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1.
J. Bras. Patol. Med. Lab. (Online) ; 58: e4482022, 2022. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1375689

ABSTRACT

ABSTRACT Introduction In Brazil, 8,000 new cases of childhood cancer are estimated each year, whose causes are still little known, although some have genetically determined factors. Approximately 70% of human cancers have alterations in the TP53 gene, which encodes the protein responsible for inhibiting the disordered growth of cells exposed to injuries. However, the frequency of alterations in the expression of TP53 in childhood cancers in Brazil remains poorly known. Objective To evaluate the expression of TP53 gene in patients with childhood cancer in northeastern of Santa Catarina, Brazil. Materials and Methods: Retrospectively, 282 patients diagnosed with cancer between 2005 and 2015 in Joinville were included. TP53 expression was evaluated by immunohistochemistry using a score based on the intensity and percentage of stained cells. Results The p53 protein was positive in 25.2% of cases, with no difference between sexes. Considering the five main groups of tumors in the sample, the expression was positive in 31.8%, 27.3%, 20%, 17.2% and 5.9% of lymphomas, nephroblastomas, neuroblastomas, tumors of the Central Nervous System and leukemias, respectively. Conclusion The prevalence of TP53 expression was evaluated in different childhood cancers in the northeastern of Santa Catarina. Positivity was higher among lymphomas and lower in leukemias, but with no significant difference among the five most frequent tumors. Further studies that allow correlation with aggressiveness and disease evolution are required.

2.
J Med Case Rep ; 15(1): 348, 2021 Jul 17.
Article in English | MEDLINE | ID: mdl-34271987

ABSTRACT

BACKGROUND: Glomangioma is a benign tumor of mesenchymal origin, derived from the glomus body. It is responsible for the thermal regulation of the dermis. The occurrence of oncogenic osteomalacia related to glomangioma is rare. Only two cases have been reported thus far. CASE PRESENTATION: A 32-year-old female, Brazilian, presented diffuse pain, during pregnancy, that developed progressively, limiting her mobility. Imaging showed a femoral neck fracture, and rheumatological laboratory examination showed hypophosphatemia. Also, the patient reported episodes of epistaxis during childhood and recurrence along with progressively right nasal obstruction. Endoscopic resection of the tumor was performed, and immunohistochemistry was conclusive for glomangioma. This case report describes the third case in which endonasal endoscopic surgery resulted in a favorable outcome. CONCLUSION: This case of glomangioma-induced oncogenic osteomalacia suggests that surgeons and clinicians should consider sinonasal tumors as a differential diagnosis of osteomalacia, and endonasal endoscopic surgery should be a possible curative resection.


Subject(s)
Glomus Tumor , Paranasal Sinus Neoplasms , Adult , Brazil , Female , Glomus Tumor/diagnosis , Glomus Tumor/diagnostic imaging , Humans , Neoplasm Recurrence, Local , Osteomalacia , Paranasal Sinus Neoplasms/diagnosis , Paranasal Sinus Neoplasms/diagnostic imaging , Paraneoplastic Syndromes
3.
BMC Plant Biol ; 20(1): 158, 2020 Apr 15.
Article in English | MEDLINE | ID: mdl-32293271

ABSTRACT

BACKGROUND: Plants reprogram metabolism and development to rapidly adapt to biotic and abiotic stress. Protein kinases play a significant role in this process by phosphorylating protein substrates that activate or inactivate signaling cascades that regulate cellular and metabolic adaptations. Despite their importance in plant biology, a notably small fraction of the plant kinomes has been studied to date. RESULTS: In this report, we describe ZmDRIK1, a stress-responsive receptor-like pseudokinase whose expression is downregulated under water restriction. We show the structural features and molecular basis of the absence of ATP binding exhibited by ZmDRIK1. The ZmDRIK1 kinase domain lacks conserved amino acids that are essential for phosphorylation activity. The crystal structure of the ZmDRIK1 kinase domain revealed the presence of a spine formed by the side chain of the triad Leu240, Tyr363, and Leu375 that occludes the ATP binding pocket. Although ZmDRIK1 is unable to bind nucleotides, it does bind the small molecule ENMD-2076 which, in a cocrystal structure, revealed the potential to serve as a ZmDRIK1 inhibitor. CONCLUSION: ZmDRIK1 is a novel receptor-like pseudokinase responsive to biotic and abiotic stress. The absence of ATP binding and consequently, the absence of phosphorylation activity, was proven by the crystal structure of the apo form of the protein kinase domain. The expression profiling of the gene encoding ZmDRIK1 suggests this kinase may play a role in downregulating the expression of stress responsive genes that are not necessary under normal conditions. Under biotic and abiotic stress, ZmDRIK1 is down-regulated to release the expression of these stress-responsive genes.


