into the human body and act as potent toxicants, mainly on endocrine and metabolic status. In the last decade, several epidemiological studies have indicated a correlation between prenatal exposure to phthalates and adverse effects on neurodevelopment in offspring. Our research aimed to assess the impact of DEHP prenatal subchronic exposure on male offspring's behavior and learning ability and identify the primary target brain structure/s of neurotoxic action. Heightened anxiety in male offspring was evident through increased rearing, frequent line crossings, hurried movements, and reduced grooming behavior. These behaviors were accompanied by a decline in recognition memory and diminished interest in exploring novel objects. Obtained data showed that prenatal oral exposure to DEHP in a selected concentration induces irreversible changes in brain structures of the male offspring, primarily in the hippocampus, that underlies significant alterations in cognitive behavior and enhanced anxiety. The molecular mechanism of DEHP-induced hippocampal neurotoxicity in the maturing male brain involves changes in phosphatase and tensin homolog (PTEN) subcellular location, which suppresses Akt/mTOR signaling, enhances GluN2B NMDA mediated synapse depression and decreases mitochondrial fusion.

Prevalence, genotyping, and molecular relatedness of methicillin-resistant Staphylococcus aureus isolated from tertiary care hospitals in Jeddah, Saudi Arabia.

Dawoud TM, A Al-Hajjaj Y, Mubarak A … +3 more , Elbehiry A, El-Tayeb M, Moussa IM

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976907 · Publisher ↗

Methicillin-resistant Staphylococcus aureus (MRSA) is a major nosocomial pathogen causing severe morbidity and mortality in hospitals globally.Transmission of MRSA occurs within the healthcare sector as a nosocomial infe... Methicillin-resistant Staphylococcus aureus (MRSA) is a major nosocomial pathogen causing severe morbidity and mortality in hospitals globally.Transmission of MRSA occurs within the healthcare sector as a nosocomial infection, primarily facilitated by healthcare workers or patients admitted to medical facilities. The objective of this study was to evaluate the genetic characterization and similarity of MRSA strains isolated from both inpatients and outpatients who visited various healthcare facilities in Jeddah, Saudi Arabia. A total of 200 MRSA strains were isolated from participants between March 2018 and June 2019. The recovered strains were characterized using both phenotypic and genotypic methods. All isolates (n=200) tested positive for the S. aureus 16S rRNA gene, with 92.5% also testing positive for the mecA gene, while 7.5% were identified as methicillin-susceptible. Furthermore, the typing and subtyping of the staphylococcal cassette chromosome mec (SCCmec) genetic element indicated that 61.6% of the MRSA strains were classified as type III (hospital-acquired), while 32.4% were identified as type IV and 6% remained of an unknown type. Subtyping of SCCmec type IV and the detection of the Panton-Valentine leukocidin (PVL) gene were also conducted. The genetic relatedness among MRSA isolates, assessed through Random Amplified Polymorphic DNA Polymerase Chain Reaction (RAPD-PCR), revealed two primary clusters, with no discernible differentiation between outpatient and inpatient strains. Additionally, Pulsed-Field Gel Electrophoresis (PFGE) fingerprinting of the examined strains identified four major clusters. The first cluster comprised three groups (16 strains), isolated from patients with respiratory and soft tissue infections. The second cluster included two groups (12 strains), all recovered from patients with respiratory, soft tissue, and urinary tract infections (UTIs). The third and fourth clusters each contained one group (6 strains and 5 strains, respectively), all isolated from outpatients. In conclusion, Antimicrobial susceptibility testing showed significant resistance to ceftriaxone, ampicillin, and amoxicillin-clavulanic acid, with vancomycin and gentamicin being the most susceptible. Multiplex PCR identified all positive MRSA strains within hours. Most isolates were SCCmec type III and type IV. The PVL gene was found in all S. aureus isolates, especially in type IV and methicillin-sensitive strains, but not in type III. RAPD-PCR analysis revealed distinct profiles for outpatient and inpatient strains.

Targeting acetate kinase of Porphyromonas gingivalis: a computational approach to identifying novel inhibitors for endodontic infection treatment.

