Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Int J Food Sci Nutr ; 60(7): 601-5, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19817639

RESUMEN

Propolis is a resinous material collected by honeybees and obtained from beehives that has anticancer effects by inducing apoptosis. The aim of this study is to investigate the effect of propolis on human telomerase reverse transcriptase (hTERT) in the leukemia cells obtained from leukemia patients. Four different bone marrow cell cultures from each of four leukemia cases were prepared. The 60 ng/ml, 30 ng/ml and 15 ng/ml working concentrations of propolis were administered to three cultures of each patient, while one culture contained only culture medium. hTERT mRNA expression levels of cells were detected at 24 h, 48 h and 72 h using the LightCycler 2.0 instrument. A significant decrease in hTERT expression levels was observed in the 60 ng/ml concentration of propolis. In conclusion, Manisa propolis may also have a potential effect on the expression of hTERT in leukemia-particularly owing to its constituent chrysin.


Asunto(s)
Médula Ósea/patología , Leucemia/patología , Própolis , Telomerasa/metabolismo , Médula Ósea/enzimología , Línea Celular Tumoral , Preescolar , Humanos , Leucemia/enzimología , ARN Mensajero/genética , Telomerasa/genética
2.
Bone Marrow Transplant ; 33(9): 931-5, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15034541

RESUMEN

Cytomegalovirus (CMV) disease remains an important cause of morbidity and mortality in patients undergoing hematopoietic stem cell transplantation (HSCT). We evaluated high-dose acyclovir (HDACV) and pre-emptive ganciclovir to prevent CMV disease in 76 children who underwent peripheral blood stem cell transplantation (PBSCT) and were at risk for CMV reactivation and disease (both recipient and donor seropositive) from May 1998 to April 2003. All received HDACV from day -9 to 6 months post transplant in conjunction with weekly CMV pp65 antigenemia monitoring. The incidence of antigenemia in this cohort was 19.7%, at a median of 22 days post-PBSCT. The frequencies were 26.4 and 4.4% in allogeneic and autologous groups, respectively (P=0.03). Patients with nonmalignant disease had higher CMV antigenemia than those with malignant disease (30.8 vs 8.1%, P=0.02). Age at PBSCT, sex, graft-versus-host disease (GVHD) prophylaxis regimen and presence of acute GVHD did not affect the risk of CMV antigenemia. None of the patients who had positive pp65 antigenemia developed CMV disease during the study period. We conclude that pp65 antigenemia-guided HDACV and pre-emptive ganciclovir may prevent CMV disease in children undergoing PBSCT.


Asunto(s)
Aciclovir/administración & dosificación , Antivirales/uso terapéutico , Infecciones por Citomegalovirus/prevención & control , Ganciclovir/administración & dosificación , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Neoplasias/terapia , Adolescente , Niño , Preescolar , Estudios de Cohortes , Quimioterapia Combinada , Femenino , Enfermedad Injerto contra Huésped , Humanos , Lactante , Masculino , Fosfoproteínas/química , Factores de Riesgo , Factores de Tiempo , Resultado del Tratamiento , Proteínas de la Matriz Viral/química
3.
Pediatr Hematol Oncol ; 18(6): 397-406, 2001 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11554235

RESUMEN

Tropisetron and granisetron are selective serotonin (5-HT3) antagonists that have been proven effective in the prevention of nausea and vomiting in adults and children receiving cancer chemotherapy. This prospective, randomised study was designed to compare the efficacy of the two agents in the prevention of vomiting and nausea in children receiving highly emetogenic chemotherapy for various malignancies. A total of 51 children (mean age: 7.7 +/- 4.8 year) were studied in 133 chemotherapy cycles. In 66 chemotherapy cycles, the children received tropisetron as an antiemetic agent in a dose of 0.2 mg/kg/24 h intravenously and, in 67 cycles, they received granisetron 40 micrograms/kg/24 h intravenously before cytotoxic drug administration during the days they received chemotherapy. The response per 24 h of chemotherapy was defined as complete (no nausea and vomiting), partial (1-4 events of vomiting and/or nausea), and failure (more than 4 events of vomiting and/or nausea). Efficacy of antiemetic therapy was evaluated as acute (Day 1) and overall was based on the worst day during the chemotherapy. Complete control of acute vomiting was achieved in 74% of tropisetron and 88% of granisetron patients (P = 0.04), and complete control of acute nausea in 56% and 82% respectively (p = 0.002). Overall response by means of complete control of both vomiting and nausea during the whole therapy period was 29% of tropisetron group and 55% of granisetron group (p = 0.007). The statistical analysis (depending on the emetogenicity of the chemotherapy cycles) showed increased efficacy of granisetron in highly (grade 3) emetogenic chemotherapy cycles (p = 0.002), whereas there was no difference in the very highly emetogenic cycles (p = 0.7). Also, granisetron was found to be more effective than tropisetron, especially in patients heavier than 25 kg (p = 0.02). The adverse reactions were few and mild. There were no differences in the tolerability of the two antiemetic therapy modalities. In conclusion, granisetron was found to be more effective than tropisetron in controlling nausea and vomiting in children receiving highly emetogenic chemotherapy. This increased antiemetic efficacy of ganisetron might have been related to maximal dose differences according to body weight.