Subject(s)
Adenosine Triphosphate/chemistry , Plant Proteins/chemistry , Receptor Protein-Tyrosine Kinases/chemistry , Zea mays/enzymology , Crystallography , Gene Expression Profiling , Gene Expression Regulation, Plant , Plant Proteins/antagonists & inhibitors , Plant Proteins/genetics , Protein Kinase Inhibitors/chemistry , Pyrazoles/chemistry , Pyrimidines/chemistry , Receptor Protein-Tyrosine Kinases/antagonists & inhibitors , Receptor Protein-Tyrosine Kinases/genetics , Stress, Physiological/genetics , Zea mays/genetics
4.
J Vis Exp ; (138)2018 08 25.
Article in English | MEDLINE | ID: mdl-30199012

ABSTRACT

A wide range of studies in plant biology are performed using hydroponic cultures. In this work, an in vitro hydroponic growth system designed for assessing plant responses to chemicals and other substances of interest is presented. This system is highly efficient in obtaining homogeneous and healthy seedlings of the C3 and C4 model species Arabidopsis thaliana and Setaria viridis, respectively. The sterile cultivation avoids algae and microorganism contamination, which are known limiting factors for plant normal growth and development in hydroponics. In addition, this system is scalable, enabling the harvest of plant material on a large scale with minor mechanical damage, as well as the harvest of individual parts of a plant if desired. A detailed protocol demonstrating that this system has an easy and low-cost assembly, as it uses pipette racks as the main platform for growing plants, is provided. The feasibility of this system was validated using Arabidopsis seedlings to assess the effect of the drug AZD-8055, a chemical inhibitor of the target of rapamycin (TOR) kinase. TOR inhibition was efficiently detected as early as 30 min after an AZD-8055 treatment in roots and shoots. Furthermore, AZD-8055-treated plants displayed the expected starch-excess phenotype. We proposed this hydroponic system as an ideal method for plant researchers aiming to monitor the action of plant inducers or inhibitors, as well as to assess metabolic fluxes using isotope-labeling compounds which, in general, requires the use of expensive reagents.


Subject(s)
Cost-Benefit Analysis/economics , Hydroponics/economics , Hydroponics/methods
5.
Sci Rep ; 7(1): 8305, 2017 08 16.
Article in English | MEDLINE | ID: mdl-28814797

ABSTRACT

Arabidopsis plants store part of the carbon fixed by photosynthesis as starch to sustain growth at night. Two competing hypotheses have been proposed to explain this diel starch turnover based on either the measurement of starch abundance with respect to circadian time, or the sensing of sugars to feedback to the circadian oscillator to dynamically adjust the timing of starch turnover. We report a phase oscillator model that permitted derivation of the ideal responses of the circadian regulation of starch breakdown to maintain sucrose homeostasis. Testing the model predictions using a sugar-unresponsive mutant of Arabidopsis demonstrated that the dynamics of starch turnover arise from the circadian clock measuring and responding to the rate of change of cellular sucrose. Our theory and experiments suggest that starch turnover is controlled by the circadian clock acting as a dynamic homeostat responding to sucrose signals to maintain carbon homeostasis.


Subject(s)
Arabidopsis/physiology , Carbohydrate Metabolism , Circadian Rhythm , Starch/metabolism , Sugars/metabolism , Homeostasis , Metabolic Networks and Pathways , Signal Transduction , Sucrose/metabolism
6.
Plant Physiol Biochem ; 68: 16-22, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23619240

ABSTRACT

Hsp90s are involved in several cellular processes, such as signaling, proteostasis, epigenetics, differentiation and stress defense. Although Hsp90s from different organisms are highly similar, they usually have small variations in conformation and function. Thus, the characterization of different Hsp90s is important to gain insight into the structure-function relationship that makes these chaperones key regulators in protein homeostasis. This work describes the characterization of a cytosolic Hsp90 from sugarcane and its comparison with Hsp90s from other plants. Previous expressed sequence tag (EST) studies in Saccharum spp. (sugarcane) predicted the presence of an mRNA coding for a cytosolic Hsp90. The corresponding cDNA was cloned, and the recombinant protein was purified and its conformation and function characterized. The structural conformation of Hsp90 was assessed by chemical cross-linking and hydrogen/deuterium exchange using mass spectrometry and hydrodynamic assays, which revealed regions accessible to solvent and that Hsp90 is an elongated dimer in solution. The in vivo expression of Hsp90 in sugarcane leaves was confirmed by western blot, and in vitro functional characterization indicated that sugarcane Hsp90 has strong chaperone activity.


