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1.
Diabet Med ; 37(1): 114-122, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31705695

RESUMO

AIMS: To examine the relative association between fasting plasma glucose vs post-load (1-h and 2-h) glucose levels based on the oral glucose tolerance test in pregnancy and large-for-gestational-age and hypertensive disorders of pregnancy outcomes. METHODS: All live singleton births between October 2008 and December 2014 in Alberta, Canada were included. Gestational diabetes mellitus was diagnosed using Diabetes Canada criteria. Logistic regression models were used to examine the association between fasting plasma glucose vs post-load values and large-for-gestational-age infants and hypertensive disorders of pregnancy after adjusting for maternal characteristics and pharmaceutical intervention in gestational diabetes pregnancies. RESULTS: Among 257 547 pregnancies, 208 344 (80.9%) had negative 50-g glucose challenge tests, 36 261 (14.1%) had negative 75-g oral glucose tolerance tests, and 12 942 (5.0%) had gestational diabetes based on either elevated fasting plasma glucose (n=4130, 1.6%) or elevated 1-h and/or 2-h oral glucose tolerance test values (n=8812, 3.4%). Large-for-gestational-age and hypertensive disorders of pregnancy rates were 8.1% and 5.1% in negative glucose challenge test pregnancies, 11.0% and 7.0% in negative oral glucose tolerance test pregnancies, 22.4% and 11.9% in gestational diabetes pregnancies with elevated fasting plasma glucose, and 9.1% and 8% in gestational diabetes pregnancies with elevated post-load levels, respectively. Among gestational diabetes pregnancies, those with elevated fasting plasma glucose were at higher risk of large-for-gestational age (adjusted odds ratio 2.66, 95% CI 2.39-2.96) and hypertensive disorders of pregnancy (adjusted odds ratio 1.51, 95% CI 1.33-1.72) outcomes relative to pregnancies with post-load glucose elevations only. Fasting plasma glucose remained significantly associated with adverse outcomes in gestational diabetes pregnancies with and without pharmacological intervention. CONCLUSIONS: Elevated fasting plasma glucose in women with gestational diabetes is a stronger predictor of large-for-gestational-age and hypertensive disorders of pregnancy outcomes than elevated post-load glucose.


Assuntos
Glicemia/metabolismo , Diabetes Gestacional/sangue , Jejum/sangue , Adulto , Alberta , Jejum/efeitos adversos , Feminino , Teste de Tolerância a Glucose , Humanos , Gravidez , Resultado da Gravidez
2.
Am J Transplant ; 16(12): 3479-3489, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27160653

RESUMO

Renal cell carcinoma (RCC) is a common malignancy following kidney transplantation. We describe RCC risk and examine RCC risk factors among US kidney recipients (1987-2010). The Transplant Cancer Match Study links the US transplant registry with 15 cancer registries. Standardized incidence ratios (SIRs) were used to compare RCC risk (overall and for clear cell [ccRCC] and papillary subtypes) to the general population. Associations with risk factors were assessed using Cox models. We identified 683 RCCs among 116 208 kidney recipients. RCC risk was substantially elevated compared with the general population (SIR 5.68, 95% confidence interval 5.27-6.13), especially for papillary RCC (SIR 13.3 versus 3.98 for ccRCC). Among kidney recipients, RCC risk was significantly elevated for blacks compared to whites (hazard ratio [HR] 1.50) and lower in females than males (HR 0.56). RCC risk increased with prolonged dialysis preceding transplantation (p-trend < 0.0001). Risk was variably associated for RCC subtypes with some medical conditions that were indications for transplantation: ccRCC risk was reduced with polycystic kidney disease (HR 0.54), and papillary RCC was increased with hypertensive nephrosclerosis (HR 2.02) and vascular diseases (HR 1.86). In conclusion, kidney recipients experience substantially elevated risk of RCC, especially for papillary RCC, and multiple factors contribute to these cancers.


Assuntos
Carcinoma de Células Renais/etiologia , Rejeição de Enxerto/etiologia , Neoplasias Renais/etiologia , Transplante de Rim/efeitos adversos , Complicações Pós-Operatórias , Adulto , Carcinoma de Células Renais/epidemiologia , Feminino , Seguimentos , Taxa de Filtração Glomerular , Rejeição de Enxerto/epidemiologia , Humanos , Incidência , Falência Renal Crônica/cirurgia , Testes de Função Renal , Neoplasias Renais/epidemiologia , Masculino , Pessoa de Meia-Idade , Prognóstico , Fatores de Risco , Estados Unidos/epidemiologia
3.
Br J Cancer ; 108(6): 1378-86, 2013 Apr 02.
Artigo em Inglês | MEDLINE | ID: mdl-23361049

RESUMO

BACKGROUND: The chromosome 9p21.3 region has been implicated in the pathogenesis of multiple cancers. METHODS: We systematically examined up to 203 tagging SNPs of 22 genes on 9p21.3 (19.9-32.8 Mb) in eight case-control studies: thyroid cancer, endometrial cancer (EC), renal cell carcinoma, colorectal cancer (CRC), colorectal adenoma (CA), oesophageal squamous cell carcinoma (ESCC), gastric cardia adenocarcinoma and osteosarcoma (OS). We used logistic regression to perform single SNP analyses for each study separately, adjusting for study-specific covariates. We combined SNP results across studies by fixed-effect meta-analyses and a newly developed subset-based statistical approach (ASSET). Gene-based P-values were obtained by the minP method using the Adaptive Rank Truncated Product program. We adjusted for multiple comparisons by Bonferroni correction. RESULTS: Rs3731239 in cyclin-dependent kinase inhibitors 2A (CDKN2A) was significantly associated with ESCC (P=7 × 10(-6)). The CDKN2A-ESCC association was further supported by gene-based analyses (Pgene=0.0001). In the meta-analyses by ASSET, four SNPs (rs3731239 in CDKN2A, rs615552 and rs573687 in CDKN2B and rs564398 in CDKN2BAS) showed significant associations with ESCC and EC (P<2.46 × 10(-4)). One SNP in MTAP (methylthioadenosine phosphorylase) (rs7023329) that was previously associated with melanoma and nevi in multiple genome-wide association studies was associated with CRC, CA and OS by ASSET (P=0.007). CONCLUSION: Our data indicate that genetic variants in CDKN2A, and possibly nearby genes, may be associated with ESCC and several other tumours, further highlighting the importance of 9p21.3 genetic variants in carcinogenesis.


Assuntos
Biomarcadores Tumorais/genética , Cromossomos Humanos Par 9/genética , Inibidor de Quinase Dependente de Ciclina p15/genética , Inibidor p16 de Quinase Dependente de Ciclina/genética , Neoplasias/genética , Polimorfismo de Nucleotídeo Único/genética , Estudos de Casos e Controles , Predisposição Genética para Doença , Humanos , Metanálise como Assunto , Prognóstico
4.
Nature ; 445(7126): 399-401, 2007 Jan 25.
Artigo em Inglês | MEDLINE | ID: mdl-17251972

RESUMO

The upper atmospheres of the four Solar System giant planets exhibit high temperatures that cannot be explained by the absorption of sunlight. In the case of Saturn the temperatures predicted by models of solar heating are approximately 200 K, compared to temperatures of approximately 400 K observed independently in the polar regions and at 30 degrees latitude. This unexplained 'energy crisis' represents a major gap in our understanding of these planets' atmospheres. An important candidate for the source of the missing energy is the magnetosphere, which injects energy mostly in the polar regions of the planet. This polar energy input is believed to be sufficient to explain the observed temperatures, provided that it is efficiently redistributed globally by winds, a process that is not well understood. Here we show, using a numerical model, that the net effect of the winds driven by the polar energy inputs is not to heat but to cool the low-latitude thermosphere. This surprising result allows us to rule out known polar energy inputs as the solution to the energy crisis at Saturn. There is either an unknown--and large--source of polar energy, or, more probably, some other process heats low latitudes directly.

