Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
ACS Chem Biol ; 19(5): 1180-1193, 2024 05 17.
Artigo em Inglês | MEDLINE | ID: mdl-38652683

RESUMO

C. elegans numr-1/2 (nuclear-localized metal-responsive) is an identical gene pair encoding a nuclear protein previously shown to be activated by cadmium and disruption of the integrator RNA metabolism complex. We took a chemical genetic approach to further characterize regulation of this novel metal response by screening 41,716 compounds and extracts for numr-1p::GFP activation. The most potent activator was chaetocin, a fungal 3,6-epidithiodiketopiperazine (ETP) with promising anticancer activity. Chaetocin activates numr-1/2 strongly in the alimentary canal but is distinct from metal exposure, because it represses canonical cadmium-responsive metallothionine genes. Chaetocin has diverse targets in cancer cells including thioredoxin reductase, histone lysine methyltransferase, and acetyltransferase p300/CBP; further work is needed to identify the mechanism in C. elegans as genetic disruption and RNAi screening of homologues did not induce numr-1/2 in the alimentary canal and chaetocin did not affect markers of integrator dysfunction. We demonstrate that disulfides in chaetocin and chetomin, a dimeric ETP analog, are required to induce numr-1/2. ETP monomer gliotoxin, despite possessing a disulfide linkage, had almost no effect on numr-1/2, suggesting a dimer requirement. Chetomin inhibits C. elegans growth at low micromolar levels, and loss of numr-1/2 increases sensitivity; C. elegans and Chaetomiaceae fungi inhabit similar environments raising the possibility that numr-1/2 functions as a defense mechanism. There is no direct orthologue of numr-1/2 in humans, but RNaseq suggests that chaetocin affects expression of cellular processes linked to stress response and metal homeostasis in colorectal cancer cells. Our results reveal interactions between metal response gene regulation and ETPs and identify a potential mechanism of resistance to this versatile class of preclinical compounds.


Assuntos
Proteínas de Caenorhabditis elegans , Caenorhabditis elegans , Homeostase , Micotoxinas , Caenorhabditis elegans/efeitos dos fármacos , Caenorhabditis elegans/genética , Caenorhabditis elegans/metabolismo , Animais , Proteínas de Caenorhabditis elegans/metabolismo , Proteínas de Caenorhabditis elegans/genética , Micotoxinas/farmacologia , Micotoxinas/metabolismo , Homeostase/efeitos dos fármacos , Antineoplásicos/farmacologia , Antineoplásicos/química , Piperazinas/farmacologia , Piperazinas/química , Humanos , Proteínas Nucleares/metabolismo , Proteínas Nucleares/genética , Cádmio/farmacologia
2.
PLoS One ; 17(8): e0272452, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35951614

RESUMO

Physiological responses to the environment, disease, and aging vary by sex in many animals, but mechanisms of dimorphism have only recently begun to receive careful attention. The genetic model nematode Caenorhabditis elegans has well-defined mechanisms of stress response, aging, and sexual differentiation. C. elegans has males, but the vast majority of research only uses hermaphrodites. We found that males of the standard N2 laboratory strain were more resistant to hyperosmolarity, heat, and a natural pro-oxidant than hermaphrodites when in mixed-sex groups. Resistance to heat and pro-oxidant were also male-biased in three genetically and geographically diverse C. elegans strains consistent with a species-wide dimorphism that is not specific to domestication. N2 males were also more resistant to heat and pro-oxidant when keep individually indicating that differences in resistance do not require interactions between worms. We found that males induce canonical stress response genes by similar degrees and in similar tissues as hermaphrodites suggesting the importance of other mechanisms. We find that resistance to heat and pro-oxidant are influenced by the sex differentiation transcription factor TRA-1 suggesting that downstream organ differentiation pathways establish differences in stress resistance. Environmental stress influences survival in natural environments, degenerative disease, and aging. Understanding mechanisms of stress response dimorphism can therefore provide insights into sex-specific population dynamics, disease, and longevity.


Assuntos
Proteínas de Caenorhabditis elegans , Transtornos do Desenvolvimento Sexual , Animais , Caenorhabditis elegans/metabolismo , Proteínas de Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/metabolismo , Feminino , Longevidade , Masculino , Espécies Reativas de Oxigênio/metabolismo , Caracteres Sexuais
3.
Rev. cienc. med. Pinar Rio ; 16(1): 181-187, ene.-feb. 2012.
Artigo em Espanhol | LILACS | ID: lil-739713

RESUMO

Los teratocarcinomas representan aproximadamente entre el 3-5% de los tumores intracraneales en la infancia. Su manifestación clínica puede variar desde un estado asintomático hasta un amplio espectro de síntomas neurológicos, visuales y endocrinos. Se presenta el caso de una paciente femenina de 9 años de edad atendida en el Hospital Pediátrico "Pepe Portilla" de Pinar del Río, por un cuadro de cefalea, vómitos y pérdida brusca de la visión, a la cual se le realizan varias investigaciones y se le diagnostica un teratocarcinoma con componente de coriocarcinoma. Se opera y logra una evolución satisfactoria.


Teratocarcinomas represent 3-5% of the intracranial tumors in childhood approximately. Their clinical manifestations can vary from an asymptomatic status to a wide spectrum of neurological, visual and endocrine symptoms. A 9 year-old female patient presenting headache, vomits and sudden loss of vision attended to "Pepe Portilla" Children Hospital, Pinar del Rio. Several medical examinations were performed, diagnosing a Teratocarcinoma with a component of choriocarcinoma; the patient underwent a surgery having a satisfactory evolution.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA