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1.
Sci Adv ; 10(36): eado8422, 2024 Sep 06.
Article de Anglais | MEDLINE | ID: mdl-39241066

RÉSUMÉ

This study experimentally demonstrates the coexistence and transition between weak and strong wave turbulence during the interaction of acoustic waves and turbulent flows. We identify conditions under which different wave turbulence regimes occur based on the wave number of the turbulent flow and acoustic waves. As the sound frequency increases, strong wave turbulence dominates, requiring a specific scaling factor to reconcile the spectra with the weak turbulence theory. Our analysis using the wave turbulence framework is confirmed by experimental results, providing deep insights into the complex interaction between acoustics and turbulence.

2.
J Hazard Mater ; 479: 135663, 2024 Nov 05.
Article de Anglais | MEDLINE | ID: mdl-39217931

RÉSUMÉ

Groundwater contaminated by potentially toxic elements has become an increasing global concern for human health. Therefore, it is crucial to identify the sources and health risks of potentially toxic elements, especially in arid areas. Despite the necessity, there is a notable research gap concerning the sources and risks of these elements within multi-layer aquifers in such regions. To address this gap, 54 phreatic and 24 confined groundwater samples were collected from an arid area in Northwest China. This study aimed to trace the sources and evaluate the human health risks of potentially toxic elements by natural background level (NBL), positive matrix factorization (PMF) model, and health risk model. Findings revealed exceeding levels of potentially toxic elements existed in phreatic and confined aquifers. Source apportionment and NBL results indicated that mineral dissolution, evaporation, redox reactions, and human activities were the main factors for elevated concentrations of potentially toxic elements. High Fe and Mn concentrations were attributed to reduction environments, while F accumulation resulted from slow runoff, and irrigation from the Yellow River. Due to high F levels, more than one-third of groundwater samples (phreatic: 33.14 %, confined: 56.22 %) posed non-carcinogenic health risks to population groups. Adults displayed higher carcinogenic risks (phreatic: 19.47 %, confined: 34.16 %) than infants (phreatic: 0 %, confined: 0 %) and children (phreatic: 1.26 %, confined: 7.97 %) owing to the toxic elements of Cr. The confined aquifer presented greater health risks than the phreatic aquifer. Consequently, controlling the levels of F and Cr in multi-layered aquifers is key to reducing health risks. These findings provide valuable insights into protecting groundwater from contamination by potentially toxic elements in multi-layered aquifers worldwide.


Sujet(s)
Surveillance de l'environnement , Nappe phréatique , Polluants chimiques de l'eau , Nappe phréatique/analyse , Nappe phréatique/composition chimique , Chine , Appréciation des risques , Polluants chimiques de l'eau/analyse , Humains
3.
J Med Chem ; 67(18): 16056-16071, 2024 Sep 26.
Article de Anglais | MEDLINE | ID: mdl-39230932

RÉSUMÉ

The histone lysine methyltransferase NSD2 has been recognized as an attractive target for cancer treatment, due to the functional implication of its dysregulation in the initiation and progression of many cancers. Although considerable efforts have been made to develop NSD2 small-molecule inhibitors, highly potent and selective ones are still rarely available till now. Here, we report the discovery of a series of novel NSD2 inhibitors via an extensive SAR exploration of the privileged quinazoline scaffold within compound 8. The most promising compound 42 showed excellent NSD2 enzymatic inhibitory activity and good antiproliferative activity in cells. In addition, it demonstrated favorable pharmacokinetic properties and significantly inhibited the tumor growth in a RS411 tumor xenograft model with good safety. Taken together, compound 42 could be a promising NSD2 inhibitor and deserves further investigation.