Boreak N, Jafari SA, Alotaibi HM … +7 more , Abbas TSA, Bokar AM, Muaddi HB, Alshammakhy R, Almughallis GA, Judayba MHA, Hakami EM

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976906 · Publisher ↗

This study explores a novel approach to treating endodontic infections by targeting the acetate kinase (Ack) enzyme of Porphyromonas gingivalis, a key pathogen in these infections. Using computational methods, we develop... This study explores a novel approach to treating endodontic infections by targeting the acetate kinase (Ack) enzyme of Porphyromonas gingivalis, a key pathogen in these infections. Using computational methods, we developed an apo receptor-based E-pharmacophore model of P. gingivalis Ack and screened the ZINC Lead-Like database containing over 1.8 million compounds. High-throughput virtual screening and molecular dynamics simulations identified ZINC001306857494 as a promising lead compound, demonstrating stable binding to the Ack active site with a binding free energy of -41.66 kcal/mol. The compound forms multiple hydrogen bonds with highly conserved residues, including Leu119, His180, and Arg241. Molecular dynamics simulations over 250 ns confirmed the stability of the protein-ligand complex, with sustained interactions throughout the simulation period. This study presents a potential new scaffold for developing Ack inhibitors, offering a promising avenue for treating endodontic infections caused by P. gingivalis.

Electronic structures of isoquercitrin and its pharmacokinetic exploration with Dengue virus 1 NS5 methyl transferase.

Alwabli AS

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976905 · Publisher ↗

An enzyme called dengue virus (DENV) non-structural protein 5 (NS5) methyltransferase (MTase) aids in the virus's replication by encasing viral RNA. Here, we report on the impact of the dengue virus (DENV) protein NS5 me... An enzyme called dengue virus (DENV) non-structural protein 5 (NS5) methyltransferase (MTase) aids in the virus's replication by encasing viral RNA. Here, we report on the impact of the dengue virus (DENV) protein NS5 methyltransferase domain (NS5-MTase). This study investigates the structural, electronic, and biological properties of isoquercitrin using Density Functional Theory (DFT). Frontier molecular orbital energies were evaluated to assess the reactivity of the compounds, while molecular electrostatic potential mapping provided insights into charge distribution. In-silico ADME and toxicity analyses were conducted to determine the drug-likeness and safety profiles of the compound. Molecular docking simulations examined the binding interactions between Isoquercitrin and its target protein. To evaluate the potential of Isoquercitrin as a drug candidate, aspects such as absorption, distribution, metabolism, excretion, toxicity (ADMET), drug-likeness, and compound accessibility were analyzed. The ADME and toxicity results revealed promising drug-like properties and low toxicity, underscoring the compound's therapeutic potential.

Immune cells mediated the causal relationship between perturbational phenotyping of human blood cells and neuropathy pain: a two-sample and mediated mendelian randomized study.

Chen Q, Zhong T, Liu J … +3 more , Cai D, Gao H, Chen M

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976904 · Publisher ↗

Current research reveals a complex relationship between blood cells(BC) and neuropathic pain(NP), though the underlying biological mechanisms remain unclear. This study applies Mendelian randomization (MR) to investigate... Current research reveals a complex relationship between blood cells(BC) and neuropathic pain(NP), though the underlying biological mechanisms remain unclear. This study applies Mendelian randomization (MR) to investigate causal relationships between BC and three major types of NP: diabetic peripheral neuropathy(PDPN), postherpetic neuralgia(PHN), and trigeminal neuralgia(TN). We also explore the potential mediating role of immune cells in these associations. We employed a two-sample, two-step Mendelian randomization study using the inverse variance weighted method to investigate the causal effect of BC on three major types of NP, as well as the mediating role of immune cells in the association between BC and NP. Additionally, we utilized a two-step Mendelian randomization design to explore the mediating effect of immune cells. We identified 13 distinct blood cell phenotypes under various perturbation conditions that have a significant causal relationship with NP. Additionally, we discovered 127 immune cells that exhibit a notable causal connection with NP. Through Mendelian Randomization (MR) and two-step Mendelian Randomization analyses, we found the following results: Three blood cell phenotypes were associated with PDPN, three with PHN, and seven with TN, with platelet, red blood cell, monocyte, and neutrophil responses showing significant correlations with NP risks. Immune cell analyses revealed 36 phenotypes increasing and 31 decreasing PDPN risk, 16 increasing and 21 decreasing PHN risk, and 18 increasing and 13 decreasing TN risk, with HLA DR on DCs, PB/PC AC, and CD39+ CD4+ %T cell showing the strongest associations, respectively. Mediation analysis identified immune cells, such as CD39+ resting Treg and HLA DR+ CD4+ %lymphocyte, mediating PBC effects on NP risks. Sensitivity analyses confirmed no significant heterogeneity or pleiotropy, and reverse MR analyses found no reverse causal relationships. This study provides new evidence for the causal relationship between blood cell phenotypes and neuropathic pain and proposes immune factors with potential mediating effects. However, this finding needs to be further demonstrated by more extensive clinical studies.

Green synthesis and antibacterial activity of silver and gold nanoparticles using crude flavonoids extracted from Bombax ceiba flowers.

