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1.
In Vivo ; 37(6): 2768-2775, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37905618

RESUMEN

BACKGROUND/AIM: We aimed to compare the clinicopathological outcomes in patients with locally advanced rectal cancer after short- or long-course concurrent chemoradiotherapy (CCRT) followed by delayed surgery. PATIENTS AND METHODS: The records of 94 patients with cT3-4N0-2M0 rectal cancer who received CCRT between 2010 and 2017 were reviewed. Short-course radiotherapy (RT) was delivered with a median total dose of 25 Gy in five fractions (n=27), and long-course RT was delivered with a median total dose of 50.4 Gy in 28 fractions (n=67). The following concurrent chemotherapy regimens were administered: 5-fluorouracil plus leucovorin in 58 and capecitabine in 24; in 12 cases agents were unknown. The median interval between CCRT and surgery was 8 weeks. Adjuvant chemotherapy was administered after surgery in 80 patients (5-fluorouracil plus leucovorin, n=54; capecitabine, n=9; other, n=14; and unknown, n=3). Propensity-score matching analysis was conducted. RESULTS: The median follow-up duration was 4.3 years. There were no statistically significant differences between the short- and long-course RT groups in sphincter preservation (85.2% vs. 92.5%, p=0.478), pathological complete remission (18.5% vs. 14.9%, p=0.905), downstaging (44.4% vs. 26.9%, p=0.159), and negative circumferential resection margin (92.6% vs. 89.6%, p=0.947) rates. No differences were found in survival outcomes between the short- and long-course groups at 3 years (overall survival: 91.8% vs. 88.1%, p=0.790; disease-free survival, 75.2% vs. 72.5%, p=0.420; locoregional relapse-free survival, 90.5% vs. 98.4%, p=0.180; and distant metastasis-free survival, 79.6% vs. 73.5%, p=0.490). Similar results were observed after PSM. CONCLUSION: Clinically, short-course CCRT may be a feasible alternative to long-course CCRT in patients with locally advanced rectal cancer.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica , Neoplasias del Recto , Humanos , Capecitabina , Leucovorina , Resultado del Tratamiento , Protocolos de Quimioterapia Combinada Antineoplásica/efectos adversos , Terapia Neoadyuvante/métodos , Estadificación de Neoplasias , Recurrencia Local de Neoplasia/patología , Quimioradioterapia/métodos , Neoplasias del Recto/patología , Fluorouracilo
2.
J Autoimmun ; 121: 102647, 2021 07.
Artículo en Inglés | MEDLINE | ID: mdl-33991884

RESUMEN

BACKGROUND: We aimed to evaluate the association between autoimmune disease (AID) and lymphoma incidence in the Korean population. We also aimed to compare the overall survival (OS) in patients with AID-associated lymphoma (AAL) with that in patients with lymphoma without AID. MATERIAL AND METHODS: We used National Sample Cohort 2002-2015 provided by National Health Insurance Service. Among 1,011,638 patients, 994,496 were recruited for the final cohort: 130,987 patients (13.2%) in the AID group and 863,509 (86.8%) in control. Lymphoma was diagnosed in 1162 patients and 322 patients with accompanying AID, irrespective of the time point of diagnosis, were defined as AAL. Of those, patients who experienced lymphoma development at least one year after AID diagnosis were defined as post-AID lymphoma (N = 155). RESULTS: The median follow-up duration was 13.7 years. AAL accounted for 0.03% of total and 27.7% of lymphoma cases. AID patients experienced more Epstein-Barr virus (0.02 vs. 0.01%, P = 0.027) or Helicobacter pylori infection (63.9 vs. 41.4%, P < 0.001) than the control group did. AID was associated with a 1.45-fold increased risk of lymphoma. The median time interval from AID to AAL was 10.9 months. The risk of lymphoma increased in the order of: psoriasis (adjusted odds ratio [AOR] 1.61), systemic lupus erythematosus (AOR 3.99), multiple sclerosis (AOR 4.52), and sarcoidosis (AOR 26.37). Sjogren syndrome was not related to lymphoma in this cohort. The 5-year OS in AAL was not different from that in lymphoma patients without AID (60.9 vs. 61.5%, P = 0.970). CONCLUSIONS: The association patterns in AAL in Korean population were different from those of Western countries. Further studies on lymphomatogenesis from distinct baseline characteristics (e.g. chronic infection status) would elucidate the difference based on race and ethnicity.


Asunto(s)
Enfermedades Autoinmunes/complicaciones , Linfoma/epidemiología , Adulto , Anciano , Enfermedades Autoinmunes/inmunología , Carcinogénesis/inmunología , Femenino , Estudios de Seguimiento , Humanos , Incidencia , Linfoma/inmunología , Masculino , Persona de Mediana Edad , Programas Nacionales de Salud/estadística & datos numéricos , República de Corea/epidemiología , Estudios Retrospectivos
3.
J Food Sci ; 84(6): 1600-1608, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-31132143