Sujet(s)
Histone-lysine N-methyltransferase , Histone-lysine N-methyltransferase/antagonistes et inhibiteurs , Histone-lysine N-methyltransferase/métabolisme , Humains , Animaux , Relation structure-activité , Quinazolines/pharmacologie , Quinazolines/composition chimique , Quinazolines/synthèse chimique , Quinazolines/pharmacocinétique , Souris , Découverte de médicament , Prolifération cellulaire/effets des médicaments et des substances chimiques , Lignée cellulaire tumorale , Antinéoplasiques/pharmacologie , Antinéoplasiques/composition chimique , Antinéoplasiques/synthèse chimique , Antinéoplasiques/pharmacocinétique , Protéines de répression/antagonistes et inhibiteurs , Protéines de répression/métabolisme , Antienzymes/pharmacologie , Antienzymes/composition chimique , Antienzymes/synthèse chimique , Antienzymes/pharmacocinétique , Tests d'activité antitumorale sur modèle de xénogreffe , Souris nude , Rats
4.
Virus Res ; 349: 199461, 2024 Nov.
Article de Anglais | MEDLINE | ID: mdl-39278352

RÉSUMÉ

Human parechovirus (HPeV) is a common virus that can cause severe infections in newborns. Due to the limited knowledge of the prevalence of HPeV in different cities in China and the unknown association between HPeV infection and clinical characteristics of newborns, this research investigated the epidemiological and clinical characteristics of HPeV infection in hospitalized neonates in Changsha. From August to October 2023, 145 anal swab samples from 96 newborns and 38 pharyngeal swab samples from 33 newborns in the neonatal intensive care unit (NICU) were collected. The prevalence of HPeV was detected by reverse transcription-polymerase chain reaction (RT-PCR). The genomes of HPeV were sequenced and the viral protein 1 (VP1) region was used for genotyping. Phylogenetic analysis and recombination analysis of HPeV genome were performed. Finally, HPeV was detected in 10 out of 44 patients in October, all of them were HPeV-1. The sequenced 4 genomes of HPeV showed high genetic diversity with known strains. Additionally, a HPeV-1 recombinant strain was detected. Compared with HPeV negative patients, HPeV patients had higher prevalence of abdominal pain and diarrhea, intracranial hemorrhage, and purulent meningitis. Compared with HPeV negative patients, HPeV patients had higher peripheral blood lymphocytes, albumin, globulin, pH and lower peripheral blood neutrophils and hemoglobin. HPeV is an important viral cause of newborn infections and appears to be increasing in prevalence in recent years. Characteristic clinical pictures exist in HPeV infections, and further research is needed to accumulate more cases to obtain a comprehensive understanding of HPeV infections.


Sujet(s)
Variation génétique , Génotype , Parechovirus , Phylogenèse , Infections à Picornaviridae , Parechovirus/génétique , Parechovirus/classification , Parechovirus/isolement et purification , Humains , Infections à Picornaviridae/épidémiologie , Infections à Picornaviridae/virologie , Nouveau-né , Chine/épidémiologie , Mâle , Femelle , Prévalence , Génome viral
5.
Turk J Gastroenterol ; 35(4): 266-279, 2024 04.
Article de Anglais | MEDLINE | ID: mdl-39128063

RÉSUMÉ

BACKGROUND/AIMS: In this study, we evaluated the efficacy and safety of transcatheter arterial chemoembolization (TACE) combined with hepatic arterial infusion chemotherapy (HAIC) compared to TACE monotherapy for the treatment of unresectable hepatocellular carcinoma (HCC). MATERIALS AND METHODS: Relevant studies were systematically searched in PubMed, Embase, Web of Science, and Cochrane Library databases until September 1, 2023. Our analysis included 7 cohort studies encompassing a total of 630 patients. RESULTS: The results demonstrated that the TACE plus HAIC group exhibited significantly improved prognosis compared to the TACE alone group, as evidenced by superior rates of complete response, partial response, progressive disease, objective response rate, and disease control rate. Moreover, the TACE group displayed a lower risk of platelet reduction and vomiting when compared to the TACE plus HAIC group. None of the 7 studies reported any intervention-related mortality. CONCLUSION: In conclusion, the combination of TACE and HAIC may be recommended as a viable option for patients with unresectable HCC, given its evident enhancements in survival and tumor response rates without significant differences in adverse events when compared to TACE monotherapy. Nevertheless, additional randomized controlled trials and studies involving Western cohorts are warranted to further validate these findings.


