RÉSUMÉ
Nephrotoxicity is a common adverse effect induced by various chemicals, necessitating the development of reliable toxicity screening models for nephrotoxicity assessment. In this study, we assessed a group of nephrotoxicity indicators derived from different toxicity pathways, including conventional endpoints and kidney tubular injury biomarkers such as clusterin (CLU), kidney injury molecule-I (KIM-1), osteopontin (OPN), and neutrophil gelatinase-associated lipocalin (NGAL), using HK-2 and induced pluripotent stem cells (iPSCs)-derived renal proximal tubular epithelial-like cells (PTLs). Among the biomarkers tested, OPN emerged as the most discerning and precise marker. The predictive potential of OPN was tested using a panel of 10 nephrotoxic and 5 non-nephrotoxic compounds. The results demonstrated that combining OPN with the half-maximal inhibitory concentration (IC50) enhanced the diagnostic accuracy in both cellular models. Additionally, PTLs cells showed superior predictive efficacy for nephrotoxicity compared to HK-2 cells in this investigation. The two cellular models were utilized to evaluate the nephrotoxicity of lanthanum. The findings indicated that lanthanum possesses nephrotoxic properties; however, the degree of nephrotoxicity was relatively low, consistent with the outcomes of in vivo experiments.
Sujet(s)
Lanthane , Ostéopontine , Humains , Ostéopontine/métabolisme , Lanthane/toxicité , Lanthane/métabolisme , Rein , Tubules rénaux/métabolisme , Marqueurs biologiques/métabolismeRÉSUMÉ
The outbreak of COVID-19 has impacted the shipping industry while the extent of the impact is still not fully understood. To quantitatively investigate the relationship between pandemic-related factors and port operations, a panel regression analysis is conducted using data from three important Asian ports, Shenzhen, Hong Kong, and Singapore. Daily data from the Automatic Identification System (AIS), Oxford COVID-19 Government Response Tracker (OxCGRT) database, and port authorities from January 2020 to December 2021 are utilized. Local newly confirmed cases of ports tend to negatively impact cargo throughput, while worldwide newly confirmed cases outside of ports tend to positively impact cargo throughput. Overall, the policy implications are that ports with better control of COVID-19 reap the benefits of more cargo throughput. In addition, countermeasures against COVID-19 and other epidemics should be designed deliberately to minimize the side-effect on port operations and maritime transportation.
RÉSUMÉ
Cadmium accumulates in the kidney and causes inflammation. The NLRP3 inflammasome has been linked to the pathogenesis of inflammation. Hyperoside (HYP) possesses potent nephroprotective properties against of kidney injury. This study aimed to research the effects and related mechanism of HYP on Cd-induced kidney damage. Wide-type and NLRP3-/- mice were used to determine the role of NLRP3 inflammasome in Cd-induced renal dysfunction. Female C57BL/6 were treated with Cd (50 m,g/L) and HYP (25, 50 mg/kg) for 12 weeks. In vitro experiments, the human renal proximal-tubule epithelial cells (RPTEC/TERT1) were pretreated with HYP (50-200 µM) before exposure to Cd. NLRP3 deficiency attenuated Cd-induced NLRP3 activation, inflammation and kidney injury in mice. HYP treatment significantly alleviated Cd-induced kidney injury by decreasing indexes of kidney function, reducing pro-inflammatory cytokines release, decreasing ROS production and suppressing NLRP3 inflammasome activation. Moreover, treatment with siRNA targeting NLRP3 blocked the anti-inflammatory protective effect of HYP in Cd-treated cells. Additionally, HYP markedly inhibited Cd-induced MAPK/NF-κB pathway stimulation in vitro and in vivo. The findings indicated HYP conferred protection against Cd-induced kidney inflammation via suppression of NLRP3 inflammasome mediated by ROS/MAPK/NF-κB signaling. Our results thus support the notion of developing HYP as promising therapeutic candidate for Cd-induced kidney injury.