5.
Carcinogenesis ; 32(2): 182-9, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21037224

RESUMO

Associations between bladder cancer risk and NAT2 and GSTM1 polymorphisms have emerged as some of the most consistent findings in the genetic epidemiology of common metabolic polymorphisms and cancer, but their interaction with tobacco use, intensity and duration remain unclear. In a New England population-based case-control study of urothelial carcinoma, we collected mouthwash samples from 1088 of 1171 cases (92.9%) and 1282 of 1418 controls (91.2%) for genotype analysis of GSTM1, GSTT1 and NAT2 polymorphisms. Odds ratios and 95% confidence intervals of bladder cancer among New England Bladder Cancer Study subjects with one or two inactive GSTM1 alleles (i.e. the 'null' genotype) were 1.26 (0.85-1.88) and 1.54 (1.05-2.25), respectively (P-trend = 0.008), compared with those with two active copies. GSTT1 inactive alleles were not associated with risk. NAT2 slow acetylation status was not associated with risk among never (1.04; 0.71-1.51), former (0.95; 0.75-1.20) or current smokers (1.33; 0.91-1.95); however, a relationship emerged when smoking intensity was evaluated. Among slow acetylators who ever smoked at least 40 cigarettes/day, risk was elevated among ever (1.82; 1.14-2.91, P-interaction = 0.07) and current heavy smokers (3.16; 1.22-8.19, P-interaction = 0.03) compared with rapid acetylators in each category; but was not observed at lower intensities. In contrast, the effect of GSTM1-null genotype was not greater among smokers, regardless of intensity. Meta-analysis of the NAT2 associations with bladder cancer showed a highly significant relationship. Findings from this large USA population-based study provided evidence that the NAT2 slow acetylation genotype interacts with tobacco smoking as a function of exposure intensity.


Assuntos
Arilamina N-Acetiltransferase/genética , Glutationa Transferase/genética , Fumar/efeitos adversos , Neoplasias da Bexiga Urinária/etiologia , Acetilação , Adulto , Idoso , Estudos de Casos e Controles , Feminino , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Risco , Neoplasias da Bexiga Urinária/genética
6.
Br J Cancer ; 104(11): 1797-803, 2011 May 24.
Artigo em Inglês | MEDLINE | ID: mdl-21540858

RESUMO

BACKGROUND: Occupational exposures to dusts have generally been examined in relation to cancers of the respiratory system and have rarely been examined in relation to other cancers, such as renal cell carcinoma (RCC). Although previous epidemiological studies, though few, have shown certain dusts, such as asbestos, to increase renal cancer risk, the potential for other occupational dust exposures to cause kidney damage and/or cancer may exist. We investigated whether asbestos, as well as 20 other occupational dust exposures, were associated with RCC risk in a large European, multi-center, hospital-based renal case-control study. METHODS: General occupational histories and job-specific questionnaires were reviewed by occupational hygienists for subject-specific information. Odds ratios (ORs) and 95% confidence intervals (95% CIs) between RCC risk and exposures were calculated using unconditional logistic regression. RESULTS: Among participants ever exposed to dusts, significant associations were observed for glass fibres (OR: 2.1; 95% CI: 1.1-3.9), mineral wool fibres (OR: 2.5; 95% CI: 1.2-5.1), and brick dust (OR: 1.5; 95% CI: 1.0-2.4). Significant trends were also observed with exposure duration and cumulative exposure. No association between RCC risk and asbestos exposure was observed. CONCLUSION: Results suggest that increased RCC risk may be associated with occupational exposure to specific types of dusts. Additional studies are needed to replicate and extend findings.


Assuntos
Carcinoma de Células Renais/epidemiologia , Poeira , Neoplasias Renais/epidemiologia , Doenças Profissionais/epidemiologia , Exposição Ocupacional/efeitos adversos , Idoso , Amianto/toxicidade , Carcinógenos , Estudos de Casos e Controles , Europa (Continente) , Europa Oriental , Feminino , Vidro , Humanos , Masculino , Pessoa de Meia-Idade , Fibras Minerais , Doenças Profissionais/etiologia , Medição de Risco
7.
Exp Brain Res ; 210(3-4): 423-36, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21331527

RESUMO

Numerous studies in rodents have shown that the functional efficacy of several neurotransmitter receptors and the intrinsic membrane excitability of central vestibular neurons, as well as the organization of synaptic connections within and between vestibular nuclei can be modified during postnatal development, after a lesion of peripheral vestibular organs or in vestibular-deficient mutant animals. This review mainly focuses on the intrinsic membrane properties of neurons of the medial vestibular nuclei of rodents, their postnatal maturation, and changes following experimental or congenital alterations in vestibular inputs. It also presents the concomitant modifications in the distribution of these neurons into different neuron types, which has been based on their membrane properties in relation to their anatomical, biochemical, or functional properties. The main points discussed in this review are that (1) the intrinsic membrane properties can be used to distinguish between two dominant types of neurons, (2) the system remains plastic throughout the whole life of the animal, and finally, (3) the intracellular calcium concentration has a major effect on the intrinsic membrane properties of central vestibular neurons.


