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1.
J Gen Physiol ; 155(5)2023 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-36809486

RESUMEN

KCNQ1 voltage-gated K+ channels are involved in a wide variety of fundamental physiological processes and exhibit the unique feature of being markedly inhibited by external K+. Despite the potential role of this regulatory mechanism in distinct physiological and pathological processes, its exact underpinnings are not well understood. In this study, using extensive mutagenesis, molecular dynamics simulations, and single-channel recordings, we delineate the molecular mechanism of KCNQ1 modulation by external K+. First, we demonstrate the involvement of the selectivity filter in the external K+ sensitivity of the channel. Then, we show that external K+ binds to the vacant outermost ion coordination site of the selectivity filter inducing a diminution in the unitary conductance of the channel. The larger reduction in the unitary conductance compared to whole-cell currents suggests an additional modulatory effect of external K+ on the channel. Further, we show that the external K+ sensitivity of the heteromeric KCNQ1/KCNE complexes depends on the type of associated KCNE subunits.


Asunto(s)
Canal de Potasio KCNQ1 , Canales de Potasio con Entrada de Voltaje , Canal de Potasio KCNQ1/metabolismo , Canales de Potasio con Entrada de Voltaje/metabolismo , Simulación de Dinámica Molecular , Oocitos/metabolismo , Técnicas de Placa-Clamp
2.
Int J Mol Sci ; 22(3)2021 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-33535561

RESUMEN

Radio- and chemoresistance of cancer stem cells (CSCs) is considered as one of the possible causes of adverse results of chemoradiotherapy for various malignancies, including cervical cancer. However, little is known about quantitative changes in the CSC subpopulation in the course of treatment and mechanisms for individual response of CSCs to therapy. The purpose of the study was to evaluate the association of radiation response of cervical CSCs with clinical and morphological parameters of disease and features of human papillomavirus (HPV) infection. The proportion of CD44+CD24low CSCs was determined by flow cytometry in cervical scrapings from 55 patients with squamous cell carcinoma of uterine cervix before treatment and after fractionated irradiation at a total dose of 10 Gy. Real-time PCR assay was used to evaluate molecular parameters of HPV DNA. Post-radiation increase in the CSC proportion was found in 47.3% of patients. Clinical and morphological parameters (stage, status of lymph node involvement, and histological type) were not significantly correlated with radiation changes in the CSC proportion. Single- and multifactor analyses revealed two independent indicators affecting the radiation response of CSCs: initial proportion of CSCs and physical status of HPV DNA (R = 0.86, p = 0.001 for the multiple regression model in the whole).


Asunto(s)
Alphapapillomavirus , Infecciones por Papillomavirus/complicaciones , Infecciones por Papillomavirus/radioterapia , Neoplasias del Cuello Uterino/complicaciones , Neoplasias del Cuello Uterino/radioterapia , Adulto , Anciano , Antígeno CD24/metabolismo , Carcinoma de Células Escamosas/complicaciones , Carcinoma de Células Escamosas/radioterapia , Carcinoma de Células Escamosas/virología , ADN Viral/metabolismo , Resistencia a Antineoplásicos , Femenino , Citometría de Flujo , Humanos , Receptores de Hialuranos/metabolismo , Persona de Mediana Edad , Células Madre Neoplásicas , Pronóstico , Reacción en Cadena en Tiempo Real de la Polimerasa , Análisis de Regresión , Neoplasias del Cuello Uterino/virología , Adulto Joven
3.
Oxid Med Cell Longev ; 2015: 593658, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25741405

RESUMEN

Genes encoding proteins with antioxidant properties may influence susceptibility to endometrial hyperplasia (EH) and endometrial carcinoma (ECa). Patients with EH (n = 89), EH concurrent with ECa (n = 76), ECa (n = 186), and healthy controls (n = 1110) were genotyped for five polymorphic variants in the genes involved in metabolism of lipoproteins (APOE Cys112Arg and Arg158Cys), iron (HFE Cys282Tyr and His63Asp), and catecholamines (COMT Val158Met). Patients and controls were matched by ethnicity (all Caucasians), age, body mass index (BMI), and incidence of hypertension and diabetes. The frequency of the APOE E 2 allele (158Cys) was higher in patients with EH + ECa than in controls (P = 0.0012, P(Bonferroni) = 0.018, OR = 2.58, 95% CI 1.49-4.45). The APOE E 4 allele (112Arg) was more frequently found in patients with EH than in controls and HFE minor allele G (63Asp) had a protective effect in the ECa group, though these results appeared to be nonsignificant after correction for multiple comparisons. The results of the study indicate that E 2 allele might be associated with concurrent occurrence of EH and ECa.


Asunto(s)
Apolipoproteína E2/genética , Anciano , Alelos , Índice de Masa Corporal , Diabetes Mellitus Tipo 2/epidemiología , Hiperplasia Endometrial/genética , Hiperplasia Endometrial/patología , Neoplasias Endometriales/genética , Neoplasias Endometriales/patología , Femenino , Frecuencia de los Genes , Genotipo , Haplotipos , Proteína de la Hemocromatosis , Antígenos de Histocompatibilidad Clase I/genética , Humanos , Hipertensión/epidemiología , Proteínas de la Membrana/genética , Persona de Mediana Edad , Oportunidad Relativa , Polimorfismo de Nucleótido Simple
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