Aziz N, Alhajouj SA, Basit A … +10 more , Khan IA, Alaida MF, Alzayed RM, Albalawi MA, Alshareef SA, Al-Duais MA, Sakran M, Almalki RS, El-Khouly AS, El Sabagh A

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39976903 · Publisher ↗

The present study explores the simple and eco-friendly green synthesis of silver (AgNPs) and gold (AuNPs) nanoparticles using aqueous flower extract of Bombax ceiba, commonly known as silk cotton. The extract, rich in fl... The present study explores the simple and eco-friendly green synthesis of silver (AgNPs) and gold (AuNPs) nanoparticles using aqueous flower extract of Bombax ceiba, commonly known as silk cotton. The extract, rich in flavonoids, serves as both a reducing and capping agent, facilitating the synthesis of metal nanoparticles. The synthesized nanoparticles were characterized using UV spectroscopy and scanning electron microscopy (SEM), confirming their formation and stability. The antibacterial activity of the AgNPs, AuNPs, and crude flavonoids was evaluated against several bacterial strains, including Salmonella typhi, Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus aureus, using the agar well diffusion method. Our results show that AgNPs exhibit significant antibacterial activity, particularly against Gram-negative bacteria, with a marked zone of inhibition observed for S. typhi and E. coli. The inhibition zone increased with higher concentrations of AgNPs. In contrast, AuNPs and flavonoid solutions demonstrated only mild antibacterial effects, with no significant inhibition observed at lower concentrations (1-6 µL). The antibacterial efficacy of AgNPs was comparable to that of standard antibiotics, such as Azithromycin for Gram-positive bacteria and Ciprofloxacin for Gram-negative bacteria, suggesting their potential as effective antimicrobial agents. The antibacterial activity of the synthesized nanoparticles and the crude flavonoid extract highlights the promising use of Bombax ceiba flower extract in the green synthesis of metal nanoparticles with potential biomedical applications.

Dendrimers as drug delivery vehicles: a comprehensive review.

Zorab MM, Qadir AM, Ahmed AMA

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39910946 · Publisher ↗

Dendrimers are chemical compounds that have functional groups on their surface and a hyperbranched structure. It is simple to promote the functionality of dendrimers and produce a variety of biocompatible products by alt... Dendrimers are chemical compounds that have functional groups on their surface and a hyperbranched structure. It is simple to promote the functionality of dendrimers and produce a variety of biocompatible products by altering their terminal groups. These materials have exceptional physicochemical characteristics that make them more beneficial in the administration of medications. They have a vigorous amount of potential as agents for nanomedicine applications because of their rare properties, which compose internal cavities, strong reactivity, globular form, solubility in water, and nanoscale size. They might also be synthesized easily. In-depth information about dendrimer composition and classifications, synthesis, and applications in nanomedicine, particularly drug delivery, is mentioned in this paper. Dendrimers are chiefly categorized by their functional groups, which permit for concise encapsulation of active compounds and structural imitatively of biomaterials. A rare property not often seen in other polymers serves to stabilize the surface of dendrimers to broaden their solubility in water. Dendritic molecules own a different variety of applications, such as dendrimers, dendrons, dendronized polymers, and hyperbranched polymers, which are organized based on their molecular weight. The role-play of dendrimers' is the capability to attach a broad range of chemical entities and their ability to shift pharmacokinetic and pharmacodynamic features through tailored drug delivery. To sum up, this study bolded how dendrimers' intricate structure and versatility make them excellent drug delivery vehicles since they may exactly modify their properties to reach special requirements. Drugs can be aimed at neuroinflammatory disorders and made more soluble and stable by dendrimers, which also deliver for a diversity of modes of delivery.  Additionally, they show attractive ability in gene transfection and sensor production, drawing near their potential for a difference of usages in industries including pesticide delivery and medicine. With the potential to send out gene therapy, medicine delivery, and other specialties of science and medicine, dendrimers are becoming a huge crucial in the pharmaceutical and medical industries through the next research and clinical investigations.

Biochemical profiling and antioxidant evaluation of Martynia annua and Polygonum viviparum: investigating hepatoprotective properties against abiotic stress.

