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1.
Eur J Pharmacol ; 977: 176723, 2024 Aug 15.
Article in English | MEDLINE | ID: mdl-38851560

ABSTRACT

Acute lymphoblastic leukemia (ALL), a complex malignancy, displays varying expression profiles of PIP4K2-related genes in adult patients. While PIP4K2A expression is elevated in ALL bone marrow cells compared to healthy bone marrow cells, PIP4K2B is downregulated, and PIP4K2C remains relatively unchanged. Despite the correlation between increased PIP4K2A expression and increased percentage of peripheral blood blasts, clinical outcomes do not strongly correlate with the expression of these genes. Here we investigated the therapeutic potential of three PIP4K2 inhibitors (THZ-P1-2, a131, and CC260) in ALL cell models. THZ-P1-2 emerges as the most effective inhibitor, inducing cell death and mitochondrial damage while reducing cell viability and metabolism significantly. Comparative analyses highlight the superior efficacy of THZ-P1-2 over a131 and CC260. Notably, THZ-P1-2 uniquely disrupts autophagic flux and inhibits the PI3K/AKT/mTOR pathway, indicating a distinct molecular mechanism. In summary, our findings elucidate the differential expression of PIP4K2-related genes in ALL and underscore the potential role of PIP4K2A in disease pathogenesis. The therapeutic promise of THZ-P1-2 in ALL treatment, along with its distinct effects on cell death mechanisms and signaling pathways, enriches our understanding of PIP4K2's involvement in ALL development and offers targeted therapy prospects.


Subject(s)
Phosphotransferases (Alcohol Group Acceptor) , Precursor Cell Lymphoblastic Leukemia-Lymphoma , Humans , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Phosphotransferases (Alcohol Group Acceptor)/antagonists & inhibitors , Phosphotransferases (Alcohol Group Acceptor)/genetics , Cell Line, Tumor , Signal Transduction/drug effects , Proto-Oncogene Proteins c-akt/metabolism , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , TOR Serine-Threonine Kinases/metabolism , TOR Serine-Threonine Kinases/antagonists & inhibitors , Autophagy/drug effects , Cell Survival/drug effects , Phosphatidylinositol 3-Kinases/metabolism , Enzyme Inhibitors/pharmacology , Enzyme Inhibitors/therapeutic use , Protein Kinase Inhibitors/pharmacology , Protein Kinase Inhibitors/therapeutic use , Apoptosis/drug effects
2.
Int J Mol Sci ; 24(23)2023 Nov 29.
Article in English | MEDLINE | ID: mdl-38069220

ABSTRACT

Phosphatidylinositol-5-phosphate 4-kinase type 2 (PIP4K2) protein family members (PIP4K2A, PIP4K2B, and PIP4K2C) participate in the generation of PIP4,5P2, which acts as a secondary messenger in signal transduction, a substrate for metabolic processes, and has structural functions. In patients with acute myeloid leukemia (AML), high PIP4K2A and PIP4K2C levels are independent markers of a worse prognosis. Recently, our research group reported that THZ-P1-2 (PIP4K2 pan-inhibitor) exhibits anti-leukemic activity by disrupting mitochondrial homeostasis and autophagy in AML models. In the present study, we characterized the expression of PIP4K2 in the myeloid compartment of hematopoietic cells, as well as in AML cell lines and clinical samples with different genetic abnormalities. In ex vivo assays, PIP4K2 expression levels were related to sensitivity and resistance to several antileukemia drugs and highlighted the association between high PIP4K2A levels and resistance to venetoclax. The combination of THZ-P1-2 and venetoclax showed potentiating effects in reducing viability and inducing apoptosis in AML cells. A combined treatment differentially modulated multiple genes, including TAp73, BCL2, MCL1, and BCL2A1. In summary, our study identified the correlation between the expression of PIP4K2 and the response to antineoplastic agents in ex vivo assays in AML and exposed vulnerabilities that may be exploited in combined therapies, which could result in better therapeutic responses.