Sujet(s)
Carcinome hépatocellulaire , Chimioembolisation thérapeutique , Artère hépatique , Perfusions artérielles , Tumeurs du foie , Humains , Chimioembolisation thérapeutique/méthodes , Tumeurs du foie/thérapie , Carcinome hépatocellulaire/thérapie , Perfusions artérielles/méthodes , Résultat thérapeutique , Association thérapeutique , Antinéoplasiques/administration et posologie , Femelle , Mâle
6.
Acta Orthop Traumatol Turc ; 35(4): 266-279, 2024 Jan 16.
Article de Anglais | MEDLINE | ID: mdl-39175284

RÉSUMÉ

In this study, we evaluated the efficacy and safety of transcatheter arterial chemoembolization (TACE) combined with hepatic arterial infusion chemotherapy (HAIC) compared to TACE monotherapy for the treatment of unresectable hepatocellular carcinoma (HCC). Relevant studies were systematically searched in PubMed, Embase, Web of Science, and Cochrane Library databases until September 1, 2023. Our analysis included 7 cohort studies encompassing a total of 630 patients. The results demonstrated that the TACE plus HAIC group exhibited significantly improved prognosis compared to the TACE alone group, as evidenced by superior rates of complete response, partial response, progressive disease, objective response rate, and disease control rate. Moreover, the TACE group displayed a lower risk of platelet reduction and vomiting when compared to the TACE plus HAIC group. None of the 7 studies reported any intervention-related mortality. In conclusion, the combination of TACE and HAIC may be recommended as a viable option for patients with unresectable HCC, given its evident enhancements in survival and tumor response rates without significant differences in adverse events when compared to TACE monotherapy. Nevertheless, additional randomized controlled trials and studies involving Western cohorts are warranted to further validate these findings.


Sujet(s)
Carcinome hépatocellulaire , Chimioembolisation thérapeutique , Perfusions artérielles , Tumeurs du foie , Humains , Antinéoplasiques/administration et posologie , Carcinome hépatocellulaire/thérapie , Chimioembolisation thérapeutique/méthodes , Association thérapeutique , Artère hépatique , Perfusions artérielles/méthodes , Tumeurs du foie/thérapie , Résultat thérapeutique
7.
J Med Chem ; 67(18): 16072-16087, 2024 Sep 26.
Article de Anglais | MEDLINE | ID: mdl-39008565

RÉSUMÉ

Both G9a and NSD2 have been recognized as promising therapeutic targets for cancer treatment. However, G9a inhibitors only showed moderate inhibitory activity against solid tumors and NSD2 inhibitors were limited to the treatment of hematological malignancies. Inspired by the advantages of dual-target inhibitors that show great potential in enhancing efficiency, we developed a series of highly potent G9a/NSD2 dual inhibitors to treat solid tumors. The candidate 16 demonstrated much enhanced antiproliferative activity compared to the selective G9a inhibitor 3 and NSD2 inhibitor 15. In addition, it exhibited superior potency in inhibiting colony formation, inducing cell apoptosis, and blocking cancer cell metastasis. Furthermore, it effectively inhibited the catalytic functions of both G9a and NSD2 in cells and exhibited significant antitumor efficacy in the PANC-1 xenograft model with good safety. Therefore, compound 16 as a highly potent G9a/NSD2 dual inhibitor presents an attractive anticancer drug candidate for the treatment of solid tumors.


Sujet(s)
Antinéoplasiques , Prolifération cellulaire , Antigènes d'histocompatibilité , Histone-lysine N-methyltransferase , Histone-lysine N-methyltransferase/antagonistes et inhibiteurs , Histone-lysine N-methyltransferase/métabolisme , Humains , Animaux , Antinéoplasiques/pharmacologie , Antinéoplasiques/composition chimique , Antinéoplasiques/synthèse chimique , Antinéoplasiques/usage thérapeutique , Antigènes d'histocompatibilité/métabolisme , Lignée cellulaire tumorale , Prolifération cellulaire/effets des médicaments et des substances chimiques , Souris , Apoptose/effets des médicaments et des substances chimiques , Antienzymes/pharmacologie , Antienzymes/composition chimique , Antienzymes/synthèse chimique , Antienzymes/usage thérapeutique , Relation structure-activité , Tests d'activité antitumorale sur modèle de xénogreffe , Souris nude , Tumeurs/traitement médicamenteux , Tumeurs/anatomopathologie , Découverte de médicament , Protéines de répression
8.
Chem Sci ; 15(29): 11521-11527, 2024 Jul 24.
Article de Anglais | MEDLINE | ID: mdl-39055041