Assuntos
Membrana Celular/fisiologia , Modelos Neurológicos , Células Receptoras Sensoriais/citologia , Núcleos Vestibulares/citologia , Potenciais de Ação/fisiologia , Animais , Animais Recém-Nascidos , Cálcio/metabolismo , Técnicas In Vitro , Camundongos , Camundongos Mutantes , Modelos Estatísticos , Plasticidade Neuronal/fisiologia , Ratos , Roedores , Células Receptoras Sensoriais/fisiologia , Núcleos Vestibulares/crescimento & desenvolvimento
8.
Occup Environ Med ; 67(2): 136-43, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19933307

RESUMO

OMICS technologies are relatively new biomarker discovery tools that can be applied to study large sets of biological molecules. Their application in human observational studies (HOS) has become feasible in recent years due to a spectacular increase in the sensitivity, resolution and throughput of OMICS-based assays. Although, the number of OMICS techniques is ever expanding, the five most developed OMICS technologies are genotyping, transcriptomics, epigenomics, proteomics and metabolomics. These techniques have been applied in HOS to various extents. However, their application in occupational environmental health (OEH) research has been limited. Here, we will discuss the opportunities these new techniques provide for OEH research. In addition we will address difficulties and limitations to the interpretation of the data that is generated by OMICS technologies. To illustrate the current status of the application of OMICS in OEH research, we will provide examples of studies that used OMICS technologies to investigate human health effects of two well-known toxicants, benzene and arsenic.


Assuntos
Medicina Ambiental/métodos , Genômica/métodos , Medicina do Trabalho/métodos , Arsênio/toxicidade , Benzeno/toxicidade , Biomarcadores/metabolismo , Predisposição Genética para Doença , Humanos , Doenças Profissionais/induzido quimicamente , Doenças Profissionais/genética , Proteômica/métodos
9.
Occup Environ Med ; 67(1): 47-53, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19737732

RESUMO

OBJECTIVE: Central and Eastern Europe has among the highest rates of renal cell cancer worldwide. Few studies have been conducted in these areas to investigate the possible role of occupational exposures in renal cell cancer aetiology. The purpose of this study was to examine the association of renal cell cancer with employment in specific occupations and industries. METHODS: From 1999 to 2003, we conducted a hospital-based case-control study in seven areas of the Czech Republic, Poland, Romania and Russia. A detailed occupational history was collected from renal cell cancer cases and controls, together with information on potential confounders. Odds ratios (ORs) and 95% CI of cancer risk were calculated for having ever been employed in selected jobs and industries, with follow-up analyses examining duration of employment. RESULTS: A total of 992 histologically confirmed incident renal cell cancer cases and 1459 controls were included in the analysis. An increased risk of renal cell cancer was observed for workers in agricultural labour and animal husbandry (OR 1.43; 95% CI 1.05 to 1.93), particularly among women employed as general farm workers (OR 2.73; 95% CI 1.05 to 7.13). Risk gradients for agricultural work increased with longer employment. An overall increased risk of renal cell cancer was seen among architects and engineers (OR 1.89; 95% CI 1.35 to 2.65), and mechanical engineers (OR 1.71; 95% CI 1.03 to 2.84). CONCLUSIONS: Our data suggest an association between renal cell cancer and agricultural work, particularly among female workers.


Assuntos
Carcinoma de Células Renais/epidemiologia , Neoplasias Renais/epidemiologia , Doenças Profissionais/epidemiologia , Ocupações/estatística & dados numéricos , Adulto , Idoso , Idoso de 80 Anos ou mais , Agricultura/estatística & dados numéricos , Arquitetura/estatística & dados numéricos , Estudos de Casos e Controles , República Tcheca/epidemiologia , Engenharia/estatística & dados numéricos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Polônia/epidemiologia , Fatores de Risco , Romênia/epidemiologia , Federação Russa/epidemiologia , Fatores Sexuais , Fatores de Tempo
10.
Carcinogenesis ; 29(8): 1567-71, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18566013

RESUMO

This study investigated associations between occupational pesticide exposure and renal cell carcinoma (RCC) risk. To follow-up on a previous report by Buzio et al., we also considered whether this association could be modified by glutathione S-transferase M1 and T1 (GSTM1 and GSTT1) genotypes. About 1097 RCC cases and 1476 controls from Central and Eastern Europe were interviewed to collect data on lifetime occupational histories. Occupational information for jobs held for at least 12 months duration was coded for pesticide exposures and assessed for frequency and intensity of exposure. GSTM1 and GSTT1 gene deletions were analyzed using TaqMan assays. A significant increase in RCC risk was observed among subjects ever exposed to pesticides [odds ratio (OR): 1.60; 95% confidence interval (CI): 1.00-2.55]. After stratification by genotypes, increased risk was observed among exposed subjects with at least one GSTM1 active allele (OR: 4.00; 95% CI: 1.55-10.33) but not among exposed subjects with two GSTM1 inactive alleles compared with unexposed subjects with two inactive alleles (P-interaction: 0.04). Risk was highest among exposed subjects with both GSTM1 and GSTT1 active genotypes (OR: 6.47; 95% CI: 1.82-23.00; P-interaction: 0.02) compared with unexposed subjects with at least one GSTM1 or T1 inactive genotype. In the largest RCC case-control study with genotype information conducted to date, we observed that risk associated with pesticide exposure was exclusive to individuals with active GSTM1/T1 genotypes. These findings further support the hypothesis that glutathione S-transferase polymorphisms can modify RCC risk associated with occupational pesticide exposure.


Assuntos
Carcinoma de Células Renais/classificação , Carcinoma de Células Renais/genética , Glutationa Transferase/genética , Neoplasias Renais/induzido quimicamente , Neoplasias Renais/genética , Praguicidas/toxicidade , Polimorfismo Genético , Adulto , Idoso , Idoso de 80 Anos ou mais , Carcinoma de Células Renais/enzimologia , Carcinoma de Células Renais/epidemiologia , Estudos de Casos e Controles , Europa (Continente)/epidemiologia , Feminino , Humanos , Entrevistas como Assunto , Neoplasias Renais/enzimologia , Neoplasias Renais/epidemiologia , Masculino , Pessoa de Meia-Idade , Exposição Ocupacional , Medição de Risco , Fatores de Risco , Estados Unidos/epidemiologia
11.
Br J Cancer ; 99(11): 1912-5, 2008 Dec 02.
Artigo em Inglês | MEDLINE | ID: mdl-19034282

RESUMO

In a case-control study of kidney cancer in four central European countries, with 1097 incident cases and 1476 controls, we found an increased risk for self-reported hypertension and for obesity. Additional unknown risk factors are likely to be responsible for the high rates of kidney cancer in this region.


Assuntos
Índice de Massa Corporal , Hipertensão/complicações , Neoplasias Renais/etiologia , Obesidade/complicações , Fumar/efeitos adversos , Adulto , Idoso , Estudos de Casos e Controles , Europa (Continente) , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Risco
12.
J Toxicol Environ Health A ; 71(6): 367-72, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18246496

RESUMO

Previous studies investigated the role of vitamin D intake and cancer risk. The kidney is a major organ for vitamin D metabolism, activity, and calcium homeostasis; therefore, it was hypothesized that dietary vitamin D intake and polymorphisms in the vitamin D receptor (VDR) gene may modify renal cell carcinoma (RCC) risk. Three common VDR gene polymorphisms (BsmI, FokI, TaqI) were evaluated among 925 RCC cases and 1192 controls enrolled in a hospital-based case-control study conducted in Central and Eastern Europe. Overall associations with RCC risk were not observed; however, subgroup analyses revealed associations after stratification by median age of diagnosis and family history of cancer. Among subjects over 60 yr, reduced risks were observed among carriers of the f alleles in the FokI single-nucleotide polymorphism (SNP) (odds ratio [OR] = 0.61 for Ff and OR = 0.74 for ff genotypes) compared to subjects with the FF genotype (P trend = 0.04; P interaction = 0.004). Subjects with the BB BsmI genotype and a positive family history of cancer had lower risk compared to subjects with the bb allele (OR = 0.60; 95% CI: 0.33-1.1; P trend = 0.05). Genotype associations with these subgroups were not modified when dietary sources of vitamin D or calcium were considered. Additional studies of genetic variation in the VDR gene are warranted.


Assuntos
Carcinoma de Células Renais/genética , Predisposição Genética para Doença/genética , Polimorfismo Genético/genética , Receptores de Calcitriol/genética , Adulto , Idoso , Carcinoma de Células Renais/epidemiologia , Estudos de Casos e Controles , Europa (Continente)/epidemiologia , Feminino , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade
13.
Prog Neurobiol ; 76(6): 349-92, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16263204

RESUMO

Central vestibular neurons play an important role in the processing of body motion-related multisensory signals and their transformation into motor commands for gaze and posture control. Over recent years, medial vestibular nucleus (MVN) neurons and to a lesser extent other vestibular neurons have been extensively studied in vivo and in vitro, in a range of species. These studies have begun to reveal how their intrinsic electrophysiological properties may relate to their response patterns, discharge dynamics and computational capabilities. In vitro studies indicate that MVN neurons are of two major subtypes (A and B), which differ in their spike shape and after-hyperpolarizations. This reflects differences in particular K(+) conductances present in the two subtypes, which also affect their response dynamics with type A cells having relatively low-frequency dynamics (resembling "tonic" MVN cells in vivo) and type B cells having relatively high-frequency dynamics (resembling "kinetic" cells in vivo). The presence of more than one functional subtype of vestibular neuron seems to be a ubiquitous feature since vestibular neurons in the chick and frog also subdivide into populations with different, analogous electrophysiological properties. The ratio of type A to type B neurons appears to be plastic, and may be determined by the signal processing requirements of the vestibular system, which are species-variant. The membrane properties and discharge pattern of type A and type B MVN neurons develop largely post-natally, through the expression of the underlying ion channel conductances. The membrane properties of MVN neurons show rapid and long-lasting plastic changes after deafferentation (unilateral labyrinthectomy), which may serve to maintain their level of activity and excitability after the loss of afferent inputs.


Assuntos
Membrana Celular/fisiologia , Fixação Ocular/fisiologia , Plasticidade Neuronal/fisiologia , Neurônios/fisiologia , Reflexo Vestíbulo-Ocular/fisiologia , Núcleos Vestibulares/embriologia , Núcleos Vestibulares/fisiologia , Potenciais de Ação/fisiologia , Animais , Membrana Celular/ultraestrutura , Humanos , Potenciais da Membrana/fisiologia , Neurônios/citologia , Postura/fisiologia , Vertebrados , Núcleos Vestibulares/citologia
14.
Oncogene ; 36(15): 2172-2183, 2017 04.
Artigo em Inglês | MEDLINE | ID: mdl-27819678

RESUMO

Genetic alterations associated with prostate cancer (PCa) may be identified by sequencing metastatic tumour genomes to identify molecular markers at this lethal stage of disease. Previously, we characterized somatic alterations in metastatic tumours in the methylcytosine dioxygenase ten-eleven translocation 2 (TET2), which is altered in 5-15% of myeloid, kidney, colon and PCas. Genome-wide association studies previously identified non-coding risk variants associated with PCa and melanoma. We perform fine-mapping of PCa risk across TET2 using genotypes from the PEGASUS case-control cohort and identify six new risk variants in introns 1 and 2. Oligonucleotides containing two risk variants are bound by the transcription factor octamer-binding protein 1 (Oct1/POU2F1) and TET2 and Oct1 expression are positively correlated in prostate tumours. TET2 is expressed in normal prostate tissue and reduced in a subset of tumours from the Cancer Genome Atlas (TCGA). Small interfering RNA-mediated TET2 knockdown (KD) increases LNCaP cell proliferation, migration and wound healing, verifying loss drives a cancer phenotype. Endogenous TET2 bound the androgen receptor (AR) and AR-coactivator proteins in LNCaP cell extracts, and TET2 KD increases prostate-specific antigen (KLK3/PSA) expression. Published data reveal TET2 binding sites and hydroxymethylcytosine proximal to KLK3. A gene co-expression network identified using TCGA prostate tumour RNA-sequencing identifies co-regulated cancer genes associated with 2-oxoglutarate (2-OG) and succinate metabolism, including TET2, lysine demethylase (KDM) KDM6A, BRCA1-associated BAP1, and citric acid cycle enzymes IDH1/2, SDHA/B, and FH. The co-expression signature is conserved across 31 TCGA cancers suggesting a putative role for TET2 as an energy sensor (of 2-OG) that modifies aspects of androgen-AR signalling. Decreased TET2 mRNA expression in TCGA PCa tumours is strongly associated with reduced patient survival, indicating reduced expression in tumours may be an informative biomarker of disease progression and perhaps metastatic disease.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Neoplasias da Próstata/metabolismo , Proteínas Proto-Oncogênicas/metabolismo , Receptores Androgênicos/metabolismo , Proliferação de Células/fisiologia , Proteínas de Ligação a DNA/genética , Dioxigenases , Células HEK293 , Humanos , Íntrons , Calicreínas/genética , Calicreínas/metabolismo , Ácidos Cetoglutáricos/metabolismo , Masculino , Polimorfismo de Nucleotídeo Único , Antígeno Prostático Específico/genética , Antígeno Prostático Específico/metabolismo , Neoplasias da Próstata/genética , Neoplasias da Próstata/patologia , Proteínas Proto-Oncogênicas/genética , Receptores Androgênicos/genética , Succinatos/metabolismo
15.
J Neurosci ; 19(19): 8271-80, 1999 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-10493728

RESUMO

An investigation of dendritic membrane properties was performed by whole-cell patch measurements of the biophysical properties of intact chick spinal neurons that are involved in rhythmogenesis. A whole-cell voltage clamp of the somatic membrane was used to block NMDA-induced voltage oscillations from the cell body, thus partially isolating the intrinsic oscillatory properties of dendritic membranes from those of the soma. An experimental approach was developed that takes into account the complexity of the dendritic tree in an environment as normal as possible, without the need for cell isolation or slice preparations. A computational study of the experimentally determined model showed that excitatory amino acid receptors on dendrites can dynamically control the electrotonic length of the dendrites through the activation of negative slope conductances. These experiments demonstrate the presence of NMDA receptors on the dendrites and that they induce intrinsic oscillations when the synaptic input from other cells is significantly reduced.


Assuntos
Dendritos/fisiologia , N-Metilaspartato/farmacologia , Neurônios/fisiologia , Medula Espinal/fisiologia , Animais , Membrana Celular/efeitos dos fármacos , Membrana Celular/fisiologia , Embrião de Galinha , Dendritos/efeitos dos fármacos , Técnicas In Vitro , Modelos Neurológicos , Modelos Estatísticos , Neurônios/efeitos dos fármacos , Oscilometria , Técnicas de Patch-Clamp
16.
Biochim Biophys Acta ; 375(1): 115-23, 1975 Jan 14.
Artigo em Inglês | MEDLINE | ID: mdl-1111573

RESUMO

Temperature-jump experiments on isolated myelinated nerve fibers were done using a pulsed laser system in the Q switched mode. Voltage-clamp and temperature perturbations were used to measure the relaxing ionic conductances of both the Na+ and K+ systems. It is shown that the T jump can be used to probe the K+ and Na+ conductances during non-steady state conditions and thereby elicit relaxation times for a variety of initial states. Temperature-induced K+ conductance relaxation times were consistent with voltage-clamp measurements. The temperature-perturbation experiments were done as a combination of a temperature step and impulse change due to an adsorption of carbon black particles on the nerve. The experiments support the hypothesis that the relaxation times of the K+ system are independent of the previous history of the axon. It is concluded that the K+ conductance is at least a second-order system whose relaxation spectrum is composed of two exponential terms the magnitudes of which are markedly dependent on the initial conditions.


Assuntos
Membrana Celular/fisiologia , Nós Neurofibrosos/fisiologia , Animais , Membrana Celular/efeitos dos fármacos , Condutividade Elétrica , Lasers , Potenciais da Membrana , Potássio/farmacologia , Compostos de Amônio Quaternário/farmacologia , Nós Neurofibrosos/efeitos dos fármacos , Sódio/farmacologia , Xenopus
17.
Biochim Biophys Acta ; 382(3): 286-94, 1975 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-1125236

RESUMO

Light scattering studies on the giant squid axon were done using the technique of optical mixing spectroscopy. This experimental approach is based on the use of laser light to detect the fluctuations of membrane macromolecules which are associated with conductance fluctuations. The light scattering spectra were similar to the Lorentzian-like behavior of conductance fluctuations, possibly reflecting an underlying conformational change in the specific membrane sites responsible for the potassium ion conductance. The amplitude of the spectra measured, increased when the membrane was depolarized and decreased on hyperpolarization. The spectra were fit to the sum of two terms, a (1/f component and a simple Lorentzian term. Spectra from deteriorating axons did not show sensitivity to membrane potential changes. It is shown theoretically that fluctuations due to the voltage-dependent variable, n, of the Hodgkin-Huxley formalism are identical to the voltage fluctuations. The derived power spectrum is that of a second order system, capable of showing resonance peaking only if the voltage dependence of the potassium rate of constants is included in the analysis. The lack of resonance peaking in the observed light scattering spectra, indicates that the data are best described by a damped second order system.


Assuntos
Axônios/ultraestrutura , Membranas/ultraestrutura , Animais , Decapodiformes , Látex , Luz , Matemática , Microesferas , Poliestirenos , Espalhamento de Radiação , Análise Espectral
18.
J Gen Physiol ; 54(1): 33-52, 1969 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-5792364

RESUMO

Unidirectional chloride effluxes from small bundles of muscle fibers were measured under equilibrium conditions. It was found that chloride effluxes are described by the constant field theory with a chloride permeability constant, P(cl), which is independent of the chloride concentration and the membrane potential. The value of P(cl) at neutral pH was found to be 5 x 10(-6) cm/sec. Chloride movements were markedly depressed at low pH and increased at high pH. It is concluded that chloride fluxes are independent of each other over a wide pH range. The effect of nitrate on the chloride effluxes was measured. It was found that both external and internal nitrate alone reduced the chloride efflux with the external nitrate appearing more effective than internal nitrate due to the nonequilibrium nature of the experimental conditions. Under equilibrium conditions the reduction of the chloride efflux by nitrate was greater than the external nitrate effect, both of which were dependent on the relative proportion of nitrate in the bathing solution. These results are consistent with the hypothesis that the inhibition of the chloride movements by nitrate is essentially symmetrical with regard to the inside and outside surfaces of the muscle membranes. The relative action of nitrate on the chloride efflux was independent of the external pH despite marked changes in the absolute values of the fluxes measured.


Assuntos
Permeabilidade da Membrana Celular , Cloretos/metabolismo , Músculos/fisiologia , Animais , Anuros , Concentração de Íons de Hidrogênio , Potenciais da Membrana , Métodos , Nitratos/farmacologia , Radioisótopos
19.
J Gen Physiol ; 60(1): 1-19, 1972 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-4537778

RESUMO

A voltage clamp for single muscle fibers has been developed. Stability of the system was achieved when an artificial node was created by enclosing a single muscle fiber in a petroleum jelly seal which served as an analogue of the myelin sheath. Typical voltage clamp records were obtained with large inward transient currents followed by a delayed rectification of the outward currents. These currents looked qualitatively similar when the transverse tubular system was destroyed. Errors in current measurement, especially those due to anomalous rectification, are discussed.


Assuntos
Músculos/fisiologia , Rana pipiens/fisiologia , Potenciais de Ação , Animais , Anuros , Eletrofisiologia/instrumentação , Técnicas In Vitro , Matemática , Potenciais da Membrana , Bainha de Mielina/fisiologia , Vaselina , Soluções/fisiologia
20.
Artigo em Inglês | MEDLINE | ID: mdl-7827589

RESUMO

It is well established that inorganic arsenic is causally associated with lung cancer via inhalation and skin cancer via ingestion. Epidemiological evidence based on studies in Taiwan suggests that ingestion of inorganic arsenic may also cause other more fatal internal cancers, with the highest relative risks reported for bladder cancer. Here, we have used a biological marker of response, the micronucleus assay in exfoliated bladder cells, to evaluate the possible genotoxic effects of chronic arsenic ingestion on the bladder. The overall objective of this study was to compare the frequency of micronucleated cells in exfoliated bladder and buccal cells between a group of 18 individuals in Nevada who chronically ingested high levels of inorganic arsenic from their well water (average level, 1,312 micrograms/liter) and an individually matched control group with low exposure to arsenic (average level, 16 micrograms/liter). A 1.8-fold increase (90% confidence interval, 1.06-2.99) was observed in the weighted mean frequency of micronucleated bladder cells in the exposed group (2.79 per 1000 cells) compared with the unexposed group (1.57 per 1000 cells). In addition, the frequency of micronucleated bladder cells was positively associated with the urinary concentration of inorganic arsenic plus its methylated metabolites (Spearman correlation = 0.33; P = 0.03). In contrast, there was no increase in micronucleated buccal cells associated with arsenic ingestion (frequency ratio = 1.0; 90% confidence interval, 0.65-1.53). The results of this study provide evidence that chronic ingestion of high levels of inorganic arsenic in drinking water is associated with an increased frequency of micronucleated bladder cells. These findings are consistent with a genotoxic effect of arsenic on bladder cells, but a larger study is needed to confirm them.


Assuntos
Arsênio/efeitos adversos , Testes para Micronúcleos , Neoplasias da Bexiga Urinária/induzido quimicamente , Poluentes Químicos da Água/efeitos adversos , Adolescente , Adulto , Idoso , Arsênio/farmacocinética , Transformação Celular Neoplásica/induzido quimicamente , Transformação Celular Neoplásica/patologia , Relação Dose-Resposta a Droga , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Nevada , Fatores de Risco , Neoplasias da Bexiga Urinária/patologia
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