Sujet(s)
Inflammasomes , Facteur de transcription NF-kappa B , Humains , Femelle , Souris , Animaux , Facteur de transcription NF-kappa B/métabolisme , Inflammasomes/métabolisme , Protéine-3 de la famille des NLR contenant un domaine pyrine/génétique , Protéine-3 de la famille des NLR contenant un domaine pyrine/métabolisme , Cadmium/toxicité , Cadmium/métabolisme , Espèces réactives de l'oxygène/métabolisme , Souris de lignée C57BL , Transduction du signal , Rein , Inflammation/métabolismeRÉSUMÉ
Diabetic retinopathy (DR) is a common chronic fundus disease, which has four different kinds of microvessel structure and microvascular lesions: microaneurysms (MAs), hemorrhages (HEs), hard exudates, and soft exudates. Accurate detection and counting of them are a basic but important work. The manual annotation of these lesions is a labor-intensive task in clinical analysis. To solve the problem, we proposed a novel segmentation method for different lesions in DR. Our method is based on a convolutional neural network and can be divided into encoder module, attention module, and decoder module, so we refer it as EAD-Net. After normalization and augmentation, the fundus images were sent to the EAD-Net for automated feature extraction and pixel-wise label prediction. Given the evaluation metrics based on the matching degree between detected candidates and ground truth lesions, our method achieved sensitivity of 92.77%, specificity of 99.98%, and accuracy of 99.97% on the e_ophtha_EX dataset and comparable AUPR (Area under Precision-Recall curve) scores on IDRiD dataset. Moreover, the results on the local dataset also show that our EAD-Net has better performance than original U-net in most metrics, especially in the sensitivity and F1-score, with nearly ten percent improvement. The proposed EAD-Net is a novel method based on clinical DR diagnosis. It has satisfactory results on the segmentation of four different kinds of lesions. These effective segmentations have important clinical significance in the monitoring and diagnosis of DR.
Sujet(s)
Algorithmes , Rétinopathie diabétique/diagnostic , Exsudats et transsudats/imagerie diagnostique , Fond de l'oeil , Interprétation d'images assistée par ordinateur/méthodes , , Rétinopathie diabétique/imagerie diagnostique , HumainsRÉSUMÉ
Organic impurities in compound libraries are known to often cause false-positive signals in screening campaigns for new leads, but organic impurities do not fully account for all false-positive results. We discovered inorganic impurities in our screening library that can also cause positive signals for a variety of targets and/or readout systems, including biochemical and biosensor assays. We investigated in depth the example of zinc for a specific project and in retrospect in various HTS screens at Roche and propose a straightforward counter screen using the chelator TPEN to rule out inhibition caused by zinc.
RÉSUMÉ
A series of pyrimidodiazepines was identified as potent Polo-like kinase 1 (PLK1) inhibitors. The synthesis and SAR are discussed. The lead compound 7 (RO3280) has potent inhibitory activity against PLK1, good selectivity against other kinases, and excellent in vitro cellular potency. It showed strong antitumor activity in xenograft mouse models.
Sujet(s)
Antinéoplasiques/pharmacologie , Azépines/pharmacologie , Protéines du cycle cellulaire/antagonistes et inhibiteurs , Tumeurs expérimentales/traitement médicamenteux , Inhibiteurs de protéines kinases/pharmacologie , Protein-Serine-Threonine Kinases/antagonistes et inhibiteurs , Protéines proto-oncogènes/antagonistes et inhibiteurs , Pyrimidines/pharmacologie , Animaux , Antinéoplasiques/synthèse chimique , Antinéoplasiques/composition chimique , Azépines/synthèse chimique , Azépines/composition chimique , Protéines du cycle cellulaire/métabolisme , Lignée cellulaire tumorale , Prolifération cellulaire/effets des médicaments et des substances chimiques , Relation dose-effet des médicaments , Humains , Souris , Structure moléculaire , Inhibiteurs de protéines kinases/synthèse chimique , Inhibiteurs de protéines kinases/composition chimique , Protein-Serine-Threonine Kinases/métabolisme , Protéines proto-oncogènes/métabolisme , Pyrimidines/synthèse chimique , Pyrimidines/composition chimique , Stéréoisomérie , Relation structure-activité ,RÉSUMÉ
In a discovery effort to find safe and effective DGAT-1 inhibitors, we have identified 2-phenyloxazole 4-carboxamide 1 as a conformationally constrained analog of a hydrazide hit, which was previously identified from high-throughput screening. Further optimization of this series has led to chemically more stable 2-phenyloxazole-based DGAT-1 inhibitor 25 with improved solubility, cell-based activity, and pharmacokinetic properties. Compound 25 also demonstrated in vivo efficacy in a diet-induced obesity (DIO) rat model.