RÉSUMÉ

The industrial production of nylon 6 usually includes synthesizing caprolactam through the cyclohexanone-hydroxylamine route. This approach requires complex protocols, elevated temperatures, noble metal catalysts and the use of hazardous strong acids or hydroxylamine. Additionally, a significant quantity of ammonium sulphate is generated during the synthesis procedure. This study aims to develop an electrochemical reduction system for the conversion of ADN generated from the electrolytic dimerization of acrylonitrile (AN) to 6-aminocapronitrile (ACN), a precursor of nylon 6. This system utilizes a cost-effective Cu nanomaterial under eco-friendly conditions, avoiding lengthy and harsh processes, eliminating NH2OH use, and reducing low-value ammonium sulfate generation. This electrosynthesis method maintains approximately 85% ACN selectivity at 40-100 mA cm-2 when passing the charge required for 37% theoretical conversion. When extending the reaction time to achieve an 80% conversion, ACN selectivity still reached 81.6%, exceeding the theoretical value of non-selective hydrogenation by 20%. The pseudo-first-order reaction kinetic modeling proves that the reaction rate constant for ADN hydrogenation is significantly greater than that for ACN hydrogenation, highlighting the selectivity advantage of the system for ACN. This study establishes the foundation for developing a continuous electrolysis process to produce the nylon 6 precursor from AN feedstock.

9.
J Environ Manage ; 366: 121825, 2024 Aug.
Article de Anglais | MEDLINE | ID: mdl-38996604

RÉSUMÉ

Chelator-assisted phytoremediation is an efficacious method for promoting the removal efficiency of heavy metals (HMs). The effects of N, N-bis(carboxymethyl)-L-glutamic acid (GLDA) and polyaspartic acid (PASP) on Cd uptake and pyrene removal by Solanum nigrum L. (S. nigrum) were compared in this study. Using GLDA or PASP, the removal efficiency of pyrene was over 98%. And PASP observably raised the accumulation and transport of Cd by S. nigrum compared with GLDA. Meanwhile, both GLDA and PASP markedly increased soil dehydrogenase activities (DHA) and microbial activities. DHA and microbial activities in the PASP treatment group were 1.05 and 1.06 folds of those in the GLDA treatment group, respectively. Transcriptome analysis revealed that 1206 and 1684 differentially expressed genes (DEGs) were recognized in the GLDA treatment group and PASP treatment group, respectively. Most of the DEGs found in the PASP treatment group were involved in the metabolism of carbohydrates, the biosynthesis of brassinosteroid and flavonoid, and they were up-regulated. The DEGs related to Cd transport were screened, and ABCG3, ABCC4, ABCG9 and Nramp5 were found to be relevant with the reduction of Cd stress in S. nigrum by PASP. Furthermore, with PASP treated, transcription factors (TFs) related to HMs such as WRKY, bHLH, AP2/ERF, MYB were down-regulated, while more MYB and bZIP TFs were up-regulated. These TFs associated with plant stress resistance would work together to induce oxidative stress. The above results indicated that PASP was more conducive for phytoremediation of Cd-pyrene co-contaminated soil than GLDA.


Sujet(s)
Dépollution biologique de l'environnement , Cadmium , Pyrènes , Polluants du sol , Cadmium/métabolisme , Polluants du sol/métabolisme , Pyrènes/métabolisme , Sol/composition chimique , Peptides/métabolisme , Analyse de profil d'expression de gènes , Acide glutamique/métabolisme
10.
BMJ Open ; 14(6): e083052, 2024 Jun 10.
Article de Anglais | MEDLINE | ID: mdl-38858141