Asunto(s)
Antieméticos/administración & dosificación , Protocolos de Quimioterapia Combinada Antineoplásica/efectos adversos , Granisetrón/administración & dosificación , Indoles/administración & dosificación , Náusea/tratamiento farmacológico , Vómitos/tratamiento farmacológico , Adolescente , Antieméticos/toxicidad , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Niño , Preescolar , Femenino , Granisetrón/toxicidad , Humanos , Indoles/toxicidad , Lactante , Masculino , Náusea/inducido químicamente , Náusea/prevención & control , Estudios Prospectivos , Equivalencia Terapéutica , Resultado del Tratamiento , Tropisetrón , Vómitos/inducido químicamente , Vómitos/prevención & control
4.
Pediatr Int ; 42(6): 642-6, 2000 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11192521

RESUMEN

BACKGROUND: The aim of the present study was to evaluate the efficacy of treatment with recombinant interferon (IFN)-alpha2b in 12 children with chronic hepatitis B who had previously undergone therapy for cancer. METHODS: Nine children had acute leukemias and the other three children had solid tumors. The mean (+/-SD) age of the children was 8.4+/-3.8 years (range 4-16 years). All cases were hepatitis B virus (HBV)-DNA positive and 11 were hepatitis B e antigen (HBeAg) positive. One was anti-HBe positive (mutant strain). Four cases were anti-delta IgG positive. Liver biopsy revealed chronic hepatitis B in 11 patients and cirrhosis in one patient. Interferon-alpha2b was given at a dose of 5 MU/m2 three times a week, subcutaneously, for 12 months. RESULTS: Elimination of serum HBV-DNA was obtained in three cases, but a further three patients demonstrated a marked decrease in HBV-DNA levels after therapy. Three of 11 patients seroconverted from HBeAg to anti-HBe. Alanine aminotransferase (ALT) levels returned to normal in three of nine cases in whom the ALT levels were high before treatment. At the end of therapy, the mean histologic activity index score was significantly diminished (P = 0.0039). CONCLUSIONS: In conclusion, a 12 month course of IFN-alpha2b induces some beneficial effects on virologic, biochemical and histologic indices in children with chronic hepatitis B who have previously undergone therapy for cancer.


Asunto(s)
Hepatitis B Crónica/tratamiento farmacológico , Interferón-alfa/uso terapéutico , Adolescente , Niño , Preescolar , Femenino , Hepatitis B Crónica/sangre , Hepatitis B Crónica/complicaciones , Humanos , Interferón alfa-2 , Interferón-alfa/efectos adversos , Leucemia/complicaciones , Hígado/patología , Masculino , Neoplasias/complicaciones , Proteínas Recombinantes , Resultado del Tratamiento
5.
Clin Nucl Med ; 24(4): 267-70, 1999 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-10466525

RESUMEN

Tc-99m sestamibi, originally developed for myocardial studies, has been used as a tumor-seeking agent. Recently, the agent also was reported to be a functional tracer to predict multidrug resistance-related p-glycoprotein expression in tumor tissue. The current report presents the authors' experience with sestamibi tumor scintigraphy in a neuroblastoma. Although I-131 MIBG tumor imaging and Tc-99m MDP bone scanning accurately demonstrated the extent of the disease, Tc-99m sestamibi showed no accumulation in primary and metastatic foci. Lack of sestamibi uptake was initially thought to be suggestive of failure to respond to chemotherapy because of p-glycoprotein expression. However, the patient responded well to chemotherapy and complete remission was achieved. The failure of Tc-99m sestamibi to detect a neuroblastoma and the lack of sestamibi accumulation in the tumor may not always be related to chemotherapy resistance.


Asunto(s)
Neoplasias Óseas/diagnóstico por imagen , Reacciones Falso Negativas , Neoplasias del Mediastino/diagnóstico por imagen , Neuroblastoma/diagnóstico por imagen , Radiofármacos , Tecnecio Tc 99m Sestamibi , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Neoplasias Óseas/tratamiento farmacológico , Neoplasias Óseas/patología , Neoplasias Óseas/secundario , Preescolar , Resistencia a Antineoplásicos , Proteínas de Unión al GTP/genética , Regulación Neoplásica de la Expresión Génica , Humanos , Masculino , Neoplasias del Mediastino/tratamiento farmacológico , Neoplasias del Mediastino/patología , Estadificación de Neoplasias , Neuroblastoma/tratamiento farmacológico , Neuroblastoma/patología , Neuroblastoma/secundario , Cintigrafía , Inducción de Remisión , Medronato de Tecnecio Tc 99m
6.
Acta Paediatr Jpn ; 39(2): 215-7, 1997 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9141257

RESUMEN

Two hundred and twenty-four children aged 6 months to 5 years, with rectal temperatures greater than or equal to 30 degrees (104 degrees F), were randomly treated with sponging alone or with medication including a single oral dose of aspirin 15 mg/kg, or paracetamol 15 mg/kg, or ibuprofen 8 mg/kg. Twenty-three children were excluded from the final analysis because they did not complete the study. Demographic characteristics of the patients were found to be comparable in all groups. Rectal temperatures were recorded every 30 min for a 3 h period. During the first 30 min of intervention, sponging was found to be more effective than all of the three medications. After 60 min, the effects of each medication became superior to sponging with tepid water in reducing body temperature. Twenty-three children were excluded from the final analysis because they did not complete the study. Comparing the effect of the three different medications, it was seen that the antipyretic efficacy of aspirin and ibuprofen were significantly more than paracetamol 3 h after intervention (P < 0.05). For the management of fever over 39 degrees C, it is therefore recommended to give children an antipyretic drug, preferably ibuprofen, and at the same time to begin sponging to provide a rapid and sustained antipyresis


Asunto(s)
Analgésicos no Narcóticos/uso terapéutico , Baños , Fiebre/terapia , Acetaminofén/uso terapéutico , Aspirina/uso terapéutico , Preescolar , Femenino , Humanos , Ibuprofeno/uso terapéutico , Lactante , Masculino , Temperatura , Resultado del Tratamiento , Agua
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...