Sujet(s)
Diacylglycerol O-acyltransferase/antagonistes et inhibiteurs , Découverte de médicament , Antienzymes , Oxazoles/composition chimique , Oxazoles/pharmacologie , Administration par voie orale , Animaux , Poids , Diacylglycerol O-acyltransferase/composition chimique , Modèles animaux de maladie humaine , Activation enzymatique/effets des médicaments et des substances chimiques , Antienzymes/composition chimique , Antienzymes/pharmacologie , Antienzymes/usage thérapeutique , Humains , Concentration inhibitrice 50 , Souris , Structure moléculaire , Obésité/traitement médicamenteux , Oxazoles/usage thérapeutique , Rats , Solubilité , Relation structure-activitéRÉSUMÉ
Diacylglycerol acyltransferase-1 (DGAT-1) is the enzyme that catalyzes the final and committed step of triglyceride formation, namely, the acylation of diacylglycerol with acyl coenzyme A. DGAT-1 deficient mice demonstrate resistance to weight gain on high fat diet, improved insulin sensitivity, and reduced liver triglyceride content. Inhibition of DGAT-1 thus represents a potential novel approach for the treatment of obesity, dyslipidemia, and metabolic syndrome. In this communication, we report the identification of the lead structure 6 and our lead optimization efforts culminating in the discovery of potent, selective, and orally efficacious carboxylic acid derivatives of 2-phenyl-5-trifluoromethyloxazole-4-carboxamides. In particular, compound 29 (DGAT-1 enzyme assay, IC(50) = 57 nM; CHO-K1 cell triglyceride formation assay, EC(50) = 0.5 µM) demonstrated dose dependent inhibition of weight gain in diet induced obese (DIO) rats (0.3, 1, and 3 mg/kg, p.o., qd) during a 21-day efficacy study. Furthermore, compound 29 demonstrated improved glucose tolerance determined by an oral glucose tolerance test (OGTT).
Sujet(s)
Amides/composition chimique , Amides/pharmacologie , Acides carboxyliques/composition chimique , Diabète/traitement médicamenteux , Diacylglycerol O-acyltransferase/antagonistes et inhibiteurs , Découverte de médicament , Obésité/traitement médicamenteux , Oxazoles/composition chimique , Oxazoles/pharmacologie , Administration par voie orale , Amides/administration et posologie , Amides/pharmacocinétique , Animaux , Lignée cellulaire , Diabète/enzymologie , Chiens , Antienzymes/administration et posologie , Antienzymes/composition chimique , Antienzymes/pharmacocinétique , Antienzymes/pharmacologie , Canaux potassiques éther-à-go-go/antagonistes et inhibiteurs , Humains , Concentration inhibitrice 50 , Mâle , Souris , Obésité/enzymologie , Oxazoles/administration et posologie , Oxazoles/pharmacocinétique , RatsRÉSUMÉ
A novel series of quinolinyl-methylene-thiazolinones has been identified as potent and selective cyclin-dependent kinase 1 (CDK1) inhibitors. Their synthesis and structure activity relationships (SAR) are described. Representative compounds from this class reversibly inhibit CDK1 activity in vitro, and block cell cycle progression in human tumor cell lines, suggesting a potential use as antitumor agents.