RÉSUMÉ

INTRODUCTION: Ixodes ticks are pivotal in transmitting diseases like Lyme disease and human granulocytic anaplasmosis, caused by Borrelia burgdorferi and Anaplasma phagocytophilum, respectively. These pathogens not only affect humans through single or multiple tick bites but also pose risks to animal hosts, leading to potential coinfections. Despite regional studies indicating significant prevalence, their global coinfection data remain sparse. This study aims to bridge this gap through a systematic review and meta-analysis of B. burgdorferi and A. phagocytophilum coinfections in Ixodes ticks worldwide. Addressing data limitations and study variability, it seeks to provide a nuanced understanding of coinfection patterns, their epidemiological implications and inform targeted prevention strategies. METHODS AND ANALYSIS: Following Preferred Reporting Items for Systematic Review and Meta-analysis Protocols 2015 guidelines and PROSPERO registration, this study will undertake a thorough database search without constraints on language or publication date, using standardised screening and data extraction protocols. The quality and bias of studies will be evaluated using Joanna Briggs Institute tools. In the statistical analysis phase, conducted in R, we will initially determine the use of fixed or random-effects models based on the assessment of data heterogeneity. This choice will guide the framework for subsequent analyses. Within the selected model's framework, we will perform subgroup analyses and meta-regression to investigate the effects of various factors, ensuring that each step is tailored to the initial model selection to maintain analytical consistency. ETHICS AND DISSEMINATION: As this study does not involve clinical research or data collection from subjects, ethical approval is not required. We will uphold ethical standards in synthesising and reporting data. Study outcomes will be published in peer-reviewed journals, communicating findings to the scientific community and contributing to the understanding of Ixodes tickborne diseases. PROSPERO REGISTRATION NUMBER: CRD42023449735.


Sujet(s)
Anaplasma phagocytophilum , Borrelia burgdorferi , Co-infection , Ixodes , Maladie de Lyme , Méta-analyse comme sujet , Revues systématiques comme sujet , Anaplasma phagocytophilum/isolement et purification , Ixodes/microbiologie , Animaux , Borrelia burgdorferi/isolement et purification , Co-infection/épidémiologie , Maladie de Lyme/épidémiologie , Humains , Prévalence , Plan de recherche , Ehrlichiose/épidémiologie
11.
STAR Protoc ; 5(2): 103113, 2024 Jun 21.
Article de Anglais | MEDLINE | ID: mdl-38843400

RÉSUMÉ

Chicken cone cells are an excellent model for studying the regulation of lipid droplet dynamics. Here, we present a protocol for studying cone cell lipid droplets from in vivo and ex vitro cultured retinas of chicken embryos. We describe steps for dissecting chicken retinas, electroporating retinas, culturing retinas ex vivo and in vitro, and staining lipid droplets with neutral lipid dye. This protocol is also applicable to investigating other organelles in retinas. For complete details on the use and execution of this protocol, please refer to Pan et al.1.


Sujet(s)
Poulets , Gouttelettes lipidiques , Cellules photoréceptrices en cône de la rétine , Animaux , Gouttelettes lipidiques/métabolisme , Embryon de poulet , Cellules photoréceptrices en cône de la rétine/métabolisme , Cellules photoréceptrices en cône de la rétine/cytologie , Rétine/cytologie , Rétine/métabolisme
12.
Environ Sci Pollut Res Int ; 31(27): 39155-39176, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38809406

RÉSUMÉ

An in-depth understanding of nitrate-contaminated surface water and groundwater quality and associated risks is important for groundwater management. Hydrochemical characteristics and driving forces of groundwater quality and non-carcinogenic risks of nitrate were revealed by the integrated approaches of self-organizing map analysis, spatial visualization by geography information system, entropy and irrigation water quality indices, and human health risk model. Groundwater samples were categorized into two clusters by SOM analysis. Cluster I including three samples were Ca-SO4 type and cluster II of remaining 136 samples were Ca-HCO3 type. Hydrochemical compositions of two cluster samples were dominated by water-rock interaction: (1) calcite and gypsum dissolution for cluster I samples and (2) calcite dissolution, silicate weathering, and positive cation exchange for cluster II samples. Nitrate contamination occurred in both cluster I and II samples, primarily induced by agricultural nitrogen fertilizer. The EWQI results showed that 90.97% in total groundwater samples were suitable for drinking purpose, while the IWQI results demonstrated that 65.03% in total groundwater samples were appropriate for irrigation purpose. The HHR model and Monte Carlo simulation indicated that the non-carcinogenic nitrated risk was highest in children. Exposure frequency was the most sensitive factor (86.33% in total) influencing the total non-carcinogenic risk, indicated by sensitivity analysis. Compared with the two clusters of groundwater, surface water has a shorter circulation cycle and lower ion concentrations resulting in better water quality. This study can provide scientific basis for groundwater quality evaluation in other parts of the world.