RESUMEN

Considering the anti-photoaging effect of antioxidant compounds, we investigated the protective capacity of grape peel extract (GPE) and resveratrol on ultraviolet (UV)-induced skin wrinkle formation. Total phenolic, total anthocyanin, and total flavonoid content in GPE prepared from peel of Campbell Early variety were 23.96 ± 0.09, 3.27 ± 0.40, and 1.24 ± 0.09 mg/g dry weight, respectively. Additionally, trans-resveratrol and piceid content of the resulting GPE were 117.14 ± 19.97 and 85.23 ± 8.89 µg/g dry weight, respectively. Oral administration of either 2 g GPE or 2 mg resveratrol per kg body weight in mice attenuated UVB-induced epidermal thickening (the thickness was reduced by about 63% and 55% with GPE and resveratrol consumption prior to exposure to UVB, respectively, compared to only UVB-treated condition) and had marginally protective effect on wrinkle formation of skin exposed to UVB. As introduction of either GPE or resveratrol induced Nrf2-dependent antioxidant enzymes including heme oxygenase-1 (HO-1) in liver and skin as well as inhibited metalloproteinases, it is highly probable that the extract or resveratrol mitigated UVB-induced photoaging through activation of Nrf2/HO-1 signaling pathway. PRACTICAL APPLICATION: This study proved that resveratrol and the extract of grape peel, a common by-product of grape juice processing, provide effective protection from UV-induced skin wrinkle formation. Therefore, grape peel extract, which contains an appreciable amount of bioactive compound resveratrol, can be utilized as functional food ingredient for the manufacture of inner beauty products.


Asunto(s)
Hemo-Oxigenasa 1/metabolismo , Factor 2 Relacionado con NF-E2/metabolismo , Extractos Vegetales/administración & dosificación , Resveratrol/administración & dosificación , Envejecimiento de la Piel/efectos de los fármacos , Vitis/química , Animales , Antioxidantes/administración & dosificación , Modelos Animales de Enfermedad , Femenino , Flavonoides/administración & dosificación , Flavonoides/análisis , Frutas/química , Glucósidos/administración & dosificación , Glucósidos/análisis , Hemo-Oxigenasa 1/genética , Humanos , Ratones , Ratones Pelados , Factor 2 Relacionado con NF-E2/genética , Resveratrol/análisis , Transducción de Señal/efectos de los fármacos , Transducción de Señal/efectos de la radiación , Envejecimiento de la Piel/genética , Envejecimiento de la Piel/efectos de la radiación , Estilbenos/administración & dosificación , Estilbenos/análisis , Rayos Ultravioleta
4.
J Sci Food Agric ; 99(8): 4043-4053, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30737796

RESUMEN

BACKGROUND: Resveratrol, an extensively recognized phytochemical that belongs to the stilbene family, is abundant in grape peel which is discarded as a by-product during grape juice processing. RESULTS: In this study, we established that pre-heating grape peel above 75 °C significantly improved the extractability of resveratrol and its glucoside piceid. In particular, thermal heating of grape peel at 95 °C for 10 min, followed by treatment with a mixture of exo-1,3-ß-glucanase and pectinases at 50 °C for 60 min, dramatically increased the conversion of piceid into resveratrol and the overall extractability of this phytochemical by 50%. Furthermore, thermal pre-treatment promoted a substantial increase in the total phenol, flavonoid, and anthocyanin concentrations in the grape peel extract. Ultimately, resveratrol-enriched grape peel extract significantly augmented the antioxidant response in vitro, possibly by attenuating the accumulation of intracellular reactive oxygen species via the Nrf2 signaling pathway. CONCLUSION: The method developed in this study for preparing grape peel extract introduces a potential low-cost green processing for the industrial fortification of food products with resveratrol and other health-beneficial antioxidants. © 2019 Society of Chemical Industry.


Asunto(s)
Antioxidantes/química , Manipulación de Alimentos/métodos , Extractos Vegetales/química , Resveratrol/química , Vitis/química , Antioxidantes/aislamiento & purificación , Biocatálisis , Manipulación de Alimentos/instrumentación , Frutas/química , Glucano 1,3-beta-Glucosidasa/química , Calor , Extractos Vegetales/aislamiento & purificación , Poligalacturonasa/química , Resveratrol/aislamiento & purificación , Residuos/análisis
5.
Scanning ; 33(4): 211-21, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21538394

RESUMEN

This study examined the surface nanostructures of three orbital implants: nonporous poly(methyl methacrylate) (PMMA), porous aluminum oxide and porous polyethylene. The morphological characteristics of the orbital implants surfaces were observed by atomic force microscopy (AFM). The AFM topography, phase shift and deflection images of the intact implant samples were obtained. The surface of the nonporous PMMA implant showed severe scratches and debris. The surface of the aluminum oxide implant showed a porous structure with varying densities and sizes. The PMMA implant showed nodule nanostructures, 215.56 ± 52.34 nm in size, and the aluminum oxide implant showed crystal structures, 730.22 ± 341.02 nm in size. The nonporous PMMA implant showed the lowest roughness compared with other implant biomaterials, followed by the porous aluminum oxide implant. The porous polyethylene implant showed the highest roughness and severe surface irregularities. Overall, the surface roughness of orbital implants might be associated with the rate of complications and cell adhesion.


Asunto(s)
Óxido de Aluminio/química , Imagenología Tridimensional/métodos , Microscopía de Fuerza Atómica/métodos , Nanoestructuras/ultraestructura , Implantes Orbitales , Polietilenos/química , Polimetil Metacrilato/química , Materiales Biocompatibles/química , Microscopía Electrónica de Rastreo , Proyectos Piloto , Porosidad , Propiedades de Superficie
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