Sujet(s)
Protéine-kinase CDC2/antagonistes et inhibiteurs , Thiazoles/synthèse chimique , Antinéoplasiques/synthèse chimique , Antinéoplasiques/pharmacologie , Lignée cellulaire tumorale , Tests de criblage d'agents antitumoraux , Humains , Inhibiteurs de protéines kinases/synthèse chimique , Inhibiteurs de protéines kinases/pharmacologie , Relation structure-activité , Thiazoles/pharmacologieRÉSUMÉ
The cyclin-dependent protein kinases are key regulators of cell cycle progression. Aberrant expression or altered activity of distinct cyclin-dependent kinase (CDK) complexes results in escape of cells from cell cycle control, leading to unrestricted cell proliferation. CDK inhibitors have the potential to induce cell cycle arrest and apoptosis in cancer cells, and identifying small-molecule CDK inhibitors has been a major focus in cancer research. Several CDK inhibitors are entering the clinic, the most recent being selective CDK2 and CDK4 inhibitors. We have identified a diaminopyrimidine compound, R547, which is a potent and selective ATP-competitive CDK inhibitor. In cell-free assays, R547 effectively inhibited CDK1/cyclin B, CDK2/cyclin E, and CDK4/cyclin D1 (K(i) = 1-3 nmol/L) and was inactive (K(i) > 5,000 nmol/L) against a panel of >120 unrelated kinases. In vitro, R547 effectively inhibited the proliferation of tumor cell lines independent of multidrug resistant status, histologic type, retinoblastoma protein, or p53 status, with IC(50)s = 0.60 mumol/L. The growth-inhibitory activity is characterized by a cell cycle block at G(1) and G(2) phases and induction of apoptosis. R547 reduced phosphorylation of the cellular retinoblastoma protein at specific CDK phosphorylation sites at the same concentrations that induced cell cycle arrest, suggesting a potential pharmacodynamic marker for clinical use. In vivo, R547 showed antitumor activity in all of the models tested to date, including six human tumor xenografts and an orthotopic syngeneic rat model. R547 was efficacious with daily oral dosing as well as with once weekly i.v. dosing in established human tumor models and at the targeted efficacious exposures inhibited phosphorylation of the retinoblastoma protein in the tumors. The selective kinase inhibition profile and the preclinical antitumor activity of R547 suggest that it may be promising for development for use in the treatment of solid tumors. R547 is currently being evaluated in phase I clinical trials.
Sujet(s)
Antinéoplasiques/pharmacologie , Kinases cyclines-dépendantes/antagonistes et inhibiteurs , Pyrimidines/pharmacologie , Animaux , Antinéoplasiques/pharmacocinétique , Antinéoplasiques/usage thérapeutique , Apoptose , Lignée cellulaire tumorale , Prolifération cellulaire/effets des médicaments et des substances chimiques , Essais cliniques de phase I comme sujet , Kinases cyclines-dépendantes/métabolisme , Femelle , Phase G1/effets des médicaments et des substances chimiques , Phase G2/effets des médicaments et des substances chimiques , Gènes MDR/effets des médicaments et des substances chimiques , Humains , Souris , Souris nude , Phosphorylation/effets des médicaments et des substances chimiques , Pyrimidines/pharmacocinétique , Pyrimidines/usage thérapeutique , Rats , Rats de lignée F344 , Rétinoblastome/traitement médicamenteux , Rétinoblastome/métabolisme , Protéine p53 suppresseur de tumeur/métabolismeRÉSUMÉ
The cyclin-dependent kinases (CDKs) and their cyclin partners are key regulators of the cell cycle. Since deregulation of CDKs is found with high frequency in many human cancer cells, pharmacological inhibition of CDKs with small molecules has the potential to provide an effective strategy for the treatment of cancer. The 2,4-diamino-5-ketopyrimidines 6 reported here represent a novel class of potent and ATP-competitive inhibitors that selectively target the cyclin-dependent kinase family. This diaminopyrimidine core with a substituted 4-piperidine moiety on the C2-amino position and 2-methoxybenzoyl at the C5 position has been identified as the critical structure responsible for the CDK inhibitory activity. Further optimization has led to a good number of analogues that show potent inhibitory activities against CDK1, CDK2, and CDK4 but are inactive against a large panel of serine/threonine and tyrosine kinases (K(i) > 10 microM). As one of these representative analogues, compound 39 (R547) has the best CDK inhibitory activities (K(i) = 0.001, 0.003, and 0.001 microM for CDK1, CDK2, and CDK4, respectively) and excellent in vitro cellular potency, inhibiting the growth of various human tumor cell lines including an HCT116 cell line (IC(50) = 0.08 microM). An X-ray crystal structure of 39 bound to CDK2 has been determined in this study, revealing a binding mode that is consistent with our SAR. Compound 39 demonstrates significant in vivo efficacy in the HCT116 human colorectal tumor xenograft model in nude mice with up to 95% tumor growth inhibition. On the basis of its superior overall profile, 39 was chosen for further evaluation and has progressed into Phase I clinical trial for the treatment of cancer.