Sujet(s)
Irrigation agricole , Nappe phréatique , Apprentissage machine , Analyse spatiale , Polluants chimiques de l'eau , Qualité de l'eau , Nappe phréatique/composition chimique , Appréciation des risques , Polluants chimiques de l'eau/analyse , Eau de boisson/composition chimique , Humains , Surveillance de l'environnement/méthodes , Nitrates/analyse
13.
Sci Total Environ ; 935: 173276, 2024 Jul 20.
Article de Anglais | MEDLINE | ID: mdl-38796023

RÉSUMÉ

Identifying the natural background levels (NBLs), threshold values (TVs), sources and health risks of potentially toxic elements in groundwater is crucial for ensuring the water security of residents in highly urbanized areas. In this study, 96 groundwater samples were collected in urban area of Sichuan Basin, SW China. The concentrations of potentially toxic elements (Li, Fe, Cu, Zn, Al, Pb, B, Ba and Ni) were analyzed for investigating the NBLs, TVs, sources and health risks. The potentially toxic elements followed the concentration order of Fe > Ba > B > Al > Zn > Li > Cu > Ni > Pb. The NBLs and TVs indicated the contamination of potentially toxic elements mainly occurred in the northern and central parts of the study area. The Positive Matrix Factorization (PMF) model identified elevated concentrations of Fe, Al, Li, and B were found to determine groundwater quality. The primary sources of Fe, Al, Pb, and Ni were attributed to the dissolution of oxidation products, with Fe additionally affected by anthropogenic reduction environments. Li and B were determined to be originated from the weathering of tourmaline. High levels of Ni and Cu concentrations were derived from electronic waste leakage, while excessive Ba and Zn were linked to factory emissions and tire wear. The reasonable maximum exposure (RME) of hazard index (HI) was higher than safety standard and reveal the potential health risks in the southwestern study area. Sensitivity analysis demonstrated the Li concentrations possessed the highest weight contributing to health risk. This study provides a valuable information for source-specific risk assessments of potentially toxic elements in groundwater associated with urban areas.


Sujet(s)
Surveillance de l'environnement , Nappe phréatique , Polluants chimiques de l'eau , Nappe phréatique/composition chimique , Polluants chimiques de l'eau/analyse , Chine , Appréciation des risques , Urbanisation , Humains , Métaux lourds/analyse , Villes
14.
JASA Express Lett ; 4(5)2024 May 01.
Article de Anglais | MEDLINE | ID: mdl-38717466

RÉSUMÉ

Machine learning enabled auscultating diagnosis can provide promising solutions especially for prescreening purposes. The bottleneck for its potential success is that high-quality datasets for training are still scarce. An open auscultation dataset that consists of samples and annotations from patients and healthy individuals is established in this work for the respiratory diagnosis studies with machine learning, which is of both scientific importance and practical potential. A machine learning approach is examined to showcase the use of this new dataset for lung sound classifications with different diseases. The open dataset is available to the public online.


Sujet(s)
Auscultation , Apprentissage machine , Bruits respiratoires , Humains , Auscultation/méthodes , Bruits respiratoires/classification
15.
J Robot Surg ; 18(1): 176, 2024 Apr 17.
Article de Anglais | MEDLINE | ID: mdl-38630145