Subject(s)
Cytosol/metabolism , HSP90 Heat-Shock Proteins/chemistry , HSP90 Heat-Shock Proteins/metabolism , Plant Proteins/chemistry , Plant Proteins/metabolism , Saccharum/chemistry , Amino Acid Sequence , Cloning, Molecular , HSP90 Heat-Shock Proteins/genetics , Mass Spectrometry/methods , Models, Molecular , Molecular Chaperones/chemistry , Molecular Chaperones/metabolism , Molecular Sequence Data , Plant Leaves/metabolism , Plant Proteins/genetics , Protein Conformation , Protein Structure, Tertiary , Sequence Homology, Amino Acid
7.
J Proteomics ; 75(10): 2790-802, 2012 Jun 06.
Article in English | MEDLINE | ID: mdl-22236519

ABSTRACT

In the cell, proteins interact within a network in which a small number of proteins are highly connected nodes or hubs. A disturbance in the hub proteins usually has a higher impact on the cell physiology than a disturbance in poorly connected nodes. In eukaryotes, the cytosolic Hsp90 is considered to be a hub protein as it interacts with molecular chaperones and co-chaperones, and has key regulatory proteins as clients, such as transcriptional factors, protein kinases and hormone receptors. The large number of Hsp90 partners suggests that Hsp90 is involved in very important functions, such as signaling, proteostasis and epigenetics. Some of these functions are dysregulated in cancer, making Hsp90 a potential target for therapeutics. The number of Hsp90 interactors appears to be so large that a precise answer to the question of how many proteins interact with this chaperone has no definitive answer yet, not even if the question refers to specific Hsp90s as one of the human cytosolic forms. Here we review the major chaperones and co-chaperones that interact with cytosolic Hsp90s, highlighting the latest findings regarding client proteins and the role that posttranslational modifications have on the function and interactions of these molecular chaperones. This article is part of a Special Issue entitled: Proteomics: The clinical link.


Subject(s)
HSP90 Heat-Shock Proteins/metabolism , Molecular Targeted Therapy/trends , Neoplasms/therapy , Protein Interaction Mapping , Amino Acid Sequence , Cytosol/metabolism , HSP90 Heat-Shock Proteins/chemistry , Humans , Models, Molecular , Molecular Chaperones/chemistry , Molecular Chaperones/isolation & purification , Molecular Chaperones/metabolism , Molecular Sequence Data , Molecular Targeted Therapy/methods , Neoplasms/metabolism , Protein Binding/physiology , Protein Interaction Domains and Motifs/physiology , Protein Interaction Mapping/methods , Sequence Homology, Amino Acid
8.
Int J Biol Macromol ; 49(5): 1022-30, 2011 Dec 01.
Article in English | MEDLINE | ID: mdl-21903129

ABSTRACT

The Clp/Hsp100 AAA+ chaperone family is involved in recovering aggregated proteins and little is known about other orthologs of the well studied ClpB from Escherichia coli and Hsp104 from Saccharomyces cerevisiae. Plant Hsp101 is a good model for understanding the relationship between the structure and function of Hsp100 proteins and to investigate the role of these chaperones in disaggregation processes. Here, we present the cloning and purification of a sugarcane ortholog, SHsp101, which is expressed in sugarcane cells and is a folded hexamer that is capable of binding nucleotides. Thus SHsp101 has the structural and functional characteristics of the Clp/Hsp100 AAA+ family.


Subject(s)
Molecular Chaperones/metabolism , Plant Proteins/metabolism , Recombinant Proteins/metabolism , Saccharum/chemistry , Transcription Factors/metabolism , Amino Acid Sequence , Chimera/genetics , Cloning, Molecular , Endopeptidase Clp , Escherichia coli/chemistry , Escherichia coli/genetics , Escherichia coli Proteins/chemistry , Escherichia coli Proteins/genetics , Escherichia coli Proteins/metabolism , Heat-Shock Proteins/chemistry , Heat-Shock Proteins/genetics , Heat-Shock Proteins/metabolism , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Chaperones/genetics , Molecular Chaperones/isolation & purification , Molecular Sequence Data , Nucleotides/metabolism , Plant Proteins/genetics , Plant Proteins/isolation & purification , Plasmids , Polymerization , Protein Binding , Protein Folding , Protein Structure, Tertiary , Recombinant Proteins/genetics , Recombinant Proteins/isolation & purification , Saccharomyces cerevisiae/chemistry , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/chemistry , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/metabolism , Saccharum/genetics , Structure-Activity Relationship , Transcription Factors/genetics , Transcription Factors/isolation & purification , Ultracentrifugation
9.
Rev. bras. otorrinolaringol ; 65(2,pt.1): 172-4, mar.-abr. 1999. ilus
Article in Portuguese | LILACS | ID: lil-239877

ABSTRACT

Os autores apresentam um caso de neurofibroma acometendo a cavidade nasal, sendo esta uma localizaçäo pouco frequente desta neoplasia benigna, porém com possibilidade de malignizaçäo especialmente nos pacientes com neurofibromatose (doença de Von Recklinghausen). Originam-se das bainhas nervosas, e entre 25 a 45 por cento dos casos acometem a regiäo da cabeça e pescoço. Destes, apenas 4 por cento têm origem nas fossas nasais e seios paranasais. O tratamento consiste em remoçäo cirúrgica completa


Subject(s)
Humans , Male , Middle Aged , Nasal Cavity , Nasal Septum , Neurofibroma , Nose Neoplasms , Epistaxis , Nasal Obstruction , Neurofibroma/surgery , Olfaction Disorders
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