Sujet(s)
Antinéoplasiques/pharmacologie , Kinases cyclines-dépendantes/antagonistes et inhibiteurs , Antienzymes/pharmacologie , Antienzymes/pharmacocinétique , Pyrimidines/pharmacologie , Pyrimidines/pharmacocinétique , Animaux , Antinéoplasiques/pharmacocinétique , Lignée cellulaire tumorale , Phénomènes chimiques , Chimie physique , Kinase-2 cycline-dépendante/composition chimique , Conception de médicament , Femelle , Humains , Indicateurs et réactifs , Cinétique , Souris , Souris nude , Modèles moléculaires , Relation structure-activité , Diffraction des rayons XRÉSUMÉ
RO4396686 is a small molecule KDR, FGFR, and PDGFR inhibitor with good pharmacokinetic properties in rodents. In a mouse corneal neovascularization assay, this compound inhibited VEGF-induced angiogenesis. Tested in a H460a xenograft tumor model this agent effected significant tumor growth inhibition at doses as low as 50mg/kg.
Sujet(s)
Inhibiteurs de l'angiogenèse/pharmacologie , Tumeurs expérimentales/vascularisation , Néovascularisation pathologique , Pyrimidines/pharmacologie , Inhibiteurs de l'angiogenèse/composition chimique , Animaux , Souris , Souris nude , Rats , Rat Wistar , Récepteur facteur croissance fibroblaste/antagonistes et inhibiteurs , Récepteurs aux facteurs de croissance dérivés des plaquettes/antagonistes et inhibiteurs , Facteur de croissance endothéliale vasculaire de type A/physiologie , Récepteur-2 au facteur croissance endothéliale vasculaire/antagonistes et inhibiteursRÉSUMÉ
(+/-)-1-(anti-3-Hydroxy-cyclopentyl)-3-(4-methoxy-phenyl)-7-phenylamino-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one (RO4383596) is a potent and selective inhibitor of the pro-angiogenic receptor tyrosine kinases KDR, FGFR, and PDGFR. This agent has an excellent pharmacokinetic profile and is highly efficacious in rodent models of angiogenesis upon oral administration.
Sujet(s)
Inhibiteurs de l'angiogenèse/pharmacologie , Inhibiteurs de protéines kinases/pharmacologie , Protein-tyrosine kinases/antagonistes et inhibiteurs , Pyrimidinones/pharmacologie , Administration par voie orale , Inhibiteurs de l'angiogenèse/synthèse chimique , Inhibiteurs de l'angiogenèse/métabolisme , Animaux , Néovascularisation cornéenne/traitement médicamenteux , Femelle , Humains , Immunotransfert , Souris , Souris de lignée C57BL , Souris nude , Inhibiteurs de protéines kinases/synthèse chimique , Inhibiteurs de protéines kinases/pharmacocinétique , Pyrimidinones/synthèse chimique , Pyrimidinones/pharmacocinétique , Rats , Rat Wistar , Récepteur facteur croissance fibroblaste/antagonistes et inhibiteurs , Récepteurs aux facteurs de croissance dérivés des plaquettes/antagonistes et inhibiteurs , Cellules cancéreuses en culture , Récepteur-2 au facteur croissance endothéliale vasculaire/antagonistes et inhibiteursRÉSUMÉ
A novel class of 3,5,6-trisubstituted naphthostyril analogues was designed and synthesized to study the structure-activity relationship for inhibition of cyclin-dependent kinase 2 (CDK2). These compounds, particularly molecules with side-chain modifications providing additional hydrogen bonding capability, were demonstrated to be potent CDK2 inhibitors with cellular activities consistent with CDK2 inhibition. These molecules inhibited tumor cell proliferation and G1-S and G2-M cell-cycle progression in vitro. The X-ray crystal structure of a 2-aminoethyleneamine derivative bound to CDK2, refined to 2.5A resolution, is presented.