RÉSUMÉ

The objective is to preliminary evaluated postoperative leukocyte counts as a surrogate for the surgical stress response in NSCLC patients who underwent RATS or VATS for further prospective analyses with proper assessment of surgical stress response and tissue trauma. We retrospectively analyzed patients with stageI-IIIA NSCLC who underwent RATS or VATS at a hospital between 8 May 2020 and 31 December 2021. Analysis of leukocytes (including neutrophils and lymphocytes) and albumin on postoperative days (PODs) 1 and 3 in patients with NSCLC treated with RATS or VATS after propensity score matching (PSM). In total, 1824 patients (565 RATS and 1259 VATS) were investigated. The two MIS groups differed significantly with regard to operative time (p < 0.001), chronic lung disease (p < 0.001), the type of pulmonary resection (p < 0.001), the excision site of lobectomy (p = 0.004), and histology of the tumor (p = 0.028). After PSM, leukocyte and neutrophil levels in the RATS group were lower than those in the VATS group on PODs 1 and 3, with those on POD 3 (p < 0.001) being particularly notable. While lymphocyte levels in the RATS group were significantly lower than those in the VATS group only at POD 1 (p = 0.016). There was no difference in albumin levels between the RATS and VATS groups on PODs 1 and 3. The surgical stress response and tissue trauma was less severe in NSCLC patients who underwent RATS than in those who underwent VATS, especially reflected in the neutrophils of leukocytes.


Sujet(s)
Carcinome pulmonaire non à petites cellules , Tumeurs du poumon , Interventions chirurgicales robotisées , Robotique , Humains , Chirurgie thoracique vidéoassistée , Études rétrospectives , Interventions chirurgicales robotisées/méthodes , Numération des leucocytes , Carcinome pulmonaire non à petites cellules/chirurgie , Albumines , Tumeurs du poumon/chirurgie
16.
Eur J Med Chem ; 267: 116171, 2024 Mar 05.
Article de Anglais | MEDLINE | ID: mdl-38301329

RÉSUMÉ

The ubiquitous methyltransferases employing SAM as the methyl donor have emerged as potential targets in many disease treatments, especially in anticancer. Therefore, developing SAM-competitive inhibitors of methyltransferases is of great interest to the drug research. To explore this direction, herein, we rationally designed a series of nucleoside derivatives as potent PRMT5 inhibitors with novel scaffold. The representative compounds A2 and A8 exhibited highly potent PRMT5 inhibition activity as well as good selectivity over other PRMTs and PKMTs. Further cellular experiments revealed that compounds A2 and A8 potently reduced the level of sDMA and inhibited the proliferation of Z-138 and MOLM-13 cell lines by inducing apoptosis. Moreover, compounds A8 which had favorable pharmacokinetic properties exhibited potent antitumor efficacy without the loss of body weight in a subcutaneous MOLM-13 xenograft model. In summary, our efforts provided a series of novel nucleoside analogs as potent PRMT5 inhibitors and may also offer a new strategy to develop SAM analogs as other methyltransferases' inhibitors.


Sujet(s)
Antienzymes , Nucléosides , Humains , Nucléosides/pharmacologie , Relation structure-activité , Lignée cellulaire tumorale , Antienzymes/pharmacologie , Antienzymes/métabolisme , Methyltransferases/métabolisme , Protein-arginine N-methyltransferases
17.
J Med Chem ; 67(4): 2466-2486, 2024 Feb 22.
Article de Anglais | MEDLINE | ID: mdl-38316017

RÉSUMÉ

Adenoviral E1A binding protein 300 kDa (p300) and its closely related paralog CREB binding protein (CBP) are promising therapeutic targets for human cancer. Here, we report the first discovery of novel potent small-molecule PROTAC degraders of p300/CBP against hepatocellular carcinoma (HCC), one of the most common solid tumors. Based upon the clinical p300/CBP bromodomain inhibitor CCS1477, a conformational restriction strategy was used to optimize the linker to generate a series of PROTACs, culminating in the identification of QC-182. This compound effectively induces p300/CBP degradation in the SK-HEP-1 HCC cells in a dose-, time-, and ubiquitin-proteasome system-dependent manner. QC-182 significantly downregulates p300/CBP-associated transcriptome in HCC cells, leading to more potent cell growth inhibition compared to the parental inhibitors and the reported degrader dCBP-1. Notably, QC-182 potently depletes p300/CBP proteins in mouse SK-HEP-1 xenograft tumor tissue. QC-182 is a promising lead compound toward the development of p300/CBP-targeted HCC therapy.