E-Habiba U, Qureshi ZH, Farooq B … +12 more , Jabeen R, Kazmi MB, Qammar N, Rafi Qamar, Hafiz Muhammad Rashad Javeed, Shahzad M, Albalawi M, Mohammed Ali Al-Duais, Hayam A Alwabsi, Ahmad El Askary, Mohamed M Zayed, Nermin I Rizk

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39910945 · Publisher ↗

The liver is the second largest organ in the body, playing a crucial role in maintaining homeostasis and regulating metabolism. However, the prevalence of liver diseases has been rising steadily due to an increase in bot... The liver is the second largest organ in the body, playing a crucial role in maintaining homeostasis and regulating metabolism. However, the prevalence of liver diseases has been rising steadily due to an increase in both infectious and non-infectious factors. Medicinal plants offer a remarkable opportunity to enhance our healthcare system by addressing various diseases through their ability to control oxidative stress and support metabolic processes. This revision improves readability while retaining the original meaning. In the present study, purified methanol extracts of Martynia annua and Polygonum viviparum at different concentrations were used to explore the antioxidant and hepatoprotective potential against abiotic stress on liver cells.  Firstly total flavonoids and total phenolic contents of both plants were measured and then their antioxidant activities were determined through DPPH radical scavenging activity and FRAP assay. Moreover, bioactive compounds and in vitro hepatoprotective potential among these plants were determined through LC-MS and Liver Slice Culture assay respectively. In P. viviparum high amounts of TPC and TFC were observed with maximum antioxidant potential in terms of DPPH inhibition at 84% and high ferric-reducing ability at 240 mg/mL. The presence of different phytoconstituents like Myricetin, Gallic acid, Ferulic acid, Chlorogenic acid, Sweroside, Morroniside, Echonoside, Swertiamarin and Protocatechuic acid were confirmed in M. annua and P. viviparum in LC-MS study. The maximum hepatoprotective potential in terms of minimum cytotoxicity 6% and 9% were observed in M. annua and P. viviparum respectively. It was revealed that both plants have stunning hepatoprotective properties to prevent liver from toxicants and their related complications due to high antioxidant potential and active metabolites.

A critical evaluation of biochemical markers for the diagnosis of acute pancreatitis.

Alshahrani MM

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39910944 · Publisher ↗

Acute pancreatitis (AP) is a common but poorly understood gastrointestinal illness. One explanation for this lack of awareness is the absence of clear recommendations on the use of biochemical markers to identify this il... Acute pancreatitis (AP) is a common but poorly understood gastrointestinal illness. One explanation for this lack of awareness is the absence of clear recommendations on the use of biochemical markers to identify this illness. This is because knowledge in this field is always expanding. Serum amylase and lipase are two extensively utilized biochemical indicators in the diagnosis of AP. The lack of agreement on the optimal use of these markers, notably amylase and lipase, has an impact on diagnostic outcomes. Through a critical study of the current literatures, this review intends to explore in depth the use of biochemical markers in the diagnosis of AP. A comprehensive review of the literature had a glance at biochemical indicators in the context of AP diagnosis, diving into topics including pancreatic anatomy, functions, pathology, mechanisms of AP, etiologies, symptoms, and also diagnostic approaches. This review revealed areas of agreement and disagreement about biochemical indicators in the diagnosis of AP, as well as potential future research directions.

IL-38 attenuates renal ischemia/reperfusion injury through suppressing inflammation in mice.

Liang D, Dai L, Sun H … +1 more , Li L

Cell Mol Biol (Noisy-le-grand) · 2025 Feb · PMID 39910943 · Publisher ↗

Inflammation plays an important role in the pathogenesis of renal ischemia/reperfusion injury (IRI). Interleukin-38 (IL-38) is an emerging cytokine with multiple functions involved in infection and immunity. The present... Inflammation plays an important role in the pathogenesis of renal ischemia/reperfusion injury (IRI). Interleukin-38 (IL-38) is an emerging cytokine with multiple functions involved in infection and immunity. The present study aimed to determine whether IL-38 attenuates renal IR injury in an animal model and to identify the underlying mechanisms. For this purpose, the renal IRI model was induced by left renal pedicle clamping for 45 min and right nephrectomy in mice. All mice were intraperitoneally injected with vehicle or IL-38. Renal histology, function, apoptosis and inflammatory cytokines were assessed. mRNAs were detected by Real-time PCR. The proteins were measured by Western blot. Results showed that the expression of IL-38 mRNA and protein in kidney tissue was significantly increased at 6 h and reached a peak at 24 h after renal IRI, along with the kidney dysfunction. IL-38 significantly decreased renal IRI, as reflected by the attenuation of renal dysfunction, tubular damage and cellular apoptosis. Thus, IL-38 markedly ameliorated the survival rate after renal IRI. In addition, IL-38 significantly increased the level of cytoplasmic IκB-α and suppressed the nuclear translocation of NF-κB, which inhibited the expression and release of inflammatory cytokines. In conclusion, IL-38 significantly protects against renal IRI probably by inhibiting pro-inflammatory reactions.
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