Subject(s)
Antineoplastic Agents , Leukemia, Myeloid, Acute , Humans , Cell Line, Tumor , Proto-Oncogene Proteins c-bcl-2/metabolism , Leukemia, Myeloid, Acute/drug therapy , Leukemia, Myeloid, Acute/genetics , Leukemia, Myeloid, Acute/metabolism , Bridged Bicyclo Compounds, Heterocyclic/pharmacology , Bridged Bicyclo Compounds, Heterocyclic/therapeutic use , Apoptosis , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Phosphotransferases (Alcohol Group Acceptor)/pharmacology
3.
Hematol., Transfus. Cell Ther. (Impr.) ; 44(4): 582-594, Oct.-dec. 2022. tab, ilus
Article in English | LILACS | ID: biblio-1421521

ABSTRACT

ABSTRACT Introduction: Systemic Mastocytosis comprises a group of neoplastic diseases characterized by clonal expansion and infiltration of mast cells into several organs. The diagnosis and treatment of this disease may be challenging for non-specialists. Objective: Make suggestions or recommendations in Systemic Mastocytosis based in a panel of Brazilian specialists. Method and results: An online expert panel with 18 multidisciplinary specialists was convened to propose recommendations on the diagnosis and treatment of Systemic Mastocytosis in Brazil. Recommendations were based on discussions of topics and multiple-choice questions and were graded using the Oxford Centre for Evidence-Based Medicine 2011 Levels of Evidence Chart. Conclusion: Twenty-two recommendations or suggestions were proposed based on a literature review and graded according to the findings.


Subject(s)
Mastocytosis, Systemic/diagnosis , Mastocytosis, Systemic/therapy , Child , Adult
4.
Hematol Transfus Cell Ther ; 44(4): 582-594, 2022.
Article in English | MEDLINE | ID: mdl-35688791

ABSTRACT

INTRODUCTION: Systemic Mastocytosis comprises a group of neoplastic diseases characterized by clonal expansion and infiltration of mast cells into several organs. The diagnosis and treatment of this disease may be challenging for non-specialists. OBJECTIVE: Make suggestions or recommendations in Systemic Mastocytosis based in a panel of Brazilian specialists. METHOD AND RESULTS: An online expert panel with 18 multidisciplinary specialists was convened to propose recommendations on the diagnosis and treatment of Systemic Mastocytosis in Brazil. Recommendations were based on discussions of topics and multiple-choice questions and were graded using the Oxford Centre for Evidence-Based Medicine 2011 Levels of Evidence Chart. CONCLUSION: Twenty-two recommendations or suggestions were proposed based on a literature review and graded according to the findings.

6.
Nanomedicine ; 13(8): 2475-2484, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28842374

ABSTRACT

Opportunistic bacteria that cause life-threatening infections are still a central problem associated with a healthcare setting. Bacteriophage capsid immobilization on nanostructured polymers maximizes its tail exposure and looks promising in applications toward skin-infections as alternative to antibiotics standardly used. The main goal of this work was to investigate the covalent immobilization of vB_Pae_Kakheti25 bacteriophage capsid on polycaprolactone (PCL) nanofibers (non-woven textile), as a potential effective antimicrobial, laundry resistant and non-toxic dressing for biomedical use. Surface analyses showed that the immobilization of vB_Pae_Kakheti25 bacteriophage capsid on PCL nanofibres oriented bacteriophage tails to interact with bacteria. Furthermore, antimicrobial assays showed a very effective 6 log bacterial reduction, which was equivalent to 99.9999%, after immediate and 2 hours of contact, even following 25 washing cycles (due to covalent bond). The activity of PCL-vB_Pae_Kakheti25 against P. aeruginosa was immediate and its reduction was complete.


Subject(s)
Anti-Infective Agents/pharmacology , Bacteriophages , Bandages , Capsid Proteins/pharmacology , Immobilized Proteins/pharmacology , Wound Infection/prevention & control , Animals , Anti-Infective Agents/chemistry , BALB 3T3 Cells , Bacteriophages/chemistry , Bandages/microbiology , Bandages/virology , Capsid Proteins/chemistry , Cell Line , Humans , Immobilized Proteins/chemistry , Mice , Models, Molecular , Nanofibers/chemistry , Nanofibers/ultrastructure , Polyesters/chemistry , Pseudomonas Infections/prevention & control , Pseudomonas aeruginosa/drug effects
7.
J Microbiol Biotechnol ; 27(4): 747-758, 2017 Apr 28.
Article in English | MEDLINE | ID: mdl-28104899

ABSTRACT

Chronic wounds, pressure sores, lesions, and infections of microbial origin in bedridden, paralyzed, or malnutrition patients remain the object of study of many researchers. A variety of factors behind the development of these disorders are related to the patient's immune system, making it unable to respond effectively to the treatment of the wound. These factors can be properly controlled, giving particular importance to the ethiology and stage of the wound, as well as the time periods corresponding to the replacement of the dressings. The present research reports a novel foam/soft material, L-Cys-g-PCL, with an application for decubitus/pressure ulcers, especially for wounds with a difficult healing process due to infections and constant oxidation of the soft tissues. During this work, the interactions between S. aureus and L-Cys-g-PCL foam were studied under conditions that simulate decubitus ulcers; namely, pH and exudate. The effects of duration of grafting (1 or 8 h) and pH (7.0 and 8.9) on wettability, surface energy, swelling, and porosity were also evaluated. Results showed an effective microbicidal activity exhibiting an inhibition ratio of 99.73% against S. aureus. This new L-Cys-g-PCL soft material showed saftey to contact skin, ability to be shaped to fill in sunken holes (craters) - pressure ulcers stage III - and to act as a smart material responsive to pH, which can be tailored to develop better swelling properties at alkaline pH where exudates are normally higher, so as to address exudate self-cleaning and prevention of desiccation..


Subject(s)
Amino Acids/chemistry , Amino Acids/pharmacology , Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Pressure Ulcer/drug therapy , Administration, Oral , Animals , BALB 3T3 Cells , Calorimetry , Cell Survival/drug effects , Chemistry, Pharmaceutical , Cysteine/chemistry , Cysteine/therapeutic use , Drug Compounding/methods , Hydrogen-Ion Concentration , Mice , Microscopy, Electron, Scanning , Polyesters/chemistry , Spectrophotometry, Infrared , Staphylococcus aureus/drug effects , Wound Healing
8.
Blood Cells Mol Dis ; 54(1): 44-50, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25175566

ABSTRACT

Cerebrovascular disease (CVD) is a severe complication associated with sickle cell anemia. Abnormal transcranial Doppler (TCD) identifies some children at high risk, but other markers would be helpful. This cohort study was aimed at evaluating the effects of genetic biomarkers on the risk of developing CVD in children from Minas Gerais, Brazil. Clinical and hematological data were retrieved from children's records. Outcomes studied were overt ischemic stroke and CVD (overt ischemic stroke, transient ischemic attack, abnormal TCD, or abnormal cerebral angiography). Out of 411 children, 386 (93.9%) had SS genotype, 23 (5.6%) had Sß(0)-thal and two had severe Sß(+)-thal (0.5%). Frequency of CVD was lower in Sß-thal group (p=0.05). No effect of VCAM-1 polymorphism on stroke or CVD risks was detected. Cumulative incidence of stroke was significantly higher for children with TNF-α A allele (p=0.02) and lower for children with HBA deletion (p=0.02). However, no association between CVD and TNF-α -308G>A was found. CVD cumulative incidence was significantly lower for children with HBA deletion (p=0.004). This study found no association between VCAM1 c.1238G>C and stroke. An association between stroke and TNF-α -308A allele has been suggested. Our results have confirmed the protective role of HBA deletion against stroke and CVD.


Subject(s)
Anemia, Sickle Cell/genetics , Brain Ischemia/genetics , Polymorphism, Genetic , Stroke/genetics , Tumor Necrosis Factor-alpha/genetics , Vascular Cell Adhesion Molecule-1/genetics , alpha-Thalassemia/genetics , Alleles , Anemia, Sickle Cell/complications , Anemia, Sickle Cell/diagnostic imaging , Brain Ischemia/diagnostic imaging , Brain Ischemia/etiology , Child , Female , Follow-Up Studies , Hemoglobin A/genetics , Humans , Male , Retrospective Studies , Stroke/etiology , Ultrasonography , alpha-Thalassemia/complications , alpha-Thalassemia/diagnostic imaging
9.
Acta Biomater ; 9(2): 5208-15, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22995406

ABSTRACT

Helicobacter pylori infection has been associated with several gastric diseases. This bacterium colonizes the gastric mucosa of half of the world's population, and available treatments are unsuccessful in practically one in every five patients. Mucoadhesive polymers, such as chitosan, are being investigated as gastric drug delivery systems. However, since chitosan is also known for its antimicrobial properties, this work aims to evaluate H. pylori interactions with chitosan under simulated gastric environments, namely using various pHs (2.6, 4 and 6), pepsin and urea. To enable the visualization of adherent bacteria, ultrathin chitosan films were produced by spin-coating on gold/glass surfaces, cross-linked with genipin and characterized by Fourier transform infrared reflection absorption spectroscopy, ellipsometry and electrokinetic analysis. Films with homogeneous thickness of 11.7±0.6 nm were produced, and were stable and protonated at all the pHs used. Furthermore, they adsorbed pepsin in all these pHs, in contrast to urea, of which a small adsorption was only observed at pH 6. H. pylori binding to chitosan was higher at pH2.6 although most of adherent bacteria were dead. The presence of pepsin decreased bacterial adhesion, but increased its viability while in a more stressed morphology (coccoid form). The presence of urea did not affect the amount, morphology or viability of chitosan-adherent bacteria. In suspension, the decrease in pH changed H. pylori zeta potential from negative to positive. Moreover, bacteria were only culturable when incubated in pH 6 with and without urea (without pepsin). This work demonstrates that chitosan has the capacity to bind and kill H. pylori in a range of pHs independently of urea. This opens new perspectives for the application of chitosan-based materials to the elimination of H. pylori gastric colonization, though pepsin might appear to be an obstacle.


Subject(s)
Bacterial Adhesion/drug effects , Chitosan/pharmacology , Helicobacter pylori/physiology , Mucus/chemistry , Stomach/microbiology , Adhesiveness/drug effects , Buffers , Helicobacter pylori/drug effects , Helicobacter pylori/ultrastructure , Hydrogen-Ion Concentration , Microbial Viability/drug effects , Pepsin A/pharmacology , Spectroscopy, Fourier Transform Infrared , Urea/pharmacology
10.
Rev. bras. ecocardiogr. imagem cardiovasc ; 25(4): 285-291, out.-dez. 2012. ilus, tab
Article in Portuguese | LILACS | ID: lil-653986

ABSTRACT

Objetivo: Avaliar a medida da ECMIC em idosos portadores de EVAo, de forma a tentar estabelecer uma relação entre a EVAo e a Aterosclerose de Carótidas. Método: Estudo seccional observacional baseado na demanda espontânea do Serviço de Ecocardiografia do Centro Clínico Vingt-un Rosado, município de Mossoró-RN, no período de novembro de 2.009 a junho de 2.010. Foram excluídos com história de evento e/ou doença cardiovascular prévios. Foram considerados portadores de aumento da ECMIC, aqueles que tiveram uma medida da ECMIC ≥ 10mm. A análise estatística foi realizada pelo método do Teste Exato de Fisher, considerando significância estatística para um p < 0,05. Resultados: Foram avaliados 105 pacientes, dos quais 37 preenchiam os critérios de exclusão do estudo. Entre os 68 pacientes analisados, foram 18 (26,4%) homens e 50 mulheres (73,5%), com média de idade de 71,9 anos. 56 pacientes (82,3%) tinham EVAo, sendo 16 do sexo masculino (28,5%) e 40 do sexo feminino (71,4%); e 40 apresentavam aumento da ECMI, com prevalência significativamente maior nos pacientes portadores de EVAo (p < 00,5). Conclusão: Os resultados sugerem que idosos portadores de EVAo devem ser mais bem avaliados para detecção de ateromatose subclínica.


Subject(s)
Humans , Male , Female , Aged , Aged , Coronary Disease/complications , Carotid Artery Diseases/complications , Tunica Media/pathology , Aortic Valve/abnormalities , Echocardiography/methods , Echocardiography , Risk Factors
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