Sujet(s)
Carcinome hépatocellulaire , Tumeurs du foie , Humains , Animaux , Souris , Protéine CBP/composition chimique , Carcinome hépatocellulaire/traitement médicamenteux , Tumeurs du foie/traitement médicamenteux , Domaines protéiques , Facteurs de transcription CBP-p300/métabolisme
18.
Sci China Life Sci ; 67(2): 230-257, 2024 Feb.
Article de Anglais | MEDLINE | ID: mdl-38212460

RÉSUMÉ

The endoplasmic reticulum (ER), which is composed of a continuous network of tubules and sheets, forms the most widely distributed membrane system in eukaryotic cells. As a result, it engages a variety of organelles by establishing membrane contact sites (MCSs). These contacts regulate organelle positioning and remodeling, including fusion and fission, facilitate precise lipid exchange, and couple vital signaling events. Here, we systematically review recent advances and converging themes on ER-involved organellar contact. The molecular basis, cellular influence, and potential physiological functions for ER/nuclear envelope contacts with mitochondria, Golgi, endosomes, lysosomes, lipid droplets, autophagosomes, and plasma membrane are summarized.


Sujet(s)
Réticulum endoplasmique , Mitochondries , Réticulum endoplasmique/métabolisme , Humains , Animaux , Mitochondries/métabolisme , Appareil de Golgi/métabolisme , Lysosomes/métabolisme , Endosomes/métabolisme , Transduction du signal , Membrane cellulaire/métabolisme , Autophagosomes/métabolisme , Enveloppe nucléaire/métabolisme , Gouttelettes lipidiques/métabolisme
19.
Cell Chem Biol ; 31(1): 177-183.e17, 2024 01 18.
Article de Anglais | MEDLINE | ID: mdl-38194973

RÉSUMÉ

N6-methyladenosine (m6A) methylation is the most abundant type of RNA modification that is mainly catalyzed by the METTL3-METTL14 methyltransferase complex. This complex has been linked to multiple cancers and is considered a promising therapeutic target for acute myeloid leukemia (AML). However, only a few METTL3 inhibitors targeting the catalytic activity were developed recently. Here, we present the discovery of WD6305 as the potent and selective proteolysis-targeting chimera (PROTAC) degrader of METTL3-METTL14 complex. WD6305 suppresses m6A modification and the proliferation of AML cells, and promotes apoptosis much more effectively than its parent inhibitor. WD6305 also affects a variety of signaling pathways related to the development and proliferation of AML. Collectively, our study reveals PROTAC degradation of METTL3-METTL14 complex as a potential anti-leukemic strategy and provides desirable chemical tool for further understanding METTL3-METTL14 protein functions.


Sujet(s)
Adénosine , Leucémie aigüe myéloïde , Humains , Methyltransferases/génétique , Methyltransferases/métabolisme , Méthylation , Leucémie aigüe myéloïde/traitement médicamenteux , Leucémie aigüe myéloïde/génétique
20.
Immunity ; 57(3): 513-527.e6, 2024 Mar 12.
Article de Anglais | MEDLINE | ID: mdl-38262419

RÉSUMÉ

Accumulation of senescent cells in organs and tissues is a hallmark of aging and known to contribute to age-related diseases. Although aging-associated immune dysfunction, or immunosenescence, is known to contribute to this process, the underlying mechanism remains elusive. Here, we report that type 2 cytokine signaling deficiency accelerated aging and, conversely, that the interleukin-4 (IL-4)-STAT6 pathway protected macrophages from senescence. Mechanistically, activated STAT6 promoted the expression of genes involved in DNA repair both via homologous recombination and Fanconi anemia pathways. Conversely, STAT6 deficiency induced release of nuclear DNA into the cytoplasm to promote tissue inflammation and organismal aging. Importantly, we demonstrate that IL-4 treatment prevented macrophage senescence and improved the health span of aged mice to an extent comparable to senolytic treatment, with further additive effects when combined. Together, our findings support that type 2 cytokine signaling protects macrophages from immunosenescence and thus hold therapeutic potential for improving healthy aging.


Sujet(s)
Vieillissement de la cellule , Interleukine-4 , Animaux , Souris , Interleukine-4/métabolisme , Vieillissement/génétique , Macrophages